Our Expert Team
Our multidisciplinary team of professionals comprises physicians, genetic counselors, nurses and social workers particularly trained to address the concerns of a family with a history or risk for a genetic disorder or birth defect. This team provides detailed evaluation of the family history, clinical genetics examinations, prenatal examination (for pregnant couples) and performance of a number of genetic tests, risk assessment and counseling.
Program Leadership
 David L. Rimoin, MD, PhD Director, Medical Genetics Institute |  Jerome I. Rotter, MD Director of Research and Co-Director, Medical Genetics Institute; Director, Division of Medical Genetics |
 Xiao-Ning Chen, MD Associate Director, Molecular Genetics Laboratory |  Daniel H. Cohn, PhD Director, Collagen Molecular Laboratory |
 Nathan Fischel-Ghodsian, MD Director, Molecular Hematology |  Mark O. Goodarzi, MD, PhD Attending Physician, Medical Genetics Institute; Department of Obstetrics and Gynecology; Division of Endocrinology, Diabetes and Metabolism |
 Ora Gordon, MD Director, GenRISKŪ Adult Genetics Program |  John M. Graham, Jr., MD, ScD Director, Clinical Genetics and Dysmorphology |
 Xiuqing Guo, PhD |  Julie R. Korenberg, MD, PhD Director, Pediatrics Research; Director, Neurogenetics |
 Miklos Peterfy, PhD Director, Laboratory of Murine Models for Metabolic Disease, Medical Genetics Institute |  Yaron Rabinowitz, MD Director, Ophthalmology Research |
 Leslie J. Raffel, MD Associate Director, Common Diseases Genetics Program |  Kent Taylor, PhD Laboratory Operations Director, Phenotyping/Genotyping Laboratory |
 William Wilcox, MD, PhD Director, Inborn Errors of Metabolism; Director, Skeletal Dysplasia Morphology Laboratory |
