Integrating genome-wide association study and expression quantitative trait loci data identifies NEGR1 as a causal risk gene of major depression disorder
Authors:
- 1 March 2020
- journal article
- research article
- Published by Elsevier in Journal of Affective Disorders
- Vol. 265, 679-686
Abstract
No abstract availableKeywords
Funding Information
- National Key Research and Development Program of China (2015CB856404)
- National Key Research and Development Program of China (2016YFC1307000)
- Natural Science Foundation of Shandong Province (ZR2019BH001)
- Peking University (PKU2018LCXQ008)
- National Natural Science Foundation of China (81901358)
- Jining Medical University
This publication has 40 references indexed in Scilit:
- A novel non-rapid-eye movement and rapid-eye-movement parasomnia with sleep breathing disorder associated with antibodies to IgLON5: a case series, characterisation of the antigen, and post-mortem studyThe Lancet Neurology, 2014
- Characterizing the genetic basis of methylome diversity in histologically normal human lung tissueNature Communications, 2014
- Beyond GWASs: Illuminating the Dark Road from Association to FunctionThe American Journal of Human Genetics, 2013
- Psychiatric patient stratification using biosignatures based on cerebrospinal fluid protein expression clustersJournal of Psychiatric Research, 2013
- The Genotype-Tissue Expression (GTEx) projectNature Genetics, 2013
- Epigenome-Wide Scans Identify Differentially Methylated Regions for Age and Age-Related Phenotypes in a Healthy Ageing PopulationPLOS Genetics, 2012
- Cognitive dysfunction in psychiatric disorders: characteristics, causes and the quest for improved therapyNature Reviews Drug Discovery, 2012
- Trait-Associated SNPs Are More Likely to Be eQTLs: Annotation to Enhance Discovery from GWASPLOS Genetics, 2010
- Epidemiology of Major Depressive DisorderArchives of General Psychiatry, 2005
- Genetic Epidemiology of Major Depression: Review and Meta-AnalysisAmerican Journal of Psychiatry, 2000