Jill Fahrner, MD

Dr. Tao Wang is an associate professor of pediatrics at the Johns Hopkins University School of Medicine. His areas of clinical expertise include global developmental delays and intellectual disability neurobehavioral disorders in children, and genetic and genomic syndromes and inborn errors of metabolism. Dr. Wang earned his M.D. from Zhongshan Medical University in China and a Ph.D. in human genetics from Johns Hopkins University. He completed his residency in pediatrics at Tufts -New England Medical Center Hospitals and performed fellowships in clinical genetics at Johns Hopkins University School of Medicine and clinical biochemical genetics at Kennedy Krieger Institute. His research interests include x-linked intellectual disabilities (XLID), autism spectrum disorders (ASDs) and inborn errors of metabolism of the central nervous system.Dr. Wang is the associate director of the Medical Genetics Residency and Fellowship Program and a preceptor in the Predoctoral Training Program in Human Genetics.

Dr. Julie Hoover-Fong is a Professor of Genetic Medicine and Pediatrics and Director of the Greenberg Center for Skeletal Dysplasias at Johns Hopkins University. Dr. Hoover-Fong holds a bachelor’s degree in Human Nutrition from The Ohio State University, where she also completed her medical degree. She received her Ph.D. in the Graduate Training Program in Clinical Investigation at the Johns Hopkins University School of Medicine and Bloomberg School of Public Health. Dr. Hoover-Fong completed a pediatric internship and residency at Washington University in St. Louis and a fellowship in medical genetics at Johns Hopkins University in Baltimore. She joined the Johns Hopkins University faculty in 2002 and progressed to Professor of Genetic Medicine and Pediatrics in 2019.She practices and oversees the clinical operations, research and educational ventures for the patients, families and healthcare providers served by the Greenberg Center. Her clinical team develops and improves diagnostic and treatment guidelines for comprehensive care of patients with all types of bone conditions including dwarfism, orofacial clefting, craniosynostosis and more. Dr. Hoover-Fong also mentors and teaches medical students, residents and genetic medicine trainees. As an active clinical researcher, Dr. Hoover-Fong is the Principal Investigator of multiple global clinical trials for achondroplasia, the first multi-center, investigator-initiated natural history study for achondroplasia, and multiple clinical studies for patients with orofacial clefting, hypophosphatasia and other conditions. She is also a co-investigator on the ELSI and Phenotype Review Committees for the Mendel Project, a whole exome sequencing venture to identify the genetic cause of Mendelian conditions. From an institutional service perspective, Dr. Hoover-Fong serves on the Johns Hopkins Associate Professor Promotions Committee and the Advisory Committee for the Graduate Training Program in Clinical Investigation. She serves on the Medical Advisory Board of the Little People of America, is a member of the Miller-Coulson Academy of Clinical Excellence at Johns Hopkins University and is a charter member of the International Skeletal Dysplasia Management Consortium, publishing best practice guidelines for patients with skeletal dysplasias.