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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)
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
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Juberg-Hayward Syndrome: Unraveling the Genetic Threads of a Rare Disorder
Explore Juberg-Hayward Syndrome, a rare genetic disorder. Learn how ESCO2 mutations are diagnosed through genetic testing for better management and family planning.
Vitagene
How to download your Vitagene DNA data and upload your raw DNA file to get free genetic analysis reports for health, wellness, and ancestry. Get more from your Vitagene DNA test!
Advancements in Understanding Achondrogenesis Type II Through Genetic Testing
Rare and severe, Achondrogenesis Type II's diagnosis is enhanced by genetic testing, revealing COL2A1 mutations and offering insights for affected families.
Waardenburg Wisdom: Navigating Genetic Testing for Waardenburg Syndrome Type 2A
Unravel Waardenburg Syndrome Type 2A through genetic testing, confirming diagnoses, aiding family planning, and personalizing management for improved care.
Premature Chromatid Separation Trait: Unlocking the Genetic Code for Better Health Outcomes
Explore the role of genetic testing in managing Premature Chromatid Separation trait, a rare condition impacting chromosomal stability and offering insights for personalized care.
Premature Chromatid Separation: Genetic Testing's Role in Understanding and Managing PCS
Explore PCS, a rare genetic disorder affecting chromatid separation. Genetic testing aids in diagnosis, management, and personalized treatment strategies.