Exploring Ehlers-Danlos Syndrome, Classic Type, 1: The Role of Genetic Testing
Unlock the potential of genetic testing for Ehlers-Danlos Syndrome, Classic Type, with early diagnosis, personalized treatment, and informed family planning.
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
Ehlers-Danlos Syndrome, Classic Type, 2: Exploring the Role of Genetic Testing
Understand Ehlers-Danlos Syndrome, classic type 2, and how genetic testing aids diagnosis, informs treatment, guides family planning, and boosts research insights.
Familial Exudative Vitreoretinopathy: Decoding the Genetic Blueprint for Better Diagnosis and Management
Explore how genetic testing advances the diagnosis and management of Familial Exudative Vitreoretinopathy, uncovering mutations like the new NDP gene variant.
Finding Clarity: Understanding Familial Idiopathic Steroid-Resistant Nephrotic Syndrome
Explore Familial Idiopathic Steroid-Resistant Nephrotic Syndrome, its genetic roots, diagnosis through testing, personalized treatments, and implications for family planning.
Facing Familial Isolated Restrictive Cardiomyopathy: The Role of Genetic Testing in Early Detection and Management
Explore the role of genetic testing in diagnosing familial isolated restrictive cardiomyopathy, focusing on the FLNC variant for early detection and effective management.
Familial Melanoma: Unveiling the Genetic Maze
Unlock insights into familial melanoma with genetic testing. Learn how identifying gene mutations aids in prevention, surveillance, and informed family decisions.
Fanconi Anemia: Unlocking the Mysteries with Genetic Testing
Explore the role of genetic testing in diagnosing Fanconi anemia. Learn about genetic mutations, carrier identification, and tailored treatment strategies for FA.
Fathoming Fetal and Neonatal Alloimmune Thrombocytopenia: The Role of Genetic Testing
Explore how genetic testing aids in diagnosing fetal and neonatal alloimmune thrombocytopenia, identifying platelet antigen incompatibilities for personalized care.