Stuart K. Shapira, MD, PhD
Chief Medical Officer and Associate Director for Science
Stuart K. Shapira, MD, PhD became Associate Director for Science in the National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, in March 2013. Prior to this role, Dr. Shapira served as a medical officer on the Pediatric Genetics Team in NCBDDD. His research activities included birth defects epidemiology, dysmorphology of autism, gene and nutritional interactions for adverse reproductive outcomes, and newborn screening.
Dr. Shapira received his PhD degree in Genetics and his MD degree, both from the University of Chicago. He completed a residency in Pediatrics and a clinical fellowship in Genetics and Metabolism at Boston Childrens Hospital. He also completed dual research fellowships in Genetics and Metabolism, and in Allergy and Immunology at Harvard Medical School. Dr. Shapira is board-certified in Clinical Genetics, Biochemical Genetics, and Molecular Genetics.
Prior to joining the National Center on Birth Defects and Developmental Disabilities in 2005, Dr. Shapira practiced clinical genetics and metabolic genetics at Baylor College of Medicine in Houston and at the University of Texas Health Science Center in San Antonio. He currently serves as CDC liaison to the Committee on Genetics for the American Academy of Pediatrics, as chairman of the Dysmorphology Workgroup for the Centers for Autism and Developmental Disabilities Research and Epidemiology, and as a member of the Editorial Board for the American Journal of Medical Genetics.
Dr. Shapira has authored and coauthored more than 100 journal articles, book chapters, and abstracts, and he has been an invited speaker at numerous regional, national, and international scientific conferences.
- Page last reviewed: January 3, 2018
- Page last updated: April 13, 2017
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