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Porcu, E.* ; Rüeger, S.* ; Lepik, K.* ; eQTLGen Consortium (Müller-Nurasyid, M. ; Strauch, K.) ; BIOS Consortium* ; Santoni, F.A.* ; Reymond, A.* ; Kutalik, Z.*

Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits.

Nat. Commun. 10:3300 (2019)
Publ. Version/Full Text Research data DOI
Open Access Gold
Creative Commons Lizenzvertrag
Genome-wide association studies (GWAS) have identified thousands of variants associated with complex traits, but their biological interpretation often remains unclear. Most of these variants overlap with expression QTLs, indicating their potential involvement in regulation of gene expression. Here, we propose a transcriptome-wide summary statistics-based Mendelian Randomization approach (TWMR) that uses multiple SNPs as instruments and multiple gene expression traits as exposures, simultaneously. Applied to 43 human phenotypes, it uncovers 3,913 putatively causal gene-trait associations, 36% of which have no genome-wide significant SNP nearby in previous GWAS. Using independent association summary statistics, we find that the majority of these loci were missed by GWAS due to power issues. Noteworthy among these links is educational attainment-associated BSCL2, known to carry mutations leading to a Mendelian form of encephalopathy. We also find pleiotropic causal effects suggestive of mechanistic connections. TWMR better accounts for pleiotropy and has the potential to identify biological mechanisms underlying complex traits.
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Publication type Article: Journal article
Document type Scientific Article
Keywords Instrumental Variables; Variants; Disease; Association; Mutation; Statistics; Expression; Pleiotropy; Obesity; Family
ISSN (print) / ISBN 2041-1723
e-ISSN 2041-1723
Quellenangaben Volume: 10, Issue: 1, Pages: , Article Number: 3300 Supplement: ,
Publisher Nature Publishing Group
Publishing Place London
Reviewing status Peer reviewed