Doctor

Dr. Wojcik is a neonatologist and clinical geneticist at Boston Children's Hospital and an associate professor in pediatrics at Harvard Medical School who specializes both clinically and academically in rare diseases affecting the fetus and neonate with a particular focus on genomic medicine implementation. Following her pediatric residency, she pursued combined fellowship training in both neonatology and genetics and subsequently obtained her Master of Public Health degree to augment her clinical effectiveness and health services research. She currently serves as the Director of the Neonatal Genomics Program at Boston Children's Hospital and the Medical Director of the Manton Center for Orphan Disease Research as well as the Assistant Director for Robert's Program on Sudden Unexplained Death in Pediatrics. Dr. Wojcik's research focuses on the application of genomic medicine in the perinatal setting, particularly related to genetic diagnosis in the neonatal intensive care unit, understanding genetic causes of perinatal mortality via genomic autopsy, and addressing inequities in rare disease genomics. In her clinical practice, she attends in the neonatal intensive care unit at Boston Children's Hospital and on the inpatient genetics service, consults prenatally for complex fetal cases, and runs a multidisciplinary developmental follow-up clinic for infants with genetic conditions.