Bacteremia Susceptibility: Decoding the Genetic Blueprint to Combat a Silent Threat
Explore how genetic testing reveals predispositions to bacteremia type 2, guiding personalized treatments and enhancing infection control against resistant strains.
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
Breaking Through BAP1-Related Tumor Predisposition Syndrome: The Role of Genetic Testing
Explore the role of genetic testing in managing BAP1-TPDS, a syndrome linked to increased cancer risk, by offering early detection, personalized treatment, and informed decisions.
Breaking Barriers with Genetic Testing: Understanding Baraitser-Winter Syndrome 2
Explore how genetic testing aids in diagnosing Baraitser-Winter Syndrome 2, offering accurate diagnosis, personalized care, and critical family planning insights.
Breaking Down Brown-Vialetto-van Laere Syndrome 2: Genetic Testing's Role in Diagnosis and Treatment
Explore how genetic testing aids in diagnosing and managing Brown-Vialetto-van Laere syndrome 2, a rare disorder linked to SLC52A2 gene mutations.
Charting the Course of Charcot-Marie-Tooth Disease Dominant Intermediate E Through Genetic Testing
Genetic testing enhances diagnosis and treatment of Charcot-Marie-Tooth Disease E, revealing specific mutations for personalized care and improved prognosis.
Chronic Challenges: Understanding Chilblain Lupus 2 Through Genetic Testing
Explore chilblain lupus 2, a rare autoimmune disorder. Discover how genetic testing identifies variants for personalized treatment and better disease management.
Cracking the Code: Understanding Childhood Encephalopathy Due to Thiamine Pyrophosphokinase Deficiency
Unlock insights into childhood encephalopathy due to TPK deficiency. Genetic testing aids in diagnosis, early detection, and personalized treatment strategies.
Chromosome 2p16.3 Deletion Syndrome: Unraveling the Genetic Threads of an Enigmatic Disorder
Explore Chromosome 2p16.3 Deletion Syndrome and its link to Lynch syndrome. Discover how genetic testing aids diagnosis and personalized healthcare plans.