Seckel Syndrome 7: Unraveling the Genetic Threads of a Rare Disorder
Explore Seckel syndrome 7, a rare genetic disorder. Learn how genetic testing aids early diagnosis, personalized treatment, and informed family planning.
Brandon Colby, MD
MD · MBA
Physician specializing in genetic analysis and personalized preventive medicine, and author of Outsmart Your Genes.
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 degree 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
- BA in Genetics with Honors, University of Michigan · 2000
- MD, Mount Sinai School of Medicine · 2004
- MBA, Stanford University Graduate School of Business · 2007
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 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
Seckel Syndrome 8: Unraveling the Genetic Threads of a Rare Disorder
Explore genetic testing's role in diagnosing Seckel Syndrome 8, a rare disorder. Learn about early intervention, personalized care, and family planning.
Solving the Puzzle of Short Stature with Microcephaly and Distinctive Facies: The Role of Genetic Testing
Explore how genetic testing can help diagnose short stature with microcephaly and distinctive facies, offering early intervention, treatment options, and family planning insights.
Short Stature-Onychodysplasia-Facial Dysmorphism-Hypotrichosis Syndrome: Decoding the Genetic Puzzle
Unlock the mysteries of SOFDH with genetic testing. Explore diagnosis, early intervention, and family planning for this rare disorder in our comprehensive guide.
Short Stature-Optic Atrophy-Pelger-Huët Anomaly Syndrome: The Role of Genetic Testing in Diagnosis and Management
Explore the role of genetic testing in diagnosing and managing SOPH syndrome, focusing on the NBAS gene's impact on growth, vision, and family planning.
Sinoatrial Node Dysfunction and Deafness: Unraveling the Genetic Threads
Explore how genetic testing aids in diagnosing Sinoatrial Node Dysfunction and Deafness, highlighting genetic mutations, personalized treatment, and family planning.
Specific Language Impairment 5: Unraveling Genetic Threads in Communication Challenges
Uncover how genetic testing aids in diagnosing Specific Language Impairment 5, informing personalized treatments, and supporting family planning for better outcomes.
Solving Spermatogenic Failure 10: The Promise of Genetic Testing
Solve male infertility challenges with genetic testing. Addressing Spermatogenic Failure 10, genetic insights offer personalized treatments and guide family planning.