EUR cohort
Evidence from:
primary |
all sources
Related entities (28)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| 1000 Genomes Project | interacts_with | EUR | — | 1 |
| 1000 Genomes Project | associated_with | EUR | — | 2 |
| AGDS | associated_with | EUR | — | 1 |
| auditory | associated_with | EUR | — | 1 |
| EUR | interacts_with | 1000 Genomes Project | — | 1 |
| EUR | associated_with | 1KGP | — | 1 |
| EUR | associated_with | AFR | 2.78e-21 | 1 |
| EUR | interacts_with | AFR | — | 2 |
| EUR | interacts_with | EAs | — | 1 |
| EUR | interacts_with | His | — | 1 |
| EUR | interacts_with | lateral amygdala | — | 1 |
| EUR | associated_with | lateral amygdala | 3.52e-20 | 1 |
| EUR | associated_with | PAU | — | 1 |
| EUR | interacts_with | rs9829896 | — | 1 |
| EUR | interacts_with | SAS | — | 1 |
| EUR | associated_with | SRE | — | 1 |
| EUR | expressed_in | UKB | — | 1 |
| EUR | associated_with | UK Biobank | — | 1 |
| genome-wide significant SNPs | associated_with | EUR | 0 | 1 |
| HapMap3 | associated_with | EUR | — | 1 |
| His | associated_with | EUR | — | 1 |
| lead SNP | associated_with | EUR | — | 1 |
| MVP | associated_with | EUR | — | 1 |
| PAU | associated_with | EUR | — | 1 |
| PAU PRS | expressed_in | EUR | — | 1 |
| PMBB | associated_with | EUR | — | 1 |
| Twin cohort | associated_with | EUR | — | 1 |
| variant | associated_with | EUR | — | 1 |
Mentioned in (25)
Papers in which this entity is mentioned.
- Mapping the genetic landscape across 14 psychiatric disorders. (2026)
- Meta-analysis reveals differences in somatic alterations by genetic ancestry across common cancers. (2025)
- Functional analysis of cancer-associated germline risk variants. (2025)
- Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI. (2024)
- MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups. (2024)
- Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank. (2024)
- Clinical, genomic, and neurophysiological correlates of lifetime suicide attempts among individuals with alcohol dependence. (2024)
- Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR. (2024)
- Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder. (2024)
- A harmonized public resource of deeply sequenced diverse human genomes. (2024)
- Biobank-scale methods and projections for sparse polygenic prediction from machine learning. (2023)
- Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals. (2023)
- Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology. (2023)
- A saturated map of common genetic variants associated with human height. (2022)
- The complete sequence of a human genome. (2022)
- Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease. (2022)
- Using a developmental perspective to examine the moderating effects of marriage on heavy episodic drinking in a young adult sample enriched for risk. (2021)
- Rapid genotype imputation from sequence with reference panels. (2021)
- Genotypes of informative loci from 1000 Genomes data allude evolution and mixing of human populations. (2021)
- Genetics of substance use disorders in the era of big data. (2021)
- Meta-Analysis of Genetic Influences on Initial Alcohol Sensitivity. (2018)
- KAT2B polymorphism identified for drug abuse in African Americans with regulatory links to drug abuse pathways in human prefrontal cortex. (2016)
- A global reference for human genetic variation. (2015)
- Fast and accurate genotype imputation in genome-wide association studies through pre-phasing. (2012)
- Using whole-genome sequencing to evaluate copy number variants of the LPA Kringle-IV type 2 domain with DRAGEN
Merged raw entities (3)
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 |
|---|---|---|---|
| eur | cohort | 25 | 135 |
| european ancestry ld reference | cohort | — | — |
| eur sequence data | cohort | — | — |