UK Biobank cohort

Aliases

British-ancestry UK Biobank, UK Biobank British samples, UK Biobank reference samples, UK Biobank samples, UK Biobank target samples, UK Biobank34, UKB, UKB GWAS summary statistics, UKB dataset, UKB individuals, UKB sample, UKB team, UKBB, non-British European ancestry UK Biobank

Related entities (88)

Mentioned in (93)

Papers in which this entity is mentioned.

• Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis. (2026)
• Specificity, length and luck drive gene rankings in association studies. (2026)
• Associations between common genetic variants and income provide insights about the socio-economic health gradient. (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)
• Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. (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)
• Transcription start sites experience a high influx of heritable variants fueled by early development. (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)
• Alcohol Use Disorder Polygenic Score Compared With Family History and ADH1B. (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)
• The Polygenic Score Catalog: new functionality and tools to enable FAIR research. (2024)
• Recent advances in polygenic scores: translation, equitability, methods and FAIR tools. (2024)
• Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder. (2024)
• An overview of DNA methylation-derived trait score methods and applications. (2023)
• Biobank-scale methods and projections for sparse polygenic prediction from machine learning. (2023)
• Genetic nurture effects for alcohol use disorder. (2023)
• Pitfalls of predicting age-related traits by polygenic risk scores. (2023)
• Multiomic prioritisation of risk genes for anorexia nervosa. (2023)
• Unsupervised discovery of ancestry-informative markers and genetic admixture proportions in biobank-scale datasets. (2023)
• Polygenic scoring accuracy varies across the genetic ancestry continuum. (2023)
• Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses. (2023)
• Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals. (2023)
• Associations Between Cannabis Use, Polygenic Liability for Schizophrenia, and Cannabis-related Experiences in a Sample of Cannabis Users. (2023)
• Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology. (2023)
• Multi-trait genome-wide association study of opioid addiction: OPRM1 and beyond. (2022)
• Genetic architecture of 11 major psychiatric disorders at biobehavioral, functional genomic and molecular genetic levels of analysis. (2022)
• Item-Level Genome-Wide Association Study of the Alcohol Use Disorders Identification Test in Three Population-Based Cohorts. (2022)
• A saturated map of common genetic variants associated with human height. (2022)
• Variant interpretation using population databases: Lessons from gnomAD. (2022)
• Reproducible brain-wide association studies require thousands of individuals. (2022)
• Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease. (2022)
• Principal Component Analyses (PCA)-based findings in population genetic studies are highly biased and must be reevaluated. (2022)
• Closing the life-cycle of normative modeling using federated hierarchical Bayesian regression. (2022)
• Gene-based polygenic risk scores analysis of alcohol use disorder in African Americans. (2022)
• Inferring population structure in biobank-scale genomic data. (2022)
• Multi-environment gene interactions linked to the interplay between polysubstance dependence and suicidality. (2021)
• Large-scale collaboration in ENIGMA-EEG: A perspective on the meta-analytic approach to link neurological and psychiatric liability genes to electrophysiological brain activity. (2021)
• Polygenic risk scores for alcohol involvement relate to brain structure in substance-naïve children: Results from the ABCD study. (2021)
• Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions. (2021)
• Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. (2021)
• Frequent LPA KIV-2 Variants Lower Lipoprotein(a) Concentrations and Protect Against Coronary Artery Disease. (2021)
• Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction. (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)
• Rapid genotype imputation from sequence with reference panels. (2021)
• Genetics of substance use disorders in the era of big data. (2021)
• gene network in the prefrontal cortex is associated with total brain volume in childhood. (2020)
• Interpretation of risk loci from genome-wide association studies of Alzheimer's disease. (2020)
• Polygenic risk scores: from research tools to clinical instruments. (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)
• The mutational constraint spectrum quantified from variation in 141,456 humans. (2020)
• ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries. (2020)
• Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits. (2020)
• Transcriptomic signatures across human tissues identify functional rare genetic variation. (2020)
• White matter disturbances in major depressive disorder: a coordinated analysis across 20 international cohorts in the ENIGMA MDD working group. (2020)
• Polygenic prediction via Bayesian regression and continuous shrinkage priors. (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)
• Association of a Schizophrenia-Risk Nonsynonymous Variant With Putamen Volume in Adolescents: A Voxelwise and Genome-Wide Association Study. (2019)
• The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
• Sex differences in the developing brain: insights from multimodal neuroimaging. (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)
• Psychosocial moderation of polygenic risk for cannabis involvement: the role of trauma exposure and frequency of religious service attendance. (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)
• Genome-Wide Association Study Meta-Analysis of the Alcohol Use Disorders Identification Test (AUDIT) in Two Population-Based Cohorts. (2019)
• Longitudinally Mapping Childhood Socioeconomic Status Associations with Cortical and Subcortical Morphology. (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)
• The Gene Encoding Protocadherin 9 (PCDH9), a Novel Risk Factor for Major Depressive Disorder. (2018)
• Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer's disease susceptibility. (2018)
• Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. (2018)
• Human Genetics of Addiction: New Insights and Future Directions. (2018)
• Extending the Human Connectome Project across ages: Imaging protocols for the Lifespan Development and Aging projects. (2018)
• Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. (2018)
• The development of brain white matter microstructure. (2018)
• Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112 117). (2017)
• G = E: What GWAS Can Tell Us about the Environment. (2016)
• Reference-based phasing using the Haplotype Reference Consortium panel. (2016)
• Genome-wide association study identifies 74 loci associated with educational attainment. (2016)
• Fast and accurate long-range phasing in a UK Biobank cohort. (2016)
• Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank. (2015)
• NIH toolbox for assessment of neurological and behavioral function. (2013)
• Managing incidental findings and research results in genomic research involving biobanks and archived data sets. (2012)
• A general factor of brain white matter integrity predicts information processing speed in healthy older people. (2010)

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