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A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia
Schizophrenia is a complex highly heritable disorder. Genome-wide association studies (GWAS) have identified multiple loci that influence the risk of developing schizophrenia, although the causal variants driving these associations and their impacts on specific genes are largely unknown. We identify...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7416679/ https://www.ncbi.nlm.nih.gov/pubmed/31691811 http://dx.doi.org/10.1093/hmg/ddz253 |
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author | Hall, Lynsey S Medway, Christopher W Pain, Oliver Pardiñas, Antonio F Rees, Elliott G Escott-Price, Valentina Pocklington, Andrew Bray, Nicholas J Holmans, Peter A Walters, James T R Owen, Michael J O’Donovan, Michael C |
author_facet | Hall, Lynsey S Medway, Christopher W Pain, Oliver Pardiñas, Antonio F Rees, Elliott G Escott-Price, Valentina Pocklington, Andrew Bray, Nicholas J Holmans, Peter A Walters, James T R Owen, Michael J O’Donovan, Michael C |
author_sort | Hall, Lynsey S |
collection | PubMed |
description | Schizophrenia is a complex highly heritable disorder. Genome-wide association studies (GWAS) have identified multiple loci that influence the risk of developing schizophrenia, although the causal variants driving these associations and their impacts on specific genes are largely unknown. We identify a significant correlation between schizophrenia risk and expression at 89 genes in the dorsolateral prefrontal cortex (P ≤ 9.43 × 10(−6)), including 20 novel genes. Genes whose expression correlate with schizophrenia were enriched for those involved in abnormal CNS synaptic transmission (P(FDR) = 0.02) and antigen processing and presentation of peptide antigen via MHC class I (P(FDR) = 0.02). Within the CNS synaptic transmission set, we identify individual significant candidate genes to which we assign direction of expression changes in schizophrenia. The findings provide strong candidates for experimentally probing the molecular basis of synaptic pathology in schizophrenia. |
format | Online Article Text |
id | pubmed-7416679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-74166792020-08-12 A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia Hall, Lynsey S Medway, Christopher W Pain, Oliver Pardiñas, Antonio F Rees, Elliott G Escott-Price, Valentina Pocklington, Andrew Bray, Nicholas J Holmans, Peter A Walters, James T R Owen, Michael J O’Donovan, Michael C Hum Mol Genet Association Studies Article Schizophrenia is a complex highly heritable disorder. Genome-wide association studies (GWAS) have identified multiple loci that influence the risk of developing schizophrenia, although the causal variants driving these associations and their impacts on specific genes are largely unknown. We identify a significant correlation between schizophrenia risk and expression at 89 genes in the dorsolateral prefrontal cortex (P ≤ 9.43 × 10(−6)), including 20 novel genes. Genes whose expression correlate with schizophrenia were enriched for those involved in abnormal CNS synaptic transmission (P(FDR) = 0.02) and antigen processing and presentation of peptide antigen via MHC class I (P(FDR) = 0.02). Within the CNS synaptic transmission set, we identify individual significant candidate genes to which we assign direction of expression changes in schizophrenia. The findings provide strong candidates for experimentally probing the molecular basis of synaptic pathology in schizophrenia. Oxford University Press 2020-01-01 2019-11-06 /pmc/articles/PMC7416679/ /pubmed/31691811 http://dx.doi.org/10.1093/hmg/ddz253 Text en © The Author(s) 2019. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Association Studies Article Hall, Lynsey S Medway, Christopher W Pain, Oliver Pardiñas, Antonio F Rees, Elliott G Escott-Price, Valentina Pocklington, Andrew Bray, Nicholas J Holmans, Peter A Walters, James T R Owen, Michael J O’Donovan, Michael C A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia |
title | A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia |
title_full | A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia |
title_fullStr | A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia |
title_full_unstemmed | A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia |
title_short | A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia |
title_sort | transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia |
topic | Association Studies Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7416679/ https://www.ncbi.nlm.nih.gov/pubmed/31691811 http://dx.doi.org/10.1093/hmg/ddz253 |
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