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Office
975 West Walnut Street
IB 130
Indianapolis, IN 46202Phone+1 317-944-3966Fax+1 317-968-1354
Summary
- Dr. Brett Graham is a medical geneticist in Indianapolis, IN. He received his medical degree from Emory University School of Medicine and has been in practice 19 years. He specializes in clinical genetics and medical biochemical genetics and is experienced in mitochondrial diseases, inborn errors of metabolism, medical biochemical genetics, pediatric genetics, and medical genetics. He has more than 100 publications and over 500 citings.
Education & Training
- Baylor College of MedicineFellowship, Medical Biochemical Genetics, 2001 - 2003
- Baylor College of Medicine (Houston)Residency, Pediatrics, 1998 - 2001
- Emory UniversityPhD, Genetics and Molecular Biology, 1991 - 1998
- Emory University School of MedicineClass of 1998
Certifications & Licensure
- IN State Medical License 2017 - 2025
- TX State Medical License 2003 - 2018
- American Board of Medical Genetics and Genomics Clinical Genetics
- American Board of Medical Genetics and Genomics Medical Biochemical Genetics
Publications & Presentations
PubMed
- 86 citationsRecurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 MutationsSeema R. Lalani, Pengfei Liu, Jill A. Rosenfeld, Levi B. Watkin, Theodore Chiang
American Journal of Human Genetics. 2016-02-04 - 118 citationsDe novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndromeMatthew N. Bainbridge, Hao Hu, Donna M. Muzny, Luciana Musante, James R. Lupski
Genome Medicine. 2013-02-05 - 157 citationsMutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum-associated degradation pathwayGregory M. Enns, Vandana Shashi, Matthew N. Bainbridge, Michael J. Gambello, Farah R. Zahir
Genetics in Medicine. 2014-10-01
Grant Support
- Determination of pathogenetic mechanisms in cortex-specific Sucla2 deficiency as a model for mitochondrial encephalopathyNational Institute of Neurological Disorders and Stroke2022–2027
- Succinyl-Coa Synthetase Deficiency: A Model To Study Mitochondrial DNA (MTDNA) DENational Institute Of General Medical Sciences2012
- Genetic Screens For Mitochondrial Phenotypes In ES CellsNational Institute Of Arthritis And Musculoskeletal And Skin Diseases2005–2007
- Drosophila Vdac'S Role In Mitochondrial FunctionEunice Kennedy Shriver National Institute Of Child Health &Human Development2003–2007
- The Role Of Mitochondrial Vdacs In Apoptosis.National Institute Of General Medical Sciences2002–2003
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