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 benefits of genetic testing for diagnosing and managing X-linked Intellectual Disability 1 (XLID1). Learn how early intervention and personalized treatments can…
Discover the role of genetic testing in diagnosing Kniest Dysplasia, a rare bone disorder, and learn how personalized treatment plans improve patient outcomes.
Discover the genetic causes of lactic acidosis, including SURF1, YARS2, CREBBP, and PDHB mutations. Learn how genetic testing aids in diagnosis and improves patient outcomes.
Discover the importance of Langereis blood group in various health conditions and learn how genetic testing can help diagnose, assess risk, and guide treatment methods. (158…
Discover the role of genetic testing in diagnosing Left Ventricular Noncompaction 3, identifying at-risk family members, guiding prognosis, and managing overlapping…
Discover the role of genetic testing in diagnosing Li-Fraumeni Syndrome, guiding personalized cancer surveillance, and informing family planning decisions.
Discover the role of genetic testing in diagnosing Long QT Syndrome types 2 and 3, the importance of understanding digenic inheritance, and potential treatment options.
Discover the role of genetic testing in diagnosing Long QT Syndrome 3/6, digenic, guiding treatment strategies, and screening family members for this rare cardiac disorder.