Dr. Amanda Barone Pritchard is an Associate Professor of Pediatrics in the Division of Pediatric Genetics, Metabolism, and Genomic Medicine within the Department of Pediatrics at University of Michigan Health. In addition to providing clinical care, her research interests include clinical trials in inborn errors of metabolism and delineation of new genetic disorders. She is the medical geneticist in the Multidisciplinary Ophthalmic Genetics Clinic (MOGC) at the University of Michigan Kellogg Eye Center.

Dr. Pritchard also serves as Program Director for the Medical Biochemical Genetics Fellowship and Associate Program Director Medical Genetics and Genomics Residency programs at the University of Michigan. She is a fellow of the ACMG and elected member of the Executive Committee of Council on Genetics of the American Academy of Pediatrics.