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.
Discover the role of genetic testing in identifying SmQTL3, a factor linked to smoking behavior & cardiovascular disease risk, and its impact on personalized treatment.
Discover the importance of SSQTL1 genetic testing for diagnosing and managing associated health conditions. Learn about recent research, risk assessment, and family planning.
Discover the role of genetic testing in diagnosing Three Vessel Coronary Disease (3VD) and personalizing treatment plans to improve heart health and long-term outcomes.
Discover the role of somatic mutations in Thrombocythemia 2, and learn how genetic testing aids in accurate diagnosis, personalized treatment, and family planning.
Discover the role of genetic testing in diagnosing Tietz Syndrome, a rare genetic disorder causing albinism & hearing loss. Learn about its benefits, limitations, and impact on…
Discover the importance of genetic testing in diagnosing and managing Usher Syndrome Type ID/F, enabling early intervention, targeted treatment, and informed family planning.
Discover the role of genetic testing in diagnosing Usher Syndrome Type IIC, a rare genetic disorder causing hearing loss & vision impairment. Learn about treatment options &…
Discover the role of genetic testing in diagnosing Wieacker-Wolff Syndrome, a rare neuromuscular disorder. Learn about ZC4H2 gene mutations, severity assessment, and management…