eQTLGen Consortium cohort
Evidence from:
primary |
all sources
Related entities (4)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| eQTLGen Consortium | expressed_in | brain | — | 2 |
| eQTLGen Consortium | associated_with | OCD | — | 1 |
| GWAS | associated_with | eQTLGen Consortium | — | 3 |
| SNP | associated_with | eQTLGen Consortium | — | 2 |
Mentioned in (20)
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)
- ASEP: Gene-based detection of allele-specific expression across individuals in a population by RNA sequencing. (2020)
- Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
- Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. (2018)
- Annotation-free quantification of RNA splicing using LeafCutter. (2018)
- The impact of structural variation on human gene expression. (2017)
- 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)
- Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants. (2014)
- The Genotype-Tissue Expression (GTEx) project. (2013)
Merged raw entities (14)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| eqtl | variant | 29 | 55 |
| eqtl | phenotype | 14 | 32 |
| eqtls | variant | 12 | 13 |
| eqtls | phenotype | 6 | 7 |
| eqtlgen | cohort | 5 | 14 |
| eqtl | drug | 4 | 6 |
| eqtlgen consortium | cohort | 4 | 7 |
| eqtl snp | variant | 3 | 4 |
| eqtls | drug | 2 | 2 |
| eqtls | cohort | — | — |
| eqtl snps | cohort | — | — |
| expression qtl | cohort | — | — |
| expression quantitative trait loci | cohort | — | — |
| expression quantitative trait locus | cohort | — | — |