disease risk phenotype
Evidence from:
primary |
all sources
Related entities (5)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| common variants | risk_factor_for | disease risk | — | 1 |
| genetic variants | biomarker_for | disease risk | — | 1 |
| genetic variants | risk_factor_for | disease risk | — | 2 |
| rare variation | risk_factor_for | disease risk | — | 1 |
| risk allele | risk_factor_for | disease risk | — | 1 |
Mentioned in (28)
Papers in which this entity is mentioned.
- The Polygenic Score Catalog: new functionality and tools to enable FAIR research. (2024)
- An overview of DNA methylation-derived trait score methods and applications. (2023)
- Pruning and thresholding approach for methylation risk scores in multi-ancestry populations. (2023)
- Biobank-scale methods and projections for sparse polygenic prediction from machine learning. (2023)
- Epigenome-wide change and variation in DNA methylation in childhood: trajectories from birth to late adolescence. (2021)
- Enter the Matrix: Factorization Uncovers Knowledge from Omics. (2018)
- Annotation-free quantification of RNA splicing using LeafCutter. (2018)
- The placenta and neurodevelopment: sex differences in prenatal vulnerability. (2016)
- Enacting the molecular imperative: How gene-environment interaction research links bodies and environments in the post-genomic age. (2016)
- The Placenta as a Mediator of Stress Effects on Neurodevelopmental Reprogramming. (2016)
- Sex differences and stress across the lifespan. (2015)
- A gene-based association method for mapping traits using reference transcriptome data. (2015)
- Obstructive heart defects associated with candidate genes, maternal obesity, and folic acid supplementation. (2015)
- The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. (2014)
- Genic intolerance to functional variation and the interpretation of personal genomes. (2013)
- Evolution and functional impact of rare coding variation from deep sequencing of human exomes. (2012)
- Maternal nutritional status, C(1) metabolism and offspring DNA methylation: a review of current evidence in human subjects. (2012)
- Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011)
- Gene set analysis of genome-wide association studies: methodological issues and perspectives. (2011)
- Epigenetics and psychoneuroimmunology: mechanisms and models. (2011)
- Gene--environment-wide association studies: emerging approaches. (2010)
- Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America. (2009)
- A groupwise association test for rare mutations using a weighted sum statistic. (2009)
- Interaction between the serotonin transporter gene (5-HTTLPR), stressful life events, and risk of depression: a meta-analysis. (2009)
- Finding the missing heritability of complex diseases. (2009)
- Genomewide association studies: history, rationale, and prospects for psychiatric disorders. (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 |
|---|---|---|---|
| disease risk | phenotype | 27 | 31 |
| disease risks | phenotype | 1 | 1 |