Yaning Wu, MD, PhD, FACMG
- Director, Genetics and Genomics Diagnostic Laboratory, Division of Human Genetics
- Assistant Professor, UC Department of Pediatrics
About
MD: China Medical University, Shenyang, China,
PhD: The University of Texas at Austin, Austin, TX,
Fellowship: Clinical Molecular Genetics and Clinical Cytogenetics, Children’s Hospital of Philadelphia, Philadelphia, PA,
Certifications: American Board of Medical Genetics and Genomics in Clinical Cytogenetics and Genomics, 2015; American Board of Medical Genetics and Genomics in Clinical Molecular Genetics and Genomics, 2017; American Board of Medical Genetics in Clinical Molecular Genetics, 2015
Services and Specialties
Research Areas
Publications
A de novo SATB2 mutation in monozygotic twins with cleft palate, dental anomalies, and developmental delay. American Journal of Medical Genetics, Part A. 2017; 173(3):809-812.
Hearing loss, coloboma and left ventricular enlargement in a boy with an interstitial 10q26 deletion. American Journal of Medical Genetics, Part C: Seminars in Medical Genetics. 2016; 172(2):109-116.
A de novo interstitial deletion of 7q31.2q31.31 identified in a girl with developmental delay and hearing loss. American Journal of Medical Genetics, Part C: Seminars in Medical Genetics. 2016; 172(2):102-108.
Drosophila Nipped-B Mutants Model Cornelia de Lange Syndrome in Growth and Behavior. PLoS Genetics. 2015; 11(11):e1005655.
Compound heterozygote CDK5RAP2 mutations in a Guatemalan/Honduran child with autosomal recessive primary microcephaly, failure to thrive and speech delay. American Journal of Medical Genetics, Part A. 2015; 167(6):1414-1417.
Clinical, developmental and molecular update on Cornelia de Lange syndrome and the cohesin complex: abstracts from the 2014 Scientific and Educational Symposium. American Journal of Medical Genetics, Part A. 2015; 167(6):1179-1192.
A Drosophila model for Angelman syndrome. Proceedings of the National Academy of Sciences of the United States of America. 2008; 105(34):12399-12404.
Drosophila klaroid encodes a SUN domain protein required for Klarsicht localization to the nuclear envelope and nuclear migration in the eye. Fly. 2007; 1(2):75-85.
Association of alpha 2-macroglobulin polymorphisms and Alzheimer disease in Mainland Han Chinese. Journal of the Neurological Sciences. 2004; 217(1):13-15.
[Apolipoprotein E gene polymorphisms and Alzheimer disease]. Journal of Genetics and Genomics. 2003; 30(12):1167-1170.
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