Andrea Gropman, MD, FANA
St. Jude Children's Research Hospital
Dr. Andrea Gropman is a neurogeneticist and international expert in Urea Cycle Disorders, Smith-Magenis syndrome, chromosome aneuploidies, and mitochondrial disorders research brain biomarkers of injury using multimodal imaging. She serves on several committees: the American College of Medica Genetics Therapeutics Committee, the Society for Inherited Metabolic Disorders Education Committee, the American Neurological Association Annual Meeting Programing Committee, and the American Society of Human Genetics Public Education and Awareness Outreach Committee. She is a past chair of the ANA Neurogenetics Special Interest Group and currently chairs the Neurogenetics Special Interest Group at Congress of Neurological Surgeons. Dr. Gropman is also principal investigator of the Urea Cycle Rare Disease Consortium.