disease susceptibility phenotype
Evidence from:
primary |
all sources
Related entities (5)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| candidate genes | risk_factor_for | disease susceptibility | — | 1 |
| cases | associated_with | disease susceptibility | — | 1 |
| controls | associated_with | disease susceptibility | — | 1 |
| non-synonymous SNP | risk_factor_for | disease susceptibility | — | 1 |
| rare variation | risk_factor_for | disease susceptibility | — | 1 |
Mentioned in (15)
Papers in which this entity is mentioned.
- The GenomeAsia 100K Project enables genetic discoveries across Asia. (2019)
- Identification of novel candidate disease genes from de novo exonic copy number variants. (2017)
- Alcohol Dependence Genetics: Lessons Learned From Genome-Wide Association Studies (GWAS) and Post-GWAS Analyses. (2015)
- A gene-based association method for mapping traits using reference transcriptome data. (2015)
- DNA methylation contributes to natural human variation. (2013)
- Dosage transmission disequilibrium test (dTDT) for linkage and association detection. (2013)
- The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation. (2013)
- Evolution and functional impact of rare coding variation from deep sequencing of human exomes. (2012)
- Gene set analysis of genome-wide association studies: methodological issues and perspectives. (2011)
- Marker selection for genetic case-control association studies. (2009)
- Maternal nutrient supplementation counteracts bisphenol A-induced DNA hypomethylation in early development. (2007)
- PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007)
- Co-occurring risk factors for alcohol dependence and habitual smoking: update on findings from the Collaborative Study on the Genetics of Alcoholism. (2006)
- SNPs3D: candidate gene and SNP selection for association studies. (2006)
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 |
|---|---|---|---|
| disease susceptibility | phenotype | 15 | 20 |
| genetic susceptibility to disease | phenotype | — | — |