Back to Search Start Over

Large-Scale Identification of Common Trait and Disease Variants Affecting Gene Expression

Authors :
Barbara K. Lipska
Mads E. Hauberg
Pamela Sklar
Hiroyoshi Toyoshiba
Oscar Franzén
Johan Björkegren
Laurent Essioux
Chang-Gyu Hahn
Panos Roussos
Raquel E. Gur
Bernie Devlin
Benjamin A. Logsdon
Timothy J. Vyse
Keisuke Hirai
David L. Morris
Vahram Haroutunian
Wen Zhang
Hardik Shah
Douglas M. Ruderfer
Solveig K. Sieberts
Arno Ruusalepp
Mette A. Peters
Kristen K. Dang
Joseph D. Buxbaum
Menachem Fromer
Thanneer M. Perumal
Milind Mahajan
Enrico Domenici
Lara M. Mangravite
David A. Lewis
Lambertus Klei
Jessica S. Johnson
Eric E. Schadt
Claudia Giambartolomei
Source :
Hauberg, M E, Zhang, W, Giambartolomei, C, Franzen, O, Morris, D L, Vyse, T J, Ruusalepp, A, Sklar, P, Schadt, E E, Bjorkegren, J L M, Roussos, P & CommonMind Consortium 2017, ' Large-Scale Identification of Common Trait and Disease Variants Affecting Gene Expression ', American Journal of Human Genetics, vol. 100, no. 6, pp. 885-894 . https://doi.org/10.1016/j.ajhg.2017.04.016
Publication Year :
2017

Abstract

Genome-wide association studies (GWASs) have identified a multitude of genetic loci involved with traits and diseases. However, it is often unclear which genes are affected in such loci and whether the associated genetic variants lead to increased or decreased gene function. To mitigate this, we integrated associations of common genetic variants in 57 GWASs with 24 studies of expression quantitative trait loci (eQTLs) from a broad range of tissues by using a Mendelian randomization approach. We discovered a total of 3,484 instances of gene-trait-associated changes in expression at a false-discovery rate

Details

Language :
English
Database :
OpenAIRE
Journal :
Hauberg, M E, Zhang, W, Giambartolomei, C, Franzen, O, Morris, D L, Vyse, T J, Ruusalepp, A, Sklar, P, Schadt, E E, Bjorkegren, J L M, Roussos, P & CommonMind Consortium 2017, ' Large-Scale Identification of Common Trait and Disease Variants Affecting Gene Expression ', American Journal of Human Genetics, vol. 100, no. 6, pp. 885-894 . https://doi.org/10.1016/j.ajhg.2017.04.016
Accession number :
edsair.doi.dedup.....ed1f231aec65e910d6410f23c998f2be
Full Text :
https://doi.org/10.1016/j.ajhg.2017.04.016