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 genetic testing for hereditary motor and sensory neuropathy with optic atrophy. Diagnose, manage progression, and guide treatment decisions effectively.
Uncover the role of genetic testing in diagnosing Hereditary Spastic Paraplegia. Explore benefits for treatment, family planning, and insights into gene interactions.
Explore how genetic testing aids in diagnosing Hermansky-Pudlak Syndrome, offering personalized treatment and supporting family planning, especially in Puerto Rico.
Explore how genetic testing revolutionizes the diagnosis, treatment, and management of homocystinuria without methylmalonic aciduria for tailored, effective care.
Explore how genetic testing aids in diagnosing hyaline body myopathy, providing early detection, personalized treatments, and improved management of this rare disorder.
"Explore hyperprolinemia's impact on kidneys, its genetic roots, and management strategies. Learn how genetic testing aids early diagnosis and personalized care."
Explore how genetic testing aids in accurate diagnosis, early intervention, and personalized treatment of Hypotrichosis-Lymphedema-Telangiectasia-Renal Defect Syndrome.
Unlock insights into hypotrichosis simplex with genetic testing. Discover how it aids diagnosis, guides family planning, and offers personalized treatment options.