Mendelian randomization integrating GWAS and eQTL data revealed genes pleiotropically associated with major depressive disorder

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Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions

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Identification of the primate-specific gene BTN3A2 as an additional schizophrenia risk gene in the MHC loci

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

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Mendelian randomization analysis revealed potential causal factors for systemic lupus erythematosus

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Integrating genome-wide association study and expression quantitative trait loci data identifies NEGR1 as a causal risk gene of major depression disorder

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Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

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Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways

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Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

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Integrative analysis of omics summary data reveals putative mechanisms underlying complex traits

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Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood

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Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways

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Evolutionary and polymorphism analyses reveal the central role of BTN3A2 in the concerted evolution of the BTN3 gene family

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An xQTL map integrates the genetic architecture of the human brain's transcriptome and epigenome

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Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield

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Schizophrenia risk from complex variation of complement component 4

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Identification of 15 genetic loci associated with risk of major depression in individuals of European descent

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Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets

(2016) Zhihong Zhu et al.   NATURE GENETICS

Gene expression elucidates functional impact of polygenic risk for schizophrenia

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Purification and Characterization of Progenitor and Mature Human Astrocytes Reveals Transcriptional and Functional Differences with Mouse

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Predicting gene targets from integrative analyses of summary data from GWAS and eQTL studies for 28 human complex traits

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Mendelian randomization: where are we now and where are we going?

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Schizophrenia and Depression Co-Morbidity: What We have Learned from Animal Models

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Mendelian randomization: genetic anchors for causal inference in epidemiological studies

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An RNA-Sequencing Transcriptome and Splicing Database of Glia, Neurons, and Vascular Cells of the Cerebral Cortex

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The Genetics of Major Depression

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Five Years of GWAS Discovery

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Plasma Levels of Complement 4a Protein are Increased in Alzheimerʼs Disease

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Genome-Wide Association Study of Major Recurrent Depression in the U.K. Population

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How do natural killer T cells help B cells?

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Mendelian Randomization

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Common variants on chromosome 6p22.1 are associated with schizophrenia

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