case/control status phenotype
Evidence from:
primary |
all sources
Related entities (7)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| African-Americans | associated_with | case/control status | — | 1 |
| age | associated_with | case/control status | — | 1 |
| case-control sample | associated_with | case/control status | — | 1 |
| case/control status | associated_with | brain | — | 1 |
| secondary phenotype | associated_with | case/control status | — | 1 |
| sex | associated_with | case/control status | — | 1 |
| SNP | associated_with | case/control status | — | 2 |
Mentioned in (13)
Papers in which this entity is mentioned.
- Tutorial: a guide to performing polygenic risk score analyses. (2020)
- Genomic structural equation modelling provides insights into the multivariate genetic architecture of complex traits. (2019)
- Collider scope: when selection bias can substantially influence observed associations. (2018)
- Obstructive heart defects associated with candidate genes, maternal obesity, and folic acid supplementation. (2015)
- Maternal obesity and tobacco use modify the impact of genetic variants on the occurrence of conotruncal heart defects. (2014)
- Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder. (2014)
- Polygenic risk scores for smoking: predictors for alcohol and cannabis use? (2014)
- Associations between maternal genotypes and metabolites implicated in congenital heart defects. (2012)
- Quality control parameters on a large dataset of regionally dissected human control brains for whole genome expression studies. (2011)
- Incorporating age at onset of smoking into genetic models for nicotine dependence: evidence for interaction with multiple genes. (2010)
- Multiple cholinergic nicotinic receptor genes affect nicotine dependence risk in African and European Americans. (2010)
- Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. (2009)
- Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. (2007)
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 |
|---|---|---|---|
| case/control status | phenotype | 8 | 8 |
| case-control status | phenotype | 4 | 5 |
| control status | phenotype | 1 | 1 |