causal variant cohort

Evidence from: primary | all sources

Related entities (4)

Subject	Relation	Object	p-value	Evidence
case-control phenotypes	associated_with	causal variant	—	1
causal variant	associated_with	SNP	—	1
functional SNP	associated_with	causal variant	—	1
genetic variants	associated_with	causal variant	—	1

Mentioned in (13)

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)
An overview of DNA methylation-derived trait score methods and applications. (2023)
A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies. (2023)
Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals. (2023)
Research Review: A guide to computing and implementing polygenic scores in developmental research. (2022)
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. (2021)
Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
Elevated polygenic burden for autism is associated with differential DNA methylation at birth. (2018)
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)
Gene--environment-wide association studies: emerging approaches. (2010)
Meta-analysis in genome-wide association studies. (2009)

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	—	—