Rachel Fisher, M.S., L.C.G.C.

Rachel joined the University in 2015 and specializes in pediatric genetic counseling. She spends half of her time in the general pediatric clinic and the other half of her time is dedicated to coordination of follow up care for infants with abnormal newborn screening results for lysosomal storage disorders. In addition, she supervises students and is involved in research related to whole exome sequencing and Pompe disease.