A Fine-Mapping Study of 7 Top Scoring Genes from a GWAS for Major Depressive Disorder

Major depressive disorder (MDD) is a psychiatric disorder that is characterized -amongst others- by persistent depressed mood, loss of interest and pleasure and psychomotor retardation. Environmental circumstances have proven to influence the aetiology of the disease, but MDD also has an estimated 40% heritability, probably with a polygenic background. In 2009, a genome wide association study (GWAS) was performed on the Dutch GAIN-MDD cohort. A non-synonymous coding single nucleotide polymorphism (SNP) rs2522833 in the PCLO gene became only nominally significant after post-hoc analysis with an... Mehr ...

Verfasser: Verbeek, E.C.
Bakker, I.M.C.
Bevova, M.R.
Bochdanovits, Z.
Rizzu, P.
Sondervan, D.
Willemsen, G.
de Geus, E.J.C.
Smit, J.H.
Penninx, B.W.J.H.
Boomsma, D.I.
Hoogendijk, W.J.G.
Heutink, P.
Dokumenttyp: Artikel
Erscheinungsdatum: 2012
Reihe/Periodikum: Verbeek , E C , Bakker , I M C , Bevova , M R , Bochdanovits , Z , Rizzu , P , Sondervan , D , Willemsen , G , de Geus , E J C , Smit , J H , Penninx , B W J H , Boomsma , D I , Hoogendijk , W J G & Heutink , P 2012 , ' A Fine-Mapping Study of 7 Top Scoring Genes from a GWAS for Major Depressive Disorder ' , PLoS ONE , vol. 7 , no. 5 , e37384 , pp. e37384 . https://doi.org/10.1371/journal.pone.0037384
Schlagwörter: /dk/atira/pure/keywords/cohort_studies/netherlands_twin_register_ntr_ / name=Netherlands Twin Register (NTR)
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-29210777
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : https://research.vu.nl/en/publications/1279d778-3b5c-4385-9c8b-4a0cfc36b58a

Major depressive disorder (MDD) is a psychiatric disorder that is characterized -amongst others- by persistent depressed mood, loss of interest and pleasure and psychomotor retardation. Environmental circumstances have proven to influence the aetiology of the disease, but MDD also has an estimated 40% heritability, probably with a polygenic background. In 2009, a genome wide association study (GWAS) was performed on the Dutch GAIN-MDD cohort. A non-synonymous coding single nucleotide polymorphism (SNP) rs2522833 in the PCLO gene became only nominally significant after post-hoc analysis with an Australian cohort which used similar ascertainment. The absence of genome-wide significance may be caused by low SNP coverage of genes. To increase SNP coverage to 100% for common variants (m.a.f.>0.1, r