complex traits phenotype
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Related entities (26)
Mentioned in (72)
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)
- Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology. (2023)
- Research Review: A guide to computing and implementing polygenic scores in developmental research. (2022)
- Mother-child similarity in brain morphology: A comparison of structural characteristics of the brain's reading network. (2022)
- Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. (2021)
- Genetic association study of childhood aggression across raters, instruments, and age. (2021)
- Genetics of substance use disorders in the era of big data. (2021)
- Functionally informed fine-mapping and polygenic localization of complex trait heritability. (2020)
- Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease. (2020)
- 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)
- Genomic structural equation modelling provides insights into the multivariate genetic architecture of complex traits. (2019)
- Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
- Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. (2018)
- Critical Issues in the Inclusion of Genetic and Epigenetic Information in Prevention and Intervention Trials. (2018)
- Incorporating Functional Genomic Information to Enhance Polygenic Signal and Identify Variants Involved in Gene-by-Environment Interaction for Young Adult Alcohol Problems. (2018)
- Genetic effects on gene expression across human tissues. (2017)
- Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations. (2017)
- BECon: a tool for interpreting DNA methylation findings from blood in the context of brain. (2017)
- LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis. (2017)
- RNA splicing is a primary link between genetic variation and disease. (2016)
- 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)
- A global reference for human genetic variation. (2015)
- Gene-Environment Interaction Effects of Peer Deviance, Parental Knowledge and Stressful Life Events on Adolescent Alcohol Use. (2015)
- Epigenomic annotation of genetic variants using the Roadmap Epigenome Browser. (2015)
- A global reference for human genetic variation. (2015)
- Guidelines for investigating causality of sequence variants in human disease. (2014)
- Heritability and molecular-genetic basis of the P3 event-related brain potential: a genome-wide association study. (2014)
- 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)
- In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. (2014)
- PolymiRTS Database 3.0: linking polymorphisms in microRNAs and their target sites with human diseases and biological pathways. (2014)
- Genome-wide variation of cytosine modifications between European and African populations and the implications for complex traits. (2013)
- Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity. (2013)
- Dosage transmission disequilibrium test (dTDT) for linkage and association detection. (2013)
- A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines. (2013)
- Hand in glove: brain and skull in development and dysmorphogenesis. (2013)
- Common liability to addiction and "gateway hypothesis": theoretical, empirical and evolutionary perspective. (2012)
- Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. (2012)
- The aggregate effect of dopamine genes on dependence symptoms among cocaine users: cross-validation of a candidate system scoring approach. (2012)
- Population-specificity of human DNA methylation. (2012)
- Uncovering hidden variance: pair-wise SNP analysis accounts for additional variance in nicotine dependence. (2011)
- Mechanisms that underlie co-variation of the brain and face. (2011)
- Genome-wide association study identifies five new schizophrenia loci. (2011)
- Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA. (2011)
- Distribution of allele frequencies and effect sizes and their interrelationships for common genetic susceptibility variants. (2011)
- Genome wide association for addiction: replicated results and comparisons of two analytic approaches. (2010)
- Statistical analysis strategies for association studies involving rare variants. (2010)
- Finding the missing heritability of complex diseases. (2009)
- The future of genetics in psychology and psychiatry: microarrays, genome-wide association, and non-coding RNA. (2009)
- Geographic patterns of genome admixture in Latin American Mestizos. (2008)
- COGA phenotypes and linkages on chromosome 2. (2005)
- Precision and error of three-dimensional phenotypic measures acquired from 3dMD photogrammetric images. (2005)
- Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes. (2005)
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 | — | — |