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.
Genetic testing aids early NCL diagnosis, understanding intrafamilial variability, guiding treatment, and family planning, thus enhancing patient outcomes and care.
Gain insights into Okur-Chung Syndrome, a genetic disorder linked to the CSNK2A1 gene. Discover how genetic testing ensures accurate diagnosis and personalized care.
Explore Optic Atrophy 11, a rare genetic disorder affecting vision. Learn how genetic testing aids in diagnosis, family planning, and potential treatments.
Genetic testing for Orofaciodigital Syndrome XV aids in early diagnosis, personalized care, and research advancements, improving lives with this rare genetic disorder.
Explore how genetic testing aids in early detection, personalized treatment, and family planning for Patterned Macular Dystrophy 3, offering hope and insights.
Explore Peeling Skin Syndrome 5, a rare genetic disorder. Learn how genetic testing aids in diagnosis, treatment, and understanding its progression.
Explore how genetic testing aids in the early diagnosis and management of PERCHING syndrome, improving outcomes through tailored treatments and advanced research.
Explore the role of genetic testing in diagnosing Periventricular Nodular Heterotopia 7, uncovering its genetic roots, and guiding family planning and treatment.