Analyzing Amyotrophic Lateral Sclerosis Type 20: The Role of Genetic Testing
Uncover ALS Type 20's genetic roots. Explore the role of genetic testing in early detection, treatment personalization, and familial risk assessment.
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
Advancing Understanding: Genetic Testing for Ataxia with Oculomotor Apraxia Type 3
Unlock the role of genetic testing in diagnosing and managing Ataxia with Oculomotor Apraxia Type 3. Learn about early diagnosis, tailored treatments, and family planning.
Understanding Autism, Susceptibility to, 18: The Role of Genetic Testing
Explore the link between CHD8 mutations and autism. Understand how genetic testing aids in diagnosis, personalized care, and targeted interventions for ASD.
Understanding Autism Susceptibility 19: The Role of Genetic Testing
Explore how genetic testing reveals Autism Susceptibility 19, aiding early diagnosis, personalized interventions, and informed family planning decisions.
A Deep Dive into Autosomal Dominant Hypocalcemia 2: The Genetic Testing Revolution
Explore Autosomal Dominant Hypocalcemia 2, a rare disorder due to GNA11 mutations. Genetic testing aids in diagnosis, treatment, and informs family planning.
Addressing Autosomal Recessive Congenital Ichthyosis 10: The Role of Genetic Testing
Explore ARCI10, a rare genetic skin disorder. Learn how genetic testing offers diagnostic clarity, personalized treatments, and aids in research and family planning.
Advancements in Understanding Autosomal Recessive Congenital Ichthyosis 9 Through Genetic Testing
Explore how genetic testing enhances early diagnosis and management of ARCI9, revealing the role of the CERS3 gene mutation in this rare skin disorder.
Genetic Insights: Understanding Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2T
Explore the impact of genetic testing in diagnosing LGMD2T, from early detection and personalized treatment to family planning and advancing research.