Beverly Hay

Beverly Hay, MD is an Associate Professor at UMass Chan Medical School, affiliated with the T.H. Chan School of Medicine's Pediatrics department, specializing in Pediatric Genetics. Her roles include clinical research and academic leadership in pediatric genetic disorders and newborn screening programs.

Education: BA in Microbiology from University of California, Santa Barbara; MD from Jefferson Medical College.

Research focuses on genetic screening for disorders like Spinal Muscular Atrophy (SMA), Severe Combined Immunodeficiency (SCID), and congenital anomalies linked to chromosome deletions (e.g., 22q11). She contributes to statewide newborn screening initiatives and has co-authored studies on immunodeficiency treatments and genetic syndromes.

Publications highlight her work in neonatal screening protocols, SCID management, and case studies involving genetic skin and blood disorders.

Collaborations include co-authors such as Anne Marie Comeau and Karen Wiss, and her networks include researchers focused on immunodeficiency and genetic syndromes.