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  5. Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ
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Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/20844
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dc.contributor.authorElbaz, A.en
dc.contributor.authorRoss, O. A.en
dc.contributor.authorIoannidis, J. P.en
dc.contributor.authorSoto-Ortolaza, A. I.en
dc.contributor.authorMoisan, F.en
dc.contributor.authorAasly, J. O.en
dc.contributor.authorAnnesi, G.en
dc.contributor.authorBozi, M.en
dc.contributor.authorBrighina, L.en
dc.contributor.authorChartier-Harlin, M. C.en
dc.contributor.authorDestee, A.en
dc.contributor.authorFerrarese, C.en
dc.contributor.authorFerraris, A.en
dc.contributor.authorGibson, J. M.en
dc.contributor.authorGispert, S.en
dc.contributor.authorHadjigeorgiou, G. M.en
dc.contributor.authorJasinska-Myga, B.en
dc.contributor.authorKlein, C.en
dc.contributor.authorKruger, R.en
dc.contributor.authorLambert, J. C.en
dc.contributor.authorLohmann, K.en
dc.contributor.authorvan de Loo, S.en
dc.contributor.authorLoriot, M. A.en
dc.contributor.authorLynch, T.en
dc.contributor.authorMellick, G. D.en
dc.contributor.authorMutez, E.en
dc.contributor.authorNilsson, C.en
dc.contributor.authorOpala, G.en
dc.contributor.authorPuschmann, A.en
dc.contributor.authorQuattrone, A.en
dc.contributor.authorSharma, M.en
dc.contributor.authorSilburn, P. A.en
dc.contributor.authorStefanis, L.en
dc.contributor.authorUitti, R. J.en
dc.contributor.authorValente, E. M.en
dc.contributor.authorVilarino-Guell, C.en
dc.contributor.authorWirdefeldt, K.en
dc.contributor.authorWszolek, Z. K.en
dc.contributor.authorXiromerisiou, G.en
dc.contributor.authorMaraganore, D. M.en
dc.contributor.authorFarrer, M. J.en
dc.date.accessioned2015-11-24T19:10:35Z-
dc.date.available2015-11-24T19:10:35Z-
dc.identifier.issn1531-8249-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/20844-
dc.rightsDefault Licence-
dc.subjectAdulten
dc.subjectAge of Onseten
dc.subjectAgeden
dc.subjectAged, 80 and overen
dc.subjectCase-Control Studiesen
dc.subjectFemaleen
dc.subject*Genetic Predisposition to Diseaseen
dc.subjectHumansen
dc.subjectLogistic Modelsen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectOdds Ratioen
dc.subjectParkinson Disease/*geneticsen
dc.subjectPolymorphism, Single Nucleotide/*geneticsen
dc.subjectRetrospective Studiesen
dc.subjectalpha-Synuclein/*geneticsen
dc.subjecttau Proteins/*geneticsen
dc.titleIndependent and joint effects of the MAPT and SNCA genes in Parkinson diseaseen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primary10.1002/ana.22321-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/21391235-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/store/10.1002/ana.22321/asset/22321_ftp.pdf?v=1&t=h0je1s7i&s=e655486443030c9791c940c9a36aa9987cf4acda-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate2011-
heal.abstractOBJECTIVE: We studied the independent and joint effects of the genes encoding alpha-synuclein (SNCA) and microtubule-associated protein tau (MAPT) in Parkinson disease (PD) as part of a large meta-analysis of individual data from case-control studies participating in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) consortium. METHODS: Participants of Caucasian ancestry were genotyped for a total of 4 SNCA (rs2583988, rs181489, rs356219, rs11931074) and 2 MAPT (rs1052553, rs242557) single nucleotide polymorphism (SNPs). Individual and joint effects of SNCA and MAPT SNPs were investigated using fixed- and random-effects logistic regression models. Interactions were studied on both a multiplicative and an additive scale, and using a case-control and case-only approach. RESULTS: Fifteen GEO-PD sites contributed a total of 5,302 cases and 4,161 controls. All 4 SNCA SNPs and the MAPT H1-haplotype-defining SNP (rs1052553) displayed a highly significant marginal association with PD at the significance level adjusted for multiple comparisons. For SNCA, the strongest associations were observed for SNPs located at the 3' end of the gene. There was no evidence of statistical interaction between any of the 4 SNCA SNPs and rs1052553 or rs242557, neither on the multiplicative nor on the additive scale. INTERPRETATION: This study confirms the association between PD and both SNCA SNPs and the H1 MAPT haplotype. It shows, based on a variety of approaches, that the joint action of variants in these 2 loci is consistent with independent effects of the genes without additional interacting effects.en
heal.journalNameAnn Neurolen
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
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