<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Barton A</submitter><funding>Versus Arthritis</funding><funding>Medical Research Council</funding><funding>Wellcome Trust</funding><pagination>2274-9</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2465799</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(15)</volume><pubmed_abstract>Rheumatoid arthritis (RA) is an archetypal, common, complex autoimmune disease with both genetic and environmental contributions to disease aetiology. Two novel RA susceptibility loci have been reported from recent genome-wide and candidate gene association studies. We, therefore, investigated the evidence for association of the STAT4 and TRAF1/C5 loci with RA using imputed data from the Wellcome Trust Case Control Consortium (WTCCC). No evidence for association of variants mapping to the TRAF1/C5 gene was detected in the 1860 RA cases and 2930 control samples tested in that study. Variants mapping to the STAT4 gene did show evidence for association (rs7574865, P = 0.04). Given the association of the TRAF1/C5 locus in two previous large case-control series from populations of European desc</pubmed_abstract><journal>Human molecular genetics</journal><pubmed_title>Re-evaluation of putative rheumatoid arthritis susceptibility genes in the post-genome wide association study era and hypothesis of a key pathway underlying susceptibility.</pubmed_title><pmcid>PMC2465799</pmcid><funding_grant_id>17552</funding_grant_id><funding_grant_id>G0000934</funding_grant_id><funding_grant_id>18475</funding_grant_id><funding_grant_id>090532</funding_grant_id><pubmed_authors>Stevens HE</pubmed_authors><pubmed_authors>Hordon L</pubmed_authors><pubmed_authors>Nimmo ER</pubmed_authors><pubmed_authors>Cardin NJ</pubmed_authors><pubmed_authors>Bentley D</pubmed_authors><pubmed_authors>McGuffin P</pubmed_authors><pubmed_authors>Taylor L</pubmed_authors><pubmed_authors>Mathew CG</pubmed_authors><pubmed_authors>Groves CJ</pubmed_authors><pubmed_authors>Lango 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hypothesis of a key pathway underlying susceptibility.</name><description>Rheumatoid arthritis (RA) is an archetypal, common, complex autoimmune disease with both genetic and environmental contributions to disease aetiology. Two novel RA susceptibility loci have been reported from recent genome-wide and candidate gene association studies. We, therefore, investigated the evidence for association of the STAT4 and TRAF1/C5 loci with RA using imputed data from the Wellcome Trust Case Control Consortium (WTCCC). No evidence for association of variants mapping to the TRAF1/C5 gene was detected in the 1860 RA cases and 2930 control samples tested in that study. Variants mapping to the STAT4 gene did show evidence for association (rs7574865, P = 0.04). Given the association of the TRAF1/C5 locus in two previous large case-control series from populations of European desc</description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Aug</publication><modification>2026-04-29T11:37:19.981Z</modification><creation>2019-03-27T00:15:50Z</creation></dates><accession>S-EPMC2465799</accession><cross_references><pubmed>18434327</pubmed><doi>10.1093/hmg/ddn128</doi></cross_references></HashMap>