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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
- 118 citationsMutations in FBXL4 Cause Mitochondrial Encephalopathy and a Disorder of Mitochondrial DNA MaintenancePenelope E. Bonnen, John W. Yarham, Arnaud Besse, Ping Wu, Eissa Faqeih
American Journal of Human Genetics. 2013-09-05 - 47 citationsBacteria, yeast, worms, and flies: exploiting simple model organisms to investigate human mitochondrial diseases.Shane L. Rea, Brett H. Graham, Eiko Nakamaru-Ogiso, Adwitiya Kar, Marni J. Falk
Developmental Disabilities Research Reviews. 2010-06-01 - 137 citationsMARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome.Julia Wang, Rami Al-Ouran, Yanhui Hu, Seon Young Kim, Ying-Wooi Wan
American Journal of Human Genetics. 2017-06-01
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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