causal variant cohort
Evidence from:
primary |
all sources
Related entities (2)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| case-control phenotypes | associated_with | causal variant | — | 1 |
| causal variant | associated_with | SNP | — | 1 |
Mentioned in (7)
Papers in which this entity is mentioned.
- A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies. (2025)
- Principles and methods for transferring polygenic risk scores across global populations. (2024)
- A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies. (2023)
- Research Review: A guide to computing and implementing polygenic scores in developmental research. (2022)
- Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
- Genetic linkage analysis in the age of whole-genome sequencing. (2015)
- Common biological networks underlie genetic risk for alcoholism in African- and European-American populations. (2013)
Merged raw entities (2)
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 |
|---|---|---|---|
| causal variant | variant | 13 | 15 |
| causal variant | cohort | — | — |