Understanding Lynch Syndrome: Diagnosis and the Role of Genetic Testing
Explore how Lynch syndrome, a genetic disorder increasing cancer risk, is diagnosed through family history, clinical evaluations, and essential genetic testing.
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
Understanding Malignant Peritoneal Mesothelioma: Diagnosis and the Role of Genetic Testing
Boost early detection & treatment of Malignant Peritoneal Mesothelioma with genetic testing. Learn about symptoms, diagnosis, and personalized treatment options.
Understanding, Diagnosing, and Using Genetic Testing for Malignant Tumors of the Testis
Explore how genetic testing aids in diagnosing and treating malignant testis tumors. Learn about risk factors, diagnosis methods, and personalized treatment plans.
Understanding, Diagnosing, and Using Genetic Testing for Melnick-Fraser Syndrome
Explore the role of genetic testing in diagnosing Melnick-Fraser Syndrome. Learn about its symptoms, clinical evaluation, and the importance of early intervention.
Understanding, Diagnosing, and Using Genetic Testing for Meretoja Syndrome
Explore Meretoja Syndrome, a rare genetic disorder. Learn about its symptoms, diagnosis, and how genetic testing helps in better management and family planning.
Understanding, Diagnosing, and Utilizing Genetic Testing for Movement Disorders
Explore movement disorders, their diagnosis, and how genetic testing can identify genetic mutations, personalize treatment, and assist in family planning and research.
Understanding, Diagnosing, and Using Genetic Testing for Multiple Congenital Exostosis
Genetic testing confirms Multiple Congenital Exostosis, a rare genetic disorder with benign bone tumors. Learn about diagnosis, risk assessment, and personalized treatment.
Understanding, Diagnosing, and Using Genetic Testing for Nanophthalmia
Uncover the role of genetic testing in diagnosing nanophthalmia. Learn about clinical exams, imaging studies, and vital insights to manage this rare eye condition effectively.