Follicular Lymphoma: Unraveling the Genetic Code for Better Outcomes
Genetic testing enhances follicular lymphoma care by identifying mutations, predicting treatment response, and monitoring progression for personalized therapies.
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
Gardner Syndrome: Genetic Testing as a Gateway to Early Detection and Management
Unlock early diagnosis and personalized care for Gardner syndrome with genetic testing. Monitor polyps, prevent cancer, and plan families with tailored strategies.
Harnessing the Power of Genetics: Understanding Hemochromatosis Type 2
Explore Hemochromatosis Type 2, a rare genetic disorder. Discover how genetic testing aids in early detection, family screening, and personalized treatment.
Hemoglobin D Disease: Deciphering Diagnosis Through Genetic Testing
Unlock precise Hemoglobin D disease diagnosis with genetic testing. Explore its role in family planning, personalized treatment, and groundbreaking research.
Hope for Hemolytic Anemia: Genetic Testing and Glutathione Reductase Deficiency
Explore how genetic testing aids in diagnosing and managing hemolytic anemia caused by glutathione reductase deficiency, offering early detection and personalized care.
Hereditary Hemorrhagic Telangiectasia: Harnessing Genetic Testing for Better Management
Explore the role of genetic testing in managing hereditary hemorrhagic telangiectasia. Understand early diagnosis, family risk, and personalized treatments.
Hereditary Inclusion Body Myopathy-Joint Contractures-Ophthalmoplegia Syndrome: Understanding and Navigating Genetic Testing
Unlock the potential of genetic testing for HIBM-JCOS to aid early diagnosis, personalized treatment plans, and informed family planning decisions.
Hereditary Methemoglobinemia: Unraveling the Genetic Threads of a Rare Blood Disorder
Explore hereditary methemoglobinemia—a rare blood disorder—its genetic causes, symptoms, and how genetic testing offers accurate diagnosis and personalized treatment plans.