Understanding ATTRV122I Amyloidosis: The Role of Genetic Testing in Diagnosis and Management
Explore ATTRV122I amyloidosis with insights on genetic testing for early diagnosis, family screening, and tailored treatments, enhancing patient management.
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
Advancements in Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease: The Role of Genetic Testing
Explore how genetic testing uncovers genetic mutations in Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease, aiding early diagnosis and personalized treatment.
Decoding the Silence: Understanding Autosomal Dominant Nonsyndromic Hearing Loss
Explore autosomal dominant nonsyndromic hearing loss, its genetic roots, and how advanced genetic testing, like identifying the CEACAM16 variant, aids diagnosis.
Understanding Autosomal Erythropoietic Protoporphyria: The Role of Genetic Testing in Diagnosis and Management
Explore the crucial role of genetic testing in diagnosing and managing autosomal erythropoietic protoporphyria, a rare disorder causing severe photosensitivity.
Advancing Understanding: Genetic Testing for Autosomal Recessive Non-Syndromic Intellectual Disability
Explore the impact of genetic testing in diagnosing ARNID, focusing on a key TRAPPC9 mutation discovery, offering new insights and hope for affected families.
Axenfeld-Rieger Syndrome: Unraveling Genetics for Better Management
Explore the genetic roots of Axenfeld-Rieger Syndrome. Learn how genetic testing aids early diagnosis, personalized treatments, and informed family planning.
Beta Thalassemia: Bridging the Gap with Genetic Testing
Genetic testing in beta Thalassemia aids early diagnosis, personalized treatments, and informed family planning, improving outcomes for those with this genetic blood disorder.
Breaking Down Bosley-Salih-Alorainy Syndrome: The Role of Genetic Testing
Explore Bosley-Salih-Alorainy Syndrome. Genetic testing enables early diagnosis, personalized treatment, and empowers families with critical genetic counseling insights.