
Systemic Solutions: Genetic Testing for Systemic Lupus Erythematosus
SLE is an autoimmune disease affecting multiple organs. Genetic testing may point to predisposition, personalize treatment and support wider research participation.

MD · MBA
Physician specializing in genetic analysis and personalized preventive medicine, and author of Outsmart Your Genes.
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).
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.

SLE is an autoimmune disease affecting multiple organs. Genetic testing may point to predisposition, personalize treatment and support wider research participation.

Genetic testing can flag variants tied to lupus risk and help distinguish SLE from other autoimmune diseases; diagnosis still rests on clinical findings and lab tests.

Discover the importance of understanding MTHFR Thermolabile Polymorphism, its diagnosis through genetic testing, personalized treatment plans, and ongoing research for improved…
A gene is a segment of DNA that holds the instructions for making a protein. Learn how genes work and why they matter for genetic testing.
Chromosomes are coiled DNA and protein packages inside the cell nucleus. Humans carry 23 pairs, 22 autosome pairs plus XX or XY, one of each pair from each parent.
Four chemical bases (A, T, G and C) pair along a double helix packaged into chromosomes, with half of a person's DNA inherited from each biological parent.

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Uncover the role of genetic testing in diagnosing Ehlers-Danlos Syndrome, classic type. Learn about pinpointing mutations, early intervention, and family planning.