Understanding, Diagnosing, and Using Genetic Testing for Dementia
Genetic testing identifies dementia risk factors, confirms diagnoses, and personalizes treatment plans. Learn how genetics can help manage dementia more effectively.
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
Understanding, Diagnosing, and Using Genetic Testing for Disease
Discover how genetic testing enhances disease diagnosis and treatment. Learn about symptoms, genetic mutations, risk assessment, and personalized treatment plans.
Unraveling Endometrial Neoplasm: Understanding, Diagnosing, and the Role of Genetic Testing
Effective management of endometrial neoplasm: Understand symptoms, diagnosis, and the crucial role of genetic testing in risk assessment, personalized treatment, and monitoring.
Understanding, Diagnosing, and Using Genetic Testing for Epithelial-stromal TGFBI Dystrophy
Explore how genetic testing aids in diagnosing Epithelial-stromal TGFBI Dystrophy, predicting its progression, family planning, and personalizing treatment strategies.
Understanding, Diagnosing, and Using Genetic Testing for Esophageal Atresia
Explore esophageal atresia, its diagnosis, and the crucial role of genetic testing in identifying syndromes, guiding treatment, and understanding inheritance patterns.
Understanding, Diagnosing, and Using Genetic Testing for Essential Hypertension
Genetic testing in essential hypertension reveals risk factors, personalizes treatment, and aids prevention. Learn how understanding genetic links can improve hypertension…
Understanding Familial Erythrocytosis: Diagnosis and the Role of Genetic Testing
Familial erythrocytosis is a rare genetic disorder with increased red blood cells. Learn about its diagnosis, symptoms, and how genetic testing can guide treatment and family…
Understanding, Diagnosing, and Using Genetic Testing for Familial Hemiplegic Migraine
Unlock the potential of genetic testing for Familial Hemiplegic Migraine. Learn about diagnosis, genetic mutations, personalized treatment plans, and family planning options.