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dc.contributor.authorAlcina, Antonio-
dc.contributor.authorFernández, Óscar-
dc.contributor.authorGonzález, Juan Ramón-
dc.contributor.authorCatalá-Rabasa, Antonio-
dc.contributor.authorFedetz, María-
dc.contributor.authorNdagire, D.-
dc.contributor.authorLeyva, Laura-
dc.contributor.authorGuerrero, Miguel-
dc.contributor.authorArnal, Carmen-
dc.contributor.authorDelgado, Concepción-
dc.contributor.authorLucas, Miguel-
dc.contributor.authorIzquierdo, Guillermo-
dc.contributor.authorMatesanz, F.-
dc.identifierdoi: 10.1038/ejhg.2009.240-
dc.identifierissn: 1018-4813-
dc.identifiere-issn: 1476-5438-
dc.identifier.citationEuropean Journal of Human Genetics 18(7): 827- 831 (2010)-
dc.description.abstractA recent genome-wide association study conducted by the International Multiple Sclerosis Genetic Consortium (IMSGC) identified, among others, a number of putative multiple sclerosis (MS) susceptibility variants at position 1p22. Twenty-one SNPs positively associated with MS were located at the GFI-EVI5-RPL5-FAM69A locus. In this study, we performed an analysis and fine mapping of this locus, genotyping eight Tag-SNPs in 732 MS patients and 974 controls from Spain. We observed an association with MS in three of eight Tag-SNPs: rs11804321 (P=0.008, OR=1.29; 95% CI1.08-1.54), rs11808092 (P=0.048, OR=1.19; 95% CI1.03-1.39) and rs6680578 (P=0.0082, OR=1.23; 95% CI1.07-1.41). After correcting for multiple comparisons and using logistic regression analysis to test the addition of each SNP to the most associated SNPs, we observed that rs11804321 alone was sufficient to model the association. This Tag-SNP captures two SNPs in complete linkage disequilibrium (r2= 1), both located within the 17th intron of the EVI5 gene. Our findings agree with the corresponding data of the recent IMSGC study and present new genetic evidence that points to EVI5 as a factor of susceptibility to MS. © 2010 Macmillan Publishers Limited All rights reserved.-
dc.description.sponsorshipFinancial support for the study was provided by the Ministerio de Ciencia e Innovación-Fondos Feder (Grant SAF2009–11491) and Junta de Andalucía (P07-CVI-02551) to A. Alcina, and by Fondo de Investigación Sanitaria (PI081636) to F. Matesanz. María Fedetz is a holder of a fellowship from Fundación IMABIS. Dorothy Ndagire is a holder of AECI-Ministerio de Asuntos Exteriores fellowship.-
dc.publisherNature Publishing Group-
dc.titleTag-SNP analysis of the GFI1-EVI5-RPL5-FAM69 risk locus for multiple sclerosis-
dc.description.versionPeer Reviewed-
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