Profile

MD, Peking Union Medical College
PhD, University of Texas Southwestern Medical Center



Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.

iCite Analysis       Copy PMIDs To Clipboard

  1. Leon E, Jamal SM, Zou YS, Milunsky JM. Partial trisomy 8 mosaicism due to a pseudoisodicentric chromosome 8. Am J Med Genet A. 2011 Jul; 155A(7):1740-4.View Related Profiles. PMID: 21671393; DOI: 10.1002/ajmg.a.34073;
     
  2. Flynn M, Zou YS, Milunsky A. Whole gene duplication of the PQBP1 gene in syndrome resembling Renpenning. Am J Med Genet A. 2011 Jan; 155A(1):141-4.View Related Profiles. PMID: 21204222; DOI: 10.1002/ajmg.a.33756;
     
  3. Flynn M, Zou YS, Milunsky A. Whole gene duplication of the PQBP1 gene in syndrome resembling Renpenning. Am J Med Genet A. 2010 Dec 9.View Related Profiles. PMID: 21154627; DOI: 10.1002/ajmg.a.33756;
     
  4. Leon E, Zou YS, Milunsky JM. Mosaic Down syndrome in a patient with low-level mosaicism detected by microarray. Am J Med Genet A. 2010 Dec; 152A(12):3154-6.View Related Profiles. PMID: 21108401; DOI: 10.1002/ajmg.a.33739;
     
  5. Huang XL, Zou YS, Maher TA, Newton S, Milunsky JM. A de novo balanced translocation breakpoint truncating the autism susceptibility candidate 2 (AUTS2) gene in a patient with autism. Am J Med Genet A. 2010 Aug; 152A(8):2112-4. PMID: 20635338; DOI: 10.1002/ajmg.a.33497;
     
  6. Zou YS, Newton S, Milunsky JM. A complex maternal rearrangement results in a pure 10.8 Mb duplication of the 5q13.1-q14.1 region in an affected son. Am J Med Genet A. 2010 Feb; 152A(2):498-503. PMID: 20101702; DOI: 10.1002/ajmg.a.33266;
     
  7. Zou YS, Milunsky JM. Developmental disability and hypomelanosis of Ito in a female with 7.3 Mb de novo duplication of Xp11.3-p11.4 and random X inactivation. Am J Med Genet A. 2009 Nov; 149A(11):2573-7. PMID: 19876908; DOI: 10.1002/ajmg.a.33066;
     
  8. Quadrelli R, Quadrelli A, Milunsky A, Zou YS, Huang XL, Viera E, Mechoso B, Bellini S, Costabel M, Vaglio A. A 14-year follow-up of a case detected prenatally of partial trisomy 13q21.32-qter and monosomy 18q22.3-qter as a result of a maternal complex chromosome rearrangement involving chromosomes 6, 13, and 18. Genet Test Mol Biomarkers. 2009 Jun; 13(3):387-93.View Related Profiles. PMID: 19473082; DOI: 10.1089/gtmb.2008.0120;
     
  9. Zou YS, Huang XL, Ito M, Newton S, Milunsky JM. Further delineation of the critical region for the 9p-duplication syndrome. Am J Med Genet A. 2009 Feb; 149A(2):272-6. PMID: 19161157; DOI: 10.1002/ajmg.a.32607;
     

This graph shows the total number of publications by year, by first, middle/unknown, or last author.



Contact for Mentoring: