eQTLGen Consortium cohort

Aliases

cis-eQTL, eQTL SNPs, eQTLs, expression QTL, expression Quantitative Trait Loci, expression quantitative trait loci, expression quantitative trait locus

Related entities (47)

Mentioned in (50)

Papers in which this entity is mentioned.

• Advancing regulatory variant effect prediction with AlphaGenome. (2026)
• Modeling heterogeneity in single-cell perturbation states enhances detection of response eQTLs. (2025)
• Massively parallel reporter assay investigates shared genetic variants of eight psychiatric disorders. (2025)
• Functional analysis of cancer-associated germline risk variants. (2025)
• Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. (2025)
• Nucleotide Transformer: building and evaluating robust foundation models for human genomics. (2025)
• Global impact of unproductive splicing on human gene expression. (2024)
• Single-cell RNA sequencing of peripheral blood links cell-type-specific regulation of splicing to autoimmune and inflammatory diseases. (2024)
• A saturated map of common genetic variants associated with human height. (2022)
• Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. (2021)
• Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. (2021)
• ASEP: Gene-based detection of allele-specific expression across individuals in a population by RNA sequencing. (2020)
• Sex differences in the genetic architecture of obsessive-compulsive disorder. (2019)
• CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar Disorder. (2019)
• Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
• Genome-Wide Association Study Meta-Analysis of the Alcohol Use Disorders Identification Test (AUDIT) in Two Population-Based Cohorts. (2019)
• Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. (2018)
• Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types. (2018)
• Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. (2018)
• Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer's disease susceptibility. (2018)
• Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. (2018)
• Human Genetics of Addiction: New Insights and Future Directions. (2018)
• Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. (2018)
• Annotation-free quantification of RNA splicing using LeafCutter. (2018)
• Genetic effects on gene expression across human tissues. (2017)
• The effect of alcohol on the differential expression of cluster of differentiation 14 gene, associated pathways, and genetic network. (2017)
• The impact of structural variation on human gene expression. (2017)
• Translating genome-wide association findings into new therapeutics for psychiatry. (2016)
• RNA splicing is a primary link between genetic variation and disease. (2016)
• The PsychENCODE project. (2015)
• Tools and best practices for data processing in allelic expression analysis. (2015)
• A gene-based association method for mapping traits using reference transcriptome data. (2015)
• A global reference for human genetic variation. (2015)
• A global reference for human genetic variation. (2015)
• Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants. (2014)
• Heritability and genomics of gene expression in peripheral blood. (2014)
• Large-scale genotyping identifies 41 new loci associated with breast cancer risk. (2013)
• Passive and active DNA methylation and the interplay with genetic variation in gene regulation. (2013)
• A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines. (2013)
• DNA methylation, genotype and gene expression: who is driving and who is along for the ride? (2013)
• The Genotype-Tissue Expression (GTEx) project. (2013)
• The Genotype-Tissue Expression (GTEx) project. (2013)
• Annotation of functional variation in personal genomes using RegulomeDB. (2012)
• Pathway analysis of genomic data: concepts, methods, and prospects for future development. (2012)
• Spatio-temporal transcriptome of the human brain. (2011)
• Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA. (2011)
• Genetics of psychiatric disorders methods: molecular approaches. (2010)
• Genetics and beyond--the transcriptome of human monocytes and disease susceptibility. (2010)

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