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 how genetic testing aids in diagnosing MSMD due to ISG15 deficiency, informing treatment, management, and family planning decisions effectively.
Explore how genetic testing aids in early diagnosis and management of Microcephaly 12, primary, autosomal recessive, empowering informed decisions and personalized care.
Explore how genetic testing aids in diagnosing Microcephaly 13, offering early intervention, family planning insights, and paving the way for future therapies.
Genetic testing deciphers MCCRP2's complexities, enhancing diagnosis, aiding family planning, and guiding treatments for microcephaly and chorioretinopathy.
Explore the role of ARHGEF7 gene mutations in Mirror Movements 3. Learn how genetic testing aids in early diagnosis, personalized treatment, and family planning.
Explore Mitochondrial Complex III Deficiency Nuclear Type 9. Genetic testing aids in diagnosis, personalized treatment, and family planning for this rare disorder.
Explore the role of genetic testing in diagnosing mitochondrial ATP synthase deficiency, aiding in early detection and personalized treatment for better management.
Explore the genetic basis of Myopathy, Centronuclear, 5, its symptoms, diagnosis, personalized treatments, and the crucial role of genetic testing in management.