001     10078
005     20210129210513.0
024 7 _ |2 pmid
|a pmid:20071346
024 7 _ |2 pmc
|a pmc:PMC2838541
024 7 _ |2 DOI
|a 10.1093/hmg/ddq009
024 7 _ |2 WOS
|a WOS:000275818500020
037 _ _ |a PreJuSER-10078
041 _ _ |a eng
082 _ _ |a 570
084 _ _ |2 WoS
|a Biochemistry & Molecular Biology
084 _ _ |2 WoS
|a Genetics & Heredity
100 1 _ |0 P:(DE-HGF)0
|a Ingason, A.
|b 0
245 _ _ |a A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia
260 _ _ |a Oxford
|b Oxford Univ. Press
|c 2010
300 _ _ |a 1379 - 1386
336 7 _ |a Journal Article
|0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|0 0
|2 EndNote
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a article
|2 DRIVER
440 _ 0 |0 9913
|a Human Molecular Genetics
|v 19
|x 0964-6906
|y 7
500 _ _ |a Funding for the project was provided by the Wellcome Trust under award 076113. Part of the genotyping of the Munich sample was done at the Genetics Research Centre (GmbH) which is a joint venture between GlaxoSmithKline Germany and the Department of Psychiatry, Ludwig-Maximilians-University. This work was funded by EU grants LSHM-CT-2006-037761 (Project SGENE) and PIAP-GA-2008-218251 (Project PsychGene). The Cardiff research was funded by grants from the MRC and the Wellcome Trust. The UCLA-Utrecht research was funded by NIH grant R01 MH078075.
520 _ _ |a The Abelson helper integration site 1 (AHI1) gene locus on chromosome 6q23 is among a group of candidate loci for schizophrenia susceptibility that were initially identified by linkage followed by linkage disequilibrium mapping, and subsequent replication of the association in an independent sample. Here, we present results of a replication study of AHI1 locus markers, previously implicated in schizophrenia, in a large European sample (in total 3907 affected and 7429 controls). Furthermore, we perform a meta-analysis of the implicated markers in 4496 affected and 18,920 controls. Both the replication study of new samples and the meta-analysis show evidence for significant overrepresentation of all tested alleles in patients compared with controls (meta-analysis; P = 8.2 x 10(-5)-1.7 x 10(-3), common OR = 1.09-1.11). The region contains two genes, AHI1 and C6orf217, and both genes-as well as the neighbouring phosphodiesterase 7B (PDE7B)-may be considered candidates for involvement in the genetic aetiology of schizophrenia.
536 _ _ |0 G:(DE-Juel1)FUEK409
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|c FUEK409
|a Funktion und Dysfunktion des Nervensystems (FUEK409)
536 _ _ |a 89571 - Connectivity and Activity (POF2-89571)
|0 G:(DE-HGF)POF2-89571
|c POF2-89571
|x 1
|f POF II T
536 _ _ |a PSYCHGENE - Copy Number Variation and Endophenotypes in Psychiatric Disorders (218251)
|0 G:(EU-Grant)218251
|c 218251
|x 2
|f FP7-PEOPLE-2007-3-1-IAPP
588 _ _ |a Dataset connected to Web of Science, Pubmed
650 _ 2 |2 MeSH
|a Adaptor Proteins, Signal Transducing: genetics
650 _ 2 |2 MeSH
|a European Continental Ancestry Group: genetics
650 _ 2 |2 MeSH
|a Genetic Markers
650 _ 2 |2 MeSH
|a Genetic Predisposition to Disease
650 _ 2 |2 MeSH
|a Genome-Wide Association Study
650 _ 2 |2 MeSH
|a Humans
650 _ 2 |2 MeSH
|a Schizophrenia: genetics
650 _ 7 |0 0
|2 NLM Chemicals
|a AHI1 protein, human
650 _ 7 |0 0
|2 NLM Chemicals
|a Adaptor Proteins, Signal Transducing
650 _ 7 |0 0
|2 NLM Chemicals
|a Genetic Markers
650 _ 7 |2 WoSType
|a J
700 1 _ |0 P:(DE-HGF)0
|a Giegling, I.
|b 1
700 1 _ |0 P:(DE-Juel1)VDB92668
|a Cichon, S.
|b 2
|u FZJ
700 1 _ |0 P:(DE-HGF)0
|a Hansen, T.
|b 3
700 1 _ |0 P:(DE-HGF)0
|a Rasmussen, H.B.
|b 4
700 1 _ |0 P:(DE-HGF)0
|a Nielsen, J.
|b 5
700 1 _ |0 P:(DE-HGF)0
|a Jürgens, G.
|b 6
700 1 _ |0 P:(DE-HGF)0
|a Muglia, P.
|b 7
700 1 _ |0 P:(DE-HGF)0
|a Hartmann, A.M.
|b 8
700 1 _ |0 P:(DE-HGF)0
|a Strengman, E.
|b 9
700 1 _ |0 P:(DE-HGF)0
|a Vasilescu, C.
|b 10
700 1 _ |0 P:(DE-HGF)0
|a Mühleisen, T.W.
|b 11
700 1 _ |0 P:(DE-HGF)0
|a Djurovic, S.
|b 12
700 1 _ |0 P:(DE-HGF)0
|a Melle, I.
|b 13
700 1 _ |0 P:(DE-HGF)0
|a Lerer, B.
|b 14
700 1 _ |0 P:(DE-HGF)0
|a Möller, H.J.
|b 15
700 1 _ |0 P:(DE-HGF)0
|a Francks, C.
|b 16
700 1 _ |0 P:(DE-HGF)0
|a Pietiläinen, O.P.
|b 17
700 1 _ |0 P:(DE-HGF)0
|a Lonnqvist, J.
|b 18
700 1 _ |0 P:(DE-HGF)0
|a Suvisaari, J.
|b 19
700 1 _ |0 P:(DE-HGF)0
|a Tuulio-Henriksson, A.
|b 20
700 1 _ |0 P:(DE-HGF)0
|a Walshe, M.
|b 21
700 1 _ |0 P:(DE-HGF)0
|a Vassos, E.
|b 22
700 1 _ |0 P:(DE-HGF)0
|a Di Forti, M.
|b 23
700 1 _ |0 P:(DE-HGF)0
|a Murray, R.
|b 24
700 1 _ |0 P:(DE-HGF)0
|a Bonetto, C.
|b 25
700 1 _ |0 P:(DE-HGF)0
|a Tosato, S.
|b 26
700 1 _ |0 P:(DE-HGF)0
|a GROUP, Investig.
|b 27
700 1 _ |0 P:(DE-HGF)0
|a Cantor, R.M.
|b 28
700 1 _ |0 P:(DE-HGF)0
|a Rietschel, M.
|b 29
700 1 _ |0 P:(DE-HGF)0
|a Craddock, N.
|b 30
700 1 _ |0 P:(DE-HGF)0
|a Owen, M.J.
|b 31
700 1 _ |0 P:(DE-HGF)0
|a Peltonen, L.
|b 32
700 1 _ |0 P:(DE-HGF)0
|a Andreassen, O.A.
|b 33
700 1 _ |0 P:(DE-HGF)0
|a Nöthen, M.M.
|b 34
700 1 _ |0 P:(DE-HGF)0
|a St. Clair, D.
|b 35
700 1 _ |0 P:(DE-HGF)0
|a Ophoff, R.A.
|b 36
700 1 _ |0 P:(DE-HGF)0
|a O'Donovan, M.
|b 37
700 1 _ |0 P:(DE-HGF)0
|a Collier, D.
|b 38
700 1 _ |0 P:(DE-HGF)0
|a Werge, T.
|b 39
700 1 _ |0 P:(DE-HGF)0
|a Rujescu, D.
|b 40
773 _ _ |0 PERI:(DE-600)1474816-2
|a 10.1093/hmg/ddq009
|g Vol. 19, p. 1379 - 1386
|p 1379 - 1386
|q 19<1379 - 1386
|t Human molecular genetics
|v 19
|x 0964-6906
|y 2010
856 7 _ |2 Pubmed Central
|u http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2838541
909 C O |o oai:juser.fz-juelich.de:10078
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