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.
Explore how genetic testing unveils causes of congenital heart defects, enabling early diagnosis, personalized treatment, and informed family planning.
Explore how genetic testing unravels congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome, aiding in diagnosis, early interventions, and family planning.
Uncover how genetic testing aids in diagnosing Congenital Nongoitrous Hypothyroidism 6, ensuring early detection, personalized treatment, and improved patient outcomes.
Explore how genetic testing aids in diagnosing Congenital Stationary Night Blindness 1E, identifies genetic variants, and informs personalized treatment plans.
Explore how genetic testing aids in diagnosing Cornelia de Lange Syndrome 4, offering insights into early intervention, personalized treatment, and family planning.
Unlock early detection of coronary heart disease with genetic testing. Learn how eNOS gene variations impact risk and enable personalized prevention strategies.
Explore how genetic testing can accurately diagnose Cortisone Reductase Deficiency 2, a rare disorder affecting cortisol metabolism, to guide treatment and counseling.
Explore how genetic testing unravels cranioectodermal dysplasia 4, aiding early diagnosis, guiding genetic counseling, and informing treatment strategies.