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Progress in Multiple Sclerosis Genetics

A genetic component in the susceptibility to multiple sclerosis (MS) has long been known, and the first and major genetic risk factor, the HLA region, was identified in the 1970’s. However, only with the advent of genome-wide association studies in the past five years did the list of risk factors fo...

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Detalles Bibliográficos
Autores principales: Goris, An, Pauwels, Ine, Dubois, Bénédicte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492804/
https://www.ncbi.nlm.nih.gov/pubmed/23730204
http://dx.doi.org/10.2174/138920212803759695
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author Goris, An
Pauwels, Ine
Dubois, Bénédicte
author_facet Goris, An
Pauwels, Ine
Dubois, Bénédicte
author_sort Goris, An
collection PubMed
description A genetic component in the susceptibility to multiple sclerosis (MS) has long been known, and the first and major genetic risk factor, the HLA region, was identified in the 1970’s. However, only with the advent of genome-wide association studies in the past five years did the list of risk factors for MS grow from 1 to over 50. In this review, we summarize the search for MS risk genes and the latest results. Comparison with data from other autoimmune and neurological diseases and from animal models indicates parallels and differences between diseases. We discuss how these translate into an improved understanding of disease mechanisms, and address current challenges such as genotype-phenotype correlations, functional mechanisms of risk variants and the missing heritability.
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spelling pubmed-34928042013-06-01 Progress in Multiple Sclerosis Genetics Goris, An Pauwels, Ine Dubois, Bénédicte Curr Genomics Article A genetic component in the susceptibility to multiple sclerosis (MS) has long been known, and the first and major genetic risk factor, the HLA region, was identified in the 1970’s. However, only with the advent of genome-wide association studies in the past five years did the list of risk factors for MS grow from 1 to over 50. In this review, we summarize the search for MS risk genes and the latest results. Comparison with data from other autoimmune and neurological diseases and from animal models indicates parallels and differences between diseases. We discuss how these translate into an improved understanding of disease mechanisms, and address current challenges such as genotype-phenotype correlations, functional mechanisms of risk variants and the missing heritability. Bentham Science Publishers 2012-12 2012-12 /pmc/articles/PMC3492804/ /pubmed/23730204 http://dx.doi.org/10.2174/138920212803759695 Text en ©2012 Bentham Science Publishers http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.5/), which permits unrestrictive use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Goris, An
Pauwels, Ine
Dubois, Bénédicte
Progress in Multiple Sclerosis Genetics
title Progress in Multiple Sclerosis Genetics
title_full Progress in Multiple Sclerosis Genetics
title_fullStr Progress in Multiple Sclerosis Genetics
title_full_unstemmed Progress in Multiple Sclerosis Genetics
title_short Progress in Multiple Sclerosis Genetics
title_sort progress in multiple sclerosis genetics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492804/
https://www.ncbi.nlm.nih.gov/pubmed/23730204
http://dx.doi.org/10.2174/138920212803759695
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