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August 2016; 2 (4) EditorialOpen Access

A new dawn for genetic association studies in multiple sclerosis

Orhun H. Kantarci
First published August 4, 2016, DOI: https://doi.org/10.1212/NXG.0000000000000093
Orhun H. Kantarci
From the Department of Neurology, Mayo Clinic, Rochester, MN.
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A new dawn for genetic association studies in multiple sclerosis
Orhun H. Kantarci
Neurol Genet Aug 2016, 2 (4) e93; DOI: 10.1212/NXG.0000000000000093

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Abstract

Before the genomics technology revolution allowed us to do genome-wide science, genetics research relied on our limited knowledge about a subject to generate hypothesis and candidate genes to study. Despite the level of naiveté, several associations with susceptibility to a complex disease such as multiple sclerosis (MS) were discovered. Of these, HLA-DRB1 and IL7R1 stand out as being confirmed and refined early by the genome-wide association studies (GWAS) that followed.2 Despite the expense and gargantuan efforts, these GWAS have successfully led to the discovery of more than 100 additional genes, albeit with smaller effect sizes, that contribute to MS susceptibility.3 This list keeps growing, but it comes with no surprise that most of these genes identified the immune system as one large candidate for MS susceptibility.

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  • Funding information and disclosures are provided at the end of the editorial. Go to Neurology.org/ng for full disclosure forms. The Article Processing Charge for this editorial was waived at the discretion of the Editor.

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  • © 2016 American Academy of Neurology

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND), which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially.

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