causal variants cohort
Evidence from:
primary |
all sources
Related entities (3)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| causal variants | risk_factor_for | Alzheimer's disease | — | 2 |
| causal variants | risk_factor_for | OCD | — | 1 |
| MiXeR | interacts_with | causal variants | — | 1 |
Mentioned in (9)
Papers in which this entity is mentioned.
- Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. (2025)
- A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies. (2025)
- Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI. (2024)
- BridgePRS leverages shared genetic effects across ancestries to increase polygenic risk score portability. (2024)
- Principles and methods for transferring polygenic risk scores across global populations. (2024)
- Recent advances in polygenic scores: translation, equitability, methods and FAIR tools. (2024)
- Research Review: A guide to computing and implementing polygenic scores in developmental research. (2022)
- Tutorial: a guide to performing polygenic risk score analyses. (2020)
- 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 variants | variant | 17 | 22 |
| causal variants | cohort | — | — |