Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Cynthia Casson Morton, Ph.D.

Co-Author

This page shows the publications co-authored by Cynthia Morton and Stanislawa Weremowicz.
Connection Strength

1.907
  1. Is HMGIC rearranged due to cryptic paracentric inversion of 12q in karyotypically normal uterine leiomyomas? Genes Chromosomes Cancer. 1999 Feb; 24(2):172-3.
    View in: PubMed
    Score: 0.211
  2. Validation of DNA probes for preimplantation genetic diagnosis (PGD) by fluorescence in situ hybridization (FISH) R1. Prenat Diagn. 2006 Nov; 26(11):1042-50.
    View in: PubMed
    Score: 0.090
  3. HMGA2 expression in uterine leiomyomata and myometrium: quantitative analysis and tissue culture studies. Genes Chromosomes Cancer. 2003 Sep; 38(1):68-79.
    View in: PubMed
    Score: 0.072
  4. 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.
    View in: PubMed
    Score: 0.070
  5. Intravenous leiomyomatosis is characterized by a der(14)t(12;14)(q15;q24). Genes Chromosomes Cancer. 2003 Feb; 36(2):205-6.
    View in: PubMed
    Score: 0.070
  6. Intravenous leiomyomatosis: molecular and cytogenetic analysis of a case. Mod Pathol. 2002 Mar; 15(3):351-6.
    View in: PubMed
    Score: 0.065
  7. Fluorescence in situ hybridization (FISH) for rapid detection of aneuploidy: experience in 911 prenatal cases. Prenat Diagn. 2001 Apr; 21(4):262-9.
    View in: PubMed
    Score: 0.061
  8. A novel conserved cochlear gene, OTOR: identification, expression analysis, and chromosomal mapping. Genomics. 2000 Jun 15; 66(3):242-8.
    View in: PubMed
    Score: 0.058
  9. Dysregulation of HMGIC in a uterine lipoleiomyoma with a complex rearrangement including chromosomes 7, 12, and 14. Genes Chromosomes Cancer. 2000 Feb; 27(2):209-15.
    View in: PubMed
    Score: 0.056
  10. Expression of HMGIY in three uterine leiomyomata with complex rearrangements of chromosome 6. Cancer Genet Cytogenet. 1999 Oct 01; 114(1):9-16.
    View in: PubMed
    Score: 0.055
  11. Localization and expression of the human estrogen receptor beta gene in uterine leiomyomata. Genes Chromosomes Cancer. 1998 Dec; 23(4):361-6.
    View in: PubMed
    Score: 0.052
  12. Cytogenetic abnormalities in uterine myomas are associated with myoma size. Mol Hum Reprod. 1998 Jan; 4(1):83-6.
    View in: PubMed
    Score: 0.049
  13. Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9. Genomics. 1997 Dec 15; 46(3):345-54.
    View in: PubMed
    Score: 0.049
  14. An ancient conserved gene expressed in the human inner ear: identification, expression analysis, and chromosomal mapping of human and mouse antiquitin (ATQ1). Genomics. 1997 Dec 01; 46(2):191-9.
    View in: PubMed
    Score: 0.049
  15. A gene similar to PKD1 maps to chromosome 4q22: a candidate gene for PKD2. Genomics. 1996 Nov 15; 38(1):1-4.
    View in: PubMed
    Score: 0.045
  16. Translocation breakpoints upstream of the HMGIC gene in uterine leiomyomata suggest dysregulation of this gene by a mechanism different from that in lipomas. Genes Chromosomes Cancer. 1996 Sep; 17(1):1-6.
    View in: PubMed
    Score: 0.045
  17. Reporting of Diagnostic Cytogenetic Results. Curr Protoc Hum Genet. 2016 Apr 01; 89:A.1D.1-A.1D.23.
    View in: PubMed
    Score: 0.043
  18. Translocations in 7q22 define a critical region in uterine leiomyomata. Cancer Genet Cytogenet. 1994 Oct; 77(1):65-8.
    View in: PubMed
    Score: 0.039
  19. Identification of genetically aberrant cell lineages in Wilms' tumors. Genes Chromosomes Cancer. 1994 May; 10(1):40-8.
    View in: PubMed
    Score: 0.038
  20. Cytogenetic evidence for a chromosome 22 tumor suppressor gene in ependymoma. Cancer Genet Cytogenet. 1992 Jul 15; 61(2):193-6.
    View in: PubMed
    Score: 0.033
  21. Reporting of diagnostic cytogenetic results. Curr Protoc Hum Genet. 2011 Jul; Appendix 1:1D.
    View in: PubMed
    Score: 0.031
  22. Localization of the human angiogenin gene to chromosome band 14q11, proximal to the T cell receptor alpha/delta locus. Am J Hum Genet. 1990 Dec; 47(6):973-81.
    View in: PubMed
    Score: 0.030
  23. The placental ribonuclease inhibitor (RNH) gene is located on chromosome subband 11p15.5. Genomics. 1990 Dec; 8(4):717-21.
    View in: PubMed
    Score: 0.030
  24. Reporting of diagnostic cytogenetic results. Curr Protoc Hum Genet. 2010 Oct; Appendix 1:1D.1-23.
    View in: PubMed
    Score: 0.030
  25. Reporting of diagnostic cytogenetic results. Curr Protoc Hum Genet. 2004 Nov; Appendix 1:Appendix 1D.
    View in: PubMed
    Score: 0.020
  26. Mutation of perinatal myosin heavy chain associated with a Carney complex variant. N Engl J Med. 2004 Jul 29; 351(5):460-9.
    View in: PubMed
    Score: 0.019
  27. A neural survival factor is a candidate oncogene in breast cancer. Proc Natl Acad Sci U S A. 2003 Sep 16; 100(19):10931-6.
    View in: PubMed
    Score: 0.018
  28. Multicolor karyotypic interpretation of a heterochromatin-associated marker chromosome in a dysmorphic girl with developmental delay. Am J Med Genet. 2002 Jul 15; 110(4):393-6.
    View in: PubMed
    Score: 0.017
  29. The sequence, expression, and chromosomal localization of a novel polycystic kidney disease 1-like gene, PKD1L1, in human. Genomics. 2002 Mar; 79(3):376-86.
    View in: PubMed
    Score: 0.016
  30. Psoriasin expression in mammary epithelial cells in vitro and in vivo. Cancer Res. 2002 Jan 01; 62(1):43-7.
    View in: PubMed
    Score: 0.016
  31. Chromosomal translocation t(8;12) induces aberrant HMGIC expression in aggressive angiomyxoma of the vulva. Genes Chromosomes Cancer. 2001 Oct; 32(2):172-6.
    View in: PubMed
    Score: 0.016
  32. STK25 is a candidate gene for pseudopseudohypoparathyroidism. Genomics. 2001 Sep; 77(1-2):2-4.
    View in: PubMed
    Score: 0.016
  33. Human calcium transport protein CaT1. Biochem Biophys Res Commun. 2000 Nov 19; 278(2):326-32.
    View in: PubMed
    Score: 0.015
  34. SMARCAD1, a novel human helicase family-defining member associated with genetic instability: cloning, expression, and mapping to 4q22-q23, a band rich in breakpoints and deletion mutants involved in several human diseases. Genomics. 2000 Oct 15; 69(2):162-73.
    View in: PubMed
    Score: 0.015
  35. Mutations in the protein kinase A R1alpha regulatory subunit cause familial cardiac myxomas and Carney complex. J Clin Invest. 2000 Sep; 106(5):R31-8.
    View in: PubMed
    Score: 0.015
  36. A t(2;19)(p13;p13.2) in a giant invasive cardiac lipoma from a patient with multiple lipomatosis. Genes Chromosomes Cancer. 2000 Jun; 28(2):133-7.
    View in: PubMed
    Score: 0.014
  37. Identification and characterization of a novel polycystin family member, polycystin-L2, in mouse and human: sequence, expression, alternative splicing, and chromosomal localization. Genomics. 2000 Mar 15; 64(3):241-51.
    View in: PubMed
    Score: 0.014
  38. Human vitamin C (L-ascorbic acid) transporter SVCT1. Biochem Biophys Res Commun. 2000 Jan 19; 267(2):488-94.
    View in: PubMed
    Score: 0.014
  39. Balanced translocation of 10q and13q, including the PTEN gene, in a boy with a human chorionic gonadotropin-secreting tumor and the Bannayan-Riley-Ruvalcaba syndrome. J Clin Endocrinol Metab. 1999 Dec; 84(12):4665-70.
    View in: PubMed
    Score: 0.014
  40. Primary parauterine leiomyoma with a t(6;14) Genes Chromosomes Cancer. 1999 Dec; 26(4):385-6.
    View in: PubMed
    Score: 0.014
  41. Functional and molecular characterization of the human neutral solute channel aquaporin-9. Am J Physiol. 1999 11; 277(5):F685-96.
    View in: PubMed
    Score: 0.014
  42. Novel isoform of lymphoid adaptor FYN-T-binding protein (FYB-130) interacts with SLP-76 and up-regulates interleukin 2 production. J Biol Chem. 1999 Oct 01; 274(40):28427-35.
    View in: PubMed
    Score: 0.014
  43. The thrombospondin-4 gene. Mamm Genome. 1999 Oct; 10(10):1010-6.
    View in: PubMed
    Score: 0.014
  44. Cloning and expression of a murine histone deacetylase 3 (mHdac3) cDNA and mapping to a region of conserved synteny between murine chromosome 18 and human chromosome 5. Mol Cell Biol Res Commun. 1999 Aug; 2(2):91-6.
    View in: PubMed
    Score: 0.014
  45. Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations. Proc Natl Acad Sci U S A. 1999 Mar 16; 96(6):2919-24.
    View in: PubMed
    Score: 0.013
  46. Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defects. J Biol Chem. 1998 Oct 02; 273(40):25967-73.
    View in: PubMed
    Score: 0.013
  47. Human ARHGDIG, a GDP-dissociation inhibitor for Rho proteins: genomic structure, sequence, expression analysis, and mapping to chromosome 16p13.3. Genomics. 1998 Oct 01; 53(1):104-9.
    View in: PubMed
    Score: 0.013
  48. The human ortholog of rhesus mannose-binding protein-A gene is an expressed pseudogene that localizes to chromosome 10. Mamm Genome. 1998 Mar; 9(3):246-9.
    View in: PubMed
    Score: 0.012
  49. Identification, localization, and expression of two novel human genes similar to deoxyribonuclease I. Genomics. 1997 Jun 15; 42(3):507-13.
    View in: PubMed
    Score: 0.012
  50. Genomic organization, complete sequence, and chromosomal location of the gene for human eotaxin (SCYA11), an eosinophil-specific CC chemokine. Genomics. 1997 May 01; 41(3):471-6.
    View in: PubMed
    Score: 0.012
  51. Structure and chromosomal assignment of the human cathepsin K gene. Genomics. 1997 Apr 15; 41(2):258-62.
    View in: PubMed
    Score: 0.012
  52. Assignment of C1QBP encoding the C1q globular domain binding protein (gC1q-R) to human chromosome 17 band p13.3 by in situ hybridization. Cytogenet Cell Genet. 1997; 77(3-4):283-4.
    View in: PubMed
    Score: 0.011
  53. Cloning of human RTEF-1, a transcriptional enhancer factor-1-related gene preferentially expressed in skeletal muscle: evidence for an ancient multigene family. Genomics. 1996 Oct 01; 37(1):68-76.
    View in: PubMed
    Score: 0.011
  54. The protein tyrosine phosphatase epsilon gene maps to mouse chromosome 7 and human chromosome 10q26. Genomics. 1996 Feb 01; 31(3):373-5.
    View in: PubMed
    Score: 0.011
  55. RSK3 encodes a novel pp90rsk isoform with a unique N-terminal sequence: growth factor-stimulated kinase function and nuclear translocation. Mol Cell Biol. 1995 Aug; 15(8):4353-63.
    View in: PubMed
    Score: 0.010
  56. Disruption of the architectural factor HMGI-C: DNA-binding AT hook motifs fused in lipomas to distinct transcriptional regulatory domains. Cell. 1995 Jul 14; 82(1):57-65.
    View in: PubMed
    Score: 0.010
  57. Genomic organization and chromosomal localization of the DUSP2 gene, encoding a MAP kinase phosphatase, to human 2p11.2-q11. Genomics. 1995 Jul 01; 28(1):92-6.
    View in: PubMed
    Score: 0.010
  58. Expression of two human skeletal calcitonin receptor isoforms cloned from a giant cell tumor of bone. The first intracellular domain modulates ligand binding and signal transduction. J Clin Invest. 1995 Jun; 95(6):2680-91.
    View in: PubMed
    Score: 0.010
  59. Trinucleotide repeats at the rad locus. Allele distributions in NIDDM and mapping to a 3-cM region on chromosome 16q. Diabetes. 1995 Feb; 44(2):243-7.
    View in: PubMed
    Score: 0.010
  60. Mapping of the human cone transducin alpha-subunit (GNAT2) gene to 1p13 and negative mutation analysis in patients with Stargardt disease. Genomics. 1995 Jan 01; 25(1):288-90.
    View in: PubMed
    Score: 0.010
  61. Characterization of human and mouse cartilage oligomeric matrix protein. Genomics. 1994 Dec; 24(3):435-9.
    View in: PubMed
    Score: 0.010
  62. Localization of serum biotinidase (BTD) to human chromosome 3 in band p25. Genomics. 1994 Aug; 22(3):662-3.
    View in: PubMed
    Score: 0.010
  63. Assignment of the gene coding for the human high-affinity glutamate transporter EAAC1 to 9p24: potential role in dicarboxylic aminoaciduria and neurodegenerative disorders. Genomics. 1994 Mar 15; 20(2):335-6.
    View in: PubMed
    Score: 0.009
  64. Isolation and chromosomal localization of the human endothelial nitric oxide synthase (NOS3) gene. Genomics. 1994 Jan 15; 19(2):350-7.
    View in: PubMed
    Score: 0.009
  65. Purification of the human NF-E2 complex: cDNA cloning of the hematopoietic cell-specific subunit and evidence for an associated partner. Mol Cell Biol. 1993 Sep; 13(9):5604-12.
    View in: PubMed
    Score: 0.009
Connection Strength
The connection strength for co-authors is the sum of the scores for each of their shared publications.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.