Lindsay Burrage, M.D., Ph.D. is a board-certified pediatrician, clinical geneticist, and biochemical geneticist. She completed pediatric residency training at Rainbow Babies and Children’s Hospital and medical genetics training at Baylor College of Medicine. She is an associate professor with tenure in the Department of Molecular and Human Genetics at Baylor College of Medicine and an attending physician in the Inborn Errors of Metabolism and Skeletal Dysplasia clinics at Texas Children’s Hospital.   In the laboratory, she investigates long-term complications and new therapeutic approaches for inborn errors of metabolism, such as urea cycle disorders, and uses these disorders as models for more common human diseases. In addition, she is a senior member of the sequence analysis team at the Baylor College of Medicine site for the Undiagnosed Diseases Network (UDN) and a principal investigator of the NIH-funded Center for Precision Medicine Models at Baylor, which generates precision animal models to end the diagnostic odyssey for patients with rare and undiagnosed diseases.  She has over 100 peer-reviewed publications and book chapters and her research in rare disorders has been awarded with the Burroughs Wellcome Fund Career Award for Medical Scientists and the Society for Pediatric Research Young Investigator Award.