Lindsay Burrage, M.D., Ph.D. is a board-certified pediatrician, clinical geneticist, and biochemical geneticist, and she is an attending physician in the Inborn Errors of Metabolism and Skeletal Dysplasia clinics at Texas Children’s Hospital.   In the laboratory, she uses inborn errors of metabolism as models for studying basic biological processes that impact more common disorders.  As an investigator in the Urea Cycle Disorders Consortium, she also has a special interest in investigating the etiology of long-term complications, such as liver disease, in individuals with urea cycle disorders.   In addition, she has participated in a variety of gene discovery projects as a leader of the sequence analysis team at the Baylor College of Medicine site for the Undiagnosed Diseases Network.  She is also leading the Clinical Translational Core of the Baylor College of Medicine Center for Precision Medicine Models. She has been awarded the Burroughs Wellcome Fund Career Award for Medical Scientists and the Society for Pediatric Research Young Investigator Award for her research in rare disorders.