phenotype phenotype
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Related entities (48)
Mentioned in (125)
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)
- Emotion, motivation, decision-making, the orbitofrontal cortex, anterior cingulate cortex, and the amygdala. (2023)
- Pruning and thresholding approach for methylation risk scores in multi-ancestry populations. (2023)
- 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)
- Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology. (2023)
- DNA methylation and general psychopathology in childhood: an epigenome-wide meta-analysis from the PACE consortium. (2023)
- GenSLMs: Genome-scale language models reveal SARS-CoV-2 evolutionary dynamics. (2022)
- Brain charts for the human lifespan. (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)
- Closing the life-cycle of normative modeling using federated hierarchical Bayesian regression. (2022)
- Genetic variants associated with longitudinal changes in brain structure across the lifespan. (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)
- Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions. (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)
- 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)
- Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
- Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
- Genome-wide association study reveals novel loci associated with body size and carcass yields in Pekin ducks. (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)
- Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. (2019)
- Identification of common genetic risk variants for autism spectrum disorder. (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)
- Collider scope: when selection bias can substantially influence observed associations. (2018)
- 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)
- Enter the Matrix: Factorization Uncovers Knowledge from Omics. (2018)
- Comprehensive Characterization of Cancer Driver Genes and Mutations. (2018)
- Incorporating Functional Genomic Information to Enhance Polygenic Signal and Identify Variants Involved in Gene-by-Environment Interaction for Young Adult Alcohol Problems. (2018)
- A Brief Critique of the TATES Procedure. (2018)
- Cohort Profile: Pregnancy And Childhood Epigenetics (PACE) Consortium. (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)
- Machine learning shows association between genetic variability in and cerebral connectivity in preterm infants. (2017)
- Extending the MR-Egger method for multivariable Mendelian randomization to correct for both measured and unmeasured pleiotropy. (2017)
- De Novo Coding Variants Are Strongly Associated with Tourette Disorder. (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)
- Testing Causal Effects of Maternal Smoking During Pregnancy on Offspring's Externalizing and Internalizing Behavior. (2016)
- Genome-wide association study identifies 74 loci associated with educational attainment. (2016)
- Possible relationship between common genetic variation and white matter development in a pilot study of preterm infants. (2016)
- Role of overlapping genetic and environmental factors in the relationship between early adolescent conduct problems and substance use in young adulthood. (2016)
- The National Birth Defects Prevention Study: A review of the methods. (2015)
- A gene-based association method for mapping traits using reference transcriptome data. (2015)
- An introductory review of parallel independent component analysis (p-ICA) and a guide to applying p-ICA to genetic data and imaging phenotypes to identify disease-associated biological pathways and systems in common complex disorders. (2015)
- Candidate gene-environment interaction research: reflections and recommendations. (2015)
- Maternal periconceptional alcohol consumption and congenital heart defects. (2015)
- HLA-VBSeq: accurate HLA typing at full resolution from whole-genome sequencing data. (2015)
- Heritability and molecular-genetic basis of resting EEG activity: a genome-wide association study. (2014)
- Genetic influences on brain developmental trajectories on neuroimaging studies: from infancy to young adulthood. (2014)
- In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. (2014)
- Testing for measured gene-environment interaction: problems with the use of cross-product terms and a regression model reparameterization solution. (2014)
- Candidate gene association studies: a comprehensive guide to useful in silico tools. (2013)
- Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity. (2013)
- Visualizing genomic information across chromosomes with PhenoGram. (2013)
- ACMG clinical laboratory standards for next-generation sequencing. (2013)
- Gene expression in the human brain: the current state of the study of specificity and spatiotemporal dynamics. (2013)
- The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation. (2013)
- Alcohol consumption in men is influenced by qualitatively different genetic factors in adolescence and adulthood. (2013)
- 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)
- Pathway analysis of genomic data: concepts, methods, and prospects for future development. (2012)
- The genetic basis of addictive disorders. (2012)
- The impact of gene-environment interaction on alcohol use disorders. (2012)
- Genome-wide efficient mixed-model analysis for association studies. (2012)
- An integrated encyclopedia of DNA elements in the human genome. (2012)
- Maternal nutritional status, C(1) metabolism and offspring DNA methylation: a review of current evidence in human subjects. (2012)
- Genome-wide search for replicable risk gene regions in alcohol and nicotine co-dependence. (2012)
- Pharmacogenetics of smoking cessation: role of nicotine target and metabolism genes. (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)
- Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. (2011)
- Molecular mechanisms of long noncoding RNAs. (2011)
- Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn. (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)
- The PhenX Toolkit: get the most from your measures. (2011)
- Large-scale analysis of acute ethanol exposure in zebrafish development: a critical time window and resilience. (2011)
- Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence. (2011)
- Genome-wide scan for self-rating of the effects of alcohol in American Indians. (2010)
- Genome wide association for addiction: replicated results and comparisons of two analytic approaches. (2010)
- Statistical analysis strategies for association studies involving rare variants. (2010)
- Fetal alcohol spectrum disorders: Extending the range of structural defects. (2010)
- The psychiatric GWAS consortium: big science comes to psychiatry. (2010)
- Conserved role of unc-79 in ethanol responses in lightweight mutant mice. (2010)
- Genome-wide association studies in diverse populations. (2010)
- Evidence for genes on chromosome 2 contributing to alcohol dependence with conduct disorder and suicide attempts. (2010)
- The genetic interpretation of area under the ROC curve in genomic profiling. (2010)
- Expansion of the human mu-opioid receptor gene architecture: novel functional variants. (2009)
- Meta-analysis in genome-wide association studies. (2009)
- Finding the missing heritability of complex diseases. (2009)
- DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources. (2009)
- Marker selection for genetic case-control association studies. (2009)
- Perceived peer delinquency and the genetic predisposition for substance dependence vulnerability. (2009)
- Interaction between two independent CNR1 variants increases risk for cocaine dependence in European Americans: a replication study in family-based sample and population-based sample. (2009)
- Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk. (2009)
- Genetic and environmental influences on externalizing behavior and alcohol problems in adolescence: a female twin study. (2009)
- Nicotinic acetylcholine receptor beta2 subunit gene implicated in a systems-based candidate gene study of smoking cessation. (2008)
- Rapid SNP discovery and genetic mapping using sequenced RAD markers. (2008)
- Genetic and environmental factors in complex neurodevelopmental disorders. (2007)
- Heterogeneity in meta-analyses of genome-wide association investigations. (2007)
- Stability of inbred mouse strain differences in behavior and brain size between laboratories and across decades. (2006)
- SNPs3D: candidate gene and SNP selection for association studies. (2006)
- Environmental programming of stress responses through DNA methylation: life at the interface between a dynamic environment and a fixed genome. (2005)
Merged raw entities (12)
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 |
|---|---|---|---|
| phenotype | phenotype | 103 | 205 |
| phenotypes | phenotype | 19 | 21 |
| y | phenotype | 9 | 11 |
| other phenotypes | phenotype | 5 | 6 |
| multiple phenotypes | phenotype | 2 | 2 |
| general factor | phenotype | 1 | 2 |
| observed phenotype | phenotype | 1 | 1 |
| four phenotypes | phenotype | — | — |
| measure | phenotype | — | — |
| outcome variable (y) | phenotype | — | — |
| phenotype values | phenotype | — | — |
| phenotypic effect | phenotype | — | — |