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 Bradley Quade.
Connection Strength

3.285
  1. Molecular pathogenesis of uterine smooth muscle tumors from transcriptional profiling. Genes Chromosomes Cancer. 2004 Jun; 40(2):97-108.
    View in: PubMed
    Score: 0.289
  2. 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: 0.266
  3. Intravenous leiomyomatosis: molecular and cytogenetic analysis of a case. Mod Pathol. 2002 Mar; 15(3):351-6.
    View in: PubMed
    Score: 0.247
  4. Corrigendum: Loss of LDAH associated with prostate cancer and hearing loss. Hum Mol Genet. 2019 05 15; 28(10):1753-1754.
    View in: PubMed
    Score: 0.204
  5. Loss of LDAH associated with prostate cancer and hearing loss. Hum Mol Genet. 2018 12 15; 27(24):4194-4203.
    View in: PubMed
    Score: 0.198
  6. Clinical, pathologic, cytogenetic, and molecular profiling in self-identified black women with uterine leiomyomata. Cancer Genet. 2018 04; 222-223:1-8.
    View in: PubMed
    Score: 0.187
  7. Disseminated peritoneal leiomyomatosis. Clonality analysis by X chromosome inactivation and cytogenetics of a clinically benign smooth muscle proliferation. Am J Pathol. 1997 Jun; 150(6):2153-66.
    View in: PubMed
    Score: 0.178
  8. Intravenous leiomyomatosis: an unusual intermediate between benign and malignant uterine smooth muscle tumors. Mod Pathol. 2016 05; 29(5):500-10.
    View in: PubMed
    Score: 0.163
  9. Expression profiling of uterine leiomyomata cytogenetic subgroups reveals distinct signatures in matched myometrium: transcriptional profilingof the t(12;14) and evidence in support of predisposing genetic heterogeneity. Hum Mol Genet. 2012 May 15; 21(10):2312-29.
    View in: PubMed
    Score: 0.123
  10. Disseminated peritoneal leiomyomatosis after laparoscopic supracervical hysterectomy with characteristic molecular cytogenetic findings of uterine leiomyoma. Genes Chromosomes Cancer. 2010 Dec; 49(12):1152-60.
    View in: PubMed
    Score: 0.113
  11. Identifying the molecular signature of the interstitial deletion 7q subgroup of uterine leiomyomata using a paired analysis. Genes Chromosomes Cancer. 2009 Oct; 48(10):865-85.
    View in: PubMed
    Score: 0.105
  12. 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.
    View in: PubMed
    Score: 0.094
  13. Characterization of apparently balanced chromosomal rearrangements from the developmental genome anatomy project. Am J Hum Genet. 2008 Mar; 82(3):712-22.
    View in: PubMed
    Score: 0.094
  14. Disruption of diacylglycerol kinase delta (DGKD) associated with seizures in humans and mice. Am J Hum Genet. 2007 Apr; 80(4):792-9.
    View in: PubMed
    Score: 0.087
  15. Confined placental mosaicism as a risk factor among newborns with fetal growth restriction. Prenat Diagn. 2006 May; 26(5):428-32.
    View in: PubMed
    Score: 0.083
  16. 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.
    View in: PubMed
    Score: 0.082
  17. Constitutional rearrangement of the architectural factor HMGA2: a novel human phenotype including overgrowth and lipomas. Am J Hum Genet. 2005 Feb; 76(2):340-8.
    View in: PubMed
    Score: 0.075
  18. Uterine leiomyomata with t(10;17) disrupt the histone acetyltransferase MORF. Cancer Res. 2004 Aug 15; 64(16):5570-7.
    View in: PubMed
    Score: 0.073
  19. 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: 0.066
  20. 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: 0.060
  21. 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: 0.054
  22. 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: 0.052
  23. HMGIC expression in human adult and fetal tissues and in uterine leiomyomata. Genes Chromosomes Cancer. 1999 Aug; 25(4):316-22.
    View in: PubMed
    Score: 0.052
  24. 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: 0.049
  25. Hereditary leiomyomatosis and renal cell cancer: Cutaneous lesions & atypical fibroids. Case Rep Womens Health. 2017 Jul; 15:31-34.
    View in: PubMed
    Score: 0.045
  26. Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomalies. Am J Hum Genet. 2012 Jul 13; 91(1):56-72.
    View in: PubMed
    Score: 0.032
  27. Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries. Cell. 2012 Apr 27; 149(3):525-37.
    View in: PubMed
    Score: 0.031
  28. The cell adhesion gene PVRL3 is associated with congenital ocular defects. Hum Genet. 2012 Feb; 131(2):235-50.
    View in: PubMed
    Score: 0.030
  29. Disruption of neurexin 1 associated with autism spectrum disorder. Am J Hum Genet. 2008 Jan; 82(1):199-207.
    View in: PubMed
    Score: 0.023
  30. NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects. PLoS Genet. 2007 May 25; 3(5):e80.
    View in: PubMed
    Score: 0.022
  31. Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux. Am J Hum Genet. 2007 Apr; 80(4):616-32.
    View in: PubMed
    Score: 0.022
  32. Candidate loci for Zimmermann-Laband syndrome at 3p14.3. Am J Med Genet A. 2007 Jan 15; 143A(2):107-11.
    View in: PubMed
    Score: 0.022
  33. Hypogonadotropic hypogonadism and cleft lip and palate caused by a balanced translocation producing haploinsufficiency for FGFR1. J Med Genet. 2005 Aug; 42(8):666-72.
    View in: PubMed
    Score: 0.020
  34. Human chromosome 7: DNA sequence and biology. Science. 2003 May 02; 300(5620):767-72.
    View in: PubMed
    Score: 0.017
  35. Integration of cytogenetic landmarks into the draft sequence of the human genome. Nature. 2001 Feb 15; 409(6822):953-8.
    View in: PubMed
    Score: 0.014
  36. Primary parauterine leiomyoma with a t(6;14) Genes Chromosomes Cancer. 1999 Dec; 26(4):385-6.
    View in: PubMed
    Score: 0.013
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.