Mapping the Mysteries: Genetic Testing for Malan Overgrowth Syndrome
Explore Malan Overgrowth Syndrome's genetic roots. Learn how genetic testing confirms diagnosis, guides treatment, and supports family planning 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
Mandibular Hypoplasia-Deafness-Progeroid Syndrome: Unraveling the Genetic Threads of a Rare Disorder
Explore how genetic testing advances the diagnosis and management of MDPL syndrome, a complex condition involving jaw underdevelopment, hearing loss, and progeroid features.
Mapping MEGF8: Unlocking the Genetic Mysteries of Carpenter Syndrome
Explore how genetic testing reveals the mysteries of MEGF8-related Carpenter syndrome, aiding in early diagnosis, personalized care, and family planning strategies.
Mapping Mendelian Susceptibility to Mycobacterial Diseases Due to Complete IL12B Deficiency
Explore IL12B deficiency's impact on Mendelian susceptibility to mycobacterial diseases. Learn how genetic testing aids diagnosis, treatment, and family planning.
Mapping the Mystery: Mendelian Susceptibility to Mycobacterial Diseases Due to Complete IL12RB1 Deficiency
Unlock insights into mycobacterial disease susceptibility through genetic testing for IL12RB1 deficiency, aiding in diagnosis, treatment strategies, and family planning.
Mysteries of Mendelian Susceptibility to Mycobacterial Diseases Due to Partial IRF8 Deficiency
Explore how genetic testing reveals the role of partial IRF8 deficiency in Mendelian susceptibility to mycobacterial diseases and enhances diagnosis and treatment.
Mendelian Mysteries: Unraveling Susceptibility to Mycobacterial Diseases Due to Partial STAT1 Deficiency
Explore how genetic testing for partial STAT1 deficiency aids in early detection, personalized treatment, and family planning for mycobacterial diseases.
Metaphyseal Chondromatosis with D-2-Hydroxyglutaric Aciduria: A Genetic Journey to Understanding
Genetic testing reveals IDH1 mutations in metaphyseal chondromatosis, enabling early diagnosis and personalized treatments, offering hope to affected families.