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Status: Bibliographieeintrag

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Verfasst von:Athanasiu, Lavinia [VerfasserIn]   i
 Mattingsdal, Morten [VerfasserIn]   i
 Kähler, Anna K. [VerfasserIn]   i
 Brown, Andrew [VerfasserIn]   i
 Gustafsson, Omar [VerfasserIn]   i
 Agartz, Ingrid [VerfasserIn]   i
 Giegling, Ina [VerfasserIn]   i
 Muglia, Pierandrea [VerfasserIn]   i
 Cichon, Sven [VerfasserIn]   i
 Rietschel, Marcella [VerfasserIn]   i
 Pietiläinen, Olli P. H. [VerfasserIn]   i
 Peltonen, Leena [VerfasserIn]   i
 Bramon, Elvira [VerfasserIn]   i
 Collier, David [VerfasserIn]   i
 Clair, David St. [VerfasserIn]   i
 Sigurdsson, Engilbert [VerfasserIn]   i
 Petursson, Hannes [VerfasserIn]   i
 Rujescu, Dan [VerfasserIn]   i
 Melle, Ingrid [VerfasserIn]   i
 Steen, Vidar M. [VerfasserIn]   i
 Djurovic, Srdjan [VerfasserIn]   i
 Andreassen, Ole A. [VerfasserIn]   i
Titel:Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort
Verf.angabe:Lavinia Athanasiu, Morten Mattingsdal, Anna K. Kähler, Andrew Brown, Omar Gustafsson, Ingrid Agartz, Ina Giegling, Pierandrea Muglia, Sven Cichon, Marcella Rietschel, Olli P.H. Pietiläinen, Leena Peltonen, Elvira Bramon, David Collier, David St. Clair, Engilbert Sigurdsson, Hannes Petursson, Dan Rujescu, Ingrid Melle, Vidar M. Steen, Srdjan Djurovic, Ole A. Andreassen
E-Jahr:2010
Jahr:24 February 2010
Umfang:6 S.
Fussnoten:Gesehen am 25.11.2022
Titel Quelle:Enthalten in: Journal of psychiatric research
Ort Quelle:Amsterdam [u.a.] : Elsevier Science, 1961
Jahr Quelle:2010
Band/Heft Quelle:44(2010), 12, Seite 748-753
ISSN Quelle:1879-1379
Abstract:We have performed a genome-wide association study (GWAS) of schizophrenia in a Norwegian discovery sample of 201 cases and 305 controls (TOP study) with a focused replication analysis in a larger European sample of 2663 cases and 13,780 control subjects (SGENE-plus study). Firstly, the discovery sample was genotyped with Affymetrix Genome-Wide Human SNP Array 6.0 and 572,888 markers were tested for schizophrenia association. No SNPs in the discovery sample attained genome-wide significance (P<8.7×10−8). Secondly, based on the GWAS data, we selected 1000 markers with the lowest P values in the discovery TOP sample, and tested these (or HapMap-based surrogates) for association in the replication sample. Sixteen loci were associated with schizophrenia (nominal P value<0.05 and concurring OR) in the replication sample. As a next step, we performed a combined analysis of the findings from these two studies, and the strongest evidence for association with schizophrenia was provided for markers rs7045881 on 9p21, rs433598 on 16p12 and rs10761482 on 10q21. The markers are located in PLAA, ACSM1 and ANK3, respectively. PLAA has not previously been described as a susceptibility gene, but 9p21 is implied as a schizophrenia linkage region. ACSM1 has been identified as a susceptibility gene in a previous schizophrenia GWAS study. The association of ANK3 with schizophrenia is intriguing in light of recent associations of ANK3 with bipolar disorder, thereby supporting the hypothesis of an overlap in genetic susceptibility between these psychopathological entities.
DOI:doi:10.1016/j.jpsychires.2010.02.002
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1016/j.jpsychires.2010.02.002
 Volltext: https://www.sciencedirect.com/science/article/pii/S0022395610000361
 DOI: https://doi.org/10.1016/j.jpsychires.2010.02.002
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:1
 3
 Genome-wide association study
 PLAA
 Psychiatric genetics
 Schizophrenia
K10plus-PPN:1823659128
Verknüpfungen:→ Zeitschrift

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