Decoding Lesch-Nyhan Syndrome: The Power of Genetic Testing
Discover the importance of genetic testing in diagnosing Lesch-Nyhan Syndrome, enabling early intervention, prenatal diagnosis, and genetic counseling for better care.
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
Decoding the Mystery of Acute Myeloid Leukemia M0 Subtype: Genetic Testing for Diagnosis and Treatment
Discover the crucial role of genetic testing in understanding, diagnosing, and treating Acute Myeloid Leukemia M0 subtype, including recent research findings and targeted…
Decoding Congenital Lipoprotein(a) Deficiency: Understanding, Diagnosing, and Using Genetic Testing
Discover the importance of genetic testing in diagnosing & managing Congenital Lipoprotein(a) deficiency, a rare inherited disorder affecting cardiovascular health.
Unlocking the Mysteries of Lissencephaly 4: A Comprehensive Guide to Genetic Testing
Discover the importance of genetic testing in diagnosing Lissencephaly 4, enabling early intervention, personalized treatment, and improved patient outcomes.
Decoding Long QT Syndrome 3: Understanding, Diagnosing, and Genetic Testing
Discover Long QT Syndrome 3, a rare genetic heart disorder, and learn how diagnosis, genetic testing, and treatment can help prevent life-threatening arrhythmias.
Decoding the Mystery of Lower Limb Muscle Weakness: Genetic Testing Unveiled
Discover the power of genetic testing in diagnosing lower limb muscle weakness and related neuromuscular disorders. Learn how it revolutionizes treatment and management strategies.
Decoding the Genetic Puzzle: Major Depressive Disorder and Citalopram Therapy Response
Discover how genetic testing for citalopram therapy response can optimize Major Depressive Disorder treatment, leading to personalized care and better outcomes.
Decoding the Mystery of Mephenytoin Poor Metabolism: Genetic Testing Unravels the Enigma
Discover the role of genetic testing in diagnosing mephenytoin poor metabolism, its benefits & limitations, and how it can improve treatment outcomes for patients.