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.
Discover the role of genetic testing in diagnosing Wieacker-Wolff Syndrome, a rare neuromuscular disorder. Learn about ZC4H2 gene mutations, severity assessment, and management…
Discover the rare genetic condition Woolly Hair, Autosomal Recessive 2, its diagnosis, and the crucial role of genetic testing in understanding and managing this hair disorder.
Discover the role of genetic testing in diagnosing X-linked intellectual disability Cabezas type, identifying gene mutations, and guiding personalized treatment plans.
Discover the importance of diagnosing Acatalasemia, Japanese type, through genetic testing and whole genome sequencing for effective treatment and improved quality of life.
Discover the potential of whole genome sequencing in diagnosing cerebral hemorrhage, identifying prognostic biomarkers, and revolutionizing treatment strategies.
Discover the importance of genetic testing, specifically whole genome sequencing, in diagnosing multifocal breast carcinoma and improving treatment plans.
Discover the power of genetic testing and whole genome sequencing in diagnosing venous malformations, unlocking personalized treatment options for improved patient outcomes.
Discover the role of genetic testing & whole genome sequencing in diagnosing WDR1 deficiency, a rare immunodeficiency causing recurrent infections & complications.