trait phenotype
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Related entities (25)
Mentioned in (88)
Papers in which this entity is mentioned.
- Specificity, length and luck drive gene rankings in association studies. (2026)
- Modeling heterogeneity in single-cell perturbation states enhances detection of response eQTLs. (2025)
- Concordance between male- and female-specific GWAS results helps define underlying genetic architecture of complex traits. (2025)
- Genome-wide association testing beyond SNPs. (2025)
- Parent-of-origin effects on complex traits in up to 236,781 individuals. (2025)
- A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies. (2025)
- BridgePRS leverages shared genetic effects across ancestries to increase polygenic risk score portability. (2024)
- MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups. (2024)
- Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank. (2024)
- Integrative polygenic risk score improves the prediction accuracy of complex traits and diseases. (2024)
- Clinical, genomic, and neurophysiological correlates of lifetime suicide attempts among individuals with alcohol dependence. (2024)
- Recent advances in polygenic scores: translation, equitability, methods and FAIR tools. (2024)
- An overview of DNA methylation-derived trait score methods and applications. (2023)
- A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies. (2023)
- Multiomic prioritisation of risk genes for anorexia nervosa. (2023)
- Guidelines for Evaluating the Comparability of Down-Sampled GWAS Summary Statistics. (2023)
- Polygenic scoring accuracy varies across the genetic ancestry continuum. (2023)
- Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology. (2023)
- Mapping brain asymmetry in health and disease through the ENIGMA consortium. (2022)
- Research Review: A guide to computing and implementing polygenic scores in developmental research. (2022)
- Genetic variants associated with longitudinal changes in brain structure across the lifespan. (2022)
- Epigenome-wide change and variation in DNA methylation in childhood: trajectories from birth to late adolescence. (2021)
- Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions. (2021)
- Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. (2021)
- Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. (2021)
- Genetic association study of childhood aggression across raters, instruments, and age. (2021)
- Interpretation of risk loci from genome-wide association studies of Alzheimer's disease. (2020)
- Tutorial: a guide to performing polygenic risk score analyses. (2020)
- Functionally informed fine-mapping and polygenic localization of complex trait heritability. (2020)
- Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks. (2020)
- Transcriptomic signatures across human tissues identify functional rare genetic variation. (2020)
- Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
- Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
- The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
- g:Profiler: a web server for functional enrichment analysis and conversions of gene lists (2019 update). (2019)
- Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
- Comprehensive analysis of structural variants in breast cancer genomes using single molecule sequencing (2019)
- Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types. (2018)
- Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. (2018)
- Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. (2018)
- Critical Issues in the Inclusion of Genetic and Epigenetic Information in Prevention and Intervention Trials. (2018)
- Twin study confirms virtually identical prenatal alcohol exposures can lead to markedly different fetal alcohol spectrum disorder outcomes-fetal genetics influences fetal vulnerability. (2018)
- An improved ATAC-seq protocol reduces background and enables interrogation of frozen tissues. (2017)
- Genetic effects on gene expression across human tissues. (2017)
- The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog). (2017)
- The impact of structural variation on human gene expression. (2017)
- A gene-based association method for mapping traits using reference transcriptome data. (2015)
- SEQMINER: An R-Package to Facilitate the Functional Interpretation of Sequence-Based Associations. (2015)
- Genetics and genomics of psychiatric disease. (2015)
- Second-generation PLINK: rising to the challenge of larger and richer datasets. (2015)
- Genetic linkage analysis in the age of whole-genome sequencing. (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)
- Genetic influences on brain developmental trajectories on neuroimaging studies: from infancy to young adulthood. (2014)
- Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. (2013)
- A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks. (2013)
- Plasma cytokine profiling in sibling pairs discordant for autism spectrum disorder. (2013)
- Structure and function of complex brain networks. (2013)
- DNA methylation, genotype and gene expression: who is driving and who is along for the ride? (2013)
- The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation. (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)
- A better prognosis for genetic association studies in mice. (2012)
- Managing incidental findings and research results in genomic research involving biobanks and archived data sets. (2012)
- Genome-wide association study of primary open angle glaucoma risk and quantitative traits. (2012)
- A comparison of approaches to account for uncertainty in analysis of imputed genotypes. (2011)
- Uncovering hidden variance: pair-wise SNP analysis accounts for additional variance in nicotine dependence. (2011)
- Linkage analysis merging replicate phenotypes: an application to three quantitative phenotypes in two African samples. (2011)
- Gene-environment interaction in psychological traits and disorders. (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)
- LocusZoom: regional visualization of genome-wide association scan results. (2010)
- Cortical thickness or grey matter volume? The importance of selecting the phenotype for imaging genetics studies. (2010)
- Statistical analysis strategies for association studies involving rare variants. (2010)
- i-GSEA4GWAS: a web server for identification of pathways/gene sets associated with traits by applying an improved gene set enrichment analysis to genome-wide association study. (2010)
- The genetic interpretation of area under the ROC curve in genomic profiling. (2010)
- Finding the missing heritability of complex diseases. (2009)
- Genomewide association studies and human disease. (2009)
- Genome-wide association studies in ADHD. (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)
- Rapid SNP discovery and genetic mapping using sequenced RAD markers. (2008)
- The changing impact of genes and environment on brain development during childhood and adolescence: initial findings from a neuroimaging study of pediatric twins. (2008)
- Maternal immune activation alters fetal brain development through interleukin-6. (2007)
- Variance decomposition using an IRT measurement model. (2007)
- Identification of risk-related haplotypes with the use of multiple SNPs from nuclear families. (2007)
- Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes. (2005)
Merged raw entities (15)
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 |
|---|---|---|---|
| trait | phenotype | 46 | 63 |
| quantitative trait | phenotype | 29 | 41 |
| quantitative traits | phenotype | 23 | 26 |
| traits | phenotype | 19 | 25 |
| disease trait | phenotype | 4 | 5 |
| multiple traits | phenotype | 2 | 5 |
| phenotypic traits | phenotype | 2 | 2 |
| biomedical trait | phenotype | 1 | 1 |
| quantitative trait results | phenotype | — | — |
| trait analyzed in gwas i | phenotype | — | — |
| trait-associated variant | phenotype | — | — |
| trait being studied | phenotype | — | — |
| trait data | phenotype | — | — |
| unique traits | phenotype | — | — |
| yi* | phenotype | — | — |