Decoding Sardinian HPFH: Understanding, Diagnosing, and Using Genetic Testing
Discover the role of genetic testing in diagnosing & managing Sardinian HPFH, a rare genetic condition, and its significance in understanding related diseases.
Dr. Brandon Colby, MD
MD · MBA
Founder & CEO, Sequencing.com
Founder of Sequencing and author of Outsmart Your Genes. An early voice in direct-to-consumer genetic testing.
About
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 BA with Honors 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
Education
- MD, Mount Sinai School of Medicine
- MBA, Stanford University Graduate School of Business
- BS in Genetics, with Honors, University of Michigan
Affiliations & Memberships
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 Dr. 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 SDHB-Related Disorders: Understanding, Diagnosing, and Using Genetic Testing
Discover the importance of genetic testing in diagnosing & managing SDHB-related disorders, enabling accurate diagnosis, early intervention, and personalized treatment plans.
Decoding the Mystery: Understanding Sensorineural Deafness and Migraine
Discover the role of genetic testing in diagnosing and treating sensorineural deafness and migraine. Learn about early intervention, targeted treatments, and family planning…
Decoding the Mystery: Understanding Sensorineural Deafness with Hypertrophic Cardiomyopathy
Discover the role of genetic testing in diagnosing & managing sensorineural deafness with hypertrophic cardiomyopathy, guiding treatment & improving outcomes.
Decoding SEPN1-Related Disorders: Understanding, Diagnosing, and Harnessing the Power of Genetic Testing
Discover the importance of understanding SEPN1-related disorders and the role of genetic testing in diagnosis, treatment, and family planning for these rare conditions.
Decoding the Mystery of Severe Hydrocephalus: Understanding, Diagnosing, and Genetic Testing
Discover the role of genetic testing in diagnosing and managing severe hydrocephalus, understanding its genetic causes, guiding treatment strategies, and informing family planning…
Unlocking the Secrets of Riboflavin-Responsive Skeletal Myopathy
Discover the importance of genetic testing in diagnosing riboflavin-responsive skeletal myopathy, guiding personalized treatment plans, and assisting in family planning decisions.
Deciphering the Complex World of SLC26A4-Related Disorders: Genetic Testing and Beyond
Discover the role of genetic testing in diagnosing SLC26A4-related disorders, guiding treatment, and identifying at-risk family members for improved management.