| Literature DB >> 30911161 |
Laura M Huckins1,2,3,4, Amanda Dobbyn5,6, Douglas M Ruderfer7, Gabriel Hoffman5,8, Weiqing Wang5,6, Antonio F Pardiñas9, Veera M Rajagopal10,11,12, Thomas D Als10,11,12, Hoang T Nguyen5,6, Kiran Girdhar5,6, James Boocock13, Panos Roussos5,6,14,8, Menachem Fromer5,6, Robin Kramer15, Enrico Domenici16, Eric R Gamazon7,17, Shaun Purcell5,6,8, Ditte Demontis10,11,12, Anders D Børglum10,11,12, James T R Walters9, Michael C O'Donovan9, Patrick Sullivan18,19, Michael J Owen9, Bernie Devlin20, Solveig K Sieberts21, Nancy J Cox7, Hae Kyung Im22, Pamela Sklar5,6,14,8, Eli A Stahl5,6,14,8.
Abstract
Transcriptomic imputation approaches combine eQTL reference panels with large-scale genotype data in order to test associations between disease and gene expression. These genic associations could elucidate signals in complex genome-wide association study (GWAS) loci and may disentangle the role of different tissues in disease development. We used the largest eQTL reference panel for the dorso-lateral prefrontal cortex (DLPFC) to create a set of gene expression predictors and demonstrate their utility. We applied DLPFC and 12 GTEx-brain predictors to 40,299 schizophrenia cases and 65,264 matched controls for a large transcriptomic imputation study of schizophrenia. We identified 413 genic associations across 13 brain regions. Stepwise conditioning identified 67 non-MHC genes, of which 14 did not fall within previous GWAS loci. We identified 36 significantly enriched pathways, including hexosaminidase-A deficiency, and multiple porphyric disorder pathways. We investigated developmental expression patterns among the 67 non-MHC genes and identified specific groups of pre- and postnatal expression.Entities:
Mesh:
Year: 2019 PMID: 30911161 PMCID: PMC7034316 DOI: 10.1038/s41588-019-0364-4
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330