Goldenhar Syndrome: Genetic Testing's Role in Diagnosis and Management
Explore how genetic testing enhances Goldenhar syndrome diagnosis, informs treatment options, and aids family planning by identifying specific genetic mutations.
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
Harnessing Genetic Testing for Hemoglobin E Disease: A Pathway to Precision Medicine
Explore how genetic testing advances diagnosis and personalized treatment of Hemoglobin E disease, improving management and family planning for affected individuals.
Hereditary Hemorrhagic Hazards: Understanding Hemorrhagic Disease Due to Alpha-1-Antitrypsin Pittsburgh Mutation
Explore the impact of the alpha-1-antitrypsin Pittsburgh mutation on hemorrhagic disease. Genetic testing aids early detection, personalized treatment, and family planning.
Harnessing Genetics: Understanding Hereditary Cancer-Predisposing Syndrome
Explore how genetic testing can identify mutations linked to Hereditary Cancer-Predisposing Syndrome, guiding prevention and personalized cancer treatment strategies.
Hereditary Episodic Ataxia: Harnessing Genetic Testing for Better Diagnosis and Management
Uncover how genetic testing enhances hereditary episodic ataxia diagnosis, offering personalized treatment and early intervention for improved patient outcomes.
Hereditary Motor and Sensory Neuropathy: Unveiling the Genetic Mysteries with Modern Testing
Unlock the potential of genetic testing in diagnosing hereditary motor and sensory neuropathy, guiding personalized treatments and informed family planning decisions.
Hereditary Sensory and Autonomic Neuropathy: Unraveling the Genetic Threads of a Complex Disorder
Uncover the genetic basis of Hereditary Sensory and Autonomic Neuropathy. Explore genetic testing's role in diagnosis, personalized treatments, and family risk assessment.
Hereditary Mysteries: Understanding Huntington Disease-Like Syndrome
Explore Huntington Disease-Like Syndrome, its genetic causes, and how genetic testing aids in precise diagnosis, personalized care, and informed family planning.