Cracking the Code: Genetic Testing for Congenital Fibrosis of Extraocular Muscles
Explore how genetic testing identifies mutations in CFEOM genes, aiding in diagnosis, treatment planning, and family decision-making for congenital eye disorders.
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 Congenital Microvillous Atrophy: The Role of Genetic Testing
Explore how genetic testing aids in diagnosing congenital microvillous atrophy, a severe intestinal disorder in newborns, by identifying key genetic mutations.
Congenital Multicore Myopathy with External Ophthalmoplegia: A Genetic Lens into a Complex Condition
Genetic testing aids in diagnosing congenital multicore myopathy with external ophthalmoplegia, offering insights into symptoms, management, and family planning.
Congenital Myopathy with Fiber Type Disproportion: Unraveling the Genetic Threads
Explore the role of genetic testing in diagnosing congenital myopathy with fiber type disproportion, a rare muscle disorder affecting muscle tone and strength.
Genetic Glimpses: Understanding Fuchs Endothelial Corneal Dystrophy
Explore the role of genetic testing in diagnosing Fuchs Endothelial Corneal Dystrophy, uncovering genetic mutations, and developing personalized treatment plans.
Decoding Dejerine-Sottas Disease: Genetic Testing's Promise
Unlock the potential of genetic testing for Dejerine-Sottas disease. Gain insights into diagnosis, family planning, and innovative treatments for this rare neuropathy.
Delving into Desbuquois Dysplasia 1: Genetic Testing as a Beacon of Hope
Explore how genetic testing aids in diagnosing Desbuquois Dysplasia 1, offering early intervention, informed family planning, and advancing research for better outcomes.
Decoding Desmoid Tumors: The Role of Genetic Testing in Diagnosis and Treatment
Dive into the role of genetic testing in understanding desmoid tumors. Enhance diagnosis, personalize treatments, and monitor recurrence for improved patient care.