Addressing Aplastic Anemia: Genetic Testing as a Guiding Light
Explore how genetic testing revolutionizes aplastic anemia care by identifying predispositions, guiding treatments, and aiding family planning for informed choices.
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
Arthrogryposis Multiplex Congenita: Genetic Insights for Improved Outcomes
Explore arthrogryposis multiplex congenita, its causes, and how genetic testing aids in diagnosing, personalizing treatment, and guiding family planning.
Atypical Coarctation of Aorta: Unveiling the Genetic Blueprint
Explore how genetic testing enhances understanding and management of atypical coarctation of the aorta, a rare vascular anomaly causing severe hypertension.
Advancements in Understanding Atypical Hemolytic-Uremic Syndrome: Genetic Testing as a Diagnostic Tool
Genetic testing revolutionizes aHUS diagnosis by identifying mutations, personalizing treatment, predicting prognosis, and aiding family planning strategies.
Autosomal Dominant Distal Hereditary Motor Neuropathy: Unraveling Genetic Mysteries
Explore the role of genetic testing in diagnosing Autosomal Dominant Distal Hereditary Motor Neuropathy, focusing on WARS gene mutations and personalized treatments.
Addressing Autosomal Dominant Non-Syndromic Intellectual Disability: The Role of Genetic Testing
Explore how genetic testing and whole exome sequencing enhance diagnosis and management of Autosomal Dominant Non-Syndromic Intellectual Disability.
Advancing Understanding: Genetic Testing for Autosomal Dominant Rhegmatogenous Retinal Detachment
Unlock early detection and personalized care for hereditary rhegmatogenous retinal detachment through advanced genetic testing, aiding in better vision preservation.
Advancing Understanding: Genetic Testing for Autosomal Recessive Cerebellar Ataxia
Explore how genetic testing identifies mutations in autosomal recessive cerebellar ataxia, enhancing diagnosis, personalized treatment, and informed family planning.