Decoding Crohn's Disease: The Power of Genetic Testing
Discover the power of genetic testing in diagnosing Crohn's disease, personalizing treatment plans, and identifying at-risk individuals for better prevention strategies.
Brandon Colby, MD
MD · MBA
Physician specializing in genetic analysis and personalized preventive medicine, and author of Outsmart Your Genes.
About Brandon
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).
Education
- BA in Genetics with Honors, University of Michigan · 2000
- MD, Mount Sinai School of Medicine · 2004
- MBA, Stanford University Graduate School of Business · 2007
Affiliations & Memberships
- Affiliate Specialist, American College of Medical Genetics and Genomics (ACMG)
- Associate, American College of Preventive Medicine (ACPM)
- Member, 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.
Articles by Brandon
Unlocking the Mystery of Digenic Deafness: GJB2/GJB3
Discover the role of GJB2/GJB3 genes in digenic deafness, the benefits of genetic testing, and its impact on diagnosis, early intervention, and family planning.
Decoding Digenic Deafness: A Comprehensive Guide to GJB2/GJB6-Related Hearing Loss
Discover the importance of genetic testing for GJB2/GJB6-related digenic deafness, including diagnosis, personalized treatment, and family planning options.
Decoding the Mystery of Descending Aortic Dissection: Genetic Testing and Beyond
Discover the role of genetic testing in diagnosing & managing descending aortic dissection, its connection to connective tissue disorders, and improving patient outcomes.
Decoding the Genetic Mysteries of Primary Cervical Dystonia
Discover the potential of genetic testing in diagnosing and managing primary cervical dystonia. Learn about recent research, risk factors, and personalized treatment strategies.
Decoding the Enigma of Endometriosis: Genetic Testing for Diagnosis and Management
Discover the role of genetic testing in diagnosing endometriosis, understanding its causes, and personalizing treatment for improved fertility outcomes.
Decoding the Mystery of Autosomal Recessive Epidermolysis Bullosa Dystrophica: Genetic Testing and Beyond
Discover the power of genetic testing in diagnosing Epidermolysis Bullosa Dystrophica, guiding treatment, prenatal diagnosis, and shaping nationwide programs.
Unlocking the Mysteries of Autosomal Recessive Epidermolysis Bullosa Dystrophica Inversa
Discover the role of genetic testing in diagnosing Epidermolysis Bullosa Dystrophica Inversa (EBDI), a rare inherited skin disorder, and its impact on family planning.