Decoding the Mystery of Congenital Indifference to Pain
Discover the rare genetic disorder, Congenital Indifference to Pain, its diagnosis, and how genetic testing plays a crucial role in managing this life-threatening condition.
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
Understanding Corneal Intraepithelial Dyskeratosis-Palmoplantar Hyperkeratosis-Laryngeal Dyskeratosis Syndrome
Discover the rare CID-PH-LD syndrome, its diagnosis process, and the crucial role of genetic testing in confirming the condition, guiding treatment, and family planning.
Decoding the Enigma of Coronary Artery Spasm 1: Genetic Testing for Susceptibility and Diagnosis
Discover the role of genetic testing in diagnosing Coronary Artery Spasm 1, its benefits, and how it can lead to personalized treatment options for patients.
Unlocking the Mysteries of Coronary Artery Spasm 2 Susceptibility: Understanding, Diagnosing, and Utilizing Genetic Testing
Discover the role of genetic testing in identifying Coronary Artery Spasm 2 susceptibility, enabling personalized diagnosis, treatment, and prevention strategies for improved…
Unlocking the Mystery: Understanding Sensorineural Deafness with Neurologic Features
Discover the role of genetic testing in diagnosing and managing sensorineural deafness with neurologic features, leading to improved treatment and quality of life.
Decoding the Genetic Enigma: Understanding and Diagnosing Early Adulthood Mortality
Discover the role of genetics in early adulthood mortality and how genetic testing can help diagnose, manage risks, and enable personalized treatment plans.
Decoding the Mysteries of Mitochondrial Complex III Deficiency
Discover the importance of genetic testing for diagnosing mitochondrial complex III deficiency, a rare genetic disorder, and how it can guide treatment plans and improve patient…
Unlocking the Mysteries of Deep Venous Thrombosis: Genetic Testing for Protection and Prevention
Discover the role of genetic testing in diagnosing deep venous thrombosis (DVT) and preventing life-threatening complications. Learn about risk factors, treatment, and recent…