Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/50214
Campo DC Valoridioma
dc.contributor.authorPino-Yanes, Maríaen_US
dc.contributor.authorCorrales, Almudenaen_US
dc.contributor.authorCumplido, Joséen_US
dc.contributor.authorPoza, Palomaen_US
dc.contributor.authorSánchez-Machín, Inmaculadaen_US
dc.contributor.authorSánchez-Palacios, Anselmoen_US
dc.contributor.authorFigueroa, Javieren_US
dc.contributor.authorAcosta-Fernández, Orlandoen_US
dc.contributor.authorBuset, Nisaen_US
dc.contributor.authorGarcía-Robaina, José Carlosen_US
dc.contributor.authorHernández, Marianoen_US
dc.contributor.authorVillar, Jesúsen_US
dc.contributor.authorCarrillo, Teresaen_US
dc.contributor.authorFlores, Carlosen_US
dc.date.accessioned2018-11-24T14:16:55Z-
dc.date.available2018-11-24T14:16:55Z-
dc.date.issued2013en_US
dc.identifier.issn1932-6203en_US
dc.identifier.urihttp://hdl.handle.net/10553/50214-
dc.description.abstractBackground: Before the advent of genome-wide association studies (GWAS), ADAM33, ADRB2, CD14, MS4A2 (alias FCER1B), IL13, IL4, IL4R, and TNF constituted the most replicated non-HLA candidate genes with asthma and related traits. However, except for the IL13-IL4 region, none of these genes have been found in close proximity of genome-wide significant hits among GWAS for asthma or related traits. Here we aimed to assess the reproducibility of these asthma associations and to test if associations were more evident considering the effect of age at diagnosis. Methodology/Principal Findings: We systematically evaluated 286 common single nucleotide polymorphisms (SNPs) of these 8 genes in a sample of 1,865 unrelated Spanish individuals (606 asthmatics and 1,259 controls). We found that variants at MS4A2, IL4R and ADAM33 genes demonstrated varying association effects with the age at diagnosis of asthma, with 10 SNPs showing study-wise significance after the multiple comparison adjustment. In addition, in silico replication with GWAS data supported the association of IL4R. Conclusions/Significance: Our results support the important role of MS4A2, IL4R and ADAM33 genes in asthma and/or atopy susceptibility. However, additional studies in larger samples sets are needed to firmly implicate these genes in asthma susceptibility, and also to identify the causal variation underlying the associations founden_US
dc.languageengen_US
dc.relation.ispartofPLoS ONEen_US
dc.sourcePLoS ONE [e-1932-6203] , v. 8(9), e73157 (Septiembre 2013)en_US
dc.subject32 Ciencias médicasen_US
dc.subject3201 Ciencias clínicasen_US
dc.subject320102 Genética clínicaen_US
dc.subject.otherAsthmaen_US
dc.subject.otherGenome-wide association studiesen_US
dc.subject.otherSingle nucleotide polymorphismsen_US
dc.subject.otherGenotypingen_US
dc.subject.otherMedical risk factorsen_US
dc.subject.otherGenetics of diseaseen_US
dc.subject.otherGenomicsen_US
dc.titleAssessing the Validity of Asthma Associations for Eight Candidate Genes and Age at Diagnosis Effectsen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1371/journal.pone.0073157en_US
dc.identifier.scopus84883651546-
dc.contributor.authorscopusid57189630546-
dc.contributor.authorscopusid36909857900-
dc.contributor.authorscopusid25622337100-
dc.contributor.authorscopusid24332950600-
dc.contributor.authorscopusid6506940514-
dc.contributor.authorscopusid7003284307-
dc.contributor.authorscopusid57202163943-
dc.contributor.authorscopusid6507398266-
dc.contributor.authorscopusid36136453800-
dc.contributor.authorscopusid6603966455-
dc.contributor.authorscopusid12794610000-
dc.contributor.authorscopusid55236061500-
dc.contributor.authorscopusid7003526269-
dc.contributor.authorscopusid7103184966-
dc.identifier.issuee73157-
dc.identifier.issue9-
dc.relation.volume8en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.description.numberofpages7en_US
dc.utils.revisionen_US
dc.date.coverdateSeptiembre 2013en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr1,74
dc.description.jcr3,534
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
dc.description.erihplusERIH PLUS
item.fulltextCon texto completo-
item.grantfulltextopen-
crisitem.author.deptGIR IUIBS: Patología médica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.orcid0000-0002-3047-8908-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameCarrillo Díaz, Teresa-
Colección:Artículos
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