Cracking the Genetic Code: Understanding and Diagnosing Cataract 43
Discover the role of genetic testing in diagnosing Cataract 43, a rare eye disorder, and how understanding its genetic basis can lead to targeted treatments and improved patient…
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
Decoding the Genetic Mysteries of Advanced Colon Cancer
Discover the role of genetic testing in diagnosing advanced colon cancer, identifying high-risk individuals, and guiding personalized treatment for better outcomes.
Decoding the Colton-null Phenotype: Genetic Testing for Understanding and Diagnosis
Discover the importance of genetic testing in diagnosing and managing the Colton-null phenotype, a rare blood group variant, for better healthcare outcomes.
Decoding the Silence: Understanding and Diagnosing Congenital Sensorineural Hearing Impairment
Discover the role of genetic testing in diagnosing congenital sensorineural hearing impairment, its genetic causes, and how early intervention can improve lives.
Decoding Cortical Tubers: Understanding, Diagnosing, and Utilizing Genetic Testing
Discover the role of genetic testing in diagnosing cortical tubers, a neurological condition linked to tuberous sclerosis complex (TSC), and its benefits in guiding treatment…
Unlocking the Mysteries of Costello Syndrome: Genetic Testing and Beyond
Discover how genetic testing aids in diagnosing Costello Syndrome, a rare genetic disorder, and explore advances in research for targeted treatments. Learn about the benefits of…
Decoding the Mystery of Nonclassifiable Autosomal Dominant Craniosynostosis: Understanding, Diagnosing, and Using Genetic Testing
Discover the role of genetic testing in diagnosing nonclassifiable autosomal dominant craniosynostosis, guiding treatment, and advancing personalized medicine.
Unlocking the Mysteries of Cranium Bifidum Occultum: Understanding, Diagnosing, and Genetic Testing
Discover the importance of understanding Cranium Bifidum Occultum, its diagnosis, genetic factors, and how genetic testing plays a crucial role in managing this rare congenital…