MD · MBA
Physician specializing in genetic analysis and personalized preventive medicine, and author of Outsmart Your Genes.
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).
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.
Discover the complexities of C-reflex enhancement, its diagnosis, and the crucial role of genetic testing in understanding and managing this neurological condition for improved…
Discover the role of genetic testing in diagnosing Epidermolysis Bullosa Pruriginosa, a rare skin disorder, and its benefits for affected individuals and families.
Explore mitochondrial epilepsy, its genetic causes, and the vital role of genetic testing in diagnosing, managing, and guiding treatment for this rare neurological disorder.
Discover the importance of understanding and diagnosing severe Multiple Epiphyseal Dysplasia 1 (MED 1) through genetic testing, enabling effective disease management and informed…
Discover the link between exercise intolerance and complex III deficiency, and learn how genetic testing can aid in diagnosing and managing this rare genetic disorder.
Discover the role of genetic testing in diagnosing exercise intolerance, muscle pain, and lactic acidemia. Learn how it guides treatment, monitors progression, and improves lives.
Discover the importance of understanding and diagnosing digenic exudative vitreoretinopathy, the role of genetic testing in confirming diagnosis, and its benefits.
Discover the importance of genetic testing in diagnosing Familial Hypertrophic Cardiomyopathy 22, enabling early detection, personalized treatment, and effective management.