Susan Hayflick, MD completed training in medical genetics at Johns Hopkins in Baltimore and joined the faculty at Oregon Health & Science University in 1993. Dr. Hayflick is a professor of Molecular and Medical Genetics, Pediatrics, and Neurology and chair of the Department of Molecular and Medical Genetics. She has led a research program on neurodegeneration with brain iron accumulation disorders (NBIA) for more than 30 years. Her group’s achievements in basic, translational, and clinical science include: discovering 6 disease genes (PANK2, PLA2G6, FA2H, WDR45, MECR, and SLC39A14); delineating their associated disease phenotypes including molecular, biochemical, and cellular pathophysiologies, and clinical natural histories; developing new clinical molecular diagnostics; creating animal models of disease; and developing rational therapeutics for inborn errors of coenzyme A biosynthesis and related disorders. She is clinically active as a medical geneticist in direct patient care and laboratory diagnostics, with ABMGG certification in Clinical Genetics, Biochemical Genetics, and Molecular Genetics.