Decoding the Genetic Mysteries of Behavior Disorders
Discover the benefits of genetic testing in diagnosing behavior disorders, personalizing treatments, predicting disease risk, and informing family planning decisions. Improve…
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
Unlocking the Secrets of Bone Mineral Density: A Journey into QTL 15
Discover the role of genetic testing in diagnosing osteoporosis, understanding bone mineral density, and developing personalized prevention & treatment strategies.
Deciphering the Mysteries of Charcot-Marie-Tooth Disease Axonal Type 2P
Discover the role of genetic testing in diagnosing Charcot-Marie-Tooth disease type 2P (CMT2P), guiding treatment plans, and advancing research for better outcomes.
Demystifying Chromosome 2q23.1 Deletion Syndrome: Understanding, Diagnosing, and Genetic Testing
Discover Chromosome 2q23.1 deletion syndrome, its symptoms, and the importance of genetic testing for diagnosis, family planning, and personalized treatment.
Decoding the Genetic Mysteries of Colorectal Cancer: Understanding, Diagnosing, and Utilizing Genetic Testing
Discover the benefits of genetic testing for colorectal cancer diagnosis, risk assessment, and treatment insights. Learn how early detection can improve outcomes and save lives.
Decoding Colostrum Secretion: A Genetic Approach to Understanding and Diagnosing the Disease
Discover the importance of colostrum secretion, its genetic factors, and how genetic testing aids in diagnosing and managing related diseases for newborns' health.
Unlocking the Mysteries of Congenital Blindness: Genetic Testing and Beyond
Explore the role of genetic testing in diagnosing congenital blindness, leading to accurate diagnosis, personalized care, and improved understanding of this rare disorder.
Decoding the Genetic Mysteries of Congenital Hemolytic Anemia
Discover the benefits of genetic testing in diagnosing congenital hemolytic anemia, enabling early intervention, personalized treatment plans, and informed family planning.