Mapping Myofibrillar Myopathy 8: The Role of Genetic Testing
Explore how genetic testing can accurately diagnose Myofibrillar Myopathy 8, personalize treatments, aid family planning, and advance MFM8 research and therapies.
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
Mapping Myopathy: Understanding Distal Myopathy with Rimmed Vacuoles Through Genetic Testing
Explore how genetic testing aids in diagnosing distal myopathy with rimmed vacuoles, contributing to personalized treatments, family planning, and future research directions.
Mapping Myopia: The Role of Genetic Testing in Autosomal Dominant Myopia 25
Explore how genetic testing aids in early myopia 25 diagnosis, personalized treatment, and family planning. Discover its impact on research and future advancements.
Mapping the Mysteries of MYPN-related Myopathy: The Role of Genetic Testing
Explore the impact of genetic testing on MYPN-related myopathy, a rare muscle disorder, from early diagnosis to personalized treatment and potential therapies.
Nasopharyngeal Carcinoma Susceptibility: Unraveling Genetic Mysteries
Explore nasopharyngeal carcinoma susceptibility and genetic testing's role in early detection, personalized treatment, and risk assessment. Learn more about NPC today.
Nephronophthisis 20: Navigating the Genetic Maze of a Kidney Disorder
Explore the genetic underpinnings of Nephronophthisis 20. Discover early diagnosis, personalized treatment, and family planning with advanced genetic testing.
Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy: A Genetic Testing Journey into Childhood-Onset Mysteries
Unravel childhood-onset neurodegeneration with genetic testing. Early diagnosis and personalized care improve outcomes for conditions like ataxia and dystonia.
Neurodevelopmental Disorder with Hypotonia, Seizures, and Absent Language: Decoding the Genetic Puzzle
Explore how genetic testing uncovers the roots of neurodevelopmental disorders, improving early diagnosis, personalized treatment, and informed family planning.