Understanding Striatal Degeneration: A Comprehensive Guide
Discover the importance of genetic testing in diagnosing striatal degeneration, guiding treatment plans, identifying at-risk family members, and advancing research.
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
Understanding, Diagnosing, and Using Genetic Testing for Nonalcoholic Fatty Liver Disease Susceptibility
Discover the role of genetic testing in diagnosing nonalcoholic fatty liver disease (NAFLD), its benefits in identifying at-risk individuals, and personalizing treatment plans for…
Decoding the Mysteries of Syndromic Microphthalmia, Dominant
Discover the importance of genetic testing in diagnosing Syndromic Microphthalmia, Dominant, a rare eye disorder, and how it benefits affected individuals and their families.
Unlocking the Mysteries of Syndromic Microphthalmia, Recessive
Discover the role of genetic testing in diagnosing and managing Syndromic Microphthalmia, Recessive - a rare eye disorder. Learn about its causes, symptoms, and treatment options.
Understanding, Diagnosing, and Using Genetic Testing for Thiamine Metabolism Dysfunction Syndrome
Discover the importance of genetic testing in diagnosing and managing Thiamine Metabolism Dysfunction Syndrome, a rare genetic disorder affecting vitamin B1 levels.
Decoding Thyroid Hormonogenesis Defect: Understanding, Diagnosing, and Genetic Testing
Discover Thyroid Hormonogenesis Defect, its symptoms, diagnosis, and the importance of genetic testing for early detection, prenatal diagnosis, and carrier testing.
Decoding TP63-Related Spectrum Disorders: Understanding, Diagnosing, and Genetic Testing
Discover the importance of understanding TP63-Related Spectrum Disorders, their diagnosis, and the benefits of genetic testing for effective management and family planning.
Understanding Transient Neonatal Diabetes, Dominant
Discover the importance of genetic testing in diagnosing Transient Neonatal Diabetes, its role in treatment planning, and its benefits for family planning.