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Updated: Feb 9, 2026

Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
Published on: July 19, 2019
Genome-wide association studies of multiple sclerosis
Chris Cotsapas1,2, Mitja Mitrovic1,2
1Departments of Neurology and Genetics Yale School of Medicine New Haven CT USA.
Abstract:
Large-scale genetic studies of multiple sclerosis have identified over 230 risk effects across the human genome, making it a prototypical common disease with complex genetic architecture. Here, after a brief historical background on the discovery and definition of the disease, we summarise the last fifteen years of genetic discoveries and map out the challenges that remain to translate these findings into an aetiological framework and actionable clinical understanding.
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