Brandon Colby, MD

MD · MBA

Physician specializing in genetic analysis and personalized preventive medicine, and author of Outsmart Your Genes.

About Brandon

Brandon Colby is a physician-expert in the fields of genetic analysis and Personalized Preventive Medicine. He holds an MD from the Mount Sinai School of Medicine, an MBA from Stanford University's Graduate School of Business, and a degree in Genetics from the University of Michigan.

Dr. Colby is the author of the book Outsmart Your Genes and has developed numerous technologies that improve the analysis, interpretation, and actionability of genome sequencing data. He is an Affiliate Specialist of the American College of Medical Genetics and Genomics (⁠ACMG), an Associate of the American College of Preventive Medicine (⁠ACPM), and a member of the National Society of Genetic Counselors (⁠NSGC).

Education

BA in Genetics with Honors, University of Michigan · 2000
MD, Mount Sinai School of Medicine · 2004
MBA, Stanford University Graduate School of Business · 2007

Affiliations & Memberships

Affiliate Specialist, American College of Medical Genetics and Genomics (ACMG)
Associate, American College of Preventive Medicine (ACPM)
Member, National Society of Genetic Counselors (NSGC)

Connect with Brandon

Articles by Brandon Colby, MD are reviewed for accuracy by Sequencing's medical and scientific team. This page is for informational purposes and does not constitute medical advice.

Articles by Brandon

Unraveling the Mystery of Phenytoin Response: A Guide to Genetic Testing

Discover the benefits of genetic testing in predicting phenytoin response for epilepsy treatment, optimizing seizure control, and minimizing adverse effects. Learn how…

Decoding the Mysteries of Phosphoglycerate Kinase Electrophoretic Variant PGK II

Discover the importance of genetic testing in diagnosing and managing phosphoglycerate kinase electrophoretic variant PGK II, a rare enzyme deficiency impacting health.

Pituitary hormone deficiency, combined 5

Decoding the Genetic Puzzle of Combined Pituitary Hormone Deficiency

Explore the role of genetic testing in diagnosing Combined Pituitary Hormone Deficiency (CPHD), its genetic basis, and how it aids in treatment and management.

Decoding the Mystery: Understanding Pol III-related Leukodystrophy

Discover the role of genetic testing in diagnosing Pol III-related leukodystrophy, a rare neurological disorder, and its impact on treatment, family planning, and research.

Decoding the Enigma of POLG-Related Disorders: A Comprehensive Guide to Understanding, Diagnosing, and Utilizing Genetic Testing

Discover the role of genetic testing in diagnosing POLG-related disorders, including whole-exome sequencing and yeast models, for better treatment & management.