Kevin E. Glinton, MD, PhD
- Genetics
Assistant Professor, Department of Molecular and Human Genetics, Baylor College of Medicine
Phone:
832-822-2100
Languages: English
Departments:
Office location:
17580 Interstate 45 South
The Woodlands, TX 77384
Get to know Kevin E. Glinton, MD, PhD
Personal Statement
As a clinician and researcher, my aim is to provide the most timely and precise diagnosis for patients. I enjoy treating children with a variety of genetic disorders but have a particular interest in the diagnosis and treatment of children with inborn errors of metabolism.
Education
| School | Education | Degree | Year |
|---|---|---|---|
| Baylor College of Medicine | Fellowship | Medical Biochemical Genetics | 2020 |
| Baylor College of Medicine | Fellowship | Medical Genetics | 2019 |
| University of Virginia Medical Center | Residency | Pediatrics | 2017 |
| Geisel School of Medicine at Dartmouth | Medical School | Doctor of Medicine | 2014 |
| University of Southern California | PhD | Doctor of Philosophy | 2010 |
Organizations
| Organization Name | Role |
|---|---|
| American Academy of Pediatrics | Fellow |
| American College of Medical Genetics | Fellow |
| American Society of Human Genetics | Member |
| Society for Inherited Metabolic Disorders | Member |
* Texas Children’s Hospital physicians’ licenses and credentials are reviewed prior to practicing at any of our facilities. Sections titled From the Doctor, Professional Organizations and Publications were provided by the physician’s office and were not verified by Texas Children’s Hospital.
Glinton, K. E., Hurst, A. C., Bowling, K. M., Cristian, I., Haynes, D., Adstamongkonkul, D., ... & Stankiewicz, P., 2021. Phenotypic expansion of the BPTF‐related neurodevelopmental disorder with dysmorphic facies and distal limb anomalies. American Journal of Medical Genetics Part A, 185(5), 1366-1378.
Turner A, Glinton K.E., Sutton V.R. Advancements in therapeutics for inborn errors of metabolism. Curr Opin Pediatr. 2022 Dec 1;34(6):559-564. doi: 10.1097/MOP.0000000000001168. Epub 2022 Aug 22. Review. PubMed PMID: 35993290.Alaimo, J.T., Glinton, K.E., Liu, N., Xiao, J., Yang, Y., Sutton, V.R. and Elsea, S.H., 2020. Integrated analysis of metabolomic profiling and exome data supplements sequence variant interpretation, classification, and diagnosis. Genetics in Medicine, 22(9), pp.1560-1566.
Glinton, K.E., Levy, H.L., Kennedy, A.D., Pappan, K.L. and Elsea, S.H., 2019. Untargeted metabolomics identifies unique though benign biochemical changes in patients with pathogenic variants in UROC1. Molecular Genetics and Metabolism Reports 18, pp.14-18.
Glinton, K.E., Benke, P.J., Lines, M.A., Geraghty, M.T., Chakraborty, P., Al-Dirbashi, O.Y., Jiang, Y., Kennedy, A.D., Grotewiel, M.S., Sutton, V.R. and Elsea, S.H., 2018. Disturbed phospholipid metabolism in serine biosynthesis defects revealed by metabolomic profiling. Molecular Genetics and Metabolism 123(3), pp.309-316.