Innovative Insights: Understanding Intellectual Disability, Autosomal Recessive 50
Explore genetic testing's role in diagnosing and managing Intellectual Disability, Autosomal Recessive 50, aiding early detection and personalized care strategies.
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
Genetic Insights into Intellectual Disability-Macrocephaly-Hypotonia-Behavioral Abnormalities Syndrome
Gain insights into intellectual disability-macrocephaly syndrome through genetic testing, offering accurate diagnoses and personalized treatment strategies.
Illuminating Intellectual Disability-Microcephaly-Strabismus-Behavioral Abnormalities Syndrome Through Genetic Testing
Discover how genetic testing aids in diagnosing and managing IMSBAS, a rare syndrome marked by intellectual and behavioral symptoms, offering insights into treatment and family…
Illuminating Isolated Focal Non-Epidermolytic Palmoplantar Keratoderma: The Role of Genetic Testing
Explore the impact of genetic testing on diagnosing and managing isolated focal non-epidermolytic palmoplantar keratoderma, a rare skin thickening condition.
Journey Through Genetics: Understanding Joubert Syndrome 23
Explore how genetic testing aids in diagnosing Joubert Syndrome 23, offering insights into symptoms, treatment guidance, and empowering family planning decisions.
Klippel-Feil Anomaly-Myopathy-Facial Dysmorphism Syndrome: Unlocking the Genetic Code
Explore how genetic testing uncovers the complexities of Klippel-Feil syndrome, offering accurate diagnosis, personalized treatments, and valuable family planning insights.
Unlocking the Mysteries of Lethal Congenital Contracture Syndrome 6: Genetic Testing as a Beacon of Hope
Explore how genetic testing aids in diagnosing Lethal Congenital Contracture Syndrome 6, offering precise mutation identification and guiding early intervention and family…
Unlocking the Mysteries of Lethal Congenital Contracture Syndrome 7: The Role of Genetic Testing
Explore the role of genetic testing in diagnosing Lethal Congenital Contracture Syndrome 7, aiding early detection, family planning, and advancing research.