complex traits phenotype
Evidence from:
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all sources
Related entities (3)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| candidate SNP | associated_with | complex traits | — | 1 |
| genetic variants | associated_with | complex traits | — | 1 |
| psychiatric disorders | associated_with | complex traits | — | 1 |
Mentioned in (28)
Papers in which this entity is mentioned.
- Consortium profile: the methylation, imaging and NeuroDevelopment (MIND) consortium. (2026)
- Specificity, length and luck drive gene rankings in association studies. (2026)
- Concordance between male- and female-specific GWAS results helps define underlying genetic architecture of complex traits. (2025)
- Parent-of-origin effects on complex traits in up to 236,781 individuals. (2025)
- BridgePRS leverages shared genetic effects across ancestries to increase polygenic risk score portability. (2024)
- Integrative polygenic risk score improves the prediction accuracy of complex traits and diseases. (2024)
- Principles and methods for transferring polygenic risk scores across global populations. (2024)
- Global impact of unproductive splicing on human gene expression. (2024)
- CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods. (2024)
- Recent advances in polygenic scores: translation, equitability, methods and FAIR tools. (2024)
- Consortium Profile: The Methylation, Imaging and NeuroDevelopment (MIND) Consortium. (2024)
- Single-cell RNA sequencing of peripheral blood links cell-type-specific regulation of splicing to autoimmune and inflammatory diseases. (2024)
- A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies. (2023)
- Biobank-scale methods and projections for sparse polygenic prediction from machine learning. (2023)
- Research Review: A guide to computing and implementing polygenic scores in developmental research. (2022)
- Genetic association study of childhood aggression across raters, instruments, and age. (2021)
- Transcriptomic signatures across human tissues identify functional rare genetic variation. (2020)
- Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
- Exploring the relationship between polygenic risk for cannabis use, peer cannabis use and the longitudinal course of cannabis involvement. (2019)
- Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
- Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
- RNA splicing is a primary link between genetic variation and disease. (2016)
- A gene-based association method for mapping traits using reference transcriptome data. (2015)
- A global reference for human genetic variation. (2015)
- Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene. (2014)
- Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants. (2014)
- Dosage transmission disequilibrium test (dTDT) for linkage and association detection. (2013)
- The aggregate effect of dopamine genes on dependence symptoms among cocaine users: cross-validation of a candidate system scoring approach. (2012)
Merged raw entities (7)
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 |
|---|---|---|---|
| complex traits | phenotype | 52 | 90 |
| complex trait | phenotype | 21 | 30 |
| complex phenotypes | phenotype | 7 | 9 |
| human complex traits | phenotype | 4 | 4 |
| complex traits (including disease) | phenotype | — | — |
| complex traits of interest | phenotype | — | — |
| polygenic trait | phenotype | — | — |