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 Nager syndrome's genetic roots, clinical challenges, and how genetic testing aids in diagnosis and personalized management for improved quality of life.
Explore how genetic testing aids in diagnosing distal hereditary motor neuronopathy (dHMN2A), offering insights into early diagnosis, family planning, and tailored care.
Early diagnosis of Neuronopathy Type 7A through genetic testing enables personalized treatment and informed family planning, improving outcomes and managing symptoms effectively.
Explore how genetic testing enhances diagnosis, management, and family planning for Nonsyndromic Congenital Nail Disorder 3, improving patient outcomes.
Explore genetic testing's role in diagnosing Noonan syndrome with multiple lentigines, guiding treatment, improving outcomes, and aiding family planning.
Explore how genetic testing aids in diagnosing oromandibular-limb hypogenesis spectrum, offering diagnostic clarity, personalized care, and insights for family planning.
Unlock insights into Palmoplantar Keratoderma-Deafness Syndrome with genetic testing. Explore accurate diagnosis, mutation variability, and personalized treatments.
Explore the impact of genetic testing on early diagnosis, personalized care, and family planning in palmoplantar keratoderma-esophageal carcinoma syndrome.