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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.

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  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. 2010 Dec 9.View Related Profiles. PMID: 21154627; 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. 2011 Jan; 155A(1):141-4.View Related Profiles. PMID: 21204222; 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;
     

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