MD · MBA
Founder & CEO, Sequencing.com
Founder of Sequencing and author of Outsmart Your Genes. An early voice in direct-to-consumer genetic testing.
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 BA with Honors 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 Dr. 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 the impact of genetic testing in diagnosing ARNID, focusing on a key TRAPPC9 mutation discovery, offering new insights and hope for affected families.
Explore the genetic roots of Axenfeld-Rieger Syndrome. Learn how genetic testing aids early diagnosis, personalized treatments, and informed family planning.
Genetic testing in beta Thalassemia aids early diagnosis, personalized treatments, and informed family planning, improving outcomes for those with this genetic blood disorder.
Explore Bosley-Salih-Alorainy Syndrome. Genetic testing enables early diagnosis, personalized treatment, and empowers families with critical genetic counseling insights.
Explore how genetic testing enhances CM-AVM1 diagnosis, treatment personalization, and family planning strategies. Unlock the potential for effective management.
Explore the role of genetic testing in esophageal carcinoma, identifying mutations, guiding treatments, predicting prognosis, and shaping personalized cancer care.
Unlock the benefits of genetic testing for Carpenter Syndrome: early diagnosis, personalized treatment plans, family planning insights, and future therapy developments.
Explore centronuclear myopathy, a rare muscle disorder, and how genetic testing aids in diagnosis, treatment guidance, and informed family planning decisions.