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 potential of genetic testing in diagnosing and managing Hyperalphalipoproteinemia 1, a rare disorder with high HDL cholesterol levels. Learn about its genetic basis…
Discover the importance of diagnosing childhood self-limiting hypercalciuria, and how genetic testing can prevent complications and guide personalized treatment plans.
Discover the importance of understanding hyperechogenic kidneys, their diagnosis, and how genetic testing plays a crucial role in personalized medicine, prenatal care, and…
Discover the role of genetic testing in diagnosing CBS-related hyperhomocysteinemia, guiding treatment plans, and informing reproductive decisions to reduce thrombotic risks.
Discover the role of genetic testing in diagnosing and treating hypoammonemia, a rare metabolic disorder. Learn about advancements in whole-genome sequencing and targeted…
Discover the role of genetic testing in diagnosing Hypotrichosis 2, a rare hair growth disorder, and learn about targeted treatments, early diagnosis benefits, and managing…
Discover Iminoglycinuria, a rare metabolic disorder with a complex digenic inheritance pattern. Learn how genetic testing aids in diagnosis, treatment, and understanding its…
Discover the latest advancements in MRXSA research, including unique DNA methylation episignatures, novel gene mutations, and the benefits of genetic testing for diagnosis and…