MD · MBA
Physician specializing in genetic analysis and personalized preventive medicine, and author of Outsmart Your Genes.
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).
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.
Explore genetic testing's vital role in diagnosing perinatal lethal hypophosphatasia and how early intervention and enzyme therapy can improve infant outcomes.
Explore Perrault syndrome, a rare genetic disorder with sensorineural deafness and ovarian dysgenesis. Learn how genetic testing aids in diagnosis and management.
Explore Phosphoenolpyruvate Carboxykinase Deficiency, its genetic roots, diagnosis via genetic testing, and personalized treatment strategies for better management.
Explore the impact of genetic testing on pilocytic astrocytoma, highlighting personalized treatment, prognostic insights, and early recurrence detection for improved care.
Explore how genetic testing transforms pilomyxoid astrocytoma management with personalized treatments, early detection, and prognostic insights for young patients.
Uncover how genetic testing enhances pineoblastoma diagnosis by identifying mutations, personalizing treatments, predicting responses, and aiding early detection.
Uncover how genetic testing is revolutionizing the diagnosis of rare Pitt-Hopkins-like syndrome, aiding in treatment, family planning, and enhancing understanding.
Explore genetic testing's crucial role in diagnosing, treating, and monitoring pituitary carcinoma, enhancing precision and personalization in patient care.