phenotype phenotype

Aliases

P, Y, disease status, four phenotypes, general factor, measure, multiple phenotypes, observed phenotype, outcome variable (Y), phenotype, phenotype of interest, phenotype values, phenotypes, phenotypic effect, trait, traits

Related entities (13)

Mentioned in (46)

Papers in which this entity is mentioned.

• Infant subcortical brain volumes associated with maternal obesity and diabetes: a large multicohort human study. (2026)
• Artificial Intelligence agents for biological research: a survey. (2026)
• Integrated in vivo combinatorial functional genomics and spatial transcriptomics of tumours to decode genotype-to-phenotype relationships. (2026)
• Concordance between male- and female-specific GWAS results helps define underlying genetic architecture of complex traits. (2025)
• Biomni: A General-Purpose Biomedical AI Agent. (2025)
• Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. (2025)
• A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies. (2025)
• Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI. (2024)
• 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)
• CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods. (2024)
• The Polygenic Score Catalog: new functionality and tools to enable FAIR research. (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)
• Guidelines for Evaluating the Comparability of Down-Sampled GWAS Summary Statistics. (2023)
• Polygenic scoring accuracy varies across the genetic ancestry continuum. (2023)
• GenSLMs: Genome-scale language models reveal SARS-CoV-2 evolutionary dynamics. (2022)
• Research Review: A guide to computing and implementing polygenic scores in developmental research. (2022)
• Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease. (2022)
• Genome-wide admixture mapping of DSM-IV alcohol dependence, criterion count, and the self-rating of the effects of ethanol in African American populations. (2021)
• Genetic association study of childhood aggression across raters, instruments, and age. (2021)
• Tutorial: a guide to performing polygenic risk score analyses. (2020)
• Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks. (2020)
• Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
• Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
• Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
• Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. (2019)
• Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. (2019)
• Enter the Matrix: Factorization Uncovers Knowledge from Omics. (2018)
• Comprehensive Characterization of Cancer Driver Genes and Mutations. (2018)
• A Brief Critique of the TATES Procedure. (2018)
• The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies. (2017)
• Genetic correlates of the development of theta event related oscillations in adolescents and young adults. (2017)
• The impact of structural variation on human gene expression. (2017)
• New insights into the generation and role of de novo mutations in health and disease. (2016)
• A gene-based association method for mapping traits using reference transcriptome data. (2015)
• Candidate gene-environment interaction research: reflections and recommendations. (2015)
• HLA-VBSeq: accurate HLA typing at full resolution from whole-genome sequencing data. (2015)
• ACMG clinical laboratory standards for next-generation sequencing. (2013)
• An integrated encyclopedia of DNA elements in the human genome. (2012)
• Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence. (2011)
• Fetal alcohol spectrum disorders: Extending the range of structural defects. (2010)
• Evidence for genes on chromosome 2 contributing to alcohol dependence with conduct disorder and suicide attempts. (2010)
• Rapid SNP discovery and genetic mapping using sequenced RAD markers. (2008)

Merged raw entities (12)

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