Decoding Dentin Dysplasia Type I: A Comprehensive Guide to Genetic Testing and Diagnosis
Discover Dentin Dysplasia Type I, a rare genetic dental disorder, and learn how genetic testing aids in diagnosis, carrier identification, and prenatal care.
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
Unraveling the Mysteries of Dermatofibrosis Lenticularis Disseminata: A Closer Look at Genetic Testing
Discover the role of genetic testing in diagnosing Dermatofibrosis Lenticularis Disseminata, a rare genetic disorder, and its potential in guiding family planning and advancing…
Decoding the Genetic Mysteries of Dilated Cardiomyopathy 1T
Unlock the genetic mysteries of Dilated Cardiomyopathy 1T (DCM1T) with genetic testing for early diagnosis, personalized treatment, and family screening. Discover the benefits &…
Decoding Dyssynergia: A Comprehensive Guide to Genetic Testing and Diagnosis
Discover the role of genetic testing in diagnosing Dyssynergia, a rare neurological disorder. Learn about its causes, symptoms, and the benefits of understanding its genetic basis.
Decoding the Mysteries of Multiple Epiphyseal Dysplasia 3 with Myopathy: Genetic Testing Unlocks Answers
Discover the role of genetic testing in diagnosing Multiple Epiphyseal Dysplasia 3 with Myopathy, identifying gene mutations, and guiding treatment strategies.
Decoding the Genetic Puzzle: Understanding Esophageal Cancer Susceptibility
Discover the role of genetic testing in identifying esophageal cancer risk factors, enabling early detection, and personalizing treatment strategies. Learn how it can…
Demystifying Ewing Sarcoma: Diagnosis, Understanding, and the Role of Genetic Testing
Discover the importance of understanding Ewing Sarcoma, its diagnosis, and the crucial role of genetic testing in guiding treatment decisions and monitoring progress.
Decoding the Enigma of Impaired Exercise Stress Response: A Genetic Testing Perspective
Discover the role of genetic testing in diagnosing and managing impaired exercise stress response. Learn about gene mutations, personalized treatments, and prevention strategies.