Fletcher CD, Dal Cin P, de Wever I, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, van den Berghe H, Vanni R, Willén H
Correlation between clinicopathological features and karyotype in spindle cell sarcomas. A report of 130 cases from the CHAMP study group. Am J Pathol. 1999 Jun; 154(6):1841-7.
Correlation between clinicopathological features and karyotype in spindle cell sarcomas. A report of 130 cases from the CHAMP study group.
Dal Cin P, Quade BJ, Weremowicz S, Morton CC, Pauwels P, Van Den Berghe H
Primary parauterine leiomyoma with a t(6;14) Genes Chromosomes Cancer. 1999 Dec; 26(4):385-6.
Primary parauterine leiomyoma with a t(6;14)
Mertens F, Dal Cin P, De Wever I, Fletcher CD, Mandahl N, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, van Den Berghe H, Vanni R, Willén H
Cytogenetic characterization of peripheral nerve sheath tumours: a report of the CHAMP study group. J Pathol. 2000 Jan; 190(1):31-8.
Cytogenetic characterization of peripheral nerve sheath tumours: a report of the CHAMP study group.
Gisselsson D, Pettersson L, Höglund M, Heidenblad M, Gorunova L, Wiegant J, Mertens F, Dal Cin P, Mitelman F, Mandahl N
Proceedings of the National Academy of Sciences of the United States of America
Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity. Proc Natl Acad Sci U S A. 2000 May 09; 97(10):5357-62.
Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity.
Fletcher CD, Fletcher JA, Dal Cin P, Ladanyi M, Woodruff JM
Diagnostic gold standard for soft tissue tumours: morphology or molecular genetics? Histopathology. 2001 Jul; 39(1):100-3.
Diagnostic gold standard for soft tissue tumours: morphology or molecular genetics?
Gisselsson D, Hibbard MK, Dal Cin P, Sciot R, Hsi BL, Kozakewich HP, Fletcher JA
PLAG1 alterations in lipoblastoma: involvement in varied mesenchymal cell types and evidence for alternative oncogenic mechanisms. Am J Pathol. 2001 Sep; 159(3):955-62.
PLAG1 alterations in lipoblastoma: involvement in varied mesenchymal cell types and evidence for alternative oncogenic mechanisms.
1q42 approximately q44 is rarely cytogenetically involved in sporadic uterine leiomyomata. Cancer Genet Cytogenet. 2002 Oct 01; 138(1):92-3.
1q42 approximately q44 is rarely cytogenetically involved in sporadic uterine leiomyomata.
Brown JR, Friedberg JW, Feng Y, Scofield S, Phillips K, Dal Cin P, Joyce R, Takvorian RW, Fisher DC, Fisher RI, Liesveld J, Marquis D, Neuberg D, Freedman AS
A phase 2 study of concurrent fludarabine and rituximab for the treatment of marginal zone lymphomas. Br J Haematol. 2009 Jun; 145(6):741-8.
A phase 2 study of concurrent fludarabine and rituximab for the treatment of marginal zone lymphomas.
Fan YS, Rowe JM, Dal Cin PD, Sandberg AA
A translocation t(9;11)(p11;q23) in T-cell acute lymphoblastic leukemia (FAB-l2). Cancer Genet Cytogenet. 1988 Apr; 31(2):263-9.
A translocation t(9;11)(p11;q23) in T-cell acute lymphoblastic leukemia (FAB-l2).
United States and Canadian Academy of Pathology.
Loss of INI1 Expression Is Characteristic of Both Conventional And Proximal-Type Epithelioid Sarcoma. United States and Canadian Academy of Pathology. 2007; San Diego, California .
Loss of INI1 Expression Is Characteristic of Both Conventional And Proximal-Type Epithelioid Sarcoma
Heidelberg:. Petrovich Z, Baert L, eds Springer Verlag
Innovations in the Management of Benign Prostatic Hyperplasia. Chromosome abnormalities in benign prostatic hyperplasia. Heidelberg:. Petrovich Z, Baert L, eds Springer Verlag. 1994; 49-56.
Innovations in the Management of Benign Prostatic Hyperplasia. Chromosome abnormalities in benign prostatic hyperplasia
Oliveira AM, Hsi B-L, Weromowicz S, Perez-Ayade AR, Rosenberg AE, Dal Cin P, Joseph N, Bridge JA, Fletcher JA.
Translocation (16;17)(q22;p13) fuses osteobalstic cadherin CDH11 to USP6 in aneurysmal bone cysts. United States and Canadian Academy of Pathology. 2004; Vancouver, Canada.
Translocation (16;17)(q22;p13) fuses osteobalstic cadherin CDH11 to USP6 in aneurysmal bone cysts
De Wever I, Ectors N, Haustermans K, Dal Cin P, Stas M, Dubin M, Geboes K.
Clinical and histological progression of a diploid pseudomyxoma peritonei of appendical origin. Belgian Week of Gatroenterology. 1994; Knokke, Belgium.
Clinical and histological progression of a diploid pseudomyxoma peritonei of appendical origin
Dal Cin P, Moreman P, De Wever I, Van den Berghe H
Is i(1)(q10) a chromosome marker in phyllodes tumor of the breast? Cancer Genet Cytogenet. 1995 Sep; 83(2):174-5.
Is i(1)(q10) a chromosome marker in phyllodes tumor of the breast?
Sciot R, Dal Cin P, Fletcher C, Samson I, Smith M, De Vos R, Van Damme B, Van den Berghe H
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
t(9;22)(q22-31;q11-12) is a consistent marker of extraskeletal myxoid chondrosarcoma: evaluation of three cases. Mod Pathol. 1995 Sep; 8(7):765-8.
t(9;22)(q22-31;q11-12) is a consistent marker of extraskeletal myxoid chondrosarcoma: evaluation of three cases.
Foschini MP, Van Eyken P, Brock PR, Casteels-Van Daele M, De Vos R, Dal Cin P, Van den Berghe H, Desmet VJ
Malignant rhabdoid tumour of the liver. A case report. Histopathology. 1992 Feb; 20(2):157-65.
Malignant rhabdoid tumour of the liver. A case report.
Lawrence B, Perez-Atayde A, Hibbard MK, Rubin BP, Dal Cin P, Pinkus JL, Pinkus GS, Xiao S, Yi ES, Fletcher CD, Fletcher JA
TPM3-ALK and TPM4-ALK oncogenes in inflammatory myofibroblastic tumors. Am J Pathol. 2000 Aug; 157(2):377-84.
TPM3-ALK and TPM4-ALK oncogenes in inflammatory myofibroblastic tumors.
Nucci MR, Drapkin R, Dal Cin P, Fletcher CD, Fletcher JA
The American journal of surgical pathology
Distinctive cytogenetic profile in benign metastasizing leiomyoma: pathogenetic implications. Am J Surg Pathol. 2007 May; 31(5):737-43.
Distinctive cytogenetic profile in benign metastasizing leiomyoma: pathogenetic implications.
Dal Cin P, van Gool S, Brock P, Proesmans W, Casteels-van Daele M, de Wever I, Baert L, van Damme B, van den Berghe H
Renal cell carcinoma in a child. Cancer Genet Cytogenet. 1991 Nov; 57(1):137-8.
Chou RC, Dinarello CA, Ferry JA, Dal Cin P
A 36-year-old woman with recurrent high-grade fevers, hypotension, and hypertriglyceridemia. Arthritis Care Res (Hoboken). 2010 Jan 15; 62(1):128-36.
A 36-year-old woman with recurrent high-grade fevers, hypotension, and hypertriglyceridemia.
Sait SN, Dal Cin P, Ovanessoff S, Sandberg AA
A uterine leiomyoma showing both t(12;14) and del(7) abnormalities. Cancer Genet Cytogenet. 1989 Feb; 37(2):157-61.
A uterine leiomyoma showing both t(12;14) and del(7) abnormalities.
Oliveira AM, Hsi BL, Weremowicz S, Rosenberg AE, Dal Cin P, Joseph N, Bridge JA, Perez-Atayde AR, Fletcher JA
USP6 (Tre2) fusion oncogenes in aneurysmal bone cyst. Cancer Res. 2004 Mar 15; 64(6):1920-3.
USP6 (Tre2) fusion oncogenes in aneurysmal bone cyst.
Joniau S, Goeman L, Kreuzbauer S, Bogaert G, Dal Cin P, Oyen R, Sciot R, van Poppel H
Benign renal mesenchymoma in the pediatric age group: a novel pathologic and karyotype entity. Urology. 2004 May; 63(5):981-4.
Benign renal mesenchymoma in the pediatric age group: a novel pathologic and karyotype entity.
Stern C, Kazmierczak B, Thode B, Rommel B, Bartnitzke S, Dal Cin P, van de Ven W, Van den Berghe H, Bullerdiek J
Leiomyoma cells with 12q15 aberrations can be transformed in vitro and show a relatively stable karyotype during precrisis period. Cancer Genet Cytogenet. 1991 Jul 15; 54(2):223-8.
Leiomyoma cells with 12q15 aberrations can be transformed in vitro and show a relatively stable karyotype during precrisis period.
Cuneo A, Van Orshoven A, Michaux JL, Boogaerts M, Louwagie A, Doyen C, Dal Cin P, Fagioli F, Castoldi G, Van den Berghe H
Morphologic, immunologic and cytogenetic studies in erythroleukaemia: evidence for multilineage involvement and identification of two distinct cytogenetic-clinicopathological types. Br J Haematol. 1990 Jul; 75(3):346-54.
Morphologic, immunologic and cytogenetic studies in erythroleukaemia: evidence for multilineage involvement and identification of two distinct cytogenetic-clinicopathological types.
Schaefer IM, Dal Cin P, Landry LM, Fletcher CDM, Hanna GJ, French CA
CIC-NUTM1 fusion: A case which expands the spectrum of NUT-rearranged epithelioid malignancies. Genes Chromosomes Cancer. 2018 09; 57(9):446-451.
CIC-NUTM1 fusion: A case which expands the spectrum of NUT-rearranged epithelioid malignancies.
Wang L, Motoi T, Khanin R, Olshen A, Mertens F, Bridge J, Dal Cin P, Antonescu CR, Singer S, Hameed M, Bovee JV, Hogendoorn PC, Socci N, Ladanyi M
Identification of a novel, recurrent HEY1-NCOA2 fusion in mesenchymal chondrosarcoma based on a genome-wide screen of exon-level expression data. Genes Chromosomes Cancer. 2012 Feb; 51(2):127-39.
Identification of a novel, recurrent HEY1-NCOA2 fusion in mesenchymal chondrosarcoma based on a genome-wide screen of exon-level expression data.
De Coppi P, Bartsch G,Perin L, Yoo JY, Dal Cin P, , Soker S, Atala A.
2nd Symposiuom on therapeutic applications of human stem cells and precursor cells.
Human embronic and fetal stem cell isolation from chorion villi and amniotic fluid. In vitro and In vivo studies. 2nd Symposiuom on therapeutic applications of human stem cells and precursor cells. 2002; Hannover, Germany.
Human embronic and fetal stem cell isolation from chorion villi and amniotic fluid. In vitro and In vivo studies
Monti S, Savage KJ, Kutok JL, Feuerhake F, Kurtin P, Mihm M, Bingyan Wu B, Pasqualucci L, Neuberg D, Aguiar RCT, Dal Cin P, Ladd C, Pinkus GS, Salles G, Harris NL, Dalla-Favera R, Habermann TM, Aster JC, Golub TR, Shipp MA.
American Society of Hematology, 47th Annual Meeting.
Molecular profiling of diffuse large B-cell lymphoma reveals discrete cluster including one characterized by host inflammatory response. American Society of Hematology, 47th Annual Meeting. 2004; San Diego, CA.
Molecular profiling of diffuse large B-cell lymphoma reveals discrete cluster including one characterized by host inflammatory response
Gibas Z, Limon J, Dal Cin P, Karakousis C, Sandberg AA.
Chromosomal rearrangements in soft tissue sarcoma. Am J Hum Genet (suppl). 1986; (A31):87.
Chromosomal rearrangements in soft tissue sarcoma
Dal Cin P, Drochmans A, Moerman PH, Van den Berghe H.
Isochromosome 12p in a mediastinal germ cell tumor. Genetics in Cancer & Development. Clin. Genet. 1990; (37):300.
Isochromosome 12p in a mediastinal germ cell tumor. Genetics in Cancer & Development
Dal Cin P, Sciot R, Fletcher CDM, De Vos R, Mandahl N, Willén H, Larson O, Van den Berghe,H.
Near-haploidy may characterize inflammatory leiomyosarcoma as a distinct entity. CTOS 3rd Annual Scientific Meeting. 1997; Milano, Italy.
Near-haploidy may characterize inflammatory leiomyosarcoma as a distinct entity
Renard M, Brock P, Kruger M, De Wever I, Smet M, Vandamme B, Dal Cin P, Casteels-Van Daele M.
Chemotherapy in congenital fibrosarcoma. International Society of Paediatric Oncology (SIOP) XXIIIrd Meeting. Med & Pediatr Oncol. 1991; (19):362.
Chemotherapy in congenital fibrosarcoma. International Society of Paediatric Oncology (SIOP) XXIIIrd Meeting
Dal Cin P, Aly MS, De Wever I, Van Damme B, Van den Berghe H
Does chromosome investigation discriminate between benign and malignant gastrointestinal leiomyomatous tumors?. Diag Oncol. 1992; 2:55-59.
Does chromosome investigation discriminate between benign and malignant gastrointestinal leiomyomatous tumors?
Ginevan KB, Fletcher JA, Dal Cin P, Cibas ES.
American Society of Cytopathology. 49TH Scientific Annual Meeting.
The value of cytogenetics as an adjunct to diagnostic fine needle aspiration cytology of nonhematopoietic neoplasms. American Society of Cytopathology. 49TH Scientific Annual Meeting. 2001; Kansas City, Missouri.
The value of cytogenetics as an adjunct to diagnostic fine needle aspiration cytology of nonhematopoietic neoplasms
Coccia M, Meltzer P, Dal Cin P, Turc Carel C, Sait S, Sandberg AA, Trent J.
80th Annual Meeting, American Association for Cancer Research
DNA sequence amplification in malignant fibrous histiocytoma. 80th Annual Meeting, American Association for Cancer Research. 1989.
DNA sequence amplification in malignant fibrous histiocytoma
Kakati S, Limon J, Dal Cin P, Pietrzak E, Kinniburgh AJ, Li FP, Sandberg AA
Abnormally banded region in a poorly differentiated sarcoma is not correlated with amplification of c-MYC or c-MOS protooncogenes. Cancer Genet Cytogenet. 1988 Aug; 34(1):111-5.
Abnormally banded region in a poorly differentiated sarcoma is not correlated with amplification of c-MYC or c-MOS protooncogenes.
Takeyama K, Monti S, Manis JP, Dal Cin P, Getz G, Beroukhim R, Dutt S, Aster JC, Alt FW, Golub TR, Shipp MA
Integrative analysis reveals 53BP1 copy loss and decreased expression in a subset of human diffuse large B-cell lymphomas. Oncogene. 2008 Jan 10; 27(3):318-22.
Integrative analysis reveals 53BP1 copy loss and decreased expression in a subset of human diffuse large B-cell lymphomas.
Antonescu CR, Nafa K, Segal NH, Dal Cin P, Ladanyi M
Clinical cancer research : an official journal of the American Association for Cancer Research
EWS-CREB1: a recurrent variant fusion in clear cell sarcoma--association with gastrointestinal location and absence of melanocytic differentiation. Clin Cancer Res. 2006 Sep 15; 12(18):5356-62.
EWS-CREB1: a recurrent variant fusion in clear cell sarcoma--association with gastrointestinal location and absence of melanocytic differentiation.
Derivative (1)t(1;19)(p13;p13) in the setting of myelofibrosis with JAK2 V617F. Cancer Genet Cytogenet. 2009 Jun; 191(2):109-10.
Derivative (1)t(1;19)(p13;p13) in the setting of myelofibrosis with JAK2 V617F.
Sandberg AA, Meloni-Ehrig AM, Van den Berghe H, Dal Cin P, Block AW
Editorial communication. Cancer Genet Cytogenet. 2010 Dec; 203(2):101.
Leon A, Staropoli JF, Hernandez JM, Longtine JA, Kuo FC, Dal Cin P
Translocation t(1;9) is a recurrent cytogenetic abnormality associated with progression of essential thrombocythemia patients displaying the JAK2 V617F mutation. Leuk Res. 2011 Sep; 35(9):1188-92.
Translocation t(1;9) is a recurrent cytogenetic abnormality associated with progression of essential thrombocythemia patients displaying the JAK2 V617F mutation.
Qian X, Hornick JL, Cibas ES, Dal Cin P, Domanski HA
Angiomatoid fibrous histiocytoma a series of five cytologic cases with literature review and emphasis on diagnostic pitfalls. Diagn Cytopathol. 2012 Aug; 40 Suppl 2:E86-93.
Angiomatoid fibrous histiocytoma a series of five cytologic cases with literature review and emphasis on diagnostic pitfalls.
Sioletic S, Dal Cin P, Fletcher CD, Hornick JL
Well-differentiated and dedifferentiated liposarcomas with prominent myxoid stroma: analysis of 56 cases. Histopathology. 2013 Jan; 62(2):287-93.
Well-differentiated and dedifferentiated liposarcomas with prominent myxoid stroma: analysis of 56 cases.
Cuneo A, Carli MG, Piva N, Faglioli F, Pazzi I, Tallarico A, Ferrari L, Wlodarska I, Aly MS, Dal Cin P, Cassiman JJ, Van den Berghe H, Castoldi, G.L.
Fluorescent in situ hybridization for the detection and monitoring of trisomy 12 in B-cell chronic lymphocytic leukaemia. FISH Meeting. 1992.
Fluorescent in situ hybridization for the detection and monitoring of trisomy 12 in B-cell chronic lymphocytic leukaemia
Rege-Cambrin G, Speleman F, Kerim S, Scaravaglio P, Carozzi F, Dal Cin P, Michaux JL, Offner F, Saglio G, Van den Berghe H
Extra translocation +der(1q9p) is a prognostic indicator in myeloproliferative disorders. Leukemia. 1991 Dec; 5(12):1059-63.
Extra translocation +der(1q9p) is a prognostic indicator in myeloproliferative disorders.
Srivastava A, Nielsen PG, Dal Cin P, Rosenberg AE
Archives of pathology & laboratory medicine
Monophasic synovial sarcoma of the liver. Arch Pathol Lab Med. 2005 Aug; 129(8):1047-9.
Monophasic synovial sarcoma of the liver.
Involvement of 6p in an endometrial polyp. Cancer Genet Cytogenet. 1991 Feb; 51(2):279-80.
Involvement of 6p in an endometrial polyp.
Debiec-Rychter M, Sciot R, Pauwels P, Schoenmakers E, Dal Cin P, Hagemeijer A
Molecular cytogenetic definition of three distinct chromosome arm 14q deletion intervals in gastrointestinal stromal tumors. Genes Chromosomes Cancer. 2001 Sep; 32(1):26-32.
Molecular cytogenetic definition of three distinct chromosome arm 14q deletion intervals in gastrointestinal stromal tumors.
Huang D, Sumegi J, Dal Cin P, Reith JD, Yasuda T, Nelson M, Muirhead D, Bridge JA
C11orf95-MKL2 is the resulting fusion oncogene of t(11;16)(q13;p13) in chondroid lipoma. Genes Chromosomes Cancer. 2010 Sep; 49(9):810-8.
C11orf95-MKL2 is the resulting fusion oncogene of t(11;16)(q13;p13) in chondroid lipoma.
Brown JR, Hanna M, Tesar B, Werner L, Pochet N, Asara JM, Wang YE, Dal Cin P, Fernandes SM, Thompson C, Macconaill L, Wu CJ, Van de Peer Y, Correll M, Regev A, Neuberg D, Freedman AS
Integrative genomic analysis implicates gain of PIK3CA at 3q26 and MYC at 8q24 in chronic lymphocytic leukemia. Clin Cancer Res. 2012 Jul 15; 18(14):3791-802.
Integrative genomic analysis implicates gain of PIK3CA at 3q26 and MYC at 8q24 in chronic lymphocytic leukemia.
J.C.E. Underwood, Ed. Current Topics in Pathology: Pathology of the Nucleus.
Karyotypic analysis of solid tumors. J.C.E. Underwood, Ed. Current Topics in Pathology: Pathology of the Nucleus. 1990.
Fletcher CDM, Unni KK, Mertens F, editors. World Health Organization Classification of TumoursPathology and Genetics of Tumours of Soft Tissue and Bone.
Plexiform fibrohistiocytic tumour. Fletcher CDM, Unni KK, Mertens F, editors. World Health Organization Classification of TumoursPathology and Genetics of Tumours of Soft Tissue and Bone. 2002; 116-117.
Ladanyi M, Lui MY, Antonescu CR, Krause-Boehm A, Meloni-Ehrig A, Argani P, Sorensen PHB, Mertens F, Mandahl N, Van den Berghe H, Sciot R, Dal Cin P, Bridge J.
Cloning of the der(17)t(X;17)(p11;q25) of alveolar soft part sarcoma identifies the ASPL/TFE3 gene fusion, a new molecular diagnostic marker. United States and Canadian Academy of Pathology. 2001; Atlanta, Georgia.
Cloning of the der(17)t(X;17)(p11;q25) of alveolar soft part sarcoma identifies the ASPL/TFE3 gene fusion, a new molecular diagnostic marker
Dal Cin P, Sciot R, Pauwels P, De Wever I, Van den Berghe H.
5th European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors
Cytogenetics revealing the diagnosis in metastases of unknown origin. 5th European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors. 1996; Baveno - Stresa, Italy.
Cytogenetics revealing the diagnosis in metastases of unknown origin
Van Poppel H, Dal Cin P, Aly MS, Van Damme B, Van den Berghe H, Baert L.
XIth Congress of the European Association of Urology
Trisomy 7 and trisomy 10 in the healthy parenchyma of RCC bearing kidneys is not a premalignant lesion. XIth Congress of the European Association of Urology. 1994; Berlin, Germany.
Trisomy 7 and trisomy 10 in the healthy parenchyma of RCC bearing kidneys is not a premalignant lesion
Chromosomes changes in pediatric tumors. 1993; South Africa.
Dal Cin P, Sciot R, De Wever I, Van Damme B, Van den Berghe H.
86th Annual Meeting of the American Association for Cancer Research.
Trisomy 21 in a solitary fibrous tumor. 86th Annual Meeting of the American Association for Cancer Research. 1995; Toronto, Canada.
Dal Cin P, Talcott J, Abrams J, Li FP, Sandberg AA
Ins(10;19) in an endometrial stromal sarcoma. Cancer Genet Cytogenet. 1988 Nov; 36(1):1-5.
Ins(10;19) in an endometrial stromal sarcoma.
Uterine Leiomyomata: Pathogenesis and Management.
Cytogenetic and Other Genetic Insights into the Pathogenesis of Uterine Leiomyomata. Uterine Leiomyomata: Pathogenesis and Management. 2005.
Cytogenetic and Other Genetic Insights into the Pathogenesis of Uterine Leiomyomata
Adem C, Gisselsson D, Dal Cin P, Nascimento AG.
Interphase cytogenetics analysis of infantile fibrosarcomas and congenital mesoblastic nephromas. United States and Canadian Academy of Pathology. 2002; Chicago, IL.
Interphase cytogenetics analysis of infantile fibrosarcomas and congenital mesoblastic nephromas
Association of Genetic Technologists, 29th Annual Meeting.
Clinical importance of fluorescence in situ hybridization in hematologic disorders. Association of Genetic Technologists, 29th Annual Meeting. 2004; Anaheim, CA.
Clinical importance of fluorescence in situ hybridization in hematologic disorders
Vanni R, Dal Cin P. Involvement of chromosome 12 in uterine leiomyoma.
Chromosome 12 Aberrations in Human Solid Tumors. Cytogenetics and Molecular Genetics. 1994; 16-26.
Chromosome 12 Aberrations in Human Solid Tumors
Hirsh Ms, Dal Cin P, Joseph N, Thomas, A, Fletcher JA, Weinstein MH.
Assesement of unselected renal epithelial tumors: independent evaluation by cytogenetics and histology. United States and Canadian Academy of Pathology. 2002; Chicago, IL.
Assesement of unselected renal epithelial tumors: independent evaluation by cytogenetics and histology
Diffuse-type giant tumour. Fletcher CDM, Unni KK, Mertens F, editors. World Health Organization Classification of TumoursPathology and Genetics of Tumours of Soft Tissue and Bone. 2002; 112-114.
Aly MS, Dal Cin P, Van de Voorde W, van Poppel H, Ameye F, Baert L, Van den Berghe H
Chromosome abnormalities in benign prostatic hyperplasia. Genes Chromosomes Cancer. 1994 Apr; 9(4):227-33.
Chromosome abnormalities in benign prostatic hyperplasia.
Soltisova D, Merkhofer E, Fergusun B, DuBois Z, McLaughlin C, Sherman L, Dal Cin P.
Association of Genetic Technologists, 28th Annual Meeting.
Unrelated chromosome abnormalities in hematological malignacies. Association of Genetic Technologists, 28th Annual Meeting. 2003; Atlanta, Georgia.
Unrelated chromosome abnormalities in hematological malignacies
Cuneo A, Ferrant A, Michaux JL, Boogaerts M, Demuynck H, Bosly A, Doyen C, Carli G, Piva N, Castoldi G, Stul M, Dal Cin P, Cassiman JJ, Van den Berghe H.
Clinical review on features and cytogenetic patterns in adult acute myeloid leukemia with lymphoid markers. Leukemia & Lymphoma Review Series. 1995; 13-19.
Clinical review on features and cytogenetic patterns in adult acute myeloid leukemia with lymphoid markers
Morfologische, immunohistochemische en cytogenetische studie van gastro-intestinale stromale tumoren. Tijdschr. Gastroenterol. 1995; 7-10.
Morfologische, immunohistochemische en cytogenetische studie van gastro-intestinale stromale tumoren
Experiencia de laboratoria en el manejo de liquidos amnioticos para del diagnostico prenatal de alteraciones cromosomicas y defectos del tubo neural. (Experience in management of amniotic fluids for diagnosis of chromosome aberrations in prenatal and neural tube defects). Acta Cient Venez. 1981; 32:299.
Experiencia de laboratoria en el manejo de liquidos amnioticos para del diagnostico prenatal de alteraciones cromosomicas y defectos del tubo neural. (Experience in management of amniotic fluids for diagnosis of chromosome aberrations in prenatal and neural tube defects)
Cuneo A, Mecucci C, Kerim S, Vandenberghe E, Dal Cin P, Van Orshoven A, Rodhain J, Bosly A, Michaux JL, Martiat P
Multipotent stem cell involvement in megakaryoblastic leukemia: cytologic and cytogenetic evidence in 15 patients. Blood. 1989 Oct; 74(5):1781-90.
Multipotent stem cell involvement in megakaryoblastic leukemia: cytologic and cytogenetic evidence in 15 patients.
Application of long-term collagenase disaggregation for the cytogenetic analysis of human solid tumors. Cancer Genet Cytogenet. 1986 Dec; 23(4):305-13.
Application of long-term collagenase disaggregation for the cytogenetic analysis of human solid tumors.
2nd International Symposium on GnRH Analogues in Cancer and Human Reproduction
Cytogenetic analysis of leiomyoma in relation to GnRH agonist treatment. 2nd International Symposium on GnRH Analogues in Cancer and Human Reproduction. 1990.
Cytogenetic analysis of leiomyoma in relation to GnRH agonist treatment
Genetica dei tumori renali. Pathologica. 1998; 90:101-07..
Rodig SJ, Healey BM, Pinkus GS, Kuo FC, Dal Cin P, Kutok JL
Mantle cell lymphoma arising within primary nodal marginal zone lymphoma: a unique presentation of two uncommon B-cell lymphoproliferative disorders. Cancer Genet Cytogenet. 2006 Nov; 171(1):44-51.
Mantle cell lymphoma arising within primary nodal marginal zone lymphoma: a unique presentation of two uncommon B-cell lymphoproliferative disorders.
De Coppi P, Bartsch G, Dal Cin P, Yoo JY, Soker S, Atala A.
Human fetal stem cell isolation from amniotic fluid. New Engalnd Section AUA. 2002; Boston, MA.
Human fetal stem cell isolation from amniotic fluid
Dal Cin P, Turc Carel C, Carr K, Sandberg AA.
Is fragile site 12q13 involved in the genesis of adipose tissue tumors ?. Am J Hum Genet (suppl). 1986; (A28):77.
Is fragile site 12q13 involved in the genesis of adipose tissue tumors ?
Dal Cin P, Fusco A, Belge G, Chiappetta G, Fedele M, Pauwels P, Bullerdiek J, Van den Berghe H.
Involvement of HMGI(Y) gene in a microfollicular adenoma of thyroid. 6th European Conference on Cytogenetics and Molecular Genetics of Human Solid Tumors. Cancer Genet Cytogent. 1999; 122:76.
Involvement of HMGI(Y) gene in a microfollicular adenoma of thyroid. 6th European Conference on Cytogenetics and Molecular Genetics of Human Solid Tumors
Chromosomal aspects of human oncogenesis. Crit Rev Oncog. 1989; 1(2):113-26.
Chromosomal aspects of human oncogenesis.
Elco CP, Mariño-Enríquez A, Abraham JA, Dal Cin P, Hornick JL
Hybrid myxoinflammatory fibroblastic sarcoma/hemosiderotic fibrolipomatous tumor: report of a case providing further evidence for a pathogenetic link. Am J Surg Pathol. 2010 Nov; 34(11):1723-7.
Hybrid myxoinflammatory fibroblastic sarcoma/hemosiderotic fibrolipomatous tumor: report of a case providing further evidence for a pathogenetic link.
Ligon AH, Morton CC, Bieber FR, Fletcher JA, Giersch AB, Kantarci S, Leach N, Lee C, Sandstrom M, Weremowicz S, Xiao S, Dal Cin P
Reporting of diagnostic cytogenetic results. Curr Protoc Hum Genet. 2010 Oct; Appendix 1:1D.1-23.
Reporting of diagnostic cytogenetic results.
Butrynski JE, D'Adamo DR, Hornick JL, Dal Cin P, Antonescu CR, Jhanwar SC, Ladanyi M, Capelletti M, Rodig SJ, Ramaiya N, Kwak EL, Clark JW, Wilner KD, Christensen JG, Jänne PA, Maki RG, Demetri GD, Shapiro GI
Crizotinib in ALK-rearranged inflammatory myofibroblastic tumor. N Engl J Med. 2010 Oct 28; 363(18):1727-33.
Crizotinib in ALK-rearranged inflammatory myofibroblastic tumor.
Metaphase harvest and cytogenetic analysis of malignant hematological specimens. Curr Protoc Hum Genet. 2003 May; Chapter 10:Unit 10.2.
Metaphase harvest and cytogenetic analysis of malignant hematological specimens.
Poitras JL, Dal Cin P, Aster JC, Deangelo DJ, Morton CC
Novel SSBP2-JAK2 fusion gene resulting from a t(5;9)(q14.1;p24.1) in pre-B acute lymphocytic leukemia. Genes Chromosomes Cancer. 2008 Oct; 47(10):884-9.
Novel SSBP2-JAK2 fusion gene resulting from a t(5;9)(q14.1;p24.1) in pre-B acute lymphocytic leukemia.
Lee CH, Mariño-Enriquez A, Ou W, Zhu M, Ali RH, Chiang S, Amant F, Gilks CB, van de Rijn M, Oliva E, Debiec-Rychter M, Dal Cin P, Fletcher JA, Nucci MR
The clinicopathologic features of YWHAE-FAM22 endometrial stromal sarcomas: a histologically high-grade and clinically aggressive tumor. Am J Surg Pathol. 2012 May; 36(5):641-53.
The clinicopathologic features of YWHAE-FAM22 endometrial stromal sarcomas: a histologically high-grade and clinically aggressive tumor.
Pathogenesis and Medical Management of Uterine Fibroids.
Cytogenetics of mesenchymal tumors of the uterus. Pathogenesis and Medical Management of Uterine Fibroids. 1999; 55-59.
Cytogenetics of mesenchymal tumors of the uterus
Dal Cin P, Sciot R, Aly MS, Stas M, De Wever I, Van Damme B, Van den Berghe H.
Human Genome Mapping Workshop 93 (HGM 93)
Some desmoid tumors are characterized by trisomy 8. Human Genome Mapping Workshop 93 (HGM 93). 1993; Kobe, Japan.
Some desmoid tumors are characterized by trisomy 8
Parry DM, Li F, Rosenberg SA, Turc Carel C, Dal Cin P, Limon J, Rao U, Sandberg AA.
Rearrangements involving Xp and 18q in soft tissue sarcomas. Am J Hum Genet (suppl). 1986; (A37):104.
Rearrangements involving Xp and 18q in soft tissue sarcomas
Qi H, Dal Cin P, García JL, Hernández JM, Van den Berghe H.
Trisomy 8 and trisomy 20 in desmoid tumours. 5th European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors. 1996; Baveno - Stresa, Italy.
Trisomy 8 and trisomy 20 in desmoid tumours
Corallini A, Gianni M, Mantovani C, Vandini A, Rimessi P, Negrini M, Giavazzi R, Bani MR, Milanesi G, Dal Cin P, Van den Berghe H, Barbanti-Brodano G.
Transformation of human cells by recombinant DNA molecules containing BK virus early region and the human activated c-H-ras or c-myc oncogenes. Cancer J. 1991; 4:24-34.
Transformation of human cells by recombinant DNA molecules containing BK virus early region and the human activated c-H-ras or c-myc oncogenes
87. Tallini G, Dal Cin P, De Wever I, Fletcher CDM, Mandahl N, Mertens F Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, Van den Berghe H, Vanni R, Willén H; Yale U., New Haven, CT; Memorial Sloan-Ketterinc Cancer Center, NY, NY; Guy's and St. Thomas' Hosp., London, U.; U. of Lund, Sweden; U. of Leuven, Belgium; and U. of Cagliari, Italy.
1995 Annual Meeting United States and Canadian Academy of Pathology
Myxoid liposarcoma represents a distinct type of liposarcoma characterized by the specific cytogenetic translocation t(12;16)(q13;p11). 1995 Annual Meeting United States and Canadian Academy of Pathology. 1995; Toronto, Canada.
Myxoid liposarcoma represents a distinct type of liposarcoma characterized by the specific cytogenetic translocation t(12;16)(q13;p11)
Dal Cin P, Turc Carel C, Limon J, Leong S, Sandberg AA.
Consistent involvement of band 12q14 in benign lipoma. Human Gene Mapping 9. 1987.
Consistent involvement of band 12q14 in benign lipoma
Bone Tumours. Genetic aspects. International Symposium Reconstruction of the Upper Limb. 1993; Leuven, Belgium.
Bone Tumours. Genetic aspects. International Symposium Reconstruction of the Upper Limb
Dal Cin P . Soft Tissue Tumors. Atlas Genet Cytogenet Oncol Haematol. January 2003.
Soft Tissue Tumors. Atlas Genet Cytogenet Oncol Haematol.
Soft Tissue Tumors. Atlas Genet Cytogenet Oncol Haematol. 2003.
American Academy Pediatrics, Section of Urology.
Human fetal stem cell isolation from amniotic fluid. American Academy Pediatrics, Section of Urology. 2001; San Francisco CA.
Aly MS, Dal Cin P, De Wever I, Moerman PH, Van den Berghe H.
Endometrial stromal sarcoma. t(7;17)(p15-21;q12-21) is a non-random chromosome change. Third European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors. Cancer Genet Cytogenet. 1992; (63):132.
Endometrial stromal sarcoma. t(7;17)(p15-21;q12-21) is a non-random chromosome change. Third European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors
Wanschura S, Belge G, Stenman G, Kools P, Dal Cin P, Schoenmakers E, Huysmans C, Van den Berghe H, Bartnitzke S, Van de Ven WJ, Bullerdiek J
Mapping of the translocation breakpoints of primary pleomorphic adenomas and lipomas within a common region of chromosome 12. Cancer Genet Cytogenet. 1996 Jan; 86(1):39-45.
Mapping of the translocation breakpoints of primary pleomorphic adenomas and lipomas within a common region of chromosome 12.
Qi H, Dal Cin P, Van de Voorde W, Elgamal AA, Van Poppel H, Baert L, Van Den Berghe H
del(1)(q12) in adenocarcinomas of the prostate. Cancer Genet Cytogenet. 1996 Mar; 87(1):79-81.
del(1)(q12) in adenocarcinomas of the prostate.
Dal Cin P, De Wolf-Peeters C, Deneffe G, Fryns JP, Van den Berghe H
Thymoma with a t(15;22)(p11;q11). Cancer Genet Cytogenet. 1996 Jul 15; 89(2):181-3.
Pauline S, Sait S, Dal Cin P, Turc Carel C, Leong SPL, Sandberg AA, Vogelstein B, Gemmill RM.
3rd International Workshop on Chromosomes in Solid Tumors
Tissie specific pulsed field gel fragment patterns in a 700 KB domain surrounding GLI. 3rd International Workshop on Chromosomes in Solid Tumors. 1989.
Tissie specific pulsed field gel fragment patterns in a 700 KB domain surrounding GLI
Durkin S, Ligon A, McLaughlin C, Dal Cin P.
Clinical Cytogenetic Analysis of Lymph Node Speciments. 2006.
Clinical Cytogenetic Analysis of Lymph Node Speciments
Cuneo A, Demuynck H, Ferrant A, Louwagie A, Doyen C, Stul M, Cassiman JJ, Dal Cin P, Carli MG, Boogaerts M, Michaux, JL, Castolde GL, Van den Berghe H.
XIIth Meeting of the International Society of Haematology
Correlation of cytoimmunological features, cytogenetic patterns and clinical outcome in Ph-positive acute leukemia. XIIth Meeting of the International Society of Haematology. 1993; Vienna, Austria..
Correlation of cytoimmunological features, cytogenetic patterns and clinical outcome in Ph-positive acute leukemia
3rd International Symposium on GnRH Analogues in Cancer and Human Redproduction.
The effect of ecapeptyl on the growht of leiomyomata. 3rd International Symposium on GnRH Analogues in Cancer and Human Redproduction. 1993.
The effect of ecapeptyl on the growht of leiomyomata
Dal Cin P, Rao U, Turc-Carel C, Sandberg AA
Translocation (7;21) in a lipoma. Cancer Genet Cytogenet. 1988 Jan; 30(1):17-22.
Kools PFJ, Dal Cin P, Schoenmakers FPM, Van den Berghe H, Van de Ven WJM.
FISH studies on ring and long-marker chromosomes from atypical lipomas and well-differentiated liposarcomas reveal involvement of region 12q13-q15. 4th European Workshop on Cytogenetics and Molecular Genetics of Human Solid tumors. Cancer Genet Cytogenet. 1994; (77):161.
FISH studies on ring and long-marker chromosomes from atypical lipomas and well-differentiated liposarcomas reveal involvement of region 12q13-q15. 4th European Workshop on Cytogenetics and Molecular Genetics of Human Solid tumors
Rassenti, LZ, Huynh L, Basak GW, Ghia E, van Dyke D, Heerema N, Zahrein D, Dal Cin P, Dell'Aquila ML, Doduru P, Byrd JC, kay NE, Rai KR, Brown JR, Wierda WG, Greaves AW, Croce Cm, Kippis TJ.
TCL1 Expersssion in Chronic Lymphocytic Lukemia corrolares with the intensity of 11q Deletions and ZAP-70. The American Society of Hematology. 2007.
TCL1 Expersssion in Chronic Lymphocytic Lukemia corrolares with the intensity of 11q Deletions and ZAP-70
Limon J, Rao U, Dal Cin P, Gibas Z, Sandberg AA
Translocation (13;22) in a hemangiopericytoma. Cancer Genet Cytogenet. 1986 Apr 15; 21(4):309-18.
Translocation (13;22) in a hemangiopericytoma.
Composite chronic myeloid leukemia and essential thrombocythemia with BCR-ABL1 fusion and CALR mutation. Am J Hematol. 2019 04; 94(4):504-505.
Composite chronic myeloid leukemia and essential thrombocythemia with BCR-ABL1 fusion and CALR mutation.
Renwick PJ, Reeves BR, Dal Cin P, Fletcher CD, Kempski H, Sciot R, Kazmierczak B, Jani K, Sonobe H, Knight JC
Two categories of synovial sarcoma defined by divergent chromosome translocation breakpoints in Xp11.2, with implications for the histologic sub-classification of synovial sarcoma. Cytogenet Cell Genet. 1995; 70(1-2):58-63.
Two categories of synovial sarcoma defined by divergent chromosome translocation breakpoints in Xp11.2, with implications for the histologic sub-classification of synovial sarcoma.
Schoenmakers EF, Kools PF, Mols R, Kazmierczak B, Bartnitzke S, Bullerdiek J, Dal Cin P, De Jong PJ, Van den Berghe H, Van de Ven WJ
Physical mapping of chromosome 12q breakpoints in lipoma, pleomorphic salivary gland adenoma, uterine leiomyoma, and myxoid liposarcoma. Genomics. 1994 Mar 15; 20(2):210-22.
Physical mapping of chromosome 12q breakpoints in lipoma, pleomorphic salivary gland adenoma, uterine leiomyoma, and myxoid liposarcoma.
Sciot R, Dal Cin P, Brock P, Moerman P, Van Damme B, De Wever I, Casteels-Van Daele M, Van den Berghe H, Desmet V
Pleuropulmonary blastoma (pulmonary blastoma of childhood): genetic link with other embryonal malignancies? Histopathology. 1994 Jun; 24(6):559-63.
Pleuropulmonary blastoma (pulmonary blastoma of childhood): genetic link with other embryonal malignancies?
Aly MS, Dal Cin P, Jiskoot P, Deneffe G, Marynen P, Van den Berghe H
Competitive in situ hybridization in a mediastinal germ cell tumor. Cancer Genet Cytogenet. 1994 Mar; 73(1):53-6.
Competitive in situ hybridization in a mediastinal germ cell tumor.
Dal Cin P, Sciot R, Fletcher CD, Hilliker C, De Wever I, Van Damme B, Van den Berghe H
Trisomy 21 in solitary fibrous tumor. Cancer Genet Cytogenet. 1996 Jan; 86(1):58-60.
Cuneo A, Castoldi G, Michaux JL, Ferrant A, Chatelain B, Louwagie A, St Jan AZ, Boogaerts M, Dal Cin P, Van den Berghe H
Differences in the chromosomal profile of AML-M0 versus AML-M1: response. Blood. 1996 Jun 15; 87(12):5381-2.
Differences in the chromosomal profile of AML-M0 versus AML-M1: response.
Soupir CP, Vergilio JA, Kelly E, Dal Cin P, Kuter D, Hasserjian RP
Identification of del(20q) in a subset of patients diagnosed with idiopathic thrombocytopenic purpura. Br J Haematol. 2009 Mar; 144(5):800-2.
Identification of del(20q) in a subset of patients diagnosed with idiopathic thrombocytopenic purpura.
Snyder EL, Sandstrom DJ, Law K, Fiore C, Sicinska E, Brito J, Bailey D, Fletcher JA, Loda M, Rodig SJ, Dal Cin P, Fletcher CD
c-Jun amplification and overexpression are oncogenic in liposarcoma but not always sufficient to inhibit the adipocytic differentiation programme. J Pathol. 2009 Jul; 218(3):292-300.
c-Jun amplification and overexpression are oncogenic in liposarcoma but not always sufficient to inhibit the adipocytic differentiation programme.
Expanding the spectrum of translocations in sclerosing epitheloid fibrosarcoma: A new case with EWSR1-CREB3L3 fusion. Genes Chromosomes Cancer. 2018 12; 57(12):675-677.
Expanding the spectrum of translocations in sclerosing epitheloid fibrosarcoma: A new case with EWSR1-CREB3L3 fusion.
Hashimura T, Tubbs RR, Connelly R, Caulfield MJ, Trindade CS, McMahon JT, Galetti TP, Edinger M, Sandberg AA, Dal Cin P
Characterization of two cell lines with distinct phenotypes and genotypes established from a patient with renal cell carcinoma. Cancer Res. 1989 Dec 15; 49(24 Pt 1):7064-71.
Characterization of two cell lines with distinct phenotypes and genotypes established from a patient with renal cell carcinoma.
When to go FISHing. Am J Clin Pathol. 2010 Mar; 133(3):351-3.
Romeo S, Duim RA, Bridge JA, Mertens F, de Jong D, Dal Cin P, Wijers-Koster PM, Debiec-Rychter M, Sciot R, Rosenberg AE, Szuhai K, Hogendoorn PC
Heterogeneous and complex rearrangements of chromosome arm 6q in chondromyxoid fibroma: delineation of breakpoints and analysis of candidate target genes. Am J Pathol. 2010 Sep; 177(3):1365-76.
Heterogeneous and complex rearrangements of chromosome arm 6q in chondromyxoid fibroma: delineation of breakpoints and analysis of candidate target genes.
Antonescu CR, Zhang L, Nielsen GP, Rosenberg AE, Dal Cin P, Fletcher CD
Consistent t(1;10) with rearrangements of TGFBR3 and MGEA5 in both myxoinflammatory fibroblastic sarcoma and hemosiderotic fibrolipomatous tumor. Genes Chromosomes Cancer. 2011 Oct; 50(10):757-64.
Consistent t(1;10) with rearrangements of TGFBR3 and MGEA5 in both myxoinflammatory fibroblastic sarcoma and hemosiderotic fibrolipomatous tumor.
Dannheim KC, Pozdnyakova O, Dal Cin P, Weinberg OK
Immunophenotypic dysplasia and aberrant T-cell antigen expression in acute myeloid leukaemia with complex karyotype and TP53 mutations. J Clin Pathol. 2018 Dec; 71(12):1051-1059.
Immunophenotypic dysplasia and aberrant T-cell antigen expression in acute myeloid leukaemia with complex karyotype and TP53 mutations.
Cao M, Carrasco RD, Dubuc AM, Dal Cin P, Fletcher JA, Xiao S
ZMYM2-FGFR1 fusion as secondary change in acute myeloid leukemia. Leuk Lymphoma. 2019 02; 60(2):556-558.
ZMYM2-FGFR1 fusion as secondary change in acute myeloid leukemia.
Schoenmakers EFPM, Kools PFJ, Mols R, Kazmierczak B, Bartnitzke S, Bullerdiek J, Dal Cin P, Van den Berghe H, Van de Ven WJM.
Physical mapping of chromosome 12q translocation breakpoints in one malignant and three benign solid tumors. 4th European Workshop on Cytogenetics and Molecular Genetics of Human Solid tumors. Cancer Genet Cytogenet. 1994; (77):201.
Physical mapping of chromosome 12q translocation breakpoints in one malignant and three benign solid tumors. 4th European Workshop on Cytogenetics and Molecular Genetics of Human Solid tumors
Mylonas KS, Kao CS, Levy D, Lordello L, Dal Cin P, Masiakos PT, Oliva E
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
Clinicopathologic Features and Chromosome 12p Status of Pediatric Sacrococcygeal Teratomas: A Multi-institutional Analysis. Pediatr Dev Pathol. 2019 May-Jun; 22(3):214-220.
Clinicopathologic Features and Chromosome 12p Status of Pediatric Sacrococcygeal Teratomas: A Multi-institutional Analysis.
Brosens IA, Johannisson E, Dal Cin P, Deprest J, Van den Berghe H.
4th International Symposium on GnRH Analogues in Cancer and Human Reproduction.
Proliferation rate and oestrogen dependency of uterine leiomyomas are dependent on the chromosomal pattern. 4th International Symposium on GnRH Analogues in Cancer and Human Reproduction. 1996; Geneva, Switzerland.
Proliferation rate and oestrogen dependency of uterine leiomyomas are dependent on the chromosomal pattern
Kazmierczak B, Dal Cin P, Vanni R, Bartnitzke S, Van den Berghe H, Bullerdiek J.
Failure to establish cell lines from uterine leiopmyomas showing the del(7) as the sole abnormality. 5th European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors. 1996; Baveno - Stresa, Italy.
Failure to establish cell lines from uterine leiopmyomas showing the del(7) as the sole abnormality
Giant cell tumour of tendon sheath. Fletcher CDM, Unni KK, Mertens F, editors. World Health Organization Classification of TumoursPathology and Genetics of Tumours of Soft Tissue and Bone. 2002; 110-111.
Kazmierczak B, Dal Cin P, Meyer-Bolte K, Van den Berghe H, Bullerdiek J.
HMG1 is not the target of 13q12 rearrangements in lipomas. 6th European Conference on Cytogenetics and Molecular Genetics of Human Solid Tumors. Cancer Genet Cytogenet. 1999; (122):83-84.
HMG1 is not the target of 13q12 rearrangements in lipomas. 6th European Conference on Cytogenetics and Molecular Genetics of Human Solid Tumors
Paulien S, Turc-Carel C, Dal Cin P, Sandberg AA, Gemmill R.
Second European Workshop on Cytogenetics and Molecular Genetics in Human Solid Tumors.
Mapping studies aroudn the 12q13-q14 region in adipose tissue tumors. Second European Workshop on Cytogenetics and Molecular Genetics in Human Solid Tumors. 1990.
Mapping studies aroudn the 12q13-q14 region in adipose tissue tumors
Antonescu CR, Dal Cin P, Nafa K, Teot LA, CFletcher CD, Ladanyi M.
EWS-CREB1 is the Predominant Gene Fusion in Angiomatoid Fibrous Histiocytoma. United States and Canadian Academy of Pathology. 2007; San Diego, California.
EWS-CREB1 is the Predominant Gene Fusion in Angiomatoid Fibrous Histiocytoma
Vanni R, Marras S, Dal Cin P, Schoenmakers E, Kazmierckzak B, Bullerdiek J, Van de Ven JWJ, Van den Berghe H.
In situ fluorescence hybridization analysis of deletion of the long arm of chromosome 7 in a uterine leiomyoma derived cell line. 5th European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors. 1996; Baveno - Stresa, Italy.
In situ fluorescence hybridization analysis of deletion of the long arm of chromosome 7 in a uterine leiomyoma derived cell line
Sciot R, Samson I, Dal Cin P, Lateur L, van Damme B, van den Berghe H, Desmet V
Giant cell rich parosteal osteosarcoma. Histopathology. 1995 Jul; 27(1):51-5.
Gibson SE, Swerdlow SH, Ferry JA, Surti U, Dal Cin P, Harris NL, Hasserjian RP
Reassessment of small lymphocytic lymphoma in the era of monoclonal B-cell lymphocytosis. Haematologica. 2011 Aug; 96(8):1144-52.
Reassessment of small lymphocytic lymphoma in the era of monoclonal B-cell lymphocytosis.
Loss of INI1 expression is characteristic of both conventional and proximal-type epithelioid sarcoma. Am J Surg Pathol. 2009 Apr; 33(4):542-50.
Pathobiology of Human Germ Cell Neoplasia
i(12p) in germ cell tumors. Pathobiology of Human Germ Cell Neoplasia. 1991; 123:107-111.
Takahashi H, Feuerhake F, Kutok J L, Monti S, Dal Cin P, Neuberg D, Aster J C, Shipp M A.
FAS death domain deletions and incereased c-Fliplong expression occur in different subtypes of diffuse large B-cell lymphoma. 1920.
FAS death domain deletions and incereased c-Fliplong expression occur in different subtypes of diffuse large B-cell lymphoma
Dal Cin P, Sandberg AA, Huben R, Li FP, Prout GR
New cytogenetic subtype of renal tumors. Cancer Genet Cytogenet. 1988 Jun; 32(2):313.
New cytogenetic subtype of renal tumors.
An interstitial deletion of chromosome 7 may characterize a subgroup of uterine leiomyoma. Cancer Genet Cytogenet. 1988 Sep; 34(2):207-8.
An interstitial deletion of chromosome 7 may characterize a subgroup of uterine leiomyoma.
Brosens I., Dal Cin P., Deprest J., Van den Berghe H.
Clinico-pathological features of uterine leiomyomas. Pathogenesis and Medical Management of Uterine Fibroids. 1999; 99-110.
Clinico-pathological features of uterine leiomyomas
Dal Cin P, Pauwels P, Van de Moosdijk CNF, Vrints L, Sciot R, Van den Berghe.
9th International Congress of Human Genetics
Cytogenetics revealing the diagnosis in a metastatic endometrial stromal sarcoma. 9th International Congress of Human Genetics. 1996; Rio de Janeiro, Brazil.
Cytogenetics revealing the diagnosis in a metastatic endometrial stromal sarcoma
Turc-Carel C, Dal Cin P, Boghosian L, Leong SP, Sandberg AA
Breakpoints in benign lipoma may be at 12q13 or 12q14. Cancer Genet Cytogenet. 1988 Nov; 36(1):131-5.
Breakpoints in benign lipoma may be at 12q13 or 12q14.
M. Vastamäki, S. Vilkki, H. Goransson, H. Jaroma, T. Raatikainen & T. Viliakka (eds.), 6th Congress of the International Federation of Societies for Surgery of the Hand (IFSSH); Monduzzi Editore, International Proceedings Division.
Cytogenetic characterization of tenosynovial giant cell tumors. M. Vastamäki, S. Vilkki, H. Goransson, H. Jaroma, T. Raatikainen & T. Viliakka (eds.), 6th Congress of the International Federation of Societies for Surgery of the Hand (IFSSH); Monduzzi Editore, International Proceedings Division. 1995; 937.
Cytogenetic characterization of tenosynovial giant cell tumors
Quade,BJ,Wang T-Y, Dal Cin P, Mutter GL,Morton CC.
Transcriptional profiling of uterine smooth muscle tumors: Progress towards new diagnostic markers. United States and Canadian Academy of Pathology. 2002; Chicago, IL.
Transcriptional profiling of uterine smooth muscle tumors: Progress towards new diagnostic markers
Vanni R, Dal Cin P, Kazmierczak B, Marras S, Bullerdiek J, Van de Ven W, Van den Berghe H.
Loss of the c-Met proto-oncogene from the deleted chromosome 7 of a uterine leiomyoma cell line. 4th European Workshop on Cytogenetics and Molecular Genetics of Human Solid tumors. Cancer Genet Cytogenet. 1994; (77):203.
Loss of the c-Met proto-oncogene from the deleted chromosome 7 of a uterine leiomyoma cell line. 4th European Workshop on Cytogenetics and Molecular Genetics of Human Solid tumors
Dal Cin P. Significance of trisomy 7 and trisomy 10 in kidney tumors and surrounding arenchyma.
Southern African Society of Human Genetics, 5th Congress. 1993; South Africa .
Southern African Society of Human Genetics, 5th Congress
Rege-Cambrin G, Scaravaglio P, Carozzi F, Saglio G, Speleman F, Dal Cin P, Van den Berghe H.
33„a Congresso Societa' Italiana di Ematologia
Traslocazione t(1q;9p) in associazione con la trasformazione acuta di syndromi mieloproliferative. 33„a Congresso Societa' Italiana di Ematologia. 1991.
Traslocazione t(1q;9p) in associazione con la trasformazione acuta di syndromi mieloproliferative
Cuneo A, Ferrant A, Michaux JL, Boogaerts M, Demuynck H, Van Orshoven A, Criel A, Stul M, Dal Cin P, Hernandez J
Cytogenetic profile of minimally differentiated (FAB M0) acute myeloid leukemia: correlation with clinicobiologic findings. Blood. 1995 Jun 15; 85(12):3688-94.
Cytogenetic profile of minimally differentiated (FAB M0) acute myeloid leukemia: correlation with clinicobiologic findings.
Turc-Carel C, Limon J, Dal Cin P, Rao U, Karakousis C, Sandberg AA
Cytogenetic studies of adipose tissue tumors. II. Recurrent reciprocal translocation t(12;16)(q13;p11) in myxoid liposarcomas. Cancer Genet Cytogenet. 1986 Dec; 23(4):291-9.
Cytogenetic studies of adipose tissue tumors. II. Recurrent reciprocal translocation t(12;16)(q13;p11) in myxoid liposarcomas.
New discriminative chromosomal marker in adipose tissue tumors. The chromosome 8q11-q13 region in lipoblastoma. Cancer Genet Cytogenet. 1994 Dec; 78(2):232-5.
New discriminative chromosomal marker in adipose tissue tumors. The chromosome 8q11-q13 region in lipoblastoma.
Fletcher CD, Akerman M, Dal Cin P, de Wever I, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, van den Berghe H, van de Ven W, Vanni R, Willen H
Correlation between clinicopathological features and karyotype in lipomatous tumors. A report of 178 cases from the Chromosomes and Morphology (CHAMP) Collaborative Study Group. Am J Pathol. 1996 Feb; 148(2):623-30.
Correlation between clinicopathological features and karyotype in lipomatous tumors. A report of 178 cases from the Chromosomes and Morphology (CHAMP) Collaborative Study Group.
Soupir CP, Vergilio JA, Dal Cin P, Muzikansky A, Kantarjian H, Jones D, Hasserjian RP
Philadelphia chromosome-positive acute myeloid leukemia: a rare aggressive leukemia with clinicopathologic features distinct from chronic myeloid leukemia in myeloid blast crisis. Am J Clin Pathol. 2007 Apr; 127(4):642-50.
Philadelphia chromosome-positive acute myeloid leukemia: a rare aggressive leukemia with clinicopathologic features distinct from chronic myeloid leukemia in myeloid blast crisis.
Han M, Rivera MN, Batten JM, Haber DA, Dal Cin P, Iafrate AJ
Wilms' tumor with an apparently balanced translocation t(X;18) resulting in deletion of the WTX gene. Genes Chromosomes Cancer. 2007 Oct; 46(10):909-13.
Wilms' tumor with an apparently balanced translocation t(X;18) resulting in deletion of the WTX gene.
Deng J, Carlson N, Takeyama K, Dal Cin P, Shipp M, Letai A
BH3 profiling identifies three distinct classes of apoptotic blocks to predict response to ABT-737 and conventional chemotherapeutic agents. Cancer Cell. 2007 Aug; 12(2):171-85.
BH3 profiling identifies three distinct classes of apoptotic blocks to predict response to ABT-737 and conventional chemotherapeutic agents.
Annals of oncology : official journal of the European Society for Medical Oncology
What should oncologists know about cytogenetics in solid tumors? Ann Oncol. 1993 Dec; 4(10):821-4.
What should oncologists know about cytogenetics in solid tumors?
Dal Cin P, Marynen P, Moerman PH, Vergote I, Van den Berghe H.
Ovarium germ cell tumor with chromosome 12 anomaly but without i(12p). 5th European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors. 1996; Baveno - Stresa, Italy.
Ovarium germ cell tumor with chromosome 12 anomaly but without i(12p)
Recurrent involvement of 11q13 in acute nonlymphocytic leukemia. Cancer Genet Cytogenet. 1987 Jun; 26(2):351-4.
Recurrent involvement of 11q13 in acute nonlymphocytic leukemia.
Cytogenetic findings in a primary leiomyosarcoma of the prostate. Cancer Genet Cytogenet. 1986 Jun; 22(2):159-67.
Cytogenetic findings in a primary leiomyosarcoma of the prostate.
Vanni R, Marras S, Schoenmakers EF, Dal Cin P, Kazmierczak B, Senger G, Bullerdiek J, Van de Ven WJ, Van den Berghe H
Molecular cytogenetic characterization of del(7q) in two uterine leiomyoma-derived cell lines. Genes Chromosomes Cancer. 1997 Mar; 18(3):155-61.
Molecular cytogenetic characterization of del(7q) in two uterine leiomyoma-derived cell lines.
Dal Cin P, Sciot R, Van Damme B, De Wever I, Van den Berghe H
Trisomy 20 characterizes a second group of desmoid tumors. Cancer Genet Cytogenet. 1995 Feb; 79(2):189.
Trisomy 20 characterizes a second group of desmoid tumors.
Dal Cin P, Sciot R, Fossion E, Van Damme B, Van den Berghe H
Chromosome abnormalities in cementifying fibroma. Cancer Genet Cytogenet. 1993 Dec; 71(2):170-2.
Chromosome abnormalities in cementifying fibroma.
Dal Cin P, Pauwels P, Sciot R, Van den Berghe H
Multiple chromosome rearrangements in a fibrosarcoma. Cancer Genet Cytogenet. 1996 Apr; 87(2):176-8.
Multiple chromosome rearrangements in a fibrosarcoma.
Yoda A, Yoda Y, Chiaretti S, Bar-Natan M, Mani K, Rodig SJ, West N, Xiao Y, Brown JR, Mitsiades C, Sattler M, Kutok JL, DeAngelo DJ, Wadleigh M, Piciocchi A, Dal Cin P, Bradner JE, Griffin JD, Anderson KC, Stone RM, Ritz J, Foà R, Aster JC, Frank DA, Weinstock DM
Functional screening identifies CRLF2 in precursor B-cell acute lymphoblastic leukemia. Proc Natl Acad Sci U S A. 2010 Jan 05; 107(1):252-7.
Functional screening identifies CRLF2 in precursor B-cell acute lymphoblastic leukemia.
Reporting of diagnostic cytogenetic results. Curr Protoc Hum Genet. 2011 Jul; Appendix 1:1D.
Essential of Molecular Genetic Pathology.Cheng L, Zhang D. eds.
Molecular testing for solid tumors. Essential of Molecular Genetic Pathology.Cheng L, Zhang D. eds. 2007.
Karakousis CP, Dal Cin P, Turc Carel C, Limon J, Sandberg AA.
Annual Meeting of the Society of Surgical Oncology
Chromosome changes in sarcomas. A new diagnostic parameter. Annual Meeting of the Society of Surgical Oncology. 1987.
Chromosome changes in sarcomas. A new diagnostic parameter
Moore SDP, Dal Cin P, Quade BJ, Herrick SR, Ince T, Parisi M, Mealiffe M, Harris DJ, Ferguson HL, Strehl S, Ligon AH, Kleinman M, Kucherlapati R, Morton CC.
American Society of Human Genetics. 52th Annual Meeting.
Tumor Genome Anatomy Project (TGAP): Gene discovery in tumors in the genome era. American Society of Human Genetics. 52th Annual Meeting. 2004; Toronto, Canada.
Tumor Genome Anatomy Project (TGAP): Gene discovery in tumors in the genome era
Cuneo A, Michaux JL, Ferrand A, Bosly A, Van Hove L, Dal Cin P, Piva N, Fagioli F, Carli MG, Castoldi GL, Van den Berghe H.
Cytogenetic and biomolecular studies in acute myeloid leukemia (AML) with lymphoid markers. 20th Annual ISEH Meeting. 1991.
Cytogenetic and biomolecular studies in acute myeloid leukemia (AML) with lymphoid markers
Drandi D, Lee C, Dal Cin P, Gribben JG.
39th Congresso Nazionale della Societa’ Italiana di Ematologia.
Array-based comparative Genomic Hybridization: A new molecular technology to study genomic imbalances in CLL. 39th Congresso Nazionale della Societa’ Italiana di Ematologia. 2003; Roma, Italy.
Array-based comparative Genomic Hybridization: A new molecular technology to study genomic imbalances in CLL
Christacos N, Dal Cin P, Morton CC, Quade BJ.
Cellular leiomyoma: a genetically distinct entity among benign uterine tumors. American Society of Human Genetics. 52th Annual Meeting. 2003; Los Angeles, CA.
Cellular leiomyoma: a genetically distinct entity among benign uterine tumors
Dal Cin P, van Poppel H, van Damme B, Baert L, Van den Berghe H
Cytogenetic investigation of synchronous bilateral renal tumors. Cancer Genet Cytogenet. 1996 Jul 01; 89(1):57-60.
Cytogenetic investigation of synchronous bilateral renal tumors.
Epithelioid sarcoma of the proximal type with complex karyotype including i(8q) Cancer Genet Cytogenet. 1999 Oct 01; 114(1):80-2.
Epithelioid sarcoma of the proximal type with complex karyotype including i(8q)
Nucci, MR,Koontz J, Pauwels P, Harbuger D, Dal Cin P, Sklar J.
Assessment of the frequency of t(7;17) in endometrial stromal neoplasia by RT-PCR and FISH. United States and Canadian Academy of Pathology. 2003; Washington, DC.
Assessment of the frequency of t(7;17) in endometrial stromal neoplasia by RT-PCR and FISH
Wanschura S, Dal Cin P, Kazmierczak B. Bartnitzke S, Van Den Berghe H., Bullerdiek, J.
Hidden paracentric inversions of chromosome 12q affecting the HMGIC gene. 7th International Workshop on Chromosomes in Solid Tumors. Cancer Genet Cytogenet. 1997; (98):168.
Hidden paracentric inversions of chromosome 12q affecting the HMGIC gene. 7th International Workshop on Chromosomes in Solid Tumors
Dal Cin P, Sciot R, Panagopoulos I, Åman P, Samson I, Mandahl N, Mitelman F, Van den Berghe H, Fletcher CDM.
Additional evidence of a variant translocation t(12;22) with EWS/CHOP fusion in myxoid liposarcoma: clinicopathological features. 7th International Workshop on Chromosomes in Solid Tumors. Cancer Genet Cytogenet. 1997; 98:157.
Additional evidence of a variant translocation t(12;22) with EWS/CHOP fusion in myxoid liposarcoma: clinicopathological features. 7th International Workshop on Chromosomes in Solid Tumors
Dei Tos A.P., Doglioni C., Piccinin S., Furlanetto A., Sciot R., Dal Cin P., Boiocchi M., Fletcher C.D.P., Tallini G.
Coordinated expression of MDM2, CDK4 and HMGI-C in atypical lipomatous tumors. United States and Canadian Academy of Pathology. 1998; Boston, MA.
Coordinated expression of MDM2, CDK4 and HMGI-C in atypical lipomatous tumors
Tallini G, Dal Cin P, De Wever I, Fletcher CDM, Mandahl N, Mertens F Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, Van den Berghe H, Vanni R, Willén H; Yale U., New Haven, CT; Memorial Sloan-Ketterinc Cancer Center, NY, NY; Guy's and St. Thomas' Hosp., London, U.; U. of Lund, Sweden; U. of Leuven, Belgium; and U. of Cagliari, Italy.
Atypical lipomatous tumors. evalutation of their relatinship and differential diagnosis with other adipose tissue tumors based on a combined morphologic-karyotypic study of cases. 1995 Annual Meeting United States and Canadian Academy of Pathology. 1995; Toronto, Canada.
Atypical lipomatous tumors. evalutation of their relatinship and differential diagnosis with other adipose tissue tumors based on a combined morphologic-karyotypic study of cases
European conference of the ESF Programme in Functional Genomics.
Comparative genomic hybridization array analysis: A new moecular cytogenetic method to study genomic imbalnce in B-CLL. European conference of the ESF Programme in Functional Genomics. 2003; Prague, Czech Republic.
Comparative genomic hybridization array analysis: A new moecular cytogenetic method to study genomic imbalnce in B-CLL
Coccia M, Meltzer P, Dal Cin P, Turc-Carel C, Sandberg AA, Trent J.
American Association for Cancer Research
A recurring DNA amplification in human sarcomas. American Association for Cancer Research. 1990.
A recurring DNA amplification in human sarcomas
Consistent involvement of band 12q14 in two different translocations in three lipomas from the same patient. Cancer Genet Cytogenet. 1988 Apr; 31(2):237-40.
Consistent involvement of band 12q14 in two different translocations in three lipomas from the same patient.
Moore SDP, Herrick SR, Ince T, Dal Cin P, Klienman M Morton CC, Quade BJ.
Cytogenetic chararacterization of uterine leiomyoma with t(10;17) involve the histone acetyltransferase MORF. American Society of Human Genetics. 52th Annual Meeting. 2003; Los Angeles, CA.
Cytogenetic chararacterization of uterine leiomyoma with t(10;17) involve the histone acetyltransferase MORF
Hibbard MK, Kozakewich HP, Dal Cin P, Sciot R, Tan X, Xiao S, Fletcher JA
PLAG1 fusion oncogenes in lipoblastoma. Cancer Res. 2000 Sep 01; 60(17):4869-72.
Aly MS, Dal Cin P, Jiskoot P, Deneffe G, Van den Berghe H.
European Society of Human Genetics 25th Annual Meeting
Competitive in situ hybridization in a mediastinal germ cell tumor. European Society of Human Genetics 25th Annual Meeting. 1993; Barcelona, Spain.
Meltzer PS, Jankowski SA, Dal Cin P, Sandberg AA, Paz IB, Coccia MA, Smith SH.
Identification and cloning of a novel amplified DNA sequence in human malignant fibrous histiocytoma derived from a region of chromosome 12 frequently rearranged in soft tissue tumors. Human Gene Mapping 11. Cytogenet Cell Genet. 1991; (58):1979.
Identification and cloning of a novel amplified DNA sequence in human malignant fibrous histiocytoma derived from a region of chromosome 12 frequently rearranged in soft tissue tumors. Human Gene Mapping 11
Hilliker C, Delabie J, Bilbe G, Brüggen J, Speleman F, Dal Cin P, Van Leuven F, Van Den Berghe H.
Proceedings of the American Association for Cancer Research
Localization of an intermediate filament associated protein expressed in the Reed-Sternberg cell to 12q24.1-q24.33. Eighty-third Annual Meeting of the American Association for Cancer Research. Proceedings of the American Association for Cancer Research. 1992; (33):398.
Localization of an intermediate filament associated protein expressed in the Reed-Sternberg cell to 12q24.1-q24.33. Eighty-third Annual Meeting of the American Association for Cancer Research
Quade BJ, Getman M, Wang T-Y, Weremowicz S, Dal Cin P, Morton CC.
American Society of Human Genetics. 49th Annual Meeting.
Exploring the dysregulation of HMGIC in uterine leiomyomata with t(12;14). American Society of Human Genetics. 49th Annual Meeting. 1999; San Francisco, CA.
Exploring the dysregulation of HMGIC in uterine leiomyomata with t(12;14)
Moore SDP, Herrick SR, Ince T, Dal Cin P, Kleinman M, Morton CC, Quade BJ.
Chromosome 10 rearrarangements in uterine leiomyomata involve the histone acetyltransferase MORF. United States and Canadian Academy of Pathology. 2004; Vancouver, Can.
Chromosome 10 rearrarangements in uterine leiomyomata involve the histone acetyltransferase MORF
Consistent chromosome changes in leiomyosarcoma. Cancer Genet Cytogenet. 1988 Oct 01; 35(1):47-50.
Consistent chromosome changes in leiomyosarcoma.
Dei Tos AP, Calonje E, Sciot R, Pauwels P, Knight JC, Dal Cin P, Fletcher CD
Immunohistochemical demonstration of glycoprotein p30/32MIC2 (CD99) in synovial sarcoma. A potential cause of diagnostic confusion. App Immunhistochem. 1995; 3:168-73.
Immunohistochemical demonstration of glycoprotein p30/32MIC2 (CD99) in synovial sarcoma. A potential cause of diagnostic confusion
Antonescu CR, K Nafa K, Dal Cin P , Ladanyi M.
EWS-CREB1: A recurrent variant fusion in clear cell sarcoma associated with gastrointestinal location and absence of melanocytic differentiation. United States and Canadian Academy of Pathology. 2006; Atlanta, Georgia.
EWS-CREB1: A recurrent variant fusion in clear cell sarcoma associated with gastrointestinal location and absence of melanocytic differentiation
Speleman F, De Potter C, Dal Cin P, Mangelschots K, Laureys G, Leroy JG, Van den Berghe H.
i(12p) in a malignant ovarian tumor. Genetics in Cancer & Development. 1989.
Kools PFJ, De Wever I, Sciot R, Dal Cin P, Van den Berghe H, Van de Ven WJM.
Amplifiaction of the high mobility group protein gene HMGI-C in atypical lipomatous tumors. Chromosome 12 Genes in Cancer. 1995; Leuven, Belgium.
Amplifiaction of the high mobility group protein gene HMGI-C in atypical lipomatous tumors. Chromosome 12 Genes in Cancer
Vanni R, Marras S, Moerman P, Andria M, Valdes E, Deprest L, Van den Berghe H, Dal Cin P.
International Workshop on Chromosomes in solid Tumors
Endometrial polyp. another benign tumor characterized by 12q14-15 changes ? 5th. International Workshop on Chromosomes in solid Tumors. 1993.
Endometrial polyp. another benign tumor characterized by 12q14-15 changes ? 5th
Dal Cin P, Sciot R, Van Poppel H, Balzarini P, Roskams T, Van den Berghe H
Chromosome changes in sarcomatoid renal carcinomas are different from those in renal cell carcinomas. Cancer Genet Cytogenet. 2002 Apr 01; 134(1):38-40.
Chromosome changes in sarcomatoid renal carcinomas are different from those in renal cell carcinomas.
Moore SD, Herrick SR, Ince TA, Kleinman MS, Dal Cin P, Morton CC, Quade BJ
Uterine leiomyomata with t(10;17) disrupt the histone acetyltransferase MORF. Cancer Res. 2004 Aug 15; 64(16):5570-7.
Uterine leiomyomata with t(10;17) disrupt the histone acetyltransferase MORF.
Acute myelocytic leukemia with t(11;17)(q23;q12-q21) involves a fusion of MLL and AF17. Cancer Genet Cytogenet. 2005 Feb; 157(1):87-9.
Acute myelocytic leukemia with t(11;17)(q23;q12-q21) involves a fusion of MLL and AF17.
Speleman F, Mangelschots K, Vercruyssen M, Dal Cin P, Aventin A, Offner F, Laureys G, Van den Berghe H, Leroy J
Analysis of whole-arm translocations in malignant blood cells by nonisotopic in situ hybridization. Cytogenet Cell Genet. 1991; 56(1):14-7.
Analysis of whole-arm translocations in malignant blood cells by nonisotopic in situ hybridization.
Dal Cin P, Sciot R, Samson I, De Smet L, De Wever I, Van Damme B, Van den Berghe H
Cytogenetic characterization of tenosynovial giant cell tumors (nodular tenosynovitis). Cancer Res. 1994 Aug 01; 54(15):3986-7.
Cytogenetic characterization of tenosynovial giant cell tumors (nodular tenosynovitis).
Vanni R, Dal Cin P, Marras S, Moerman P, Andria M, Valdes E, Deprest J, Van den Berghe H
Endometrial polyp: another benign tumor characterized by 12q13-q15 changes. Cancer Genet Cytogenet. 1993 Jul 01; 68(1):32-3.
Endometrial polyp: another benign tumor characterized by 12q13-q15 changes.
Aly MS, Dal Cin P, Moerman P, De Wever I, Devriendt K, Brock P, Casteels-Van Daele M, Van den Berghe H
Loss of the Y-chromosome in a malignant Sertoli tumor. Cancer Genet Cytogenet. 1993 Feb; 65(2):104-6.
Loss of the Y-chromosome in a malignant Sertoli tumor.
Nucci, MR, Dal Cin P, Drapkin R, Fletcher CDM, Fletcher JA.
So-called benign metastazing leiomyoma: Cytogenetic analysis confirms a distinct clinopathologic entity. United States and Canadian Academy of Pathology. 2003; Washington, DC.
So-called benign metastazing leiomyoma: Cytogenetic analysis confirms a distinct clinopathologic entity
Dal Cin P, Sciot R, Speleman F, Samson I, Laureys G, de Potter C, Meire F, van Damme B, van den Berghe H
Chromosome aberrations in fibrous dysplasia. Cancer Genet Cytogenet. 1994 Oct 15; 77(2):114-7.
Chromosome aberrations in fibrous dysplasia.
Antonescu CR, Dal Cin P, Nafa K, Teot LA, Surti U, Fletcher CD, Ladanyi M
EWSR1-CREB1 is the predominant gene fusion in angiomatoid fibrous histiocytoma. Genes Chromosomes Cancer. 2007 Dec; 46(12):1051-60.
EWSR1-CREB1 is the predominant gene fusion in angiomatoid fibrous histiocytoma.
Kelly PJ, Weiss SE, Sher DJ, Perez-Atayde AR, Dal Cin P, Choueiri TK
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Sunitinib-induced pseudoprogression after whole-brain radiotherapy for metastatic renal cell carcinoma. J Clin Oncol. 2010 Sep 01; 28(25):e433-5.
Sunitinib-induced pseudoprogression after whole-brain radiotherapy for metastatic renal cell carcinoma.
Metaphase harvest and cytogenetic analysis of malignant hematological specimens. Curr Protoc Hum Genet. 2012 Apr; Chapter 10:Unit 10.2.1-15.
Chromophobe renal cell carcinoma. Atlas Genet Cytogenet Oncol Haematol.
Chromophobe renal cell carcinoma. Atlas Genet Cytogenet Oncol Haematol. 2001.
Debiec-Rychter M, Roskam T, Van Poppel H, Dal Cin P, Lerut E, Blyweert W, Hagemeijer A.
8th European Conference on Cytogenetics and Molecular Genetics of Human Solid Tumors.
Cytogenetic findings in 292 primary renal cell tumors. 8th European Conference on Cytogenetics and Molecular Genetics of Human Solid Tumors. 2002; Barcelona, Spain .
Cytogenetic findings in 292 primary renal cell tumors
Kazmierczak B, Bartnitzke S, Dal Cin P, Vanni R, Bullerdiek J.
Chromosome 12 Aberrations in Human Solid Tumors. Cytogenetics and Molecular Genetics.
Cell lines from tumours showing 12q13-15 aberrations. Chromosome 12 Aberrations in Human Solid Tumors. Cytogenetics and Molecular Genetics. 1994; 89-102.
Cell lines from tumours showing 12q13-15 aberrations
Gisselsson D, Pettersson L, Höglund M, Hiedenblad M, Gurunova L, Wiegant J, Mertens F, Dal Cin P, Mitelman F, Mandahl N.
8th International Workshop on Chromosomes in Solid Tumors.
Chromosomal breakage-fusion-bridge events cause genetic intratumor heretogeneity. 8th International Workshop on Chromosomes in Solid Tumors. 2000; Tucson, AZ.
Chromosomal breakage-fusion-bridge events cause genetic intratumor heretogeneity
Dal Cin P. Cytogenetic investigations in endometrial polyps.
Chromosome changes in a prostatic leiomyosarcoma. Cancer Genet Cytogenet. 1988 Feb; 30(2):339-40.
Chromosome changes in a prostatic leiomyosarcoma.
Blood: Principles and Practice of Hematology.
Cytogenetics for the Hematologist. Blood: Principles and Practice of Hematology. 2003; 96-122.
Tallini G, Dal Cin P, Giancotti V, Fusco A, Van den Berghe H, Sciot R.
United States and Canadian Academy of Pathology 86th Annual Meeting
Expression of HMGI-C and HMGI(Y) in lipoma and atypical lipomatous tumors; immunohistochemical reactivity correlates with karyotypic alterations. United States and Canadian Academy of Pathology 86th Annual Meeting. 1997; Orlando,FL.
Expression of HMGI-C and HMGI(Y) in lipoma and atypical lipomatous tumors; immunohistochemical reactivity correlates with karyotypic alterations
t(16;21)(q24;q22) in therapy-related acute myelogenous leukemia arising from myelodysplastic syndromeAtlas Genet Cytogenet Oncol Haematol
t(16;21)(q24;q22) in therapy-related acute myelogenous leukemia arising from myelodysplastic syndromeAtlas Genet Cytogenet Oncol Haematol. 2007.
Dal Cin P, Sciot R, Fletcher CDM, Hilliker C, De Wever I, Van Damme B, Van den Berghe H.
12th International Chromosome Conference.
Trisomy 21 in solitary fibrous tumor. 12th International Chromosome Conference. 1995; Madrid, Spain.
Turc-Carel C, Dal Cin P, Rao U, Karakousis C, Sandberg AA
Recurrent breakpoints at 9q31 and 22q12.2 in extraskeletal myxoid chondrosarcoma. Cancer Genet Cytogenet. 1988 Jan; 30(1):145-50.
Recurrent breakpoints at 9q31 and 22q12.2 in extraskeletal myxoid chondrosarcoma.
Limon J, Dal Cin P, Sait SN, Karakousis C, Sandberg AA
Chromosome changes in metastatic human melanoma. Cancer Genet Cytogenet. 1988 Feb; 30(2):201-11.
Chromosome changes in metastatic human melanoma.
Sciot R, Dal Cin P, De Vos R, Van Damme B, De Wever I, Van den Berghe H, Desmet VJ
Alveolar soft-part sarcoma: evidence for its myogenic origin and for the involvement of 17q25. Histopathology. 1993 Nov; 23(5):439-44.
Alveolar soft-part sarcoma: evidence for its myogenic origin and for the involvement of 17q25.
Dal Cin P, Wanschura S, Christiaens MR, Van den Berghe I, Moerman P, Polito P, Kazmierczak B, Bullerdiek J, Van den Berghe H
Hamartoma of the breast with involvement of 6p21 and rearrangement of HMGIY. Genes Chromosomes Cancer. 1997 Sep; 20(1):90-2.
Hamartoma of the breast with involvement of 6p21 and rearrangement of HMGIY.
Dal Cin P, Sciot R, De Smet L, Van den Berghe H
Translocation 2;11 in a fibroma of tendon sheath. Histopathology. 1998 May; 32(5):433-5.
Translocation 2;11 in a fibroma of tendon sheath.
Dal Cin P, Sciot R, Fletcher CD, Samson I, De Vos R, Mandahl N, Willén H, Larsson O, Van den Berghe H
Inflammatory leiomyosarcoma may be characterized by specific near-haploid chromosome changes. J Pathol. 1998 May; 185(1):112-5.
Inflammatory leiomyosarcoma may be characterized by specific near-haploid chromosome changes.
Dal Cin P, Vanni R, Polito P, Van den Berghe H
[Diagnostic impact of cytogenetics for solid tumors]. Pathologica. 1998 Aug; 90(4):337-42.
[Diagnostic impact of cytogenetics for solid tumors].
Involvement of the HMGI(Y) gene in a microfollicular adenoma of the thyroid. Genes Chromosomes Cancer. 1999 Mar; 24(3):286-9.
Involvement of the HMGI(Y) gene in a microfollicular adenoma of the thyroid.
Van Poppel H, Nilsson S, Algaba F, Bergerheim U, Dal Cin P, Fleming S, Hellsten S, Kirkali Z, Klotz L, Lindblad P, Ljungberg B, Mulders P, Roskams T, Ross RK, Walker C, Wersäll P
Scandinavian journal of urology and nephrology. Supplementum
Precancerous lesions in the kidney. Scand J Urol Nephrol Suppl. 2000; (205):136-65.
Mertens F, Strömberg U, Mandahl N, Dal Cin P, De Wever I, Fletcher CD, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, Van Den Berghe H, Vanni R, Willén H
Prognostically important chromosomal aberrations in soft tissue sarcomas: a report of the Chromosomes and Morphology (CHAMP) Study Group. Cancer Res. 2002 Jul 15; 62(14):3980-4.
Prognostically important chromosomal aberrations in soft tissue sarcomas: a report of the Chromosomes and Morphology (CHAMP) Study Group.
Pentimalli F, Dentice M, Fedele M, Pierantoni GM, Cito L, Pallante P, Santoro M, Viglietto G, Dal Cin P, Fusco A
Suppression of HMGA2 protein synthesis could be a tool for the therapy of well differentiated liposarcomas overexpressing HMGA2. Cancer Res. 2003 Nov 01; 63(21):7423-7.
Suppression of HMGA2 protein synthesis could be a tool for the therapy of well differentiated liposarcomas overexpressing HMGA2.
Christacos NC, Quade BJ, Dal Cin P, Morton CC
Uterine leiomyomata with deletions of Ip represent a distinct cytogenetic subgroup associated with unusual histologic features. Genes Chromosomes Cancer. 2006 Mar; 45(3):304-12.
Uterine leiomyomata with deletions of Ip represent a distinct cytogenetic subgroup associated with unusual histologic features.
ALK expression in pseudosarcomatous myofibroblastic proliferations of the genitourinary tract. Histopathology. 2006 Apr; 48(5):569-78.
ALK expression in pseudosarcomatous myofibroblastic proliferations of the genitourinary tract.
Choueiri TK, Lim ZD, Hirsch MS, Tamboli P, Jonasch E, McDermott DF, Dal Cin P, Corn P, Vaishampayan U, Heng DY, Tannir NM
Vascular endothelial growth factor-targeted therapy for the treatment of adult metastatic Xp11.2 translocation renal cell carcinoma. Cancer. 2010 Nov 15; 116(22):5219-25.
Vascular endothelial growth factor-targeted therapy for the treatment of adult metastatic Xp11.2 translocation renal cell carcinoma.
Boghosian L, Dal Cin P, Turc-Carel C, Rao U, Karakousis C, Sait SJ, Sandberg AA
Three possible cytogenetic subgroups of leiomyosarcoma. Cancer Genet Cytogenet. 1989 Nov; 43(1):39-49.
Three possible cytogenetic subgroups of leiomyosarcoma.
Dal Cin P, Gaeta J, Huben R, Li FP, Prout GR, Sandberg AA
Renal cortical tumors. Cytogenetic characterization. Am J Clin Pathol. 1989 Oct; 92(4):408-14.
Renal cortical tumors. Cytogenetic characterization.
Sherman L, Ariynayagam S, Christy K, DuBois Z, Marzelli M, McLaughlin C, Soltisova D, Dal Cin P.
Association of Genetic Technologists, 27th Annual Meeting.
Cytogenetic and FISH analyses on chronic lymphocytic leukemias. Association of Genetic Technologists, 27th Annual Meeting. 2002; Cincinnati,OH.
Cytogenetic and FISH analyses on chronic lymphocytic leukemias
Dal Cin P, Rege-Cambrin G, Speleman F, Van Roy N, Kerim S, Scaravaglio P, Carozzi F, Michaux JL, Offner F, Saglio G, Van den Berghe H.
More precize localization of breakpoints involved in the derivative chromosome (1q9p), associated with myeloproliferative disorders. Human Gene Mapping 11. Cytogenet Cell Genet. 1991; (58):1852.
More precize localization of breakpoints involved in the derivative chromosome (1q9p), associated with myeloproliferative disorders. Human Gene Mapping 11
Dal Cin P, Kozakewich HP, Weremowicz S, Goumnerova L, Mankin HJ , Rosenberg AE, Fletcher JA.
Translocations involving 16q22 and 17p13 are found in all types of aneurysmal bone cysts. 8th International Workshop on Chromosomes in Solid Tumors. 2000; Tucson, AZ.
Translocations involving 16q22 and 17p13 are found in all types of aneurysmal bone cysts
Voordrachten "Myomatosis", Vlaamse Vereniging voor Obstetrie en Gynaecologie
Cytogenetic analysis on uterine leiomyomas. Voordrachten "Myomatosis", Vlaamse Vereniging voor Obstetrie en Gynaecologie. 1989.
Cytogenetic analysis on uterine leiomyomas
Sobre un caso de triple X (A case of 47,XXX). Acta Cient Venez. 1980; 31:135.
Sobre un caso de triple X (A case of 47,XXX)
Cytogenetics of tumors of the female reproductive tract. . Repro Med Rev. 1994; 3:1-10.
Cytogenetics of tumors of the female reproductive tract.
American Society of Hematology, 45th Annual Meeting.
Array-based comparative genomic hybridization identifies deletion at 14q32 as a new prognostic marker in chronic lymphocytic leukemia (CLL). American Society of Hematology, 45th Annual Meeting. 2003; San Diego, CA.
Array-based comparative genomic hybridization identifies deletion at 14q32 as a new prognostic marker in chronic lymphocytic leukemia (CLL)
Dal Cin P, Boghosian L, Crickard K, Sandberg AA
t(10;17) as the sole chromosome change in a uterine leiomyosarcoma. Cancer Genet Cytogenet. 1988 Jun; 32(2):263-6.
t(10;17) as the sole chromosome change in a uterine leiomyosarcoma.
Wanschura, S., Belge G, Stenman G, Schoenmakers, E, Dal Cin P, Bartnitzka, S., Van den Berghe, H., Van de Ven, W., Bullerdiek, J.
Physical mapping of 12q13-q15 translocation breakpoints of primary pleomorphic adenomas of the salivary glands, uterine leiomyomas, lipomas and derived cell lines. 6th International Workshop on Chromosomes in Solid Tumors February 19-21. Cancer Genet Cytogenet. 1995; (84):141.
Physical mapping of 12q13-q15 translocation breakpoints of primary pleomorphic adenomas of the salivary glands, uterine leiomyomas, lipomas and derived cell lines. 6th International Workshop on Chromosomes in Solid Tumors February 19-21
Knight JC, Renwick P, Reeves B, Cotter F, Dal Cin P, Kempski H, Sonobe H, Fletcher C.D.M.
Two categories of synovial sarcoma defined by t(X;18) breakpoints on chromosome Xp. 4th European Workshop on Cytogenetics and Molecular Genetics of Human Solid tumors. Cancer Genet Cytogenet. 1994; (77):161.
Two categories of synovial sarcoma defined by t(X;18) breakpoints on chromosome Xp. 4th European Workshop on Cytogenetics and Molecular Genetics of Human Solid tumors
Cytogenetic findings in a supratentorial ependymoma. Cancer Genet Cytogenet. 1988 Feb; 30(2):289-93.
Cytogenetic findings in a supratentorial ependymoma.
Groupe Français de Cytogénétique Hématologique
Isochromosome 21q in hematologic malignancies. Cancer Genet Cytogenet. 1991; 55:101-105.
Isochromosome 21q in hematologic malignancies
Nonrandom translocation in extraskeletal myxoid chondrosarcoma. Cancer Genet Cytogenet. 1987 Jun; 26(2):377.
Nonrandom translocation in extraskeletal myxoid chondrosarcoma.
Dal Cin P, De Wolf-Peeters C, Aly MS, Deneffe G, Van Mieghem W, Van Den Berghe H
Ring chromosome 6 as the only change in a thymoma. Genes Chromosomes Cancer. 1993 Apr; 6(4):243-4.
Ring chromosome 6 as the only change in a thymoma.
Dal Cin P, Vanni R, Marras S, Moerman P, Kools P, Andria M, Valdes E, Deprest J, Van de Ven W, Van den Berghe H
Four cytogenetic subgroups can be identified in endometrial polyps. Cancer Res. 1995 Apr 01; 55(7):1565-8.
Four cytogenetic subgroups can be identified in endometrial polyps.
Dal Cin P, Scoit R, De Smet L, Van Damme B, Van Den Berghe H
A new cytogenetic subgroup in tenosynovial giant cell tumors (nodular tenosynovitis) is characterized by involvement of 16q24. Cancer Genet Cytogenet. 1996 Mar; 87(1):85-7.
A new cytogenetic subgroup in tenosynovial giant cell tumors (nodular tenosynovitis) is characterized by involvement of 16q24.
Patel SS, Pinkus GS, Ritterhouse LL, Segal JP, Dal Cin P, Restrepo T, Harris MH, Stone RM, Hasserjian RP, Weinberg OK
High NPM1 mutant allele burden at diagnosis correlates with minimal residual disease at first remission in de novo acute myeloid leukemia. Am J Hematol. 2019 08; 94(8):921-928.
High NPM1 mutant allele burden at diagnosis correlates with minimal residual disease at first remission in de novo acute myeloid leukemia.
Professor of Pathology and Health Sciences and Technology, Emeritus
Jerome and Nancy Kohlberg Professor of Medicine
William Lambert Richardson Professor of Obstetrics, Gynecology and Reproductive Biology
Professor of Orthopedic Surgery, Emeritus
John Anthony Mannick Professor of Surgery, Emeritus
Professor of Anaesthesia (Pharmacology), Emeritus
Hung YP, Dong F, Dubuc AM, Dal Cin P, Bueno R, Chirieac LR
Molecular characterization of localized pleural mesothelioma. Mod Pathol. 2020 02; 33(2):271-280.
Molecular characterization of localized pleural mesothelioma.
Hafeez F, Xiao S, Dal Cin P, Krane JF, Chen P, Hayek J, Lian CG
Polymorphous sweat gland carcinoma found to have MYB rearrangement. Histopathology. 2020 04; 76(5):779-781.
Polymorphous sweat gland carcinoma found to have MYB rearrangement.
Nardi V, Ku N, Frigault MJ, Dubuc AM, Tsai HK, Amrein PC, Hobbs GS, Brunner AM, Narayan R, Burke ME, Foster J, Dal Cin P, Maus MV, Fathi AT, Hock H
Clinical response to larotrectinib in adult Philadelphia chromosome-like ALL with cryptic ETV6-NTRK3 rearrangement. Blood Adv. 2020 01 14; 4(1):106-111.
Clinical response to larotrectinib in adult Philadelphia chromosome-like ALL with cryptic ETV6-NTRK3 rearrangement.
Jan M, Grinshpun DE, Villalba JA, Dal Cin P, Sykes DB, Iafrate AJ, Ebert BL, Hobbs GS, Nardi V
A cryptic imatinib-sensitive G3BP1-PDGFRB rearrangement in a myeloid neoplasm with eosinophilia. Blood Adv. 2020 02 11; 4(3):445-448.
A cryptic imatinib-sensitive G3BP1-PDGFRB rearrangement in a myeloid neoplasm with eosinophilia.
Ouseph MM, Hasserjian RP, Dal Cin P, Lovitch SB, Steensma DP, Nardi V, Weinberg OK
Genomic alterations in patients with somatic loss of the Y chromosome as the sole cytogenetic finding in bone marrow cells. Haematologica. 2021 02 01; 106(2):555-564.
Genomic alterations in patients with somatic loss of the Y chromosome as the sole cytogenetic finding in bone marrow cells.
Xiao AW, Jia Y, Baughn LB, Pearce KE, Pitel BA, Aster JC, Dal Cin P, Xiao S
IGH rearrangement in myeloid neoplasms. Haematologica. 2020 06; 105(6):e315-e317.
Acosta AM, Sholl LM, Cin PD, Howitt BE, Otis CN, Nucci MR
Malignant tumours of the uterus and ovaries with Mullerian and germ cell or trophoblastic components have a somatic origin and are characterised by genomic instability. Histopathology. 2020 Nov; 77(5):788-797.
Malignant tumours of the uterus and ovaries with Mullerian and germ cell or trophoblastic components have a somatic origin and are characterised by genomic instability.
Kasbekar M, Nardi V, Dal Cin P, Brunner AM, Burke M, Chen YB, Connolly C, Fathi AT, Foster J, Macrae M, McAfee SL, McGregor K, Narayan R, Ramos AY, Som TT, Vartanian M, Friedman RS, Benhadji KA, Hobbs GS
Targeted FGFR inhibition results in a durable remission in an FGFR1-driven myeloid neoplasm with eosinophilia. Blood Adv. 2020 07 14; 4(13):3136-3140.
Targeted FGFR inhibition results in a durable remission in an FGFR1-driven myeloid neoplasm with eosinophilia.
Baniak N, Flood TA, Buchanan M, Dal Cin P, Hirsch MS
Carbonic anhydrase IX (CA9) expression in multiple renal epithelial tumour subtypes. Histopathology. 2020 Oct; 77(4):659-666.
Carbonic anhydrase IX (CA9) expression in multiple renal epithelial tumour subtypes.
Acosta AM, Demicco EG, Dal Cin P, Hirsch MS, Fletcher CDM, Jo VY
Pseudosarcomatous myofibroblastic proliferations of the urinary bladder are neoplasms characterized by recurrent FN1-ALK fusions. Mod Pathol. 2021 02; 34(2):469-477.
Pseudosarcomatous myofibroblastic proliferations of the urinary bladder are neoplasms characterized by recurrent FN1-ALK fusions.
Hergott CB, Dal Cin P, Hornick JL, Winer ES, Carrasco RD, Kim AS
Characteristic nuclear membrane ALK reactivity in chronic myelomonocytic leukemia with RANBP2-ALK fusion. Am J Hematol. 2023 02; 98(2):365-367.
Characteristic nuclear membrane ALK reactivity in chronic myelomonocytic leukemia with RANBP2-ALK fusion.
Terraf P, Sholl LM, Davids MS, Awad MM, Garcia EP, MacConaill LE, Dal Cin P, Kim A, Lindeman NI, Stachler M, Hwang DH, Dubuc AM
Cold Spring Harbor molecular case studies
Twists and turns from "tumor in tumor" profiling: surveillance of chronic lymphocytic leukemia (CLL) leads to detection of a lung adenocarcinoma, whose genomic characterization alters the original hematologic diagnosis. Cold Spring Harb Mol Case Stud. 2021 08; 7(4).
Twists and turns from "tumor in tumor" profiling: surveillance of chronic lymphocytic leukemia (CLL) leads to detection of a lung adenocarcinoma, whose genomic characterization alters the original hematologic diagnosis.
Acosta AM, Sholl LM, Marino-Enriquez A, Dal Cin P, Dickson BC, Gordetsky JB, Pins MR, McKenney JK, Fletcher CD
In Response to "Reexamining the molecular findings in specialized stromal tumors of the prostate". Mod Pathol. 2021 11; 34(11):2082-2083.
In Response to "Reexamining the molecular findings in specialized stromal tumors of the prostate".
Mueller SB, Dal Cin P, Le LP, Dias-Santagata D, Lennerz JK, Iafrate AJ, Marble HD, Brunner AM, Weinstock MJ, Luskin MR, De Angelo DJ, Stone RM, Nardi V
t(4;12)(q12;p13) ETV6-rearranged AML without eosinophilia does not involve PDGFRA: relevance for imatinib insensitivity. Blood Adv. 2022 01 08; 6(3):818-827.
t(4;12)(q12;p13) ETV6-rearranged AML without eosinophilia does not involve PDGFRA: relevance for imatinib insensitivity.
Chapel DB, Howitt BE, Sholl LM, Dal Cin P, Nucci MR
Atypical uterine polyps show morphologic and molecular overlap with mullerian adenosarcoma but follow a benign clinical course. Mod Pathol. 2022 01; 35(1):106-116.
Atypical uterine polyps show morphologic and molecular overlap with mullerian adenosarcoma but follow a benign clinical course.
Weinberg OK, Siddon A, Madanat YF, Gagan J, Arber DA, Dal Cin P, Narayanan D, Ouseph MM, Kurzer JH, Hasserjian RP
TP53 mutation defines a unique subgroup within complex karyotype de novo and therapy-related MDS/AML. Blood Adv. 2022 05 10; 6(9):2847-2853.
TP53 mutation defines a unique subgroup within complex karyotype de novo and therapy-related MDS/AML.
Akkari YMN, Baughn LB, Dubuc AM, Smith AC, Mallo M, Dal Cin P, Diez Campelo M, Gallego MS, Granada Font I, Haase DT, Schlegelberger B, Slavutsky I, Mecucci C, Levine RL, Hasserjian RP, Solé F, Levy B, Xu X
Guiding the global evolution of cytogenetic testing for hematologic malignancies. Blood. 2022 04 14; 139(15):2273-2284.
Guiding the global evolution of cytogenetic testing for hematologic malignancies.
Siegele BJ, Stemmer-Rachamimov AO, Lilljebjorn H, Fioretos T, Winters AC, Dal Cin P, Treece A, Gaskell A, Nardi V
N-terminus DUX4-immunohistochemistry is a reliable methodology for the diagnosis of DUX4-fused B-lymphoblastic leukemia/lymphoma (N-terminus DUX4 IHC for DUX4-fused B-ALL). Genes Chromosomes Cancer. 2022 08; 61(8):449-458.
N-terminus DUX4-immunohistochemistry is a reliable methodology for the diagnosis of DUX4-fused B-lymphoblastic leukemia/lymphoma (N-terminus DUX4 IHC for DUX4-fused B-ALL).
Costigan D, Dal Cin P, Fletcher CDM, Nucci MR, Parra-Herran C, Chapel DB
Low-grade Fibromyxoid Sarcoma of the Vulva and Vagina: Clinical, Pathologic, and Molecular Characterization of 7 Cases and Review of the Literature. Am J Surg Pathol. 2022 09 01; 46(9):1196-1206.
Low-grade Fibromyxoid Sarcoma of the Vulva and Vagina: Clinical, Pathologic, and Molecular Characterization of 7 Cases and Review of the Literature.
Arber DA, Orazi A, Hasserjian RP, Borowitz MJ, Calvo KR, Kvasnicka HM, Wang SA, Bagg A, Barbui T, Branford S, Bueso-Ramos CE, Cortes JE, Dal Cin P, DiNardo CD, Dombret H, Duncavage EJ, Ebert BL, Estey EH, Facchetti F, Foucar K, Gangat N, Gianelli U, Godley LA, Gökbuget N, Gotlib J, Hellström-Lindberg E, Hobbs GS, Hoffman R, Jabbour EJ, Kiladjian JJ, Larson RA, Le Beau MM, Loh ML, Löwenberg B, Macintyre E, Malcovati L, Mullighan CG, Niemeyer C, Odenike OM, Ogawa S, Orfao A, Papaemmanuil E, Passamonti F, Porkka K, Pui CH, Radich JP, Reiter A, Rozman M, Rudelius M, Savona MR, Schiffer CA, Schmitt-Graeff A, Shimamura A, Sierra J, Stock WA, Stone RM, Tallman MS, Thiele J, Tien HF, Tzankov A, Vannucchi AM, Vyas P, Wei AH, Weinberg OK, Wierzbowska A, Cazzola M, Döhner H, Tefferi A
International Consensus Classification of Myeloid Neoplasms and Acute Leukemias: integrating morphologic, clinical, and genomic data. Blood. 2022 09 15; 140(11):1200-1228.
International Consensus Classification of Myeloid Neoplasms and Acute Leukemias: integrating morphologic, clinical, and genomic data.
Nardi V, McAfee SL, Dal Cin P, Tsai HK, Amrein PC, Hobbs GS, Brunner AM, Narayan R, Foster J, Fathi AT, Hock H
Chemotherapy Resistance in B-ALL with Cryptic NUP214-ABL1 Is Amenable to Kinase Inhibition and Immunotherapy. Oncologist. 2022 03 04; 27(2):82-86.
Chemotherapy Resistance in B-ALL with Cryptic NUP214-ABL1 Is Amenable to Kinase Inhibition and Immunotherapy.
Acosta AM, Bridge JA, Dal Cin PS, Sholl LM, Cornejo KM, Fletcher CDM, Ulbright TM
Inflammatory and Nested Testicular Sex Cord Tumor: A Novel Neoplasm With Aggressive Clinical Behavior and Frequent EWSR1::ATF1 Gene Fusions. Am J Surg Pathol. 2023 04 01; 47(4):504-517.
Inflammatory and Nested Testicular Sex Cord Tumor: A Novel Neoplasm With Aggressive Clinical Behavior and Frequent EWSR1::ATF1 Gene Fusions.
Richardson ET, Selenica P, Pareja F, Cin PD, Hanlon E, Weigelt B, Reis-Filho JS, Hornick JL, Jo VY, Schnitt SJ
NR4A3 Expression Is Consistently Absent in Acinic Cell Carcinomas of the Breast: A Potential Nosologic Shift. Mod Pathol. 2023 06; 36(6):100144.
NR4A3 Expression Is Consistently Absent in Acinic Cell Carcinomas of the Breast: A Potential Nosologic Shift.
Wu G, Yoshida N, Liu J, Zhang X, Xiong Y, Heavican-Foral TB, Mandato E, Liu H, Nelson GM, Yang L, Chen R, Donovan KA, Jones MK, Roshal M, Zhang Y, Xu R, Nirmal AJ, Jain S, Leahy C, Jones KL, Stevenson KE, Galasso N, Ganesan N, Chang T, Wu WC, Louissaint A, Debaize L, Yoon H, Dal Cin P, Chan WC, Ho Sui SJ, Ng SY, Feldman AL, Horwitz SM, Adelman K, Fischer ES, Chen CW, Weinstock DM, Brown M
TP63 fusions drive multicomplex enhancer rewiring, lymphomagenesis, and EZH2 dependence. Sci Transl Med. 2023 09 20; 15(714):eadi7244.
TP63 fusions drive multicomplex enhancer rewiring, lymphomagenesis, and EZH2 dependence.
AlJabban A, Paik H, Aster JC, Berliner N, Brouillard J, Brown JR, Burns KH, Castillo JJ, Card J, Dal Cin P, DeAngelo DJ, Dorfman DM, Ebert BL, Garcia JS, Jacobson CA, Lakhani H, Laubach JP, Ligon AH, Lindeman NI, Lindsley RC, Lovitch SB, Luskin MR, Morgan EA, Nowak A, Petrides A, Pinkus GS, Pozdnyakova O, Steensma DP, Stone RM, Weinberg OK, Winer ES, Kim AS
Optimization of Advanced Molecular Genetic Testing Utilization in Hematopathology: A Goldilocks Approach to Bone Marrow Testing. JCO Oncol Pract. 2024 02; 20(2):220-227.
Optimization of Advanced Molecular Genetic Testing Utilization in Hematopathology: A Goldilocks Approach to Bone Marrow Testing.
Pérez Carretero C, González T, Quijada Álamo M, Rigolin GM, Dubuc A, Villaverde Ramiro Á, Rodríguez-Sánchez A, Rubio A, Dávila J, Vidal MJ, González Gascón Y Marín I, Hernández-Rivas JÁ, Benito R, Volpe V, Davids MS, Abramson JS, Cuneo A, Dal Cin P, Rodríguez-Vicente AE, Hernández-Rivas JM
Chronic lymphocytic leukemia patients with chromosome 6q deletion as the sole cytogenetic abnormality display a high frequency of RPS15 mutations and have a poor prognosis. Am J Hematol. 2024 Sep; 99(9):1845-1848.
Chronic lymphocytic leukemia patients with chromosome 6q deletion as the sole cytogenetic abnormality display a high frequency of RPS15 mutations and have a poor prognosis.
Jo VY, Antonescu CR, Zhang L, Dal Cin P, Hornick JL, Fletcher CD
Cutaneous syncytial myoepithelioma: clinicopathologic characterization in a series of 38 cases. Am J Surg Pathol. 2013 May; 37(5):710-8.
Cutaneous syncytial myoepithelioma: clinicopathologic characterization in a series of 38 cases.
The marriage of cytology and cytogenetics. Cancer Cytopathol. 2013 Jun; 121(6):279-90.
The marriage of cytology and cytogenetics.
ALK as a paradigm of oncogenic promiscuity: different mechanisms of activation and different fusion partners drive tumors of different lineages. Cancer Genet. 2013 Nov; 206(11):357-73.
ALK as a paradigm of oncogenic promiscuity: different mechanisms of activation and different fusion partners drive tumors of different lineages.
Sadrzadeh H, Kerr DA, Dal Cin P, Lindeman NI, Hasserjian RP, Ballen KK, Fathi AT
A unique PML-RARa rearrangement involving chromosomes 11, 15, and 17 in a patient with acute promyelocytic leukemia. Exp Hematol. 2013 Sep; 41(9):769-71.
A unique PML-RARa rearrangement involving chromosomes 11, 15, and 17 in a patient with acute promyelocytic leukemia.
Odintsov I, Kleijn TG, Ryall ST, Ameline B, Dong F, Szuhai K, Baumhoer D, Dal Cin P, Cleven AHG, Papke DJ
Odontogenic Myxoma Harbors Widespread Loss of Heterozygosity and Not Trisomies. Am J Surg Pathol. 2025 May 01; 49(5):523-525.
Odontogenic Myxoma Harbors Widespread Loss of Heterozygosity and Not Trisomies.
Boni A, Lisovsky M, Dal Cin P, Rosenberg AE, Srivastava A
Atypical lipomatous tumor mimicking giant fibrovascular polyp of the esophagus: report of a case and a critical review of literature. Hum Pathol. 2013 Jun; 44(6):1165-70.
Atypical lipomatous tumor mimicking giant fibrovascular polyp of the esophagus: report of a case and a critical review of literature.
Zhao M, Ryall S, Brody SJ, Harris AC, Cabral K, Brownstein C, Kim JC, Smith AC, Dal Cin P, Narayan R, Sikkink K, Schmitt A, Hobbs GS, Fathi AT, Griffin GK, Sait SNJ, Iafrate AJ, Aster JC, Graubert TA, Nardi V, Dubuc AM
Integrative cytogenetic and molecular studies unmask "chromosomal mimicry" in hematologic malignancies. Blood Adv. 2025 Mar 11; 9(5):1003-1012.
Integrative cytogenetic and molecular studies unmask "chromosomal mimicry" in hematologic malignancies.
Fitzpatrick MJ, Yuan J, Capa I, Bledsoe JR, Kibler CE, Tucker C, Shuai W, Matsumoto NP, Zhu GG, Ding Y, Wu X, Wang W, Hu Z, Jiang L, Jia Y, Zhao Y, Lin Y, Tian X, Galliani CA, Venkataraman G, Mehrotra S, Dal Cin P, Haag MM, Siegele B, Zhang W, Wang E, Castañeda-Sánchez I, Zhang QY, Perez-Atayde AR, Young KH, Sadigh S, Wang HY, Hasserjian RP, Medeiros LJ, Pan Z
Erythroblastic Sarcoma in Adults and Children: Different Pathways to the Same Destination. Mod Pathol. 2025 Aug; 38(8):100716.
Erythroblastic Sarcoma in Adults and Children: Different Pathways to the Same Destination.
Promiscuous genes involved in recurrent chromosomal translocations in soft tissue tumours. Pathology. 2014 Feb; 46(2):105-12.
Promiscuous genes involved in recurrent chromosomal translocations in soft tissue tumours.
Schoolmeester JK, Howitt BE, Hirsch MS, Dal Cin P, Quade BJ, Nucci MR
Perivascular epithelioid cell neoplasm (PEComa) of the gynecologic tract: clinicopathologic and immunohistochemical characterization of 16 cases. Am J Surg Pathol. 2014 Feb; 38(2):176-88.
Perivascular epithelioid cell neoplasm (PEComa) of the gynecologic tract: clinicopathologic and immunohistochemical characterization of 16 cases.
La Starza R, Barba G, Nofrini V, Pierini T, Pierini V, Marcomigni L, Perruccio K, Matteucci C, Storlazzi CT, Daniele G, Crescenzi B, Giansanti M, Giovenali P, Dal Cin P, Mecucci C
Multiple EWSR1-WT1 and WT1-EWSR1 copies in two cases of desmoplastic round cell tumor. Cancer Genet. 2013 Nov; 206(11):387-92.
Multiple EWSR1-WT1 and WT1-EWSR1 copies in two cases of desmoplastic round cell tumor.
Mariño-Enríquez A, Hornick JL, Dal Cin P, Cibas ES, Qian X
Dedifferentiated liposarcoma and pleomorphic liposarcoma: a comparative study of cytomorphology and MDM2/CDK4 expression on fine-needle aspiration. Cancer Cytopathol. 2014 Feb; 122(2):128-37.
Dedifferentiated liposarcoma and pleomorphic liposarcoma: a comparative study of cytomorphology and MDM2/CDK4 expression on fine-needle aspiration.
Puliyel MM, Mascarenhas L, Zhou S, Sapra A, Dal Cin P, French CA, Venkatramani R
Nuclear protein in testis midline carcinoma misdiagnosed as adamantinoma. J Clin Oncol. 2014 May 20; 32(15):e57-60.
Nuclear protein in testis midline carcinoma misdiagnosed as adamantinoma.
Yuen LD, Hasserjian RP, Fathi AT, Luskin MR, Winer ES, Dal Cin P, Kim AS, Lindsley RC, Tsai HK, Nardi V
Strategies for identifying NUP98 rearrangements in adult myeloid neoplasms. Haematologica. 2026 Feb 01; 111(2):518-534.
Strategies for identifying NUP98 rearrangements in adult myeloid neoplasms.
French CA, Rahman S, Walsh EM, Kühnle S, Grayson AR, Lemieux ME, Grunfeld N, Rubin BP, Antonescu CR, Zhang S, Venkatramani R, Dal Cin P, Howley PM
NSD3-NUT fusion oncoprotein in NUT midline carcinoma: implications for a novel oncogenic mechanism. Cancer Discov. 2014 Aug; 4(8):928-41.
NSD3-NUT fusion oncoprotein in NUT midline carcinoma: implications for a novel oncogenic mechanism.
Wu RI, Schorge JO, Dal Cin P, Cin PD, Young RH, Oliva E
International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists
Müllerian adenosarcoma of the uterus with low-grade sarcomatous overgrowth characterized by prominent hydropic change resulting in mimicry of a smooth muscle tumor. Int J Gynecol Pathol. 2014 Nov; 33(6):573-80.
Müllerian adenosarcoma of the uterus with low-grade sarcomatous overgrowth characterized by prominent hydropic change resulting in mimicry of a smooth muscle tumor.
Wojcik JB, Bellizzi AM, Dal Cin P, Bredella MA, Fletcher CD, Hornicek FJ, Deshpande V, Hornick JL, Nielsen GP
Primary sclerosing epithelioid fibrosarcoma of bone: analysis of a series. Am J Surg Pathol. 2014 Nov; 38(11):1538-44.
Primary sclerosing epithelioid fibrosarcoma of bone: analysis of a series.
Doyle LA, Wong KK, Bueno R, Dal Cin P, Fletcher JA, Sholl LM, Kuo F
Ewing sarcoma mimicking atypical carcinoid tumor: detection of unexpected genomic alterations demonstrates the use of next generation sequencing as a diagnostic tool. Cancer Genet. 2014 Jul-Aug; 207(7-8):335-9.
Ewing sarcoma mimicking atypical carcinoid tumor: detection of unexpected genomic alterations demonstrates the use of next generation sequencing as a diagnostic tool.
Howitt BE, Sholl LM, Dal Cin P, Jia Y, Yuan L, MacConaill L, Lindeman N, Kuo F, Garcia E, Nucci MR, Quade BJ
Targeted genomic analysis of Müllerian adenosarcoma. J Pathol. 2015 Jan; 235(1):37-49.
Targeted genomic analysis of Müllerian adenosarcoma.
Carey CD, Gusenleitner D, Chapuy B, Kovach AE, Kluk MJ, Sun HH, Crossland RE, Bacon CM, Rand V, Dal Cin P, Le LP, Neuberg D, Sohani AR, Shipp MA, Monti S, Rodig SJ
The Journal of molecular diagnostics : JMD
Molecular classification of MYC-driven B-cell lymphomas by targeted gene expression profiling of fixed biopsy specimens. J Mol Diagn. 2015 Jan; 17(1):19-30.
Molecular classification of MYC-driven B-cell lymphomas by targeted gene expression profiling of fixed biopsy specimens.
Movassaghian M, Sohani AR, McAfee SL, Perry AM, Dal Cin P, McLaughlin C, Fathi AT
Chromosome 17p deletion in a case of T-cell acute lymphoblastic lymphoma. Am J Hematol. 2015 Mar; 90(3):267-8.
Chromosome 17p deletion in a case of T-cell acute lymphoblastic lymphoma.
Jacobsen E, Pozdnyakova O, Redd R, Fisher DC, Dorfman DM, Dal Cin P, LaCasce A, Armand P, Hochberg E, Cote G, Shahsafaei A, Neuberg D, Brown JR, Freedman AS
Imatinib mesylate lacks efficacy in relapsed/refractory peripheral T cell lymphoma. Leuk Lymphoma. 2015 Apr; 56(4):993-8.
Imatinib mesylate lacks efficacy in relapsed/refractory peripheral T cell lymphoma.
Jalbut MM, Sohani AR, Dal Cin P, Hasserjian RP, Moran JA, Brunner AM, Fathi AT
Acute myeloid leukemia in a patient with constitutional 47,XXY karyotype. Leuk Res Rep. 2015; 4(1):28-30.
Acute myeloid leukemia in a patient with constitutional 47,XXY karyotype.
Cleven AH, Nardi V, Ok CY, Goswami M, Dal Cin P, Zheng Z, Iafrate AJ, Abdul Hamid MA, Wang SA, Hasserjian RP
High p53 protein expression in therapy-related myeloid neoplasms is associated with adverse karyotype and poor outcome. Mod Pathol. 2015 Apr; 28(4):552-63.
High p53 protein expression in therapy-related myeloid neoplasms is associated with adverse karyotype and poor outcome.
Hornick JL, Sholl LM, Dal Cin P, Childress MA, Lovly CM
Expression of ROS1 predicts ROS1 gene rearrangement in inflammatory myofibroblastic tumors. Mod Pathol. 2015 May; 28(5):732-9.
Expression of ROS1 predicts ROS1 gene rearrangement in inflammatory myofibroblastic tumors.
Nardi V, Pulluqi O, Abramson JS, Dal Cin P, Hasserjian RP
Routine conventional karyotyping of lymphoma staging bone marrow samples does not contribute clinically relevant information. Am J Hematol. 2015 Jun; 90(6):529-33.
Routine conventional karyotyping of lymphoma staging bone marrow samples does not contribute clinically relevant information.
Parra-Herran C, Quick CM, Howitt BE, Dal Cin P, Quade BJ, Nucci MR
Inflammatory myofibroblastic tumor of the uterus: clinical and pathologic review of 10 cases including a subset with aggressive clinical course. Am J Surg Pathol. 2015 Feb; 39(2):157-68.
Inflammatory myofibroblastic tumor of the uterus: clinical and pathologic review of 10 cases including a subset with aggressive clinical course.
Davids MS, Vartanov A, Werner L, Neuberg D, Dal Cin P, Brown JR
Controversial fluorescence in situ hybridization cytogenetic abnormalities in chronic lymphocytic leukaemia: new insights from a large cohort. Br J Haematol. 2015 Sep; 170(5):694-703.
Controversial fluorescence in situ hybridization cytogenetic abnormalities in chronic lymphocytic leukaemia: new insights from a large cohort.
Schoolmeester JK, Sciallis AP, Greipp PT, Hodge JC, Dal Cin P, Keeney GL, Nucci MR
Analysis of MDM2 Amplification in 43 Endometrial Stromal Tumors: A Potential Diagnostic Pitfall. Int J Gynecol Pathol. 2015 Nov; 34(6):576-83.
Analysis of MDM2 Amplification in 43 Endometrial Stromal Tumors: A Potential Diagnostic Pitfall.
Mandelker D, Dal Cin P, Jacene HA, Armand P, Stone RM, Lindeman NI
Refractory myeloid sarcoma with a FIP1L1-PDGFRA rearrangement detected by clinical high throughput somatic sequencing. Exp Hematol Oncol. 2015; 4:30.
Refractory myeloid sarcoma with a FIP1L1-PDGFRA rearrangement detected by clinical high throughput somatic sequencing.
Mirkovic J, Sholl LM, Garcia E, Lindeman N, MacConaill L, Hirsch M, Dal Cin P, Gorman M, Barletta JA, Nucci MR, McCluggage WG, Howitt BE
Targeted genomic profiling reveals recurrent KRAS mutations and gain of chromosome 1q in mesonephric carcinomas of the female genital tract. Mod Pathol. 2015 Nov; 28(11):1504-14.
Targeted genomic profiling reveals recurrent KRAS mutations and gain of chromosome 1q in mesonephric carcinomas of the female genital tract.
Adult Renal Cell Carcinoma: A Review of Established Entities from Morphology to Molecular Genetics. Surg Pathol Clin. 2015 Dec; 8(4):587-621.
Adult Renal Cell Carcinoma: A Review of Established Entities from Morphology to Molecular Genetics.
De Rienzo A, Archer MA, Yeap BY, Dao N, Sciaranghella D, Sideris AC, Zheng Y, Holman AG, Wang YE, Dal Cin PS, Fletcher JA, Rubio R, Croft L, Quackenbush J, Sugarbaker PE, Munir KJ, Battilana JR, Gustafson CE, Chirieac LR, Ching SM, Wong J, Tay LC, Rudd S, Hercus R, Sugarbaker DJ, Richards WG, Bueno R
Gender-Specific Molecular and Clinical Features Underlie Malignant Pleural Mesothelioma. Cancer Res. 2016 Jan 15; 76(2):319-28.
Gender-Specific Molecular and Clinical Features Underlie Malignant Pleural Mesothelioma.
Cytogenetics of Mesenchymal Tumors of the Female Genital Tract. Surg Pathol Clin. 2009 Dec; 2(4):813-21.
Cytogenetics of Mesenchymal Tumors of the Female Genital Tract.
Parra-Herran C, Schoolmeester JK, Yuan L, Dal Cin P, Fletcher CD, Quade BJ, Nucci MR
Myxoid Leiomyosarcoma of the Uterus: A Clinicopathologic Analysis of 30 Cases and Review of the Literature With Reappraisal of Its Distinction From Other Uterine Myxoid Mesenchymal Neoplasms. Am J Surg Pathol. 2016 Mar; 40(3):285-301.
Myxoid Leiomyosarcoma of the Uterus: A Clinicopathologic Analysis of 30 Cases and Review of the Literature With Reappraisal of Its Distinction From Other Uterine Myxoid Mesenchymal Neoplasms.
Giersch ABS, Bieber FR, Dubuc AM, Fletcher JA, Ligon AH, Mason-Suares H, Morton CC, Weremowicz S, Xiao S, Cin PD
Reporting of Diagnostic Cytogenetic Results. Curr Protoc Hum Genet. 2016 Apr 01; 89:A.1D.1-A.1D.23.
Van Dyke DL, Werner L, Rassenti LZ, Neuberg D, Ghia E, Heerema NA, Dal Cin P, Dell Aquila M, Sreekantaiah C, Greaves AW, Kipps TJ, Kay NE
The Dohner fluorescence in situ hybridization prognostic classification of chronic lymphocytic leukaemia (CLL): the CLL Research Consortium experience. Br J Haematol. 2016 Apr; 173(1):105-13.
The Dohner fluorescence in situ hybridization prognostic classification of chronic lymphocytic leukaemia (CLL): the CLL Research Consortium experience.
Kluk MJ, Ho C, Yu H, Chen BJ, Neuberg DS, Dal Cin P, Woda BA, Pinkus GS, Rodig SJ
MYC Immunohistochemistry to Identify MYC-Driven B-Cell Lymphomas in Clinical Practice. Am J Clin Pathol. 2016 Feb; 145(2):166-79.
MYC Immunohistochemistry to Identify MYC-Driven B-Cell Lymphomas in Clinical Practice.
Ordulu Z, Nucci MR, Dal Cin P, Hollowell ML, Otis CN, Hornick JL, Park PJ, Kim TM, Quade BJ, Morton CC
Intravenous leiomyomatosis: an unusual intermediate between benign and malignant uterine smooth muscle tumors. Mod Pathol. 2016 05; 29(5):500-10.
Intravenous leiomyomatosis: an unusual intermediate between benign and malignant uterine smooth muscle tumors.
Kluk MJ, Abo RP, Brown RD, Kuo FC, Dal Cin P, Pozdnyakova O, Morgan EA, Lindeman NI, DeAngelo DJ, Aster JC
Myeloid neoplasm demonstrating a STAT5B-RARA rearrangement and genetic alterations associated with all-trans retinoic acid resistance identified by a custom next-generation sequencing assay. Cold Spring Harb Mol Case Stud. 2015 Oct; 1(1):a000307.
Myeloid neoplasm demonstrating a STAT5B-RARA rearrangement and genetic alterations associated with all-trans retinoic acid resistance identified by a custom next-generation sequencing assay.
Burger JA, Landau DA, Taylor-Weiner A, Bozic I, Zhang H, Sarosiek K, Wang L, Stewart C, Fan J, Hoellenriegel J, Sivina M, Dubuc AM, Fraser C, Han Y, Li S, Livak KJ, Zou L, Wan Y, Konoplev S, Sougnez C, Brown JR, Abruzzo LV, Carter SL, Keating MJ, Davids MS, Wierda WG, Cibulskis K, Zenz T, Werner L, Dal Cin P, Kharchencko P, Neuberg D, Kantarjian H, Lander E, Gabriel S, O'Brien S, Letai A, Weitz DA, Nowak MA, Getz G, Wu CJ
Clonal evolution in patients with chronic lymphocytic leukaemia developing resistance to BTK inhibition. Nat Commun. 2016 05 20; 7:11589.
Clonal evolution in patients with chronic lymphocytic leukaemia developing resistance to BTK inhibition.
Wang SA, Tam W, Tsai AG, Arber DA, Hasserjian RP, Geyer JT, George TI, Czuchlewski DR, Foucar K, Rogers HJ, Hsi ED, Bryan Rea B, Bagg A, Dal Cin P, Zhao C, Kelley TW, Verstovsek S, Bueso-Ramos C, Orazi A
Targeted next-generation sequencing identifies a subset of idiopathic hypereosinophilic syndrome with features similar to chronic eosinophilic leukemia, not otherwise specified. Mod Pathol. 2016 08; 29(8):854-64.
Targeted next-generation sequencing identifies a subset of idiopathic hypereosinophilic syndrome with features similar to chronic eosinophilic leukemia, not otherwise specified.
Dubuc AM, Davids MS, Pulluqi M, Pulluqi O, Hoang K, Hernandez-Sánchez JM, Schlich C, Hernández-Rivas JM, Brown JR, Dal Cin P
FISHing in the dark: How the combination of FISH and conventional karyotyping improves the diagnostic yield in CpG-stimulated chronic lymphocytic leukemia. Am J Hematol. 2016 10; 91(10):978-83.
FISHing in the dark: How the combination of FISH and conventional karyotyping improves the diagnostic yield in CpG-stimulated chronic lymphocytic leukemia.
Wang SA, Patel KP, Pozdnyakova O, Peng J, Zuo Z, Dal Cin P, Steensma DP, Hasserjian RP
Acute erythroid leukemia with <20% bone marrow blasts is clinically and biologically similar to myelodysplastic syndrome with excess blasts. Mod Pathol. 2016 10; 29(10):1221-31.
Acute erythroid leukemia with <20% bone marrow blasts is clinically and biologically similar to myelodysplastic syndrome with excess blasts.
Mason EF, Brown RD, Szeto DP, Gibson CJ, Jia Y, Garcia EP, Jacobson CA, Dal Cin P, Kuo FC, Pinkus GS, Lindeman NI, Sholl LM, Aster JC, Morgan EA
Detection of activating MAP2K1 mutations in atypical hairy cell leukemia and hairy cell leukemia variant. Leuk Lymphoma. 2017 01; 58(1):233-236.
Detection of activating MAP2K1 mutations in atypical hairy cell leukemia and hairy cell leukemia variant.
Conventional cytogenetics for myeloid neoplasms in the era of next-generation-sequencing. Am J Hematol. 2017 03; 92(3):227-229.
Conventional cytogenetics for myeloid neoplasms in the era of next-generation-sequencing.
Petrova-Drus K, Hasserjian R, Pozdnyakova O, Dal Cin P, Mathew S, Margolskee E, Orazi A, Geyer JT
Clinicopathologic evaluation of cytopenic patients with isolated trisomy 8: a detailed comparison between idiopathic cytopenia of unknown significance and low-grade myelodysplastic syndrome. Leuk Lymphoma. 2017 03; 58(3):569-577.
Clinicopathologic evaluation of cytopenic patients with isolated trisomy 8: a detailed comparison between idiopathic cytopenia of unknown significance and low-grade myelodysplastic syndrome.
Sciot R, Dal Cin P, Fletcher CD, De Wever I, De Vos R, Van Damme B, Van den Berghe H
Monosomy 22 in a malignant peripheral nerve sheath tumour of the kidney in childhood: a genetic link with other malignant paediatric renal neoplasms? Histopathology. 1995 Oct; 27(4):373-6.
Monosomy 22 in a malignant peripheral nerve sheath tumour of the kidney in childhood: a genetic link with other malignant paediatric renal neoplasms?
Dal Cin P, Van Poppel H, Sciot R, De Vos R, Van Damme B, Baert L, Van den Berghe H
The t(1;12)(p36;q13) in a renal oncocytoma. Genes Chromosomes Cancer. 1996 Oct; 17(2):136-9.
The t(1;12)(p36;q13) in a renal oncocytoma.
Rosai J, Akerman M, Dal Cin P, DeWever I, Fletcher CD, Mandahl N, Mertens F, Mitelman F, Rydholm A, Sciot R, Tallini G, Van den Berghe H, Van de Ven W, Vanni R, Willen H
Combined morphologic and karyotypic study of 59 atypical lipomatous tumors. Evaluation of their relationship and differential diagnosis with other adipose tissue tumors (a report of the CHAMP Study Group). Am J Surg Pathol. 1996 Oct; 20(10):1182-9.
Combined morphologic and karyotypic study of 59 atypical lipomatous tumors. Evaluation of their relationship and differential diagnosis with other adipose tissue tumors (a report of the CHAMP Study Group).
Brosens I, Johannisson E, Dal Cin P, Deprest J, Van den Berghe H
Analysis of the karyotype and desoxyribonucleic acid content of uterine myomas in premenopausal, menopausal, and gonadotropin-releasing hormone agonist-treated females. Fertil Steril. 1996 Sep; 66(3):376-9.
Analysis of the karyotype and desoxyribonucleic acid content of uterine myomas in premenopausal, menopausal, and gonadotropin-releasing hormone agonist-treated females.
Mandahl N, Akerman M, Aman P, Dal Cin P, De Wever I, Fletcher CD, Mertens F, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, Van den Berghe H, Van de Ven W, Vanni R, Willén H
Duplication of chromosome segment 12q15-24 is associated with atypical lipomatous tumors: a report of the CHAMP collaborative study group. CHromosomes And MorPhology. Int J Cancer. 1996 Sep 04; 67(5):632-5.
Duplication of chromosome segment 12q15-24 is associated with atypical lipomatous tumors: a report of the CHAMP collaborative study group. CHromosomes And MorPhology.
Tallini G, Akerman M, Dal Cin P, De Wever I, Fletcher CD, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Sciot R, Van den Berghe H, Van den Ven W, Vanni R, Willen H
Combined morphologic and karyotypic study of 28 myxoid liposarcomas. Implications for a revised morphologic typing, (a report from the CHAMP Group). Am J Surg Pathol. 1996 Sep; 20(9):1047-55.
Combined morphologic and karyotypic study of 28 myxoid liposarcomas. Implications for a revised morphologic typing, (a report from the CHAMP Group).
Pauwels P, Dal Cin P, Van de Moosdijk CN, Vrints L, Sciot R, Van den Berghe H
Cytogenetics revealing the diagnosis in a metastatic endometrial stromal sarcoma. Histopathology. 1996 Jul; 29(1):84-7.
Dal Cin P, Sciot R, de Wever I, Brock P, Casteels-Van Daele M, Van Damme B, Van Den Berghe H
Cytogenetic and immunohistochemical evidence that giant cell fibroblastoma is related to dermatofibrosarcoma protuberans. Genes Chromosomes Cancer. 1996 Jan; 15(1):73-5.
Cytogenetic and immunohistochemical evidence that giant cell fibroblastoma is related to dermatofibrosarcoma protuberans.
Cuneo A, Ferrant A, Michaux JL, Demuynck H, Boogaerts M, Louwagie A, Doyen C, Stul M, Cassiman JJ, Dal Cin P, Castoldi G, Van den Berghe H
Philadelphia chromosome-positive acute myeloid leukemia: cytoimmunologic and cytogenetic features. Haematologica. 1996 Sep-Oct; 81(5):423-7.
Philadelphia chromosome-positive acute myeloid leukemia: cytoimmunologic and cytogenetic features.
Dal Cin P, Qi H, Sciot R, Van den Berghe H
Involvement of chromosomes 6 and 11 in a soft tissue chondroma. Cancer Genet Cytogenet. 1997 Feb; 93(2):177-8.
Involvement of chromosomes 6 and 11 in a soft tissue chondroma.
Buonamici L, Roncaroli F, Frank G, Dal Cin P, Van den Berghe H, Calbucci F, Eusebi V
[Cytogenetic analysis of hypophyseal adenoma. Study of 9 cases and review of the literature]. Pathologica. 1998 Apr; 90(2):116-9.
[Cytogenetic analysis of hypophyseal adenoma. Study of 9 cases and review of the literature].
Van den Berghe I, Dal Cin P, De Groef K, Michielssen P, Van den Berghe H
Monosomy 22 and trisomy 14 may be early events in the tumorigenesis of adult granulosa cell tumor. Cancer Genet Cytogenet. 1999 Jul 01; 112(1):46-8.
Monosomy 22 and trisomy 14 may be early events in the tumorigenesis of adult granulosa cell tumor.
Tallini G, Dorfman H, Brys P, Dal Cin P, De Wever I, Fletcher CD, Jonson K, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Samson I, Sciot R, Van den Berghe H, Vanni R, Willén H
Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study Group. J Pathol. 2002 Feb; 196(2):194-203.
Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study Group.
Nilsson M, Höglund M, Panagopoulos I, Sciot R, Dal Cin P, Debiec-Rychter M, Mertens F, Mandahl N
Virchows Archiv : an international journal of pathology
Molecular cytogenetic mapping of recurrent chromosomal breakpoints in tenosynovial giant cell tumors. Virchows Arch. 2002 Nov; 441(5):475-80.
Molecular cytogenetic mapping of recurrent chromosomal breakpoints in tenosynovial giant cell tumors.
Dal Cin P, De Wever I, Aerts R, Van Damme B, Van den Berghe H
Trisomy 8 as the only chromosome change in an epithelioid smooth muscle tumor. Genes Chromosomes Cancer. 1991 May; 3(3):235-7.
Trisomy 8 as the only chromosome change in an epithelioid smooth muscle tumor.
Sciot R, Akerman M, Dal Cin P, De Wever I, Fletcher CD, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Tallini G, Van den Berghe H, Vanni R, Willen H
Cytogenetic analysis of subcutaneous angiolipoma: further evidence supporting its difference from ordinary pure lipomas: a report of the CHAMP Study Group. Am J Surg Pathol. 1997 Apr; 21(4):441-4.
Cytogenetic analysis of subcutaneous angiolipoma: further evidence supporting its difference from ordinary pure lipomas: a report of the CHAMP Study Group.
Dal Cin P, Moerman P, Christiaens MR, Van den Berghe H
Observation of a deletion of the long arm of chromosome 6 in benign fibrocystic disease of the breast constitutes a challenging problem. Genes Chromosomes Cancer. 1996 May; 16(1):68-71.
Observation of a deletion of the long arm of chromosome 6 in benign fibrocystic disease of the breast constitutes a challenging problem.
Sciot R, Rosai J, Dal Cin P, de Wever I, Fletcher CD, Mandahl N, Mertens F, Mitelman F, Rydholm A, Tallini G, van den Berghe H, Vanni R, Willén H
Analysis of 35 cases of localized and diffuse tenosynovial giant cell tumor: a report from the Chromosomes and Morphology (CHAMP) study group. Mod Pathol. 1999 Jun; 12(6):576-9.
Analysis of 35 cases of localized and diffuse tenosynovial giant cell tumor: a report from the Chromosomes and Morphology (CHAMP) study group.
Mandahl N, Fletcher CD, Dal Cin P, De Wever I, Mertens F, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, Van Den Berghe H, Vanni R, Willén H
Comparative cytogenetic study of spindle cell and pleomorphic leiomyosarcomas of soft tissues: a report from the CHAMP Study Group. Cancer Genet Cytogenet. 2000 Jan 01; 116(1):66-73.
Comparative cytogenetic study of spindle cell and pleomorphic leiomyosarcomas of soft tissues: a report from the CHAMP Study Group.
Gisselsson D, Jonson T, Petersén A, Strömbeck B, Dal Cin P, Höglund M, Mitelman F, Mertens F, Mandahl N
Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors. Proc Natl Acad Sci U S A. 2001 Oct 23; 98(22):12683-8.
Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors.
Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer
Isochromosome (12p) in germ cell tumors. Recent Results Cancer Res. 1991; 123:107-11.
Isochromosome (12p) in germ cell tumors.
Dal Cin P, Sherman L, Marzelli M, McLaughlin C, Zukerberg L, Amrein PC
A new case of t(11;17)(q23;q21) with MLL rearrangement. Cancer Genet Cytogenet. 2004 Jan 15; 148(2):178-9.
A new case of t(11;17)(q23;q21) with MLL rearrangement.
Oliveira AM, Perez-Atayde AR, Dal Cin P, Gebhardt MC, Chen CJ, Neff JR, Demetri GD, Rosenberg AE, Bridge JA, Fletcher JA
Aneurysmal bone cyst variant translocations upregulate USP6 transcription by promoter swapping with the ZNF9, COL1A1, TRAP150, and OMD genes. Oncogene. 2005 May 12; 24(21):3419-26.
Aneurysmal bone cyst variant translocations upregulate USP6 transcription by promoter swapping with the ZNF9, COL1A1, TRAP150, and OMD genes.
Dal Cin P, Van den Berghe H, Sciot R, de Wever I
Deletion of the long arm of chromosome 7 in lipoma. Cancer Genet Cytogenet. 1997 Jul 01; 96(1):85-6.
Deletion of the long arm of chromosome 7 in lipoma.
Dal Cin P, Stas M, Sciot R, De Wever I, Van Damme B, Van den Berghe H
Translocation (X;1) reveals metastasis 31 years after renal cell carcinoma. Cancer Genet Cytogenet. 1998 Feb; 101(1):58-61.
Translocation (X;1) reveals metastasis 31 years after renal cell carcinoma.
Dal Cin P, Aly MS, Delabie J, Ceuppens JL, Van Gool S, Van Damme B, Baert L, Van Poppel H, Van den Berghe H
Trisomy 7 and trisomy 10 characterize subpopulations of tumor-infiltrating lymphocytes in kidney tumors and in the surrounding kidney tissue. Proc Natl Acad Sci U S A. 1992 Oct 15; 89(20):9744-8.
Trisomy 7 and trisomy 10 characterize subpopulations of tumor-infiltrating lymphocytes in kidney tumors and in the surrounding kidney tissue.
Howitt BE, Dal Cin P, Nucci MR, Quade BJ
Involvement of Chromosome 8 in Müllerian Adenosarcoma. Int J Gynecol Pathol. 2017 Jan; 36(1):24-30.
Involvement of Chromosome 8 in Müllerian Adenosarcoma.
Buonamici L, Roncaroli F, Fioravanti A, Losi L, Van den Berghe H, Calbucci F, Dal Cin P
Cytogenetic investigation of chordomas of the skull. Cancer Genet Cytogenet. 1999 Jul 01; 112(1):49-52.
Cytogenetic investigation of chordomas of the skull.
Dal Cin P, Sciot R, Brys P, De Wever I, Dorfman H, Fletcher CD, Jonsson K, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Samson I, Tallini G, Van den Berghe H, Vanni R, Willen H
Recurrent chromosome aberrations in fibrous dysplasia of the bone: a report of the CHAMP study group. CHromosomes And MorPhology. Cancer Genet Cytogenet. 2000 Oct 01; 122(1):30-2.
Recurrent chromosome aberrations in fibrous dysplasia of the bone: a report of the CHAMP study group. CHromosomes And MorPhology.
Kazmierczak B, Dal Cin P, Wanschura S, Bartnitzke S, Van den Berghe H, Bullerdiek J
Cloning and molecular characterization of part of a new gene fused to HMGIC in mesenchymal tumors. Am J Pathol. 1998 Feb; 152(2):431-5.
Cloning and molecular characterization of part of a new gene fused to HMGIC in mesenchymal tumors.
Dal Cin P, Pauwels P, Moerman P, Qi H, Van Den Berghe H
Hyperdiploidy in benign breast lesions. Cancer Genet Cytogenet. 1998 Mar; 101(2):162-3.
Mertens F, Fletcher CD, Dal Cin P, De Wever I, Mandahl N, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, Van den Berghe H, Vanni R, Willén H
Cytogenetic analysis of 46 pleomorphic soft tissue sarcomas and correlation with morphologic and clinical features: a report of the CHAMP Study Group. Chromosomes and MorPhology. Genes Chromosomes Cancer. 1998 May; 22(1):16-25.
Cytogenetic analysis of 46 pleomorphic soft tissue sarcomas and correlation with morphologic and clinical features: a report of the CHAMP Study Group. Chromosomes and MorPhology.
Dal Cin P, Timmerman D, Van den Berghe I, Wanschura S, Kazmierczak B, Vergote I, Deprest J, Neven P, Moerman P, Bullerdiek J, Van den Berghe H
Genomic changes in endometrial polyps associated with tamoxifen show no evidence for its action as an external carcinogen. Cancer Res. 1998 Jun 01; 58(11):2278-81.
Genomic changes in endometrial polyps associated with tamoxifen show no evidence for its action as an external carcinogen.
Sciot R, Dal Cin P, Bellemans J, Samson I, Van den Berghe H, Van Damme B
Synovial chondromatosis: clonal chromosome changes provide further evidence for a neoplastic disorder. Virchows Arch. 1998 Aug; 433(2):189-91.
Synovial chondromatosis: clonal chromosome changes provide further evidence for a neoplastic disorder.
Losi L, Polito P, Hagemeijer A, Buonamici L, Van den Berghe H, Dal Cin P
Intracranial germ cell tumour (embryonal carcinoma with teratoma) with complex karyotype including isochromosome 12p. Virchows Arch. 1998 Dec; 433(6):571-4.
Intracranial germ cell tumour (embryonal carcinoma with teratoma) with complex karyotype including isochromosome 12p.
Dal Cin P, Aly MS, De Wever I, Moerman P, Van Den Berghe H
Endometrial stromal sarcoma t(7;17)(p15-21;q12-21) is a nonrandom chromosome change. Cancer Genet Cytogenet. 1992 Oct 01; 63(1):43-6.
Endometrial stromal sarcoma t(7;17)(p15-21;q12-21) is a nonrandom chromosome change.
Polito P, Dal Cin P, Kazmierczak B, Rogalla P, Bullerdiek J, Van den Berghe H
Deletion of HMG17 in uterine leiomyomas with ring chromosome 1. Cancer Genet Cytogenet. 1999 Jan 15; 108(2):107-9.
Deletion of HMG17 in uterine leiomyomas with ring chromosome 1.
Vanni R, Marras S, Faa G, Uccheddu A, Dal Cin P, Sciot R, Samson I, Van den Berghe H
Chromosome instability in elastofibroma. Cancer Genet Cytogenet. 1999 Jun; 111(2):182-3.
Chromosome instability in elastofibroma.
Van den Hove LE, Van Gool SW, Van Poppel H, Baert L, Coorevits L, Van Damme B, Dal Cin P, Van den Berghe H, Ceuppens JL
Identification of an enriched CD4+ CD8alpha++ CD8beta+ T-cell subset among tumor-infiltrating lymphocytes in human renal cell carcinoma. Int J Cancer. 1997 Apr 10; 71(2):178-82.
Identification of an enriched CD4+ CD8alpha++ CD8beta+ T-cell subset among tumor-infiltrating lymphocytes in human renal cell carcinoma.
Brosens I, Deprest J, Dal Cin P, Van den Berghe H
Clinical significance of cytogenetic abnormalities in uterine myomas. Fertil Steril. 1998 Feb; 69(2):232-5.
Clinical significance of cytogenetic abnormalities in uterine myomas.
Dal Cin P, Lipcsei G, Hermand G, Boniver J, Van den Berghe H
Congenital mesoblastic nephroma and trisomy 11. Cancer Genet Cytogenet. 1998 May; 103(1):68-70.
Congenital mesoblastic nephroma and trisomy 11.
Gisselsson D, Höglund M, Mertens F, Johansson B, Dal Cin P, Van den Berghe H, Earnshaw WC, Mitelman F, Mandahl N
The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells. Hum Genet. 1999 Apr; 104(4):315-25.
The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells.
Solitary fibrous tumour of the pleura with t(4;15)(q13;q26) Histopathology. 1999 Jul; 35(1):94-5.
Solitary fibrous tumour of the pleura with t(4;15)(q13;q26)
Kazmierczak B, Dal Cin P, Sciot R, Van den Berghe H, Bullerdiek J
Inflammatory myofibroblastic tumor with HMGIC rearrangement. Cancer Genet Cytogenet. 1999 Jul 15; 112(2):156-60.
Inflammatory myofibroblastic tumor with HMGIC rearrangement.
Quade BJ, Dal Cin P, Neskey DM, Weremowicz S, Morton CC
Intravenous leiomyomatosis: molecular and cytogenetic analysis of a case. Mod Pathol. 2002 Mar; 15(3):351-6.
Intravenous leiomyomatosis: molecular and cytogenetic analysis of a case.
Mariño-Enríquez A, Fletcher CD, Dal Cin P, Hornick JL
Dedifferentiated liposarcoma with "homologous" lipoblastic (pleomorphic liposarcoma-like) differentiation: clinicopathologic and molecular analysis of a series suggesting revised diagnostic criteria. Am J Surg Pathol. 2010 Aug; 34(8):1122-31.
Dedifferentiated liposarcoma with "homologous" lipoblastic (pleomorphic liposarcoma-like) differentiation: clinicopathologic and molecular analysis of a series suggesting revised diagnostic criteria.
Dal Cin P, Brock P, Casteels-Van Daele M, De Wever I, Van Damme B, Van den Berghe H
Cytogenetic characterization of congenital or infantile fibrosarcoma. Eur J Pediatr. 1991 Jun; 150(8):579-81.
Cytogenetic characterization of congenital or infantile fibrosarcoma.
Kazmierczak B, Dal Cin P, Rogalla P, Van den Berghe H, Bullerdiek J
Regional fine mapping of HMG17 to chromosomal band 1p35. Cancer Genet Cytogenet. 2000 Jan 15; 116(2):164-5.
Regional fine mapping of HMG17 to chromosomal band 1p35.
Pauwels P, Sciot R, Croiset F, Rutten H, Van den Berghe H, Dal Cin P
Myofibroblastoma of the breast: genetic link with spindle cell lipoma. J Pathol. 2000 Jul; 191(3):282-5.
Myofibroblastoma of the breast: genetic link with spindle cell lipoma.
Koontz JI, Soreng AL, Nucci M, Kuo FC, Pauwels P, van Den Berghe H, Dal Cin P, Fletcher JA, Sklar J
Frequent fusion of the JAZF1 and JJAZ1 genes in endometrial stromal tumors. Proc Natl Acad Sci U S A. 2001 May 22; 98(11):6348-53.
Frequent fusion of the JAZF1 and JJAZ1 genes in endometrial stromal tumors.
French CA, Miyoshi I, Aster JC, Kubonishi I, Kroll TG, Dal Cin P, Vargas SO, Perez-Atayde AR, Fletcher JA
BRD4 bromodomain gene rearrangement in aggressive carcinoma with translocation t(15;19). Am J Pathol. 2001 Dec; 159(6):1987-92.
BRD4 bromodomain gene rearrangement in aggressive carcinoma with translocation t(15;19).
Ligon AH, DeAngelo DJ, Atkins L, Dal Cin P
Isochromosome of a deleted 20q may be a relatively common abnormality in myeloid malignancies. Cancer Genet Cytogenet. 2005 Oct 01; 162(1):89-91.
Isochromosome of a deleted 20q may be a relatively common abnormality in myeloid malignancies.
Dal Cin P, Sciot R, Samson I, De Wever I, Van den Berghe H
Osteoid osteoma and osteoblastoma with clonal chromosome changes. Br J Cancer. 1998 Aug; 78(3):344-8.
Osteoid osteoma and osteoblastoma with clonal chromosome changes.
Dal Cin P, Van den Berghe H, Buonamici L, Losi L, Roncaroli F, Calbucci F
Cytogenetic investigation in subependymoma. Cancer Genet Cytogenet. 1999 Jan 01; 108(1):84.
Cytogenetic investigation in subependymoma.
European journal of obstetrics, gynecology, and reproductive biology
Some genetic aspects of ovarian tumors. Eur J Obstet Gynecol Reprod Biol. 1998 Dec; 81(2):283-7.
Dal Cin P, Roskams T, De Vos R, Van Poppel H, Balzarini P, Van Den Berghe H
Involvement of chromosomes 1 and 18 in renal cell tumors. Cancer Genet Cytogenet. 2000 Jan 01; 116(1):54-8.
Involvement of chromosomes 1 and 18 in renal cell tumors.
Pauwels P, Ambros P, Hattinger C, Lammens M, Dal Cin P, Ribot J, Struyk A, van den Berghe H
Peripheral primitive neuroectodermal tumour of the cervix. Virchows Arch. 2000 Jan; 436(1):68-73.
Peripheral primitive neuroectodermal tumour of the cervix.
Dal Cin P, Kozakewich HP, Goumnerova L, Mankin HJ, Rosenberg AE, Fletcher JA
Variant translocations involving 16q22 and 17p13 in solid variant and extraosseous forms of aneurysmal bone cyst. Genes Chromosomes Cancer. 2000 Jun; 28(2):233-4.
Variant translocations involving 16q22 and 17p13 in solid variant and extraosseous forms of aneurysmal bone cyst.
Bloomfield CD, Archer KJ, Mrózek K, Lillington DM, Kaneko Y, Head DR, Dal Cin P, Raimondi SC
11q23 balanced chromosome aberrations in treatment-related myelodysplastic syndromes and acute leukemia: report from an international workshop. Genes Chromosomes Cancer. 2002 Apr; 33(4):362-78.
11q23 balanced chromosome aberrations in treatment-related myelodysplastic syndromes and acute leukemia: report from an international workshop.
Dal Cin P, Polito P, Van Eyken P, Sciot R, Hernandez JM, Garcia JL, Van den Berghe H
Anomalies of chromosomes 17 and 22 in giant cell fibroblastoma. Cancer Genet Cytogenet. 1997 Sep; 97(2):165-6.
Anomalies of chromosomes 17 and 22 in giant cell fibroblastoma.
The role of cytogenetics in the classification of soft tissue tumours. Virchows Arch. 1997 Aug; 431(2):83-94.
The role of cytogenetics in the classification of soft tissue tumours.
Dal Cin P, Quade BJ, Neskey DM, Kleinman MS, Weremowicz S, Morton CC
Intravenous leiomyomatosis is characterized by a der(14)t(12;14)(q15;q24). Genes Chromosomes Cancer. 2003 Feb; 36(2):205-6.
Intravenous leiomyomatosis is characterized by a der(14)t(12;14)(q15;q24).
De Wever I, Dal Cin P, Fletcher CD, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, Van Den Berghe H, Vanni R, Willén H
Cytogenetic, clinical, and morphologic correlations in 78 cases of fibromatosis: a report from the CHAMP Study Group. CHromosomes And Morphology. Mod Pathol. 2000 Oct; 13(10):1080-5.
Cytogenetic, clinical, and morphologic correlations in 78 cases of fibromatosis: a report from the CHAMP Study Group. CHromosomes And Morphology.
Vargas SO, French CA, Faul PN, Fletcher JA, Davis IJ, Dal Cin P, Perez-Atayde AR
Upper respiratory tract carcinoma with chromosomal translocation 15;19: evidence for a distinct disease entity of young patients with a rapidly fatal course. Cancer. 2001 Sep 01; 92(5):1195-203.
Upper respiratory tract carcinoma with chromosomal translocation 15;19: evidence for a distinct disease entity of young patients with a rapidly fatal course.
Dal Cin P, Rao U, Jani-Sait S, Karakousis C, Sandberg AA
Chromosomes in the diagnosis of soft tissue tumors. I. Synovial sarcoma. Mod Pathol. 1992 Jul; 5(4):357-62.
Chromosomes in the diagnosis of soft tissue tumors. I. Synovial sarcoma.
Vanni R, Fletcher CD, Sciot R, Dal Cin P, De Wever I, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Tallini G, Van Den Berghe H, Willén H
Cytogenetic evidence of clonality in cutaneous benign fibrous histiocytomas: a report of the CHAMP study group. Histopathology. 2000 Sep; 37(3):212-7.
Cytogenetic evidence of clonality in cutaneous benign fibrous histiocytomas: a report of the CHAMP study group.
Ordulu Z, Dal Cin P, Chong WW, Choy KW, Lee C, Muto MG, Quade BJ, Morton CC
Disseminated peritoneal leiomyomatosis after laparoscopic supracervical hysterectomy with characteristic molecular cytogenetic findings of uterine leiomyoma. Genes Chromosomes Cancer. 2010 Dec; 49(12):1152-60.
Disseminated peritoneal leiomyomatosis after laparoscopic supracervical hysterectomy with characteristic molecular cytogenetic findings of uterine leiomyoma.
Deletion of chromosome 20q: friend or foe? Leuk Res. 2011 Jul; 35(7):844-5.
Deletion of chromosome 20q: friend or foe?
Mosquera JM, Dal Cin P, Mertz KD, Perner S, Davis IJ, Fisher DE, Rubin MA, Hirsch MS
Diagnostic molecular pathology : the American journal of surgical pathology, part B
Validation of a TFE3 break-apart FISH assay for Xp11.2 translocation renal cell carcinomas. Diagn Mol Pathol. 2011 Sep; 20(3):129-37.
Validation of a TFE3 break-apart FISH assay for Xp11.2 translocation renal cell carcinomas.
Doyle LA, Wang WL, Dal Cin P, Lopez-Terrada D, Mertens F, Lazar AJ, Fletcher CD, Hornick JL
MUC4 is a sensitive and extremely useful marker for sclerosing epithelioid fibrosarcoma: association with FUS gene rearrangement. Am J Surg Pathol. 2012 Oct; 36(10):1444-51.
MUC4 is a sensitive and extremely useful marker for sclerosing epithelioid fibrosarcoma: association with FUS gene rearrangement.
Brosens I, Dal Cin P, Deprest J, Van den Berghe H.
Clinico-pathological features of uterine leiomyomas. "Pathogenesis and Medical Management of Uterine Fibroids": Satellite session of the 5th International Symposium on GnRH Analogues in Cancer and Human Reproduction. 1999; Geneva, Switzerland.
Clinico-pathological features of uterine leiomyomas. "Pathogenesis and Medical Management of Uterine Fibroids": Satellite session of the 5th International Symposium on GnRH Analogues in Cancer and Human Reproduction
Ligon AH, Morton CC, Bieber FR, Fletcher JA, Giersch AB, Lee C, Sandstrom M, Weremowicz S, Xiao S, Dal Cin P.
Current Protocols in Human Genetics. Drapoli NC, Haines JL, Korf BR, Morton CC, Seidman CE, Seidman JG, Smith DR, eds.
Reporting of Diagnostic Cytogenetic Results. Current Protocols in Human Genetics. Drapoli NC, Haines JL, Korf BR, Morton CC, Seidman CE, Seidman JG, Smith DR, eds. 2004; Supplement 43:A.1D.1 - A1D.27.
Fibrous dysplasia of the bone. Atlas Genet Cytogenet Oncol Haematol.
Fibrous dysplasia of the bone. Atlas Genet Cytogenet Oncol Haematol. 2001.
Aly MS, Dal Cin P, Van Poppel H, Baert L, Van Damme B, Cassiman JJ, Van den Berghe H.
European Society of Human Genetics Annual Meeting
Cytogenetic investigations in normal and malignant kidney tissues. European Society of Human Genetics Annual Meeting. 1991.
Cytogenetic investigations in normal and malignant kidney tissues
Aly MS, Dal Cin P, Van Damme B, Van Poppel H, Baert L, Van den Berghe H.
Cytogenetic study of renal cell carcinoma. 4th European Workshop on Cytogenetics and Molecular Genetics of Human Solid tumors. Cancer Genet Cytogenet. 1994; (77):191.
Cytogenetic study of renal cell carcinoma. 4th European Workshop on Cytogenetics and Molecular Genetics of Human Solid tumors
Enzinger &Weiss Soft Tissue Tumors 5th Ed. Weiss SW, Goldblum JR eds
Molecular genetics and cytogenetics analysis of soft tissue tumors. Enzinger &Weiss Soft Tissue Tumors 5th Ed. Weiss SW, Goldblum JR eds. 2007.
Molecular genetics and cytogenetics analysis of soft tissue tumors
Turc Carel C, Limon J, Dal Cin P, Sandberg AA.
Recurrent chromosome rearrangements in malignant and benign adipose tissue tumors. J Cell Biochem (suppl). 1986; 10A:42.
Recurrent chromosome rearrangements in malignant and benign adipose tissue tumors
Turc-Carel C, Dal Cin P, Carr K, Sandberg AA
Normal blood lymphocytes from patients with adipose tissue tumors with rearrangements at 12q13-q14 do not express the fragile site fra(12)(q13.1). Cancer Genet Cytogenet. 1988 Mar; 31(1):35-9.
Normal blood lymphocytes from patients with adipose tissue tumors with rearrangements at 12q13-q14 do not express the fragile site fra(12)(q13.1).
Dal Cin P, Li FP, Prout GR, Huben RP, Limon J, Ferti-Passantonopoulou A, Richie JP, Sandberg AA
Involvement of chromosomes 3 and 5 in renal cell carcinoma. Cancer Genet Cytogenet. 1988 Oct 01; 35(1):41-6.
Involvement of chromosomes 3 and 5 in renal cell carcinoma.
Kazmierczak B, Belge G, Stern C, Dal Cin P, Van den Berghe H, Bartnitzke S, Bullerdiek J.
International Workshop on Cytogenetics and Molecular Genetics of Chromosome 12 in Human Solid Tumors
Cell lines from human tumors showing the 12q13-15 aberrations. International Workshop on Cytogenetics and Molecular Genetics of Chromosome 12 in Human Solid Tumors. 1992.
Cell lines from human tumors showing the 12q13-15 aberrations
HMGI17 maps to chromosomal band 1p35 and is deleted in uterine leiomyomas with ring chromosome 1. 6th European Conference on Cytogenetics and Molecular Genetics of Human Solid Tumors. Cancer Genet Cytogenet. 1999; 122:83.
HMGI17 maps to chromosomal band 1p35 and is deleted in uterine leiomyomas with ring chromosome 1. 6th European Conference on Cytogenetics and Molecular Genetics of Human Solid Tumors
Si MW,Thorson JA, Lauwers GY, Dal Cin P, Furman J.
Hepatocellular lymphoepithelioma-like carcinoma associated with Epstein Barr Virus: a hitherto unrecognized entity. Diagnostic Mol Pathol. 2004; 13:183-9.
Hepatocellular lymphoepithelioma-like carcinoma associated with Epstein Barr Virus: a hitherto unrecognized entity
Cuneo A, Michaux JL, Ferrant A, Van Hove L, Bosly A, Stul M, Dal Cin P, Vandenberghe E, Cassiman JJ, Negrini M
Correlation of cytogenetic patterns and clinicobiological features in adult acute myeloid leukemia expressing lymphoid markers. Blood. 1992 Feb 01; 79(3):720-7.
Correlation of cytogenetic patterns and clinicobiological features in adult acute myeloid leukemia expressing lymphoid markers.
Current topics in pathology. Ergebnisse der Pathologie
Karyotypic analysis of solid tumors. Curr Top Pathol. 1990; 82:257-88.
Bovée JV, Sciot R, Dal Cin P, Debiec-Rychter M, van Zelderen-Bhola SL, Cornelisse CJ, Hogendoorn PC
Chromosome 9 alterations and trisomy 22 in central chondrosarcoma: a cytogenetic and DNA flow cytometric analysis of chondrosarcoma subtypes. Diagn Mol Pathol. 2001 Dec; 10(4):228-35.
Chromosome 9 alterations and trisomy 22 in central chondrosarcoma: a cytogenetic and DNA flow cytometric analysis of chondrosarcoma subtypes.
Balzarini P, Dal Cin P, Roskams T, Polito P, Van Poppel H, Van Damme B, Baert L, Van den Berghe H
Histology may depend on the presence of partial monosomy or partial trisomy 3 in renal cell carcinoma. Cancer Genet Cytogenet. 1998 Aug; 105(1):6-10.
Histology may depend on the presence of partial monosomy or partial trisomy 3 in renal cell carcinoma.
O'Brien KP, Seroussi E, Dal Cin P, Sciot R, Mandahl N, Fletcher JA, Turc-Carel C, Dumanski JP
Various regions within the alpha-helical domain of the COL1A1 gene are fused to the second exon of the PDGFB gene in dermatofibrosarcomas and giant-cell fibroblastomas. Genes Chromosomes Cancer. 1998 Oct; 23(2):187-93.
Various regions within the alpha-helical domain of the COL1A1 gene are fused to the second exon of the PDGFB gene in dermatofibrosarcomas and giant-cell fibroblastomas.
Sciot R, Dal Cin P, Samson I, van den Berghe H, Van Damme B
Clonal chromosomal changes in juxta-articular myxoma. Virchows Arch. 1999 Feb; 434(2):177-80.
Clonal chromosomal changes in juxta-articular myxoma.
Ladanyi M, Woodruff JM, Scheithauer BW, Bridge JA, Barr FG, Goldblum JR, Fisher C, Perez-Atayde A, Dal Cin P, Fletcher CD, Fletcher JA
Re: O'Sullivan MJ, Kyriakos M, Zhu X, Wick MR, Swanson PE, Dehner LP, Humphrey PA, Pfeifer JD: malignant peripheral nerve sheath tumors with t(X;18). A pathologic and molecular genetic study. Mod pathol 2000;13:1336-46. Mod Pathol. 2001 Jul; 14(7):733-7.
Re: O'Sullivan MJ, Kyriakos M, Zhu X, Wick MR, Swanson PE, Dehner LP, Humphrey PA, Pfeifer JD: malignant peripheral nerve sheath tumors with t(X;18). A pathologic and molecular genetic study. Mod pathol 2000;13:1336-46.
Panagopoulos I, Mertens F, Isaksson M, Domanski HA, Brosjö O, Heim S, Bjerkehagen B, Sciot R, Dal Cin P, Fletcher JA, Fletcher CD, Mandahl N
Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma. Genes Chromosomes Cancer. 2002 Dec; 35(4):340-52.
Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma.
Hirsch MS, Weinstein MH, Thomas A, Dal Cin P
Identical karyotypes in synchronous bilateral clear cell renal cell carcinomas. Cancer Genet Cytogenet. 2002 Nov; 139(1):86-7.
Identical karyotypes in synchronous bilateral clear cell renal cell carcinomas.
Genetics in renal cell carcinoma. Curr Opin Urol. 2003 Nov; 13(6):463-6.
Qi H, Dal Cin P, Hernández JM, Garcia JL, Sciot R, Fletcher C, Van Eyken P, De Wever I, Van den Berghe H
Trisomies 8 and 20 in desmoid tumors. Cancer Genet Cytogenet. 1996 Dec; 92(2):147-9.
Wang L, Pitman MB, Castillo CF, Dal Cin P, Oliva E
Choriocarcinoma involving the pancreas as first manifestation of a metastatic regressing mixed testicular germ cell tumor. Mod Pathol. 2004 Dec; 17(12):1573-80.
Choriocarcinoma involving the pancreas as first manifestation of a metastatic regressing mixed testicular germ cell tumor.
Dal Cin P, Wanschura S, Kazmierczak B, Tallini G, Dei Tos A, Bullerdiek J, Van den Berghe I, Moerman P, Van den Berghe H
Amplification and expression of the HMGIC gene in a benign endometrial polyp. Genes Chromosomes Cancer. 1998 Jun; 22(2):95-9.
Amplification and expression of the HMGIC gene in a benign endometrial polyp.
Dal Cin P, De Smet L, Sciot R, Van Damme B, Van den Berghe H
Trisomy 7 and trisomy 8 in dividing and non-dividing tumor cells in Dupuytren's disease. Cancer Genet Cytogenet. 1999 Jan 15; 108(2):137-40.
Trisomy 7 and trisomy 8 in dividing and non-dividing tumor cells in Dupuytren's disease.
Tallini G, Vanni R, Manfioletti G, Kazmierczak B, Faa G, Pauwels P, Bullerdiek J, Giancotti V, Van Den Berghe H, Dal Cin P
Laboratory investigation; a journal of technical methods and pathology
HMGI-C and HMGI(Y) immunoreactivity correlates with cytogenetic abnormalities in lipomas, pulmonary chondroid hamartomas, endometrial polyps, and uterine leiomyomas and is compatible with rearrangement of the HMGI-C and HMGI(Y) genes. Lab Invest. 2000 Mar; 80(3):359-69.
HMGI-C and HMGI(Y) immunoreactivity correlates with cytogenetic abnormalities in lipomas, pulmonary chondroid hamartomas, endometrial polyps, and uterine leiomyomas and is compatible with rearrangement of the HMGI-C and HMGI(Y) genes.
Sjöblom T, Shimizu A, O'Brien KP, Pietras K, Dal Cin P, Buchdunger E, Dumanski JP, Ostman A, Heldin CH
Growth inhibition of dermatofibrosarcoma protuberans tumors by the platelet-derived growth factor receptor antagonist STI571 through induction of apoptosis. Cancer Res. 2001 Aug 01; 61(15):5778-83.
Growth inhibition of dermatofibrosarcoma protuberans tumors by the platelet-derived growth factor receptor antagonist STI571 through induction of apoptosis.
The genetics of lipomatous tumors. Semin Diagn Pathol. 2001 Nov; 18(4):286-93.
Quade BJ, Weremowicz S, Neskey DM, Vanni R, Ladd C, Dal Cin P, Morton CC
Fusion transcripts involving HMGA2 are not a common molecular mechanism in uterine leiomyomata with rearrangements in 12q15. Cancer Res. 2003 Mar 15; 63(6):1351-8.
Fusion transcripts involving HMGA2 are not a common molecular mechanism in uterine leiomyomata with rearrangements in 12q15.
HMGA2 rearrangement in a case of vulvar aggressive angiomyxoma. Int J Gynecol Pathol. 2006 Oct; 25(4):403-7.
HMGA2 rearrangement in a case of vulvar aggressive angiomyxoma.
Alekseyenko AA, Walsh EM, Zee BM, Pakozdi T, Hsi P, Lemieux ME, Dal Cin P, Ince TA, Kharchenko PV, Kuroda MI, French CA
Ectopic protein interactions within BRD4-chromatin complexes drive oncogenic megadomain formation in NUT midline carcinoma. Proc Natl Acad Sci U S A. 2017 05 23; 114(21):E4184-E4192.
Ectopic protein interactions within BRD4-chromatin complexes drive oncogenic megadomain formation in NUT midline carcinoma.
Dal Cin P, Moerman P, De Wever I, Van den Berghe H
Numerical chromosome aberrations in fibrothecoma. Tumori. 1992 Apr 30; 78(2):140-2.
Numerical chromosome aberrations in fibrothecoma.
Dal Cin P, Sciot R, Polito P, Stas M, de Wever I, Cornelis A, Van den Berghe H
Lesions of 13q may occur independently of deletion of 16q in spindle cell/pleomorphic lipomas. Histopathology. 1997 Sep; 31(3):222-5.
Lesions of 13q may occur independently of deletion of 16q in spindle cell/pleomorphic lipomas.
Polito P, Dal Cin P, Pauwels P, Christiaens M, Van den Berghe I, Moerman P, Vrints L, Van den Berghe H
An important subgroup of phyllodes tumors of the breast is characterized by rearrangements of chromosomes 1q and 10q. Oncol Rep. 1998 Sep-Oct; 5(5):1099-102.
An important subgroup of phyllodes tumors of the breast is characterized by rearrangements of chromosomes 1q and 10q.
Dal Cin P, Gutierrez NC, Hernandez JM, Van den Berghe H
Molecular cytogenetics in angiomyolipomas. Cancer Genet Cytogenet. 1998 Oct 15; 106(2):182.
Molecular cytogenetics in angiomyolipomas.
Pauwels P, Dal Cin P, Sciot R, Lammens M, Penn O, van Nes E, Kwee WS, van den Berghe H
Primary malignant peripheral nerve sheath tumour of the heart. Histopathology. 1999 Jan; 34(1):56-9.
Primary malignant peripheral nerve sheath tumour of the heart.
Van den Berghe I, Dal Cin P, Sciot R, Vanvuchelen J, Michielssen P, Hagemeijer A, De Baene L, Van den Berghe H
Translocation (4;8) as a primary chromosome change in a hydropic leiomyoma. Histopathology. 1999 Apr; 34(4):378.
Translocation (4;8) as a primary chromosome change in a hydropic leiomyoma.
HMG1 is not rearranged by 13q12 aberrations in lipomas. Genes Chromosomes Cancer. 1999 Mar; 24(3):290-2.
HMG1 is not rearranged by 13q12 aberrations in lipomas.
Dal Cin P, De Wolf F, Klerckx P, Van Den Berghe H
The 6p21 chromosome region is nonrandomly involved in endometrial polyps. Gynecol Oncol. 1992 Sep; 46(3):393-6.
The 6p21 chromosome region is nonrandomly involved in endometrial polyps.
Roper N, DeAngelo DJ, Kuo F, Dal Cin P, Ghobrial I, Aster JC
An asymptomatic 61-year-old man with BCR-ABL-positive bone marrow following autologous transplantation for multiple myeloma. Am J Hematol. 2010 Dec; 85(12):944-6.
An asymptomatic 61-year-old man with BCR-ABL-positive bone marrow following autologous transplantation for multiple myeloma.
Antonescu CR, Zhang L, Chang NE, Pawel BR, Travis W, Katabi N, Edelman M, Rosenberg AE, Nielsen GP, Dal Cin P, Fletcher CD
EWSR1-POU5F1 fusion in soft tissue myoepithelial tumors. A molecular analysis of sixty-six cases, including soft tissue, bone, and visceral lesions, showing common involvement of the EWSR1 gene. Genes Chromosomes Cancer. 2010 Dec; 49(12):1114-24.
EWSR1-POU5F1 fusion in soft tissue myoepithelial tumors. A molecular analysis of sixty-six cases, including soft tissue, bone, and visceral lesions, showing common involvement of the EWSR1 gene.
Gisselsson D, Pålsson E, Höglund M, Domanski H, Mertens F, Pandis N, Sciot R, Dal Cin P, Bridge JA, Mandahl N
Differentially amplified chromosome 12 sequences in low- and high-grade osteosarcoma. Genes Chromosomes Cancer. 2002 Feb; 33(2):133-40.
Differentially amplified chromosome 12 sequences in low- and high-grade osteosarcoma.
Speleman F, Dal Cin P, De Potter K, Laureys G, Roels HJ, Leroy J, Van Den Berghe H
Cytogenetic investigation of a case of congenital fibrosarcoma. Cancer Genet Cytogenet. 1989 May; 39(1):21-4.
Cytogenetic investigation of a case of congenital fibrosarcoma.
Excessive centrosome abnormalities without ongoing numerical chromosome instability in a Burkitt's lymphoma. Mol Cancer. 2003 Sep 08; 2:30.
Excessive centrosome abnormalities without ongoing numerical chromosome instability in a Burkitt's lymphoma.
1Van Gool S, Brock P, Proesmans W, Dal Cin P, Van den Berghe H, Van Damme B, De Wever I, Baert L, Casteels-Van Daele M.
Renal cell carcinoma in a child. International Society of Paediatric Oncology (SIOP) XXIIIrd Meeting. Med & Pediatr Oncol. 1991; (19):392.
Renal cell carcinoma in a child. International Society of Paediatric Oncology (SIOP) XXIIIrd Meeting
Quade BJ, Wang TY, Sornberger K, Dal Cin P, Mutter GL, Morton CC
Molecular pathogenesis of uterine smooth muscle tumors from transcriptional profiling. Genes Chromosomes Cancer. 2004 Jun; 40(2):97-108.
Molecular pathogenesis of uterine smooth muscle tumors from transcriptional profiling.
Dal Cin P, Brock P, Aly MS, Casteels-Van Daele M, De Wever I, Van Damme B, Van den Berghe H
A variant (2;13) translocation in rhabdomyosarcoma. Cancer Genet Cytogenet. 1991 Sep; 55(2):191-5.
A variant (2;13) translocation in rhabdomyosarcoma.
Moore SD, Offor O, Ferry JA, Amrein PC, Morton CC, Dal Cin P
ELF4 is fused to ERG in a case of acute myeloid leukemia with a t(X;21)(q25-26;q22). Leuk Res. 2006 Aug; 30(8):1037-42.
ELF4 is fused to ERG in a case of acute myeloid leukemia with a t(X;21)(q25-26;q22).
Takahashi H, Feuerhake F, Kutok JL, Monti S, Dal Cin P, Neuberg D, Aster JC, Shipp MA
FAS death domain deletions and cellular FADD-like interleukin 1beta converting enzyme inhibitory protein (long) overexpression: alternative mechanisms for deregulating the extrinsic apoptotic pathway in diffuse large B-cell lymphoma subtypes. Clin Cancer Res. 2006 Jun 01; 12(11 Pt 1):3265-71.
FAS death domain deletions and cellular FADD-like interleukin 1beta converting enzyme inhibitory protein (long) overexpression: alternative mechanisms for deregulating the extrinsic apoptotic pathway in diffuse large B-cell lymphoma subtypes.
Dal Cin P, Qi H, Pauwels P, Backx C, Van den Berghe H
Monosomy 22 in a fibrothecoma. Cancer Genet Cytogenet. 1997 Dec; 99(2):129-31.
Dei Tos AP, Dal Cin P, Sciot R, Furlanetto A, Da Mosto MC, Giannini C, Rinaldo A, Ferlito A
The Annals of otology, rhinology, and laryngology
Synovial sarcoma of the larynx and hypopharynx. Ann Otol Rhinol Laryngol. 1998 Dec; 107(12):1080-5.
Synovial sarcoma of the larynx and hypopharynx.
Balzarini P, Tardanico R, Grigolato P, Cunico SC, Cozzoli A, Zanotelli T, Van Den Berghe H, Dal Cin P
Atypical chromosome abnormalities in a renal oncocytoma. Cancer Genet Cytogenet. 1999 Aug; 113(1):103-4.
Atypical chromosome abnormalities in a renal oncocytoma.
McCluggage WG, Sumathi VP, Nucci MR, Hirsch M, Dal Cin P, Wells M, Flanagan AM, Fisher C
Ewing family of tumours involving the vulva and vagina: report of a series of four cases. J Clin Pathol. 2007 Jun; 60(6):674-80.
Ewing family of tumours involving the vulva and vagina: report of a series of four cases.
An intragenic rearrangement of HMGA2 is not necessary for lipoma formation. Cancer Genet Cytogenet. 2004 Mar; 149(2):178-9.
An intragenic rearrangement of HMGA2 is not necessary for lipoma formation.
Is the chromosome band 1p36 another hot-spot for rearrangements in uterine leiomyoma? Genes Chromosomes Cancer. 1990 Sep; 2(3):255-6.
Is the chromosome band 1p36 another hot-spot for rearrangements in uterine leiomyoma?
Ten years of the cytogenetics of soft tissue tumors. Cancer Genet Cytogenet. 1997 May; 95(1):59-66.
Ten years of the cytogenetics of soft tissue tumors.
Pedeutour F, Quade BJ, Weremowicz S, Dal Cin P, Ali S, Morton CC
Localization and expression of the human estrogen receptor beta gene in uterine leiomyomata. Genes Chromosomes Cancer. 1998 Dec; 23(4):361-6.
Localization and expression of the human estrogen receptor beta gene in uterine leiomyomata.
Polito P, Dal Cin P, Sciot R, Brock P, Van Eyken P, Van den Berghe H
Embryonal rhabdomyosarcoma with only numerical chromosome changes. Case report and review of the literature. Cancer Genet Cytogenet. 1999 Mar; 109(2):161-5.
Embryonal rhabdomyosarcoma with only numerical chromosome changes. Case report and review of the literature.
Losi L, Buonamici L, Dal Cin P, Giannini C, Dei Tos P, Calbucci F, Eusebi V
[Cytogenetics of tumors of the central nervous system: a case study and review of the literature]. Pathologica. 1999 Aug; 91(4):249-55.
[Cytogenetics of tumors of the central nervous system: a case study and review of the literature].
Mulier S, Stas M, Delabie J, Lateur L, Gysen M, Dal Cin P, Robberecht C, De Wever I
Proliferative myositis in a child. Skeletal Radiol. 1999 Dec; 28(12):703-9.
Gisselsson D, Björk J, Höglund M, Mertens F, Dal Cin P, Akerman M, Mandahl N
Abnormal nuclear shape in solid tumors reflects mitotic instability. Am J Pathol. 2001 Jan; 158(1):199-206.
Abnormal nuclear shape in solid tumors reflects mitotic instability.
Analytical and quantitative cytology and histology
Genetics of epithelial tumors of the renal parenchyma in adults and renal cell carcinoma in children. Anal Quant Cytol Histol. 2001 Oct; 23(5):362-72.
Genetics of epithelial tumors of the renal parenchyma in adults and renal cell carcinoma in children.
Guardiola MT, Dobin SM, Dal Cin P, Donner LR
Pericentric inversion (12)(p12q13-14) as the sole chromosomal abnormality in a leiomyoma of the vulva. Cancer Genet Cytogenet. 2010 May; 199(1):21-3.
Pericentric inversion (12)(p12q13-14) as the sole chromosomal abnormality in a leiomyoma of the vulva.
McDonald AG, Dal Cin P, Ganguly A, Campbell S, Imai Y, Rosenberg AE, Oliva E
Liposarcoma arising in uterine lipoleiomyoma: a report of 3 cases and review of the literature. Am J Surg Pathol. 2011 Feb; 35(2):221-7.
Liposarcoma arising in uterine lipoleiomyoma: a report of 3 cases and review of the literature.
Diagnostico prenatal de agenesia del cuerpo callosos y de labio leporino en un feto portador de trisomia 5p. (Prenatal diagnosis of agenesis corpus callosum and cleft lip in a fetus carrier of trisomy 5p). Acta Cient Venez. 1983; 34:345.
Diagnostico prenatal de agenesia del cuerpo callosos y de labio leporino en un feto portador de trisomia 5p. (Prenatal diagnosis of agenesis corpus callosum and cleft lip in a fetus carrier of trisomy 5p)
Kakati S, Limon J, Dal Cin P, Pietrzak E, Kinniburgh J, Sandberg AA.
A homogeneously stain region on chromosome 8 in an osteosarcoma without amplification of MYC and MOS oncogenes. American Society of Human Genetics. 1987.
A homogeneously stain region on chromosome 8 in an osteosarcoma without amplification of MYC and MOS oncogenes
Dal Cin P, Christacos N, Morton CC, Quade BJ.
Cellular leiomyoma: a genetically distinct entity among benign uterine tumors. United States and Canadian Academy of Pathology. 2003; Washington, DC.
Morton CC, Dal Cin P, Neskey DM,S Weremowicz S, B.J. Quade BJ.
Third International Workshop”HMGA protein in cell differentiation and trasformation”
Are fusion transcripts involving HMGA2 a common molecular mechanism in uterine leiomyomata with trarrangements in 12q15?. Third International Workshop”HMGA protein in cell differentiation and trasformation”. 2002; Napoli,Italy.
Are fusion transcripts involving HMGA2 a common molecular mechanism in uterine leiomyomata with trarrangements in 12q15?
Qi H, Dal Cin P, Van de Voorde W, Van Poppel H, Baert L, Van den Berghe H.
Cytogenetic and fish study in 120 cases of prostate adenocarcinoma. 5th European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors. 1996; Baveno - Stresa, Italy.
Cytogenetic and fish study in 120 cases of prostate adenocarcinoma
Kazmierczak B, Wanschura S, Dal Cin P, Van den Berghe H, Bullerdiek J.
Involvement of the HMGIY gene in mesenchymal tumors with 6p21 aberrations. 7th International Workshop on Chromosomes in Solid Tumors. Cancer Genet Cytogenet. 1997; (98):151.
Involvement of the HMGIY gene in mesenchymal tumors with 6p21 aberrations. 7th International Workshop on Chromosomes in Solid Tumors
Christacos NC, Sherman L, Roy A, DeAngelo DJ, Dal Cin P
Is the cryptic interstitial deletion of 8q24 surrounding MYC a common mechanism in the formation of double minute chromosome? Cancer Genet Cytogenet. 2005 Aug; 161(1):90-2.
Is the cryptic interstitial deletion of 8q24 surrounding MYC a common mechanism in the formation of double minute chromosome?
Cuneo A, Ferrant A, Michaux JL, Boogaerts M, Demuynck H, Bosly A, Doyen CM, Carli MG, Piva N, Castoldi G, Stul M, Dal Cin P, Cassiman JJ, Van den Berghe H.
Clinical review on features and cytogenetic patterns in adult acute myeloid leukemia with lymphoid markers. Leuk Lymph. 1993; 9:285-91.
t(Y;18) in acute myeloblastic leukemia FAB type M2. Cancer Genet Cytogenet. 1986 Aug; 22(4):367-8.
t(Y;18) in acute myeloblastic leukemia FAB type M2.
Mito JK, Jo VY, Chiosea SI, Dal Cin P, Krane JF
HMGA2 is a specific immunohistochemical marker for pleomorphic adenoma and carcinoma ex-pleomorphic adenoma. Histopathology. 2017 Oct; 71(4):511-521.
HMGA2 is a specific immunohistochemical marker for pleomorphic adenoma and carcinoma ex-pleomorphic adenoma.
Diagnosis of primary renal cell carcinoma in a left supraclavicular lymph node by chromosome analysis. J Urol. 1996 Jul; 156(1):171-2.
Diagnosis of primary renal cell carcinoma in a left supraclavicular lymph node by chromosome analysis.
Monti S, Savage KJ, Kutok JL, Feuerhake F, Kurtin P, Mihm M, Wu B, Pasqualucci L, Neuberg D, Aguiar RC, Dal Cin P, Ladd C, Pinkus GS, Salles G, Harris NL, Dalla-Favera R, Habermann TM, Aster JC, Golub TR, Shipp MA
Molecular profiling of diffuse large B-cell lymphoma identifies robust subtypes including one characterized by host inflammatory response. Blood. 2005 Mar 01; 105(5):1851-61.
Molecular profiling of diffuse large B-cell lymphoma identifies robust subtypes including one characterized by host inflammatory response.
Speleman F, Dal Cin P, Van Roy N, Van Marck E, Buytaert P, Van den Berghe H, Leroy JG
Is t(6;20)(p21;q13) a characteristic chromosome change in endometrial polyps? Genes Chromosomes Cancer. 1991 Jul; 3(4):318-9.
Is t(6;20)(p21;q13) a characteristic chromosome change in endometrial polyps?
Sumegi J, Streblow R, Frayer RW, Dal Cin P, Rosenberg A, Meloni-Ehrig A, Bridge JA
Recurrent t(2;2) and t(2;8) translocations in rhabdomyosarcoma without the canonical PAX-FOXO1 fuse PAX3 to members of the nuclear receptor transcriptional coactivator family. Genes Chromosomes Cancer. 2010 Mar; 49(3):224-36.
Recurrent t(2;2) and t(2;8) translocations in rhabdomyosarcoma without the canonical PAX-FOXO1 fuse PAX3 to members of the nuclear receptor transcriptional coactivator family.
Snuderl M, Kolman OK, Chen YB, Hsu JJ, Ackerman AM, Dal Cin P, Ferry JA, Harris NL, Hasserjian RP, Zukerberg LR, Abramson JS, Hochberg EP, Lee H, Lee AI, Toomey CE, Sohani AR
B-cell lymphomas with concurrent IGH-BCL2 and MYC rearrangements are aggressive neoplasms with clinical and pathologic features distinct from Burkitt lymphoma and diffuse large B-cell lymphoma. Am J Surg Pathol. 2010 Mar; 34(3):327-40.
B-cell lymphomas with concurrent IGH-BCL2 and MYC rearrangements are aggressive neoplasms with clinical and pathologic features distinct from Burkitt lymphoma and diffuse large B-cell lymphoma.
HMGI(Y) and HMGI-C dysregulation: a common occurrence in human tumors. Adv Anat Pathol. 1999 Sep; 6(5):237-46.
HMGI(Y) and HMGI-C dysregulation: a common occurrence in human tumors.
[Telomeres: a review of the literature]. Pathologica. 1999 Apr; 91(2):121-3.
[Telomeres: a review of the literature].
Sciot R, Dorfman H, Brys P, Dal Cin P, De Wever I, Fletcher CD, Jonson K, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Samson I, Tallini G, Van den Berghe H, Vanni R, Willén H
Cytogenetic-morphologic correlations in aneurysmal bone cyst, giant cell tumor of bone and combined lesions. A report from the CHAMP study group. Mod Pathol. 2000 Nov; 13(11):1206-10.
Cytogenetic-morphologic correlations in aneurysmal bone cyst, giant cell tumor of bone and combined lesions. A report from the CHAMP study group.
Paulien S, Turc-Carel C, Dal Cin P, Jani-Sait S, Sreekantaiah C, Leong SP, Vogelstein B, Kinzler KW, Sandberg AA, Gemmill RM
Myxoid liposarcoma with t(12;16) (q13;p11) contains site-specific differences in methylation patterns surrounding a zinc-finger gene mapped to the breakpoint region on chromosome 12. Cancer Res. 1990 Dec 15; 50(24):7902-7.
Myxoid liposarcoma with t(12;16) (q13;p11) contains site-specific differences in methylation patterns surrounding a zinc-finger gene mapped to the breakpoint region on chromosome 12.
Kerim S, Stul M, Mecucci C, Vandenberghe E, Cuneo A, Dal Cin P, Michaux JL, Louwagie A, Cassiman JJ, Van den Berghe H
Rearrangement of immunoglobulin and TCR genes in lymphoid blast crisis of Ph+ chronic myeloid leukaemia. Br J Haematol. 1990 Apr; 74(4):414-9.
Rearrangement of immunoglobulin and TCR genes in lymphoid blast crisis of Ph+ chronic myeloid leukaemia.
Hodge JC, Quade BJ, Rubin MA, Stewart EA, Dal Cin P, Morton CC
Molecular and cytogenetic characterization of plexiform leiomyomata provide further evidence for genetic heterogeneity underlying uterine fibroids. Am J Pathol. 2008 May; 172(5):1403-10.
Molecular and cytogenetic characterization of plexiform leiomyomata provide further evidence for genetic heterogeneity underlying uterine fibroids.
Heerema NA, Byrd JC, Dal Cin PS, Dell' Aquila ML, Koduru PR, Aviram A, Smoley SA, Rassenti LZ, Greaves AW, Brown JR, Rai KR, Kipps TJ, Kay NE, Van Dyke DL
Stimulation of chronic lymphocytic leukemia cells with CpG oligodeoxynucleotide gives consistent karyotypic results among laboratories: a CLL Research Consortium (CRC) Study. Cancer Genet Cytogenet. 2010 Dec; 203(2):134-40.
Stimulation of chronic lymphocytic leukemia cells with CpG oligodeoxynucleotide gives consistent karyotypic results among laboratories: a CLL Research Consortium (CRC) Study.
Karakousis CP, Dal Cin P, Turc-Carel C, Limon J, Sandberg AA
Archives of surgery (Chicago, Ill. : 1960)
Chromosomal changes in soft-tissue sarcomas. A new diagnostic parameter. Arch Surg. 1987 Nov; 122(11):1257-60.
Chromosomal changes in soft-tissue sarcomas. A new diagnostic parameter.
Turc-Carel C, Dal Cin P, Limon J, Rao U, Li FP, Corson JM, Zimmerman R, Parry DM, Cowan JM, Sandberg AA
Involvement of chromosome X in primary cytogenetic change in human neoplasia: nonrandom translocation in synovial sarcoma. Proc Natl Acad Sci U S A. 1987 Apr; 84(7):1981-5.
Involvement of chromosome X in primary cytogenetic change in human neoplasia: nonrandom translocation in synovial sarcoma.
Current Protocols in Human Genetics, Drapoli NC, Haines JL, Korf BR, Morton CC, Seidman CE, Seidman JG, Smith DR, eds.
Metaphase harvest and cytogenetic analysis of malignant hematological specimen. Current Protocols in Human Genetics, Drapoli NC, Haines JL, Korf BR, Morton CC, Seidman CE, Seidman JG, Smith DR, eds. 2002; 10.2.1-10.2.12.
Metaphase harvest and cytogenetic analysis of malignant hematological specimen
Dal Cin P, Paolini P, Borberg C, Casanova J, Martinez P, Sanoja A, Bustamante A, Muro de D'Hoy E, Piras MM.
Diagnostico prenatal de alteraciones cromosomicas y de tubo neural. Experiencia recogida en cultivos de celulas amnioticas y en la determinacion de Ó fetoproteina. (prenatal diagnosis of chromosome aberrations and neural tube defects. Experience of amniotic fluid cell cultures and determination of fetoprotein.). Acta Cient Venez. 1980; 31:184.
Diagnostico prenatal de alteraciones cromosomicas y de tubo neural. Experiencia recogida en cultivos de celulas amnioticas y en la determinacion de Ó fetoproteina. (prenatal diagnosis of chromosome aberrations and neural tube defects. Experience of amniotic fluid cell cultures and determination of fetoprotein.)
Dal Cin P, Wanschura S, Kazmierczak B, Bullerdiek J, Van den Berghe I, Moerman Ph, Van den Berghe H.
Amplification of HMGIC in an endometrial polyp. 7th International Workshop on Chromosomes in Solid Tumors. Cancer Genet Cytogenet. 1997; (98):158.
Amplification of HMGIC in an endometrial polyp. 7th International Workshop on Chromosomes in Solid Tumors
Cancer Cytogenetics, Third Edition. Heim S, Mitelman F.
Urinary Tract. Cancer Cytogenetics, Third Edition. Heim S, Mitelman F. 2008.
Huben RP, Dal Cin P, Prout Jr. GR, Li P, Sandberg AA.
Annual Meeting of American Urological Society
Recurrent karyotype in renal cell carcinoma/cortical adenoma. Annual Meeting of American Urological Society. 1988.
Recurrent karyotype in renal cell carcinoma/cortical adenoma
Cytogenetic investigation Of synchronous bilateral renal tumors. 5th European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors. 1996; Baveno - Stresa, Italy.
Mertens F, Dal Cin P, De Wever I, Fletcher CDM, Mandahl N, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, Van den Berghe H, Vanni R, Willén H.
A report of the CHAMP group. 8th International Workshop on Chromosomes in Solid Tumors.
Cytogenetic characterization of peripheral nerve sheats tumors. A report of the CHAMP group. 8th International Workshop on Chromosomes in Solid Tumors. 2000; Tucson, AZ.
Cytogenetic characterization of peripheral nerve sheats tumors
Huben RP, Dal Cin P, Limon J, Yoshida M, Sandberg AA.
Cytogenetic definition of kidney tumors. J Urol. 1987; (137):252A.
Mito JK, Agoston AT, Dal Cin P, Srivastava A
Prevalence and significance of HMGA2 expression in oesophageal adenocarcinoma. Histopathology. 2017 Dec; 71(6):909-917.
Prevalence and significance of HMGA2 expression in oesophageal adenocarcinoma.
Rosenbaum MW, Pozdnyakova O, Geyer JT, Dal Cin P, Hasserjian RP
Ring chromosome in myeloid neoplasms is associated with complex karyotype and disease progression. Hum Pathol. 2017 10; 68:40-46.
Ring chromosome in myeloid neoplasms is associated with complex karyotype and disease progression.
Turc Carel C, Dal Cin P, Limon J, Gibas Z, Kakati S, Pietrzak E, Parry D, Li F, Sandberg AA.
Cytogenetic and molecular studies of adipose tissue tumors. Cancer Genet Cytogenet. 1987; (28):33.
Cytogenetic and molecular studies of adipose tissue tumors
Fourth MIC Cooperative Study Group. Meeting Report.
A Conference on the Morphologic, Immunologic, and Cytogenetic Classification of the Chronic (mature) B and T Lymphoid Leukaemias. Cancer Genet Cytogenet. 1990; 131-132.
A Conference on the Morphologic, Immunologic, and Cytogenetic Classification of the Chronic (mature) B and T Lymphoid Leukaemias
Chromosomes and Cancer. Oxford Textbook of Oncology. 1995.
Cuneo A, Castoldi G, Michaux JL, Ferrant A, Bosly A, Boogaerts M, Dal Cin P, Van den Berghe H. Adult acute myeloid leukemia
Adult acute myeloid leukemia. Blood. 1992; 80:1369-70.
Limon J, Dal Cin P, Gaeta J, Sandberg AA
Translocation t(4;11)(q35;p13) in an adrenocortical carcinoma. Cancer Genet Cytogenet. 1987 Oct; 28(2):343-8.
Translocation t(4;11)(q35;p13) in an adrenocortical carcinoma.
Limon J, Turc-Carel C, Dal Cin P, Rao U, Sandberg AA
Recurrent chromosome translocations in liposarcoma. Cancer Genet Cytogenet. 1986 May; 22(1):93-4.
Recurrent chromosome translocations in liposarcoma.
Dal Cin P, Drochmans A, Moerman P, Van den Berghe H
Isochromosome 12p in mediastinal germ cell tumor. Cancer Genet Cytogenet. 1989 Oct 15; 42(2):243-51.
Isochromosome 12p in mediastinal germ cell tumor.
Micci F, Brunetti M, Dal Cin P, Nucci MR, Gorunova L, Heim S, Panagopoulos I
Fusion of the genes BRD8 and PHF1 in endometrial stromal sarcoma. Genes Chromosomes Cancer. 2017 12; 56(12):841-845.
Fusion of the genes BRD8 and PHF1 in endometrial stromal sarcoma.
Armand P, Kim HT, Zhang MJ, Perez WS, Dal Cin PS, Klumpp TR, Waller EK, Litzow MR, Liesveld JL, Lazarus HM, Artz AS, Gupta V, Savani BN, McCarthy PL, Cahn JY, Schouten HC, Finke J, Ball ED, Aljurf MD, Cutler CS, Rowe JM, Antin JH, Isola LM, Di Bartolomeo P, Camitta BM, Miller AM, Cairo MS, Stockerl-Goldstein K, Sierra J, Savoie ML, Halter J, Stiff PJ, Nabhan C, Jakubowski AA, Bunjes DW, Petersdorf EW, Devine SM, Maziarz RT, Bornhauser M, Lewis VA, Marks DI, Bredeson CN, Soiffer RJ, Weisdorf DJ
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation
Classifying cytogenetics in patients with acute myelogenous leukemia in complete remission undergoing allogeneic transplantation: a Center for International Blood and Marrow Transplant Research study. Biol Blood Marrow Transplant. 2012 Feb; 18(2):280-8.
Classifying cytogenetics in patients with acute myelogenous leukemia in complete remission undergoing allogeneic transplantation: a Center for International Blood and Marrow Transplant Research study.
Dal Cin P, Sciot R, Aly MS, Delabie J, Stas M, De Wever I, Van Damme B, Van den Berghe H
Some desmoid tumors are characterized by trisomy 8. Genes Chromosomes Cancer. 1994 Jun; 10(2):131-5.
Dal Cin P, Moerman P, Deprest J, Brosens I, Van den Berghe H
A new cytogenetic subgroup in uterine leiomyoma is characterized by a deletion of the long arm of chromosome 3. Genes Chromosomes Cancer. 1995 Jul; 13(3):219-20.
A new cytogenetic subgroup in uterine leiomyoma is characterized by a deletion of the long arm of chromosome 3.
García JL, Hernández JM, González M, San Miguel JF, Dal Cin P, Van Den Berghe H
Translocation (15;17)(q22;q21) in a patient with Klinefelter syndrome. Cancer Genet Cytogenet. 1996 Jan; 86(1):86.
Translocation (15;17)(q22;q21) in a patient with Klinefelter syndrome.
[Genetics of renal tumors]. Pathologica. 1998 Apr; 90(2):101-7.
Hung YP, Dong F, Watkins JC, Nardi V, Bueno R, Dal Cin P, Godleski JJ, Crum CP, Chirieac LR
Identification of ALK Rearrangements in Malignant Peritoneal Mesothelioma. JAMA Oncol. 2018 Feb 01; 4(2):235-238.
Identification of ALK Rearrangements in Malignant Peritoneal Mesothelioma.
Dei Tos AP, Doglioni C, Piccinin S, Sciot R, Furlanetto A, Boiocchi M, Dal Cin P, Maestro R, Fletcher CD, Tallini G
Coordinated expression and amplification of the MDM2, CDK4, and HMGI-C genes in atypical lipomatous tumours. J Pathol. 2000 Apr; 190(5):531-6.
Coordinated expression and amplification of the MDM2, CDK4, and HMGI-C genes in atypical lipomatous tumours.
Ladanyi M, Lui MY, Antonescu CR, Krause-Boehm A, Meindl A, Argani P, Healey JH, Ueda T, Yoshikawa H, Meloni-Ehrig A, Sorensen PH, Mertens F, Mandahl N, van den Berghe H, Sciot R, Dal Cin P, Bridge J
The der(17)t(X;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25. Oncogene. 2001 Jan 04; 20(1):48-57.
The der(17)t(X;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25.
Panagopoulos I, Mertens F, Isaksson M, Limon J, Gustafson P, Skytting B, Akerman M, Sciot R, Dal Cin P, Samson I, Iliszko M, Ryoe J, Dêbiec-Rychter M, Szadowska A, Brosjö O, Larsson O, Rydholm A, Mandahl N
Clinical impact of molecular and cytogenetic findings in synovial sarcoma. Genes Chromosomes Cancer. 2001 Aug; 31(4):362-72.
Clinical impact of molecular and cytogenetic findings in synovial sarcoma.
Dal Cin P, De Wever I, Moerman P, Van den Berghe H
Translocation X;12 in mesothelioma. Cancer Genet Cytogenet. 1991 Aug; 55(1):115-8.
Wang WL, Mayordomo E, Czerniak BA, Abruzzo LV, Dal Cin P, Araujo DM, Lev DC, López-Terrada D, Lazar AJ
Fluorescence in situ hybridization is a useful ancillary diagnostic tool for extraskeletal myxoid chondrosarcoma. Mod Pathol. 2008 Nov; 21(11):1303-10.
Fluorescence in situ hybridization is a useful ancillary diagnostic tool for extraskeletal myxoid chondrosarcoma.
Carette JE, Raaben M, Wong AC, Herbert AS, Obernosterer G, Mulherkar N, Kuehne AI, Kranzusch PJ, Griffin AM, Ruthel G, Dal Cin P, Dye JM, Whelan SP, Chandran K, Brummelkamp TR
Ebola virus entry requires the cholesterol transporter Niemann-Pick C1. Nature. 2011 Aug 24; 477(7364):340-3.
Ebola virus entry requires the cholesterol transporter Niemann-Pick C1.
Lee CH, Ou WB, Mariño-Enriquez A, Zhu M, Mayeda M, Wang Y, Guo X, Brunner AL, Amant F, French CA, West RB, McAlpine JN, Gilks CB, Yaffe MB, Prentice LM, McPherson A, Jones SJ, Marra MA, Shah SP, van de Rijn M, Huntsman DG, Dal Cin P, Debiec-Rychter M, Nucci MR, Fletcher JA
14-3-3 fusion oncogenes in high-grade endometrial stromal sarcoma. Proc Natl Acad Sci U S A. 2012 Jan 17; 109(3):929-34.
14-3-3 fusion oncogenes in high-grade endometrial stromal sarcoma.
Dal Cin P, Sciot R, Panagopoulos I, Aman P, Samson I, Mandahl N, Mitelman F, Van den Berghe H, Fletcher CD
Additional evidence of a variant translocation t(12;22) with EWS/CHOP fusion in myxoid liposarcoma: clinicopathological features. J Pathol. 1997 Aug; 182(4):437-41.
Additional evidence of a variant translocation t(12;22) with EWS/CHOP fusion in myxoid liposarcoma: clinicopathological features.
Lee CH, Ali RH, Rouzbahman M, Marino-Enriquez A, Zhu M, Guo X, Brunner AL, Chiang S, Leung S, Nelnyk N, Huntsman DG, Blake Gilks C, Nielsen TO, Dal Cin P, van de Rijn M, Oliva E, Fletcher JA, Nucci MR
Cyclin D1 as a diagnostic immunomarker for endometrial stromal sarcoma with YWHAE-FAM22 rearrangement. Am J Surg Pathol. 2012 Oct; 36(10):1562-70.
Cyclin D1 as a diagnostic immunomarker for endometrial stromal sarcoma with YWHAE-FAM22 rearrangement.
Schwind S, Edwards CG, Nicolet D, Mrózek K, Maharry K, Wu YZ, Paschka P, Eisfeld AK, Hoellerbauer P, Becker H, Metzeler KH, Curfman J, Kohlschmidt J, Prior TW, Kolitz JE, Blum W, Pettenati MJ, Dal Cin P, Carroll AJ, Caligiuri MA, Larson RA, Volinia S, Marcucci G, Bloomfield CD
inv(16)/t(16;16) acute myeloid leukemia with non-type A CBFB-MYH11 fusions associate with distinct clinical and genetic features and lack KIT mutations. Blood. 2013 Jan 10; 121(2):385-91.
inv(16)/t(16;16) acute myeloid leukemia with non-type A CBFB-MYH11 fusions associate with distinct clinical and genetic features and lack KIT mutations.
Dal-Cin P, Killian S, Koh A, Lessnick SL, Petersen R, Kimonis V
American College of Medical Genetics, Annual Meeting.
A case of bilateral retinoblastoma with a constitutional unbalanced translocation (6;15)(q27;q11.2). American College of Medical Genetics, Annual Meeting. 2002; New Orleans, LA.
A case of bilateral retinoblastoma with a constitutional unbalanced translocation (6;15)(q27;q11.2)
Piovan E, Dal Cin P, Goppion G, Tenconi R, Baccichetti C.
Sister chromatid exchanges induced by bromodeoxyuridine and caffeine. Acta Med Auxol. 1977; 9:159.
Sister chromatid exchanges induced by bromodeoxyuridine and caffeine
Intravenous leiomyomatosis. Atlas Genet Cytogenet Oncol Haematol.
Intravenous leiomyomatosis. Atlas Genet Cytogenet Oncol Haematol. 2003.
Speleman F, Mannens M, Laureys G, Cuvelier C., Dal Cin P, Benoit Y, Leroy JG.
European Workshop on Cytogenetics and Molecular Genetics in Human Solid Tumors.
Cytogenetic and molecular studies in a case of mesoblastic nephroma. European Workshop on Cytogenetics and Molecular Genetics in Human Solid Tumors. 1990.
Cytogenetic and molecular studies in a case of mesoblastic nephroma
Dal Cin P, Sciot R, Kazmierczak B, Wanschura S, Samson I, Van Poppel H, Van den Berghe H, Bullerdiek J.
Fourth International Workshop (SCW12.4) on chromosome 12
Inflammatory pseudotumors with HMGIC rearrangement. Fourth International Workshop (SCW12.4) on chromosome 12. 1997; Nice, France.
Inflammatory pseudotumors with HMGIC rearrangement
Schoenmakers E, Mols R, Willems M, Dal Cin P, Bullerdiek J, Van Den Berghe H, Van de Ven W.
Strategy to maP YAC-derived sequence tagged sites in human chromosome region 12q13-15 using the newly developed hybrid cell line LIS-3/SV40/A9-B4. International Workshop on Cytogenetics and Molecular Genetics of Chromosome 12 in Human Solid Tumors. 1992.
Strategy to maP YAC-derived sequence tagged sites in human chromosome region 12q13-15 using the newly developed hybrid cell line LIS-3/SV40/A9-B4
Carcinoma of the Prostate. Innovations in Management.
Chromosome abnormalities in adenocarcinoma of the prostate. Carcinoma of the Prostate. Innovations in Management. 1996; 51-54.
Chromosome abnormalities in adenocarcinoma of the prostate
Dal Cin P, Van den Berghe H. Petrovich Z.
Carcinoma of the kidney, testis and uncommon tumors of the genitourinary tract.
Genetics of renal cell carcinoma. Carcinoma of the kidney, testis and uncommon tumors of the genitourinary tract. 1999.
Limon J, Dal Cin P, Kakati S, Huben RP, Sandberg AA
Cytogenetic findings in a primary adrenocortical carcinoma. Cancer Genet Cytogenet. 1987 Jun; 26(2):271-7.
Cytogenetic findings in a primary adrenocortical carcinoma.
Cytogenetic studies of adipose tissue tumors. I. A benign lipoma with reciprocal translocation t(3;12)(q28;q14). Cancer Genet Cytogenet. 1986 Dec; 23(4):283-9.
Cytogenetic studies of adipose tissue tumors. I. A benign lipoma with reciprocal translocation t(3;12)(q28;q14).
Dal Cin P, Kools P, De Jonge I, Moerman P, Van de Ven W, Van den Berghe H
Rearrangement of 12q14-15 in pulmonary chondroid hamartoma. Genes Chromosomes Cancer. 1993 Oct; 8(2):131-3.
Rearrangement of 12q14-15 in pulmonary chondroid hamartoma.
Pauwels P, Dal Cin P, Roumen R, van den Berghe H, Sciot R
Intramuscular mixed tumour with clonal chromosomal changes. Virchows Arch. 1999 Feb; 434(2):167-71.
Intramuscular mixed tumour with clonal chromosomal changes.
Verhandlungen der Deutschen Gesellschaft fur Pathologie
Cytogenetics of soft tissue tumours. Verh Dtsch Ges Pathol. 1998; 82:47-58.
Dal Cin P, Puts JP, Gruwez J, De Wever I, Van Damme B, Van den Berghe H.
XIX international Congress of the International Academy of Pathology & 10th World Congress of Academic and Environmental Pathology
Chromosomes changes in adipose tissue tumors. XIX international Congress of the International Academy of Pathology & 10th World Congress of Academic and Environmental Pathology. 1992.
Chromosomes changes in adipose tissue tumors
ETV6 rearrangements in patients with infantile fibrosarcomas and congenital mesoblastic nephromas by fluorescence in situ hybridization. Mod Pathol. 2001 Dec; 14(12):1246-51.
ETV6 rearrangements in patients with infantile fibrosarcomas and congenital mesoblastic nephromas by fluorescence in situ hybridization.
Reporting of diagnostic cytogenetic results. Curr Protoc Hum Genet. 2004 Nov; Appendix 1:Appendix 1D.
Speleman F, De Potter C, Dal Cin P, Mangelschots K, Ingelaere H, Laureys G, Benoit Y, Leroy J, Van Den Berghe H
i(12p) in a malignant ovarian tumor. Cancer Genet Cytogenet. 1990 Mar; 45(1):49-53.
Mertz KD, Demichelis F, Sboner A, Hirsch MS, Dal Cin P, Struckmann K, Storz M, Scherrer S, Schmid DM, Strebel RT, Probst-Hensch NM, Gerstein M, Moch H, Rubin MA
Association of cytokeratin 7 and 19 expression with genomic stability and favorable prognosis in clear cell renal cell cancer. Int J Cancer. 2008 Aug 01; 123(3):569-76.
Association of cytokeratin 7 and 19 expression with genomic stability and favorable prognosis in clear cell renal cell cancer.
Lee C, Drandi SD, Dal Cin P, Gribben JG.
Prognostic marker in CLL by array-based comparative genomic hyndidization. American Society of Human Genetics. 52th Annual Meeting. 2003; Los Angeles, CA.
Prognostic marker in CLL by array-based comparative genomic hyndidization
t(1;12)(p36;q13) in a renal oncocytoma.Chromosome 12 Genes in Cancer. 1995; Leuven, Belgium.
t(1;12)(p36;q13) in a renal oncocytoma.Chromosome 12 Genes in Cancer
Proceedings of the German Society of Pathology
Cytogenetics of soft tissue tumours. Proceedings of the German Society of Pathology. 1998; 82:47-58.
Dal Cin P, Vanni R, Marras S, Moerman PH, Kools P, Andria M, Valdes E, Deprest J, Van den Berghe H, Van de Ven W.
Four cytogenetic subgroups can be identified in endometrial polyps. 6th International Workshop on Chromosomes in Solid Tumors. Cancer Genet Cytogenet. 1995; (84):153.
Four cytogenetic subgroups can be identified in endometrial polyps. 6th International Workshop on Chromosomes in Solid Tumors
The 6p21 chromosome region is non randomly involved in endometrial polyps.Eighty-third Annual Meeting of the American Association for Cancer Research. Proceedings of the American Association for Cancer Research. 1992; (33):398.
The 6p21 chromosome region is non randomly involved in endometrial polyps.Eighty-third Annual Meeting of the American Association for Cancer Research
A de novo AML with a t(1;21)(p36;q22) in an elderly patient. Atlas Genet Cytogenet Oncol Haematol.
A de novo AML with a t(1;21)(p36;q22) in an elderly patient. Atlas Genet Cytogenet Oncol Haematol. 2007.
Cytogenetics in the diagnosis of soft tumors. Eur J Cancer suppl. 1991; (27):S5.
Cytogenetics in the diagnosis of soft tumors
Psihramis KE, Dal Cin P, Dretler SP, Prout GR, Sandberg AA
Further evidence that renal oncocytoma has malignant potential. J Urol. 1988 Mar; 139(3):585-7.
Further evidence that renal oncocytoma has malignant potential.
Hernández JM, Schoenmakers EF, Dal Cin P, Michaux L, Van de Ven WJ, Van den Berghe H
Molecular delineation of the commonly deleted segment in mature B-cell lymphoid neoplasias with deletion of 7q. Genes Chromosomes Cancer. 1997 Feb; 18(2):147-50.
Molecular delineation of the commonly deleted segment in mature B-cell lymphoid neoplasias with deletion of 7q.
Tallini G, Dal Cin P, Rhoden KJ, Chiapetta G, Manfioletti G, Giancotti V, Fusco A, Van den Berghe H, Sciot R
Expression of HMGI-C and HMGI(Y) in ordinary lipoma and atypical lipomatous tumors: immunohistochemical reactivity correlates with karyotypic alterations. Am J Pathol. 1997 Jul; 151(1):37-43.
Expression of HMGI-C and HMGI(Y) in ordinary lipoma and atypical lipomatous tumors: immunohistochemical reactivity correlates with karyotypic alterations.
Nascimento AF, Dal Cin P, Cilento BG, Perez-Atayde AR, Kozakewich HP, Nosé V
Urachal inflammatory myofibroblastic tumor with ALK gene rearrangement: a study of urachal remnants. Urology. 2004 Jul; 64(1):140-4.
Urachal inflammatory myofibroblastic tumor with ALK gene rearrangement: a study of urachal remnants.
Dal Cin P, Sneyers W, Aly MS, Segers A, Ostijn F, Van Damme B, Van Den Berghe H
Involvement of 19q13 in follicular thyroid adenoma. Cancer Genet Cytogenet. 1992 May; 60(1):99-101.
Involvement of 19q13 in follicular thyroid adenoma.
Van Dorpe J, Dal Cin P, Weremowicz S, Van Leuven F, de Wever I, Van den Berghe H, Fletcher CD, Sciot R
Translocation of the HMGI-C ( HMGA2) gene in a benign mesenchymoma (chondrolipoangioma). Virchows Arch. 2002 May; 440(5):485-90.
Translocation of the HMGI-C ( HMGA2) gene in a benign mesenchymoma (chondrolipoangioma).
Chromosome changes in soft tissue tumors: benign and malignant. Cancer Invest. 1989; 7(1):63-76.
Chromosome changes in soft tissue tumors: benign and malignant.
Herrera AF, Rodig SJ, Song JY, Kim Y, Griffin GK, Yang D, Nikolaenko L, Mei M, Bedell V, Dal Cin P, Pak C, Alyea EP, Budde LE, Chen R, Chen YB, Chan WC, Cutler CS, Ho VT, Koreth J, Krishnan A, Murata-Collins JL, Nikiforow S, Palmer J, Pihan GA, Pillai R, Popplewell L, Rosen ST, Siddiqi T, Sohani AR, Zain J, Kwak LW, Weisenburger DD, Weinstock DM, Soiffer RJ, Antin JH, Forman SJ, Nademanee AP, Armand P
Outcomes after Allogeneic Stem Cell Transplantation in Patients with Double-Hit and Double-Expressor Lymphoma. Biol Blood Marrow Transplant. 2018 03; 24(3):514-520.
Outcomes after Allogeneic Stem Cell Transplantation in Patients with Double-Hit and Double-Expressor Lymphoma.
Roehrl MH, Selig MK, Nielsen GP, Dal Cin P, Oliva E
A renal cell carcinoma with components of both chromophobe and papillary carcinoma. Virchows Arch. 2007 Jan; 450(1):93-101.
A renal cell carcinoma with components of both chromophobe and papillary carcinoma.
Nucci MR, Harburger D, Koontz J, Dal Cin P, Sklar J
Molecular analysis of the JAZF1-JJAZ1 gene fusion by RT-PCR and fluorescence in situ hybridization in endometrial stromal neoplasms. Am J Surg Pathol. 2007 Jan; 31(1):65-70.
Molecular analysis of the JAZF1-JJAZ1 gene fusion by RT-PCR and fluorescence in situ hybridization in endometrial stromal neoplasms.
Turc-Carel C, Dal Cin P, Limon J, Li F, Sandberg AA
Translocation X;18 in synovial sarcoma. Cancer Genet Cytogenet. 1986 Sep; 23(1):93.
Aly MS, Dal Cin P, Moerman P, De Wever I, Devriendt K, Brock P, Casteels-Van Damme M, Van den Berghe H.
5th International Workshop on Chromosomes in solid Tumors.
Loss of the Y-chromosome in a malignant Sertoly tumor. 5th International Workshop on Chromosomes in solid Tumors. 1993.
Loss of the Y-chromosome in a malignant Sertoly tumor
Schoenmakers EFPM, Kazmierczak B, Kools PFJ, Mols R, Dal Cin P, Bullerdiek J, Van den Berghe H, Van de Ven WJM.
Development and characterization of cell lines from a myxoid liposarcoma with t(12;16)(q13;p11.2) and trisomy 8. Chromosome 12 Aberrations in Human Solid Tumors. Cytogenetics and Molecular Genetics. 1994; 138-51.
Development and characterization of cell lines from a myxoid liposarcoma with t(12;16)(q13;p11.2) and trisomy 8
Array-based comparative Genomic Hybridization: Whole Genome Screening in CLL. International Workshop in CLL. 2003; Stresa, Italy.
Array-based comparative Genomic Hybridization: Whole Genome Screening in CLL
Dal Cin P, Turc Carel C, Limon J, Parry DM, Li FP, Sandberg AA.
Reciprocal translocations involving Xp11.2 and 18q11.2 in soft tissue sarcomas. Cancer Genet Cytogenet. 1987; (28):40.
Reciprocal translocations involving Xp11.2 and 18q11.2 in soft tissue sarcomas
The 6p21 chromosome region is non randomly involved in endometrial polyps. First International Workshop on Chromosome 6. Cytogenet Cell Genet. 1993; (62):82.
The 6p21 chromosome region is non randomly involved in endometrial polyps. First International Workshop on Chromosome 6
Some aspects of chromosomes and oncogenes in hematologic malignancies. Biol Clin Hematológia. 1989; 11:45 -51.
Some aspects of chromosomes and oncogenes in hematologic malignancies
Coccia M, Meltzer P, Dal Cin P, Turc Carel C, Sait S, Sandberg AA.
DNA sequence amplification in malignant fibrous histiocytoma tumors. 3rd International Workshop on Chromosomes in Solid Tumors. 1989.
DNA sequence amplification in malignant fibrous histiocytoma tumors
Herrmann ME, Belge G, Stern C, Dal Cin P, Bullerdiek J, Bartnitzke S.
Breakpoints and recipient chromosomes in pleomorphic adenomas, lipomas, and uterine leiomyomas - what do they tell us?. Chromosome 12 Aberrations in Human Solid Tumors. Cytogenetics and Molecular Genetics. 1994; 46-52.
Breakpoints and recipient chromosomes in pleomorphic adenomas, lipomas, and uterine leiomyomas - what do they tell us?
Cuneo A, Ferrant A, Michaux JL, Chatelain B, Stul, M, Dal Cin P, Begoni R., Matteo Rigolin G, Castoldi ., Van den Berghe, H.
Cytogenetic and clinicobiologic features of acute undifferentiated leukemia with stem cell phenotype. Study of nine cases. Second Meeting of the European Haematology Association. Brit J Haematol. Suppl 2. 1996; (93):327.
Cytogenetic and clinicobiologic features of acute undifferentiated leukemia with stem cell phenotype. Study of nine cases. Second Meeting of the European Haematology Association
Savage KJ, Monti S, Kutok JL, Cattoretti G, Neuberg D, de Laval L, Kurtin P, Dal Cin P, Ladd C, Feuerhake F, Aguiar R, Li S, Salles G, Berger F, Jing W, Pinkus G, Habermann T, Dalla-Favera R, Harris N, Aster JC, Golub T, Shipp M.
The molecular signature of mediastinal large B-cell lymphoma differs from that of other diffuse Large B-cell lymphomas and shares features with classical Hodgkin’s lymphoma. American Society of Hematology, 45th Annual Meeting. 2003; San Diego, CA.
The molecular signature of mediastinal large B-cell lymphoma differs from that of other diffuse Large B-cell lymphomas and shares features with classical Hodgkin’s lymphoma
Breakpoints 9q22 q31 and 22q12 are associated with extraskeletal myxoid chondrosarcoma. Human Gene Mapping 9. 1987.
Breakpoints 9q22 q31 and 22q12 are associated with extraskeletal myxoid chondrosarcoma
Dal Cin P, Diaz MC, Vargas A, Sanoja A, Piras R, Piras MM.
Analisis de resultados de 814 diagnosticos prenatales para alteraciones cromosomicas y defectos del tubo neural. (Analysis of 814 prenatal diagnoses for chromosomal aberrations and neural tube defects). Acta Cient Venez. 1983; 34:345.
Analisis de resultados de 814 diagnosticos prenatales para alteraciones cromosomicas y defectos del tubo neural. (Analysis of 814 prenatal diagnoses for chromosomal aberrations and neural tube defects)
Uyttebroeck A, Brock P, De Groote B, Renard M, Dal Cin P, Van den Berghe H, Casteels-Van Daele M
5q- syndrome in a child. Cancer Genet Cytogenet. 1995 Apr; 80(2):121-3.
Cuneo A, Demuynck H, Ferrant A, Louwagie A, Doyen C, Stul M, Cassiman JJ, Dal Cin P, Negrini M, Carli MG
Minor myeloid component in Ph chromosome-positive acute lymphoblastic leukaemia: correlation with cytogenetic pattern and implication for poor response to therapy. Br J Haematol. 1994 Jul; 87(3):515-22.
Minor myeloid component in Ph chromosome-positive acute lymphoblastic leukaemia: correlation with cytogenetic pattern and implication for poor response to therapy.
Sciot R, Dal Cin P, Samson I, Smith M., Fletcher C.
t(9;22)(q22-31;q11-12) is a consistent marker of extraskeletal myxoid chondrosarcoma. evalution of 3 cases. United States and Canadian Academy of Pathology. 1995; Toronto, Canada.
t(9;22)(q22-31;q11-12) is a consistent marker of extraskeletal myxoid chondrosarcoma. evalution of 3 cases
Dal Cin P, Turc Carel C, Sandberg AA, Van den Berghe H.
More precise localization of GLI gene by in situ hybridization. Human Genet Mapping 10. 1989.
More precise localization of GLI gene by in situ hybridization
Paolini P, Dal Cin P, Nascimento J, Ponce C.
Dos casos de trisomia 9p con cariotipos diferentes. 47,XX,+9q y 46,XX,dic(9)(pter„_q32..p22„_cen„_qter). (Two cases with trisomy 9p with different karyotypes. 47,XX,+9q and 46,XX,dic(9) (pter„_q32:p22„_cen„_qter). Acta Cient Venez. 1980; 31:136.
Dos casos de trisomia 9p con cariotipos diferentes. 47,XX,+9q y 46,XX,dic(9)(pter„_q32..p22„_cen„_qter). (Two cases with trisomy 9p with different karyotypes. 47,XX,+9q and 46,XX,dic(9) (pter„_q32:p22„_cen„_qter)
Neskey DM, Dal Cin P, SWeremowicz S, B.J. Quade BJ, C.C. Morton CC.
Understanding the Molecular Mechanism of Dysregulated HMGA2 Expression in Uterine Leiomyomata with 12q15 Rearrangements. American Society of Human Genetics. 51th Annual Meeting. 2002; Philadelphia, USA.
Understanding the Molecular Mechanism of Dysregulated HMGA2 Expression in Uterine Leiomyomata with 12q15 Rearrangements. American Society of Human Genetics
Trindade CS, Connelly R, Hashimura T, Sandberg AA, Dal Cin P, Tubbs R.
Establishment of two new renal cell carcinoma lines. Biological difference of cells from the primary tumor versus those of renal vein effluent. J Urol. 1987; (137):252A.
Establishment of two new renal cell carcinoma lines. Biological difference of cells from the primary tumor versus those of renal vein effluent
Speleman F, Mangelschots K, Vercruyssen M, Dal Cin P, Aventin A, Offner F, Laureys G, Leroy J, Van den Berghe H.
European Society of Human Genetics Symposium.
Analysis of whole-arm translocations in malignant hematologic cells by non-isotopic in situ hybridization. European Society of Human Genetics Symposium. 1990.
Analysis of whole-arm translocations in malignant hematologic cells by non-isotopic in situ hybridization
Dal Cin P, Wanschura, Moerman,Ph. Sciot R, Christiaens MR, Kazmierczak B, Bullerdiek J, Van den Berghe H.
Different breast tumors with involvement of different HMG genes in the same patient. 7th International Workshop on Chromosomes in Solid Tumors. Cancer Genet Cytogenet. 1997; 98:157.
Different breast tumors with involvement of different HMG genes in the same patient. 7th International Workshop on Chromosomes in Solid Tumors
Bossuyt V , Ginevan K, Dal Cin P, Fletcher J, Cibas E S.
The value of cytogenetics as an adjunct to cytology in the diagnosis of non-hematopoietic neoplasms. United States and Canadian Academy of Pathology. 2007; San Diego, California .
The value of cytogenetics as an adjunct to cytology in the diagnosis of non-hematopoietic neoplasms
Roh MH, Dal Cin P, Silverman SG, Cibas ES
The application of cytogenetics and fluorescence in situ hybridization to fine-needle aspiration in the diagnosis and subclassification of renal neoplasms. Cancer Cytopathol. 2010 Jun 25; 118(3):137-45.
The application of cytogenetics and fluorescence in situ hybridization to fine-needle aspiration in the diagnosis and subclassification of renal neoplasms.
Sait SN, Dal Cin P, Sandberg AA, Leong S, Karakousis C, Rao U, Harris K
Involvement of 6p in benign lipomas. A new cytogenetic entity? Cancer Genet Cytogenet. 1989 Feb; 37(2):281-3.
Involvement of 6p in benign lipomas. A new cytogenetic entity?
Smoley SA, Van Dyke DL, Kay NE, Heerema NA, Dell' Aquila ML, Dal Cin P, Koduru P, Aviram A, Rassenti L, Byrd JC, Rai KR, Brown JR, Greaves AW, Eckel-Passow J, Neuberg D, Kipps TJ, Dewald GW
Standardization of fluorescence in situ hybridization studies on chronic lymphocytic leukemia (CLL) blood and marrow cells by the CLL Research Consortium. Cancer Genet Cytogenet. 2010 Dec; 203(2):141-8.
Standardization of fluorescence in situ hybridization studies on chronic lymphocytic leukemia (CLL) blood and marrow cells by the CLL Research Consortium.
Cuneo A, Kerim S, Vandenberghe E, Van Orshoven A, Rodhain J, Bosly A, Zachee P, Louwagie A, Michaux JL, Dal Cin P
Translocation t(6;9) occurring in acute myelofibrosis, myelodysplastic syndrome, and acute nonlymphocytic leukemia suggests multipotent stem cell involvement. Cancer Genet Cytogenet. 1989 Oct 15; 42(2):209-19.
Translocation t(6;9) occurring in acute myelofibrosis, myelodysplastic syndrome, and acute nonlymphocytic leukemia suggests multipotent stem cell involvement.
Luskin MR, Discenza MN, Easter SR, Dal Cin P, Owen R, Ilagan B, Masiello M, Lane AA
Maternal iAMP21 acute lymphoblastic leukemia detected on prenatal cell-free DNA genetic screening. Blood Adv. 2017 Aug 22; 1(19):1491-1494.
Maternal iAMP21 acute lymphoblastic leukemia detected on prenatal cell-free DNA genetic screening.
Medeiros F, Araujo AR, Erickson-Johnson MR, Kashyap PC, Dal Cin P, Nucci M, Wang X, Bell DA, Oliveira AM
HMGA1 and HMGA2 rearrangements in mass-forming endometriosis. Genes Chromosomes Cancer. 2010 Jul; 49(7):630-4.
HMGA1 and HMGA2 rearrangements in mass-forming endometriosis.
Speleman F, De Telder V, De Potter KR, Dal Cin P, Van Daele S, Benoit Y, Leroy JG, Van den Berghe H
Cytogenetic analysis of a mesenchymal hamartoma of the liver. Cancer Genet Cytogenet. 1989 Jul 01; 40(1):29-32.
Cytogenetic analysis of a mesenchymal hamartoma of the liver.
Morphologic, immunologic, and cytogenetic classification of the chronic (mature) B and T lymphoid leukemias. Cancer Res. 1990; 2212.
Morphologic, immunologic, and cytogenetic classification of the chronic (mature) B and T lymphoid leukemias
Oliveira AM, Perez-Atayde AR, Dal Cin P, Gebhardt MC, Rosenberg RE, Bridge JA, and Fletcher JA .
Novel USP6 Tfusion omcogenes with TRAP150, ZNF9, Osteomodulin and COL1A1 in aneurysmal bone cyst variant translocations. United States and Canadian Academy of Pathology. 2005; San Antonio, Texas.
Novel USP6 Tfusion omcogenes with TRAP150, ZNF9, Osteomodulin and COL1A1 in aneurysmal bone cyst variant translocations
Current clinical Oncology. Muggia F, Olivia E.
Uterine cancer: Screening, Diagnosis, and Treatment. Current clinical Oncology. Muggia F, Olivia E. 2008.
Uterine cancer: Screening, Diagnosis, and Treatment
Chromosomes in solid tumors. 1993; South Africa .
Gole L, Kazmierczak B, Jox A, Dal Cin P, Bullerdiek J, Bartnitzke S.
Malignant tumors from cell lines derived from tumors with 12q13-15 aberrations. International Workshop on Cytogenetics and Molecular Genetics of Chromosome 12 in Human Solid Tumors. 1992.
Malignant tumors from cell lines derived from tumors with 12q13-15 aberrations
Van Poppel H, Dal Cin P, Aly MS, Delabie J, Ceuppens J, Van Damme B, Baert L, Van den Berghe H.
Euro-American Conference on Urological Cancer.
Cytogenetic investigations in normal and malignant kidney tissues. Euro-American Conference on Urological Cancer. 1992.
Knight JC, Renwick PJ, Dal Cin P, Van den Berghe H, Fletcher CD
Translocation t(12;16)(q13;p11) in myxoid liposarcoma and round cell liposarcoma: molecular and cytogenetic analysis. Cancer Res. 1995 Jan 01; 55(1):24-7.
Translocation t(12;16)(q13;p11) in myxoid liposarcoma and round cell liposarcoma: molecular and cytogenetic analysis.
Liang CW, Mariño-Enríquez A, Johannessen C, Hornick JL, Dal Cin P
Translocation (Y;12) in lipoma. Cancer Genet. 2011 Jan; 204(1):53-6.
Poitras JL, Costa D, Kluk MJ, Amrein PC, Stone RM, Lee C, Dal Cin P, Morton CC
Genomic alterations in myeloid neoplasms with novel, apparently balanced translocations. Cancer Genet. 2011 Feb; 204(2):68-76.
Genomic alterations in myeloid neoplasms with novel, apparently balanced translocations.
Van den Berghe E, De Wolf-Peeters C, Louwagie A, Thomas J, Wlodarska I, Dal Cin P, Stul M, Cassiman JJ, Mecucci C, Van den Berghe H
Chromosome 1p abnormalities in B non-Hodgkin lymphoma. Leukemia and Lymphoma. 1991; 5:193-1999.
Chromosome 1p abnormalities in B non-Hodgkin lymphoma
Hernández JM, Michaux L, Schoenmakers EFPM, Dal Cin P, Criel A, Van Orshoven A, De Wolf-Peeters C, Van de Ven WJM, Mecucci C, Van den Berghe H.
Clinical, biological and molecular characterization of del(7)(q) in B-cell chronic lymphoid malignancies.Second Meeting of the European Haematology Association. Brit. J. Haematol. 93. 1996; (Suppl. 2):283.
Clinical, biological and molecular characterization of del(7)(q) in B-cell chronic lymphoid malignancies.Second Meeting of the European Haematology Association
Faul PN, French CA, Vargas SO, Dal Cin P, Fletcher JA, Perez-Atayde AR.
Larynx as a primary site for t(15;19) carcinoma, a distinct rapidly fatal disease of young patients. United States and Canadian Academy of Pathology. 2001; Atlanta, Georgia.
Larynx as a primary site for t(15;19) carcinoma, a distinct rapidly fatal disease of young patients
Cytogenetic abnormalities and human cancer. ISI Atlas Science. Biochem. 1988; (1):273-78.
Cytogenetic abnormalities and human cancer
Non-papillary renal cell carcinoma is characterized by monosmy 3p and papillary renal cell carcinoma by trisomy 17 and other chromosome changes. XIth Congress of the European Association of Urology. 1994; Berlin, Germany.
Non-papillary renal cell carcinoma is characterized by monosmy 3p and papillary renal cell carcinoma by trisomy 17 and other chromosome changes
Sciot R, Dal Cin P, Fletcher CDM, De Wever I, Van den Berghe H.
6th International Workshop on Chromosomes in Solid Tumors.
Monosomy of chromosome 22 in a malignant peripheral nerve sheath tumor of the kidney. 6th International Workshop on Chromosomes in Solid Tumors. 1995; Tucson, AZ.
Monosomy of chromosome 22 in a malignant peripheral nerve sheath tumor of the kidney
Feuerhake F, Dal Cin P, Kurtin P, Pasqualucci L, Savage KJ, Kutok JL, Neuberg D , Aguiar RC, Monti S, Ladd C, Cattoretti G, Pinkus GS, Harris NL, Habermann T,Golub TR, Dalla-Favera R, Aster JC, Shipp MA.
Genetic heterogeneity in diffuse large B-cell lymphoma (DLBCL): Chromosomal translocations and increased copy numbers, gene amplification, and aberrant somatic hypermutation. American Society of Hematology, 45th Annual Meeting. 2003; San Diego, CA.
Genetic heterogeneity in diffuse large B-cell lymphoma (DLBCL): Chromosomal translocations and increased copy numbers, gene amplification, and aberrant somatic hypermutation
Polito P, Dal Cin P, Debiec-Rychter M , Hagemeijer A.
Methods in Molecular Biology. Cytogenetics: Methods and Protocols.G.J. Swansbury ed
Human Solid Tumors: Cytogenetics techniques. Methods in Molecular Biology. Cytogenetics: Methods and Protocols.G.J. Swansbury ed. 2003; 220:135-150.
Human Solid Tumors: Cytogenetics techniques
Turc-Carel C, Dal Cin P, Boghosian L, Terk-Zakarian J, Sandberg AA
Consistent breakpoints in region 14q22-q24 in uterine leiomyoma. Cancer Genet Cytogenet. 1988 May; 32(1):25-31.
Consistent breakpoints in region 14q22-q24 in uterine leiomyoma.
Bloomfield CD Kellie J Archer KJ, Raimondi SC, Harrison CJ, Kaneko Y,Head D, Dal Cin P, a Rowley JD.
2th International Workshop on BCA in Secondary Leukemia (IWBCASL), (Chicago, IL). Among Therapy-Associated Acute Leukemia Or Myelodysplastic Syndrome (t-AL/MDS) With Balanced Cytogenetic Abnormalities (BCA), Those Involving 11q23 Are Associated With Distinctive Prior Therapeutic Exposures And Clinical Features, Including Adverse Outcome. 43rd ASH Annual Meeting. 2001; Orlando, Fl.
2th International Workshop on BCA in Secondary Leukemia (IWBCASL), (Chicago, IL). Among Therapy-Associated Acute Leukemia Or Myelodysplastic Syndrome (t-AL/MDS) With Balanced Cytogenetic Abnormalities (BCA), Those Involving 11q23 Are Associated With Distinctive Prior Therapeutic Exposures And Clinical Features, Including Adverse Outcome
Dal Cin P, Neskey DM, Weremowicz S, Morton CC, Quade BJ.
Intravenous Leiomyomatosis: Is There A Genetic Link With Uterine Leiomyoma?. United States and Canadian Academy of Pathology. 2001; Atlanta, Georgia.
Intravenous Leiomyomatosis: Is There A Genetic Link With Uterine Leiomyoma?
Van Roy N, Laureys G, Benoit Y, Heyman P, Sariban E, Caron H, Dal Cin P, Brock P.R., Speleman F.
Molecular cytogenetic detection of chromosome 1 abnormalities and MYCN amplification in neuroblastoma interphase nuclei. Third European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors. Cancer Genet Cytogenet. 1992; (63):167.
Molecular cytogenetic detection of chromosome 1 abnormalities and MYCN amplification in neuroblastoma interphase nuclei. Third European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors
Fan YS, Baer MR, Sait SN, Dal Cin P, Prentice TC, Preisler HD, Sandberg AA
An acquired Robertsonian translocation dic(14;14)(p11;p11) in a patient with a myelodysplastic syndrome following treatment of multiple myeloma. Cancer Genet Cytogenet. 1988 Jan; 30(1):133-7.
An acquired Robertsonian translocation dic(14;14)(p11;p11) in a patient with a myelodysplastic syndrome following treatment of multiple myeloma.
Cytogenetic findings in leiomyosarcoma of the small bowel. Cancer Genet Cytogenet. 1988 Feb; 30(2):285-8.
Cytogenetic findings in leiomyosarcoma of the small bowel.
Translocations involving the X chromosome in solid tumors: presentation of two sarcomas with t(X;18)(q13;p11). Cancer Genet Cytogenet. 1986 Sep; 23(1):87-91.
Translocations involving the X chromosome in solid tumors: presentation of two sarcomas with t(X;18)(q13;p11).
Dal Cin P, Kools P, Sciot R, De Wever I, Van Damme B, Van de Ven W, Van den Berghe H
Cytogenetic and fluorescence in situ hybridization investigation of ring chromosomes characterizing a specific pathologic subgroup of adipose tissue tumors. Cancer Genet Cytogenet. 1993 Jul 15; 68(2):85-90.
Cytogenetic and fluorescence in situ hybridization investigation of ring chromosomes characterizing a specific pathologic subgroup of adipose tissue tumors.
Factor RE, Dal Cin P, Fletcher JA, Cibas ES
Cytogenetics and fluorescence in situ hybridization as adjuncts to cytology in the diagnosis of malignant mesothelioma. Cancer. 2009 Aug 25; 117(4):247-53.
Cytogenetics and fluorescence in situ hybridization as adjuncts to cytology in the diagnosis of malignant mesothelioma.
Chromosome 1p abnormalities in B non Hodgkin's lymphoma. Leuk Lymphoma. 1991; 5(2-3):193-9.
Chromosome 1p abnormalities in B non Hodgkin's lymphoma.
Doyle LA, Möller E, Dal Cin P, Fletcher CD, Mertens F, Hornick JL
MUC4 is a highly sensitive and specific marker for low-grade fibromyxoid sarcoma. Am J Surg Pathol. 2011 May; 35(5):733-41.
MUC4 is a highly sensitive and specific marker for low-grade fibromyxoid sarcoma.
Kluk MJ, Chapuy B, Sinha P, Roy A, Dal Cin P, Neuberg DS, Monti S, Pinkus GS, Shipp MA, Rodig SJ
Immunohistochemical detection of MYC-driven diffuse large B-cell lymphomas. PLoS One. 2012; 7(4):e33813.
Immunohistochemical detection of MYC-driven diffuse large B-cell lymphomas.
Ferguson B. Dubois Z, Merkhofer E, McLaughlin C, Powell K, Roy A, Sherman L, Soltisova D, Dal Cin P.
A technical approach to cytogenetic and molecular investigation of chronic lymphocytic leukemia. Association of Genetic Technologists, 29th Annual Meeting. 2004; Anaheim, CA.
A technical approach to cytogenetic and molecular investigation of chronic lymphocytic leukemia
Gibas Z, Limon J, Li FP, Karakousis C, Dal Cin P, Parry D, Sandberg AA.
Chromosomal rearrangements in soft tissue sarcomas. Cancer Genet Cytogenet. 1987; (28):33.
Chromosomal rearrangements in soft tissue sarcomas
Dal Cin P, Marynen P, Moerman P, Vergot I, Van den Berghe H
Ovarian germ cell tumor with chromosome 12 anomaly but without i(12p). Cancer Genet Cytogenet. 1996 Oct 01; 91(1):61-4.
Ovarian germ cell tumor with chromosome 12 anomaly but without i(12p).
Cuneo A, Ferrant A, Michaux JL, Bosly A, Chatelain B, Stul M, Dal Cin P, Dierlamm J, Cassiman JJ, Hossfeld DK, Castoldi G, Van den Berghe H
Cytogenetic and clinicobiological features of acute leukemia with stem cell phenotype: study of nine cases. Cancer Genet Cytogenet. 1996 Nov; 92(1):31-6.
Cytogenetic and clinicobiological features of acute leukemia with stem cell phenotype: study of nine cases.
Sciot R, Dal Cin P, Fletcher CD, Hernandez JM, Garcia JL, Samson I, Ramos L, Brys P, Van Damme B, Van den Berghe H
Inflammatory myofibroblastic tumor of bone: report of two cases with evidence of clonal chromosomal changes. Am J Surg Pathol. 1997 Oct; 21(10):1166-72.
Inflammatory myofibroblastic tumor of bone: report of two cases with evidence of clonal chromosomal changes.
Dal Cin P, Pauwels P, Poldermans LJ, Sciot R, Van den Berghe H
Clonal chromosome abnormalities in a so-called Dupuytren's subungual exostosis. Genes Chromosomes Cancer. 1999 Feb; 24(2):162-4.
Clonal chromosome abnormalities in a so-called Dupuytren's subungual exostosis.
Willén H, Akerman M, Dal Cin P, De Wever I, Fletcher CD, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, Van den Berghe H, Vanni R
Comparison of chromosomal patterns with clinical features in 165 lipomas: a report of the CHAMP study group. Cancer Genet Cytogenet. 1998 Apr 01; 102(1):46-9.
Comparison of chromosomal patterns with clinical features in 165 lipomas: a report of the CHAMP study group.
Dal Cin P, Van den Berghe H, Van Poppel H, Roskams T
Involvement of 12q12-13 is a nonrandom chromosome change in renal oncocytoma. Genes Chromosomes Cancer. 1999 Jan; 24(1):94.
Involvement of 12q12-13 is a nonrandom chromosome change in renal oncocytoma.
Balzarini P, Grigolato P, Tardanico R, Cadei M, Cunico SC, Cozzoli A, Zanotelli T, van den Berghe H, Dal Cin P
Multitechnical pathological diagnosis in chromophobe renal cell carcinoma. Oncol Rep. 1999 Mar-Apr; 6(2):295-9.
Multitechnical pathological diagnosis in chromophobe renal cell carcinoma.
Wanschura S, Dal Cin P, Kazmierczak B, Bartnitzke S, Van den Berghe H, Bullerdiek J
Hidden paracentric inversions of chromosome arm 12q affecting the HMGIC gene. Genes Chromosomes Cancer. 1997 Apr; 18(4):322-3.
Hidden paracentric inversions of chromosome arm 12q affecting the HMGIC gene.
Tejpar S, Nollet F, Li C, Wunder JS, Michils G, dal Cin P, Van Cutsem E, Bapat B, van Roy F, Cassiman JJ, Alman BA
Predominance of beta-catenin mutations and beta-catenin dysregulation in sporadic aggressive fibromatosis (desmoid tumor). Oncogene. 1999 Nov 11; 18(47):6615-20.
Predominance of beta-catenin mutations and beta-catenin dysregulation in sporadic aggressive fibromatosis (desmoid tumor).
Pauwels P, Dal Cin P, Vlasveld LT, Aleva RM, van Erp WF, Jones D
A chromosomal abnormality in hyaline vascular Castleman's disease: evidence for clonal proliferation of dysplastic stromal cells. Am J Surg Pathol. 2000 Jun; 24(6):882-8.
A chromosomal abnormality in hyaline vascular Castleman's disease: evidence for clonal proliferation of dysplastic stromal cells.
Dal Cin P, Atkins L, Ford C, Ariyanayagam S, Armstrong SA, George R, Cleary A, Morton CC
Amplification of AML1 in childhood acute lymphoblastic leukemias. Genes Chromosomes Cancer. 2001 Apr; 30(4):407-9.
Amplification of AML1 in childhood acute lymphoblastic leukemias.
Varnholt H, Vauthey JN, Dal Cin P, Marsh Rde W, Bhathal PS, Hughes NR, Lauwers GY
Biliary adenofibroma: a rare neoplasm of bile duct origin with an indolent behavior. Am J Surg Pathol. 2003 May; 27(5):693-8.
Biliary adenofibroma: a rare neoplasm of bile duct origin with an indolent behavior.
Cuneo A, Gretel Carli M, Piva N, Fagioli F, Vandenberghe E, Dal Cin P, Castoldi G, Van Den Berghe H
Clinicopathological evolution and multilineage involvement in erythroleukemia: report of a case. Haematologica. 1991 May-Jun; 76(3):235-7.
Clinicopathological evolution and multilineage involvement in erythroleukemia: report of a case.
Dal Cin P, Sciot R, Van Poppel H, Baert L, Van Damme B, Van den Berghe H
Chromosome analysis in angiomyolipoma. Cancer Genet Cytogenet. 1997 Dec; 99(2):132-4.
Dal Cin P, Dei Tos AP, Qi H, Giannini C, Furlanetto A, Longatti PL, Marynen P, Van den Berghe H
Immature teratoma of the pineal gland with isochromosome 12p. Acta Neuropathol. 1998 Jan; 95(1):107-10.
Immature teratoma of the pineal gland with isochromosome 12p.
Dal Cin P, Van Damme B, Hoogmartens M, Van Den Berghe H
Chromosome changes in a case of hibernoma. Genes Chromosomes Cancer. 1992 Sep; 5(2):178-80.
Chromosome changes in a case of hibernoma.
Kazmierczak B, Dal Cin P, Wanschura S, Borrmann L, Fusco A, Van den Berghe H, Bullerdiek J
HMGIY is the target of 6p21.3 rearrangements in various benign mesenchymal tumors. Genes Chromosomes Cancer. 1998 Dec; 23(4):279-85.
HMGIY is the target of 6p21.3 rearrangements in various benign mesenchymal tumors.
Gisselsson D, Höglund M, Mertens F, Dal Cin P, Mandahl N
Hibernomas are characterized by homozygous deletions in the multiple endocrine neoplasia type I region. Metaphase fluorescence in situ hybridization reveals complex rearrangements not detected by conventional cytogenetics. Am J Pathol. 1999 Jul; 155(1):61-6.
Hibernomas are characterized by homozygous deletions in the multiple endocrine neoplasia type I region. Metaphase fluorescence in situ hybridization reveals complex rearrangements not detected by conventional cytogenetics.
ALK expression in reactive pseudosarcomatous myofibroblastic proliferationns of the genitourinary tract. United States and Canadian Academy of Pathology. 2003; Washington, DC .
ALK expression in reactive pseudosarcomatous myofibroblastic proliferationns of the genitourinary tract
Lipomatous Tumors: Diagnosis and Primary Treatment. Surgical Oncology Series
Chromosomal abnormalities in adipose tissue tumors. Lipomatous Tumors: Diagnosis and Primary Treatment. Surgical Oncology Series. 1997; 4:31-41.
Chromosomal abnormalities in adipose tissue tumors
Bone: Aneurysmal bone cysts. Atlas Genet Cytogenet Oncol Haematol.
Bone: Aneurysmal bone cysts. Atlas Genet Cytogenet Oncol Haematol. 2002.
Durkin S, Ligon A, Kelly A, McLaughlin C, Dal Cin P.
Fishing for solutions: Adjust FISH analysis for myeloid malignancies with a non-clonal abnormality identified cytogenetically. 32nd AGT Annual Meeting. 2007; Denver, Colorado.
Fishing for solutions: Adjust FISH analysis for myeloid malignancies with a non-clonal abnormality identified cytogenetically
Dal Cin P, Speleman F, Van Roy N, Van Marck E, Buytaert P, Van den Berghe H.
4th International Workshop on Chromosomes in Solid Tumors.Cancer Genet Cytogenet
Is t(6;20)(p21;q13) a characteristic chromosome change in endometrial polyp?. 4th International Workshop on Chromosomes in Solid Tumors.Cancer Genet Cytogenet. 1991; (56):85.
Is t(6;20)(p21;q13) a characteristic chromosome change in endometrial polyp?
Trisomy 7 and trisomy 10 characterize subpopulations of tumor-infiltrating lymphocytes in kidney tumors and in the surrounding kidney tissue. 1993; South Africa.
Quade BJ, Neskey DM, Nucci MR, Dal Cin P, WangT-Y.
Müllerian Adenosarcomas not characterized by marked chromosomal or genomic nstability. United States and Canadian Academy of Pathology. 2001; Atlanta, Georgia.
Müllerian Adenosarcomas not characterized by marked chromosomal or genomic nstability
Fibrosarcoma versus cellular fibroma of the ovary. Am J Surg Pathol. 1998 Apr; 22(4):508-10.
Fibrosarcoma versus cellular fibroma of the ovary.
Dal Cin P, Bertoni F, Bacchini P, Hagemeijer A, Van den Berghe H
Fibrous dysplasia and the short arm of chromosome 12. Histopathology. 1999 Mar; 34(3):279-80.
Fibrous dysplasia and the short arm of chromosome 12.
Sciot R, Samson I, van den Berghe H, Van Damme B, Dal Cin P
Collagenous fibroma (desmoplastic fibroblastoma): genetic link with fibroma of tendon sheath? Mod Pathol. 1999 Jun; 12(6):565-8.
Collagenous fibroma (desmoplastic fibroblastoma): genetic link with fibroma of tendon sheath?
Sciot R, Dal Cin P, Hagemeijer A, De Smet L, Van Damme B, Van den Berghe H
Cutaneous sclerosing perineurioma with cryptic NF2 gene deletion. Am J Surg Pathol. 1999 Jul; 23(7):849-53.
Cutaneous sclerosing perineurioma with cryptic NF2 gene deletion.
Third International Workshop ”HMGA protein in cell differentiation and trasformation”.
HMGIC(HMGA2) in adipose tissue tumors. Third International Workshop ”HMGA protein in cell differentiation and trasformation”. 2002; Napoli,Italy.
Loss of the Y-chromosome in a malignant Sertoli tumor. Southern African Society of Human Genetics, 5th Congress. 1993; South Africa.
Dal Cin P, Roskams T, Van Poppel H, Balzarini P, Van den Berghe H
Cytogenetic investigation of transitional cell carcinomas of the upper urinary tract. Cancer Genet Cytogenet. 1999 Oct 15; 114(2):117-20.
Cytogenetic investigation of transitional cell carcinomas of the upper urinary tract.
Meltzer PS, Jankowski SA, Dal Cin P, Sandberg AA, Paz IB, Coccia MA
Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research
Identification and cloning of a novel amplified DNA sequence in human malignant fibrous histiocytoma derived from a region of chromosome 12 frequently rearranged in soft tissue tumors. Cell Growth Differ. 1991 Oct; 2(10):495-501.
Identification and cloning of a novel amplified DNA sequence in human malignant fibrous histiocytoma derived from a region of chromosome 12 frequently rearranged in soft tissue tumors.
Colwell AS, D'Cunha J, Vargas SO, Parker B, Dal Cin P, Maddaus MA
The Journal of thoracic and cardiovascular surgery
Synovial sarcoma of the pleura: a clinical and pathologic study of three cases. J Thorac Cardiovasc Surg. 2002 Oct; 124(4):828-32.
Synovial sarcoma of the pleura: a clinical and pathologic study of three cases.
Polito P, Dal Cin P, Debiec-Rychter M, Hagemeijer A
Methods in molecular biology (Clifton, N.J.)
Human solid tumors: cytogenetic techniques. Methods Mol Biol. 2003; 220:135-50.
Human solid tumors: cytogenetic techniques.
Savage KJ, Monti S, Kutok JL, Cattoretti G, Neuberg D, De Leval L, Kurtin P, Dal Cin P, Ladd C, Feuerhake F, Aguiar RC, Li S, Salles G, Berger F, Jing W, Pinkus GS, Habermann T, Dalla-Favera R, Harris NL, Aster JC, Golub TR, Shipp MA
The molecular signature of mediastinal large B-cell lymphoma differs from that of other diffuse large B-cell lymphomas and shares features with classical Hodgkin lymphoma. Blood. 2003 Dec 01; 102(12):3871-9.
The molecular signature of mediastinal large B-cell lymphoma differs from that of other diffuse large B-cell lymphomas and shares features with classical Hodgkin lymphoma.
Uyttebroeck A, De Groote B, Renard M, Brock P, Dal Cin P, Van den Berghe H, Casteels-Van Daele M.
International Society of Paediatric Oncology (SIOP) XXIVth Meeting.
The occurrence of 5q- syndrome in a child. International Society of Paediatric Oncology (SIOP) XXIVth Meeting. 1992.
The occurrence of 5q- syndrome in a child