Advancements in Understanding Acute Myeloid Leukemia with Multilineage Dysplasia
Explore how genetic testing revolutionizes AML with Multilineage Dysplasia diagnosis, prognosis, and personalized treatment for improved patient outcomes.
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
Alpha-N-acetylgalactosaminidase Deficiency Type 3: Understanding Genetic Testing's Role
Explore how genetic testing plays a crucial role in diagnosing and managing Alpha-N-acetylgalactosaminidase Deficiency Type 3, a rare lysosomal disorder.
Alport Syndrome: Advances in Genetic Testing and Diagnosis
Explore how genetic testing revolutionizes Alport syndrome diagnosis, enabling early detection, personalized treatment, and informed family planning decisions.
Amelogenesis Imperfecta: Unraveling the Genetic Threads of Tooth Enamel Disorders
Explore how genetic testing enhances the diagnosis and management of amelogenesis imperfecta, a hereditary enamel disorder, ensuring personalized dental care.
Amyloidosis: Unraveling the Genetic Threads of a Complex Disease
Explore how genetic testing aids in diagnosing amyloidosis, understanding subtypes, guiding treatments, and providing crucial insights for personalized patient care.
Androgen Resistance Syndrome: Understanding Genetic Testing's Role
Explore how genetic testing aids in diagnosing Androgen Resistance Syndrome, guiding treatment, offering psychosocial support, and enabling future family planning.
Anterior Segment Dysgenesis: Unlocking the Genetic Mysteries Through Testing
Unlocking genetic insights into anterior segment dysgenesis aids diagnosis, risk assessment, and innovative treatments, fostering better vision care in affected individuals.
Antisynthetase Syndrome: Unlocking the Genetic Code to Better Understand and Manage the Disease
Explore the role of genetic testing in diagnosing and managing Antisynthetase syndrome. Learn about genetic predisposition, targeted treatments, and genetic counseling.