Decoding Deuteranopia: Understanding, Diagnosing, and Utilizing Genetic Testing
Roughly 1% of males have deuteranopia, an X-linked recessive red-green color blindness; Ishihara and Farnsworth-Munsell tests diagnose it, OPN1MW analysis confirms it.
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
Dopamine Beta-Hydroxylase Polymorphism: DBH Variants
Variations in the DBH gene alter dopamine and norepinephrine synthesis, and studies link them to autism spectrum disorder and dementia susceptibility.
CES1-Related Altered Drug Metabolism: Gene Variants
The CES1 gene encodes carboxylesterase 1, an enzyme that processes many drugs; variants, fatty liver disease and inflammation can all shift a patient's response.
CYP2C8-Related Altered Drug Metabolism and Testing
NSAIDs, antidiabetic and anticancer drugs depend on the CYP2C8 enzyme, so gene variants, NAFLD and advanced ovarian cancer can change drug exposure and response.
Decoding Dysgenesis of the Cerebellar Vermis: A Comprehensive Guide
Disrupted development of the midline cerebellum affects coordination, posture and eye movement; prenatal MRI and postnatal imaging support the diagnosis.
Decoding Dysplasminogenemia: Understanding, Diagnosing, and Genetic Testing
Plasminogen normally dissolves blood clots, and an autosomal dominant mutation impairs it; plasminogen assays, DNA sequencing and carrier testing are explained.
Demystifying Early-Onset Coronary Artery Disease: Genetic Testing for Diagnosis and Management
Heart disease striking young adults reflects many genes and environment; susceptibility loci in Mexican families, Korean exome findings and South Asian risk are reviewed.
Decoding Early Spermatogenesis Maturation Arrest: A Guide to Genetic Testing and Diagnosis
Discover the role of genetic testing in diagnosing early spermatogenesis maturation arrest, a cause of male infertility, and its benefits for treatment and family planning.