Decoding the Genetic Mysteries of Maternally Transmitted Noninsulin-Dependent Diabetes Mellitus
Passed through mitochondrial DNA from the mother, this form of noninsulin-dependent diabetes has been linked to ND1, ND2, ND5 and tRNALeu(UUR) variants.
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
Type II Diabetes: Digenic Risk and Shared ALS Genes
Multiple genes contribute to Type II Diabetes Mellitus; the research covered includes a shared genetic basis with ALS, prevention and data-mining risk models.
Decoding the Mysteries of Late-Onset Torsion Dystonia 1: Genetic Testing for Diagnosis and Management
Discover the role of genetic testing in diagnosing and managing late-onset torsion dystonia 1, a rare movement disorder. Learn about benefits, limitations, and future research.
Decoding EEG with Focal Epileptiform Discharges: Understanding, Diagnosing, and Genetic Testing
Seen on an EEG as abnormal activity in one brain region, focal epileptiform discharges can cause seizures and often stem from genetic or structural factors.
Unlocking the Mysteries of Epilepsy, Progressive Myoclonic 3, with Intracellular Inclusions
KCTD7 mutations disrupt protein degradation and neuronal development, leading to myoclonic seizures, cognitive decline and intracellular inclusions in PME3.
Demystifying Episodic Ataxia Type 2 and Epilepsy: Insights into Diagnosis and Genetic Testing
Attacks of imbalance and dizziness can overlap with seizures, and KCNA2 and CACNA1A findings, topiramate and ketogenic diet reports connect the two.
Decoding Esophageal Squamous Cell Carcinoma: Genetic Testing and Its Implications
Discover the role of genetic testing in esophageal squamous cell carcinoma diagnosis, treatment, and personalized therapies. Learn about key genetic factors and advancements in…
Unlocking the Genetic Secrets of Autosomal Dominant Exudative Vitreoretinopathy 4
Passed on in an autosomal dominant pattern, EVR4 causes leaking retinal vessels and detachment; TSPAN12, FZD4 and LRP5 testing confirms it and guides counseling.