Lindsay Catherine Burrage MD
Medical Resident, Molecular & Human Genetics, Baylor College of Medicine
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6701 Fannin St.Houston, TX 77030
Phone+1 832-824-4280
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Education & Training
Baylor College of MedicineFellowship, Medical Biochemical Genetics, 2013 - 2014- Baylor College of MedicineResidency, Medical Genetics and Genomics, 2011 - 2013
Case Western Reserve Univ/Univ Hosps Cleveland Med Ctr/Rainbow Babies and Childrens HospitalResidency, Pediatrics, 2008 - 2011
Case Western Reserve University School of MedicineClass of 2008
Certifications & Licensure
TX State Medical License 2011 - 2027
OH State Medical License 2008 - 2012
American Board of Medical Genetics and Genomics Medical Biochemical Genetics
American Board of Pediatrics Pediatrics- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Clinical Trials
- Liver Disease in Urea Cycle Disorders Start of enrollment: 2021 Nov 04
Publications & Presentations
PubMed
- Developmental and Phenotypic Outcomes in Mild Phenylalanine Hydroxylase Deficiency.Aaron Williams, Kristian Divin, Lindsay C Burrage, William J Craigen, Fernando Scaglia
American Journal of Medical Genetics. Part A. 2026-08-01 - Bi-allelic loss-of-function variants in TMEM63B cause syndromic surfactant dysfunction disorder.Sock Hoai Chan, Audra N Iness, Jill A Rosenfeld, Mir Reza Bekheirnia, Lindsay C Burrage
American Journal of Human Genetics. 2026-07-02 - Evidence-based classification of genes implicated in skeletal disorders using the ClinGen curation framework.Ryan F Webb, Hannah McCurry, Amanda Girod, Madeline Hughes, Emma Wilcox
Journal of Bone and Mineral Research. 2026-07-01
Journal Articles
- Correction: “Congenital Hyperinsulinism as the Presenting Feature of Kabuki Syndrome: Clinical and Molecular Characterization of 10 Affected Individuals”Lindsay C Burrage, Sara Halbach, Paul Thornton, Andrew C Edmondson, Alejandro Diaz, Lisa Truong, Darrel Waggoner, Nature
- Congenital Hyperinsulinism as the Presenting Feature of Kabuki Syndrome: Clinical and Molecular Characterization of 10 Affected IndividualsAlejandro Diaz, Darrel Waggoner, Lindsay C Burrage, Sara Halbach, Andrew C Edmondson, Lisa Truong, Paul Thornton, Nature
Press Mentions
NIH Awards More Than $15 Million to Fund Two Rare Diseases ConsortiaSeptember 25th, 2025
Disease Mimicry: Genetic Diseases Can Produce Rheumatic SymptomsMarch 19th, 2019
Pegylated Enzyme Helps in Mice with Urea Cycle DisorderSeptember 25th, 2016
Grant Support
- Rare Organic Acidemias Research (ROAR) ConsortiumBAYLOR COLLEGE OF MEDICINE2025–2030
- BCM CENTER FOR PRECISION MEDICINE MODELSBAYLOR COLLEGE OF MEDICINE2020–2030
- BCM CENTER FOR PRECISION MEDICINE MODELSBAYLOR COLLEGE OF MEDICINE2020–2030
- BCM CENTER FOR PRECISION MEDICINE MODELSBAYLOR COLLEGE OF MEDICINE2020–2030
- DISSECTING THE LINK BETWEEN UREAGENESIS AND HEPATIC GLYCOGEN METABOLISMBAYLOR COLLEGE OF MEDICINE2021–2026
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