Decoding the Genetics of Profound Hearing Impairment: A Comprehensive Guide
Discover the role of genetics in profound hearing impairment, the importance of accurate diagnosis, and how genetic testing can aid in treatment and counseling.
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
Unlocking the Mysteries of Digenic Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions
Discover the importance of genetic testing in diagnosing digenic progressive external ophthalmoplegia with mtDNA deletions, guiding treatment decisions, and family planning.
Decoding the Mysteries of Progressive Microcephaly: Understanding, Diagnosing, and Using Genetic Testing
Discover the role of genetic testing in diagnosing progressive microcephaly, a rare neurological disorder. Learn about novel genetic variants and treatment guidance.
Unlocking the Mysteries of Progressive Ventriculomegaly: Understanding, Diagnosing, and Genetic Testing
Discover the importance of early diagnosis and genetic testing for progressive ventriculomegaly, a neurological condition affecting fetal brain development. Learn about targeted…
Unlocking the Mystery of Proximal Muscle Weakness in Upper Limbs
Discover the causes of proximal muscle weakness in upper limbs, the importance of genetic testing for diagnosis, personalized treatment, and advancing research.
Decoding Dexfenfluramine-Associated Pulmonary Hypertension: A Guide to Genetic Testing
Discover the role of genetic testing in diagnosing and managing dexfenfluramine-associated pulmonary hypertension, a rare condition linked to appetite suppressants.
Decoding the Mysteries of Fenfluramine-Associated Pulmonary Hypertension: Genetic Testing for Diagnosis and Management
Discover the role of genetic testing in diagnosing and managing Fenfluramine-Associated Pulmonary Hypertension. Learn about genetic risk factors and personalized treatments.
Unlocking the Mysteries of Radin Blood Group: Genetic Testing and Its Implications
Discover the Radin blood group's role in disease susceptibility & treatment through genetic testing. Learn how personalized medicine improves patient outcomes.