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.
Unlock the genetic secrets of Pontocerebellar Hypoplasia Type 9 with genetic testing. Explore diagnosis, treatment, and family planning for a brighter future.
Explore how genetic testing can diagnose Primary Ciliary Dyskinesia 18, linked to DRC1 gene, enabling early intervention and personalized treatment plans.
Explore the impact of genetic testing on diagnosing Primary Ciliary Dyskinesia 19, leading to precise treatments, improved patient care, and informed family planning.
Unlock precise diagnosis of Primary Ciliary Dyskinesia 21 with advanced genetic testing. Enhance accuracy, discover novel variants, and tailor personalized care.
Maximize precision in diagnosing pulmonary fibrosis and bone marrow failure with genetic testing, enhancing treatment strategies and predicting disease progression.
Genetic testing reveals crucial insights into Pulmonary Fibrosis and Bone Marrow Failure, helping with early diagnosis, personalized treatment, and informed family planning.
Unlock insights into Retinitis Pigmentosa and Situs Inversus with genetic testing. Enhance diagnosis, guide treatment, and inform family planning strategies.
Explore how genetic testing aids in diagnosing Schuurs-Hoeijmakers syndrome, offering precise, personalized care for autism-related developmental challenges.