Questions about using the genomic information can be directed to a special UK Biobank mailing list, which can be joined at https://www.jiscmail.ac.uk/cgi-bin/webadmin?A0=UKB-GENETICS.
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| Category ID | Description | Items |
|---|---|---|
| 264 | Genetically deduced phenotypes | 1 |
| 263 | Genotypes | +80 |
| 100319 | Imputation | 2+22 |
| 170 | Exome sequences | 18 |
| 180 | Whole genome sequences | 37 |
| 265 | Telomeres | 5 |
| Return ID | Description |
|---|---|
| 1641 | Meng, W et al; A Genome-Wide Association Study Finds Genetic Associations with Broadly-Defined Headache in UK Biobank (N = 223,773); EBioMedicine 28 2018 |
| 3457 | Legault et al; A genetic model of ivabradine recapitulates results from randomized clinical trials; PLOS ONE (2020) |
| 3583 | Couvy-Duchesne et al; A unified framework for association and prediction from vertex-wise grey-matter structure; Human Brain Mapping |
| 3462 | Lello et al; Accurate Genomic Prediction of Human Height; Genetics (2018) |
| 777 | Lessard et al; An erythroid-specific ATP2B4 enhancer mediates red blood cell hydration and malaria susceptibility; Journal of Clinical Investigation 2017 |
| 3614 | Curtis; Analysis of exome-sequenced UK Biobank subjects implicates genes affecting risk of hyperlipidaemia; Molecular Genetics and Metabolism |
| 3065 | Nave et al; Are Bigger Brains Smarter? Evidence From a Large-Scale Preregistered Study; Psychological Science (2018) |
| 3201 | Colodro-Conde et al; Association Between Population Density and Genetic Risk for Schizophrenia; JAMA Psychiatry (2018) |
| 2881 | Thompson et al; Association of maternal circulating 25(OH)D and calcium with birth weight: A mendelian randomisation analysis; PLoS Medicine (2019) |
| 3551 | Cao et al.,; Association of obesity status and metabolic syndrome with site-specific cancers: a population-based cohort study; British Journal of Cancer (2020) |
| 3432 | Hilser et al; Association of serum HDL-cholesterol and apolipoprotein A1 levels with risk of severe SARS-CoV-2 infection; Journal of Lipid Research (2021) |
| 2692 | Liu et al; Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use; Nature Genetics (2019) |
| 2921 | Stolicyn, A. et al; Automated classification of depression from structural brain measures across two independent community-based cohorts; Human Brain Mapping. 2020 |
| 3502 | Lipunova et al; Bilirubin is not associated with urinary bladder cancer risk and prognosis: A Mendelian Randomization Study in the UK Biobank; medRxiv (2020) |
| 702 | Liu et al; Case-control association mapping by proxy using family history of disease; Nature Genetics 2017 |
| 783 | Kendall et al; Cognitive performance among carriers of pathogenic copy number variants: Analysis of 152,000 UK Biobank subjects; Biological Psychiatry 2016 |
| 2885 | de Leeuw et al; Conditional and interaction gene-set analysis reveals novel functional pathways for blood pressure; Nature Communications (2018) |
| 1831 | Yengo et al; Detection and quantification of inbreeding depression for complex traits from SNP data; PNAS 2017 |
| 2904 | Yap et al; Dissection of genetic variation and evidence for pleiotropy in male pattern baldness; Nature Communications (2018) |
| 2962 | Le Guen, Y. et al; Enhancer locus in ch14q23.1 modulates brain asymmetric temporal regions involved in language; Cerebral Cortex. 2020 |
| 1456 | Ruth, K.S. et al; Events in Early Life are Associated with Female Reproductive Ageing: A UK Biobank Study; Scientific Reports. 2016 |
| 3616 | Xia et al.,; Evidence of horizontal indirect genetic effects in humans; Nature Human Behaviour (2020) |
| 2693 | Brazel et al; Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use; Biological Psychiatry (2019) |
| 3500 | Nadezda et al; External Replication of Urinary Bladder Cancer Prognostic Polymorphisms in the UK Biobank; Frontiers in Oncology (2019) |
| 3642 | Saunders et al.,; External Validation of Risk Prediction Models Incorporating Common Genetic Variants for Incident Colorectal Cancer Using UK Biobank; Cancer Prevention Research (2020) |
| 3365 | Yengo, L. et al; Extreme inbreeding in a European ancestry sample from the contemporary UK population; Nature Communications. 2019 |
| 2522 | Steven Gazal et al; Functional architecture of low-frequency variants highlights strength of negative selection across coding and non-coding annotations; Nature Genetics (2018) |
| 3149 | Weissbrod et al; Functionally informed fine-mapping and polygenic localization of complex trait heritability; Nature Genetics (2020) |
| 2709 | Pasman et al; GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal influence of schizophrenia; Nature Neuroscience, 21(9), 1161-1170 |
| 717 | Okbay et al; Gemome-wide association study identifies 74 loci associated with educational attainment; Nature 2016 |
| 1664 | Andrew McIntosh et al; Genetic and Environmental Risk for Chronic Pain and the Contribution of RiskVariants for Major Depressive Disorder: A Family-Based Mixed-Model Analysis; PLOS Medicine |
| 3460 | Yong et al; Genetic architecture of complex traits and disease risk predictors; Scientific Reports (2020) |
| 1455 | Ruth, K.S. et al; Genetic evidence that lower circulating FSH levels lengthen menstrual cycle, increase age at menopause and impact female reproductive health; Human Reproduction, 2016 |
| 2711 | Wei et al; Genetic mapping and evolutionary analysis of human-expanded cognitive networks; Nature Communications (2019) |
| 718 | Okbay et al; Genetic variants associated with subjective well-being, depressive symptoms,and neuroticism identified through genome-wide analysis; Nature Genetics 2016 |
| 2174 | Marioni et al; Genetic variants linked to education predict longevity; PNAS (2016) |
| 3050 | Sanchez-Roige et al; Genome-Wide Association Study Meta-Analysis of the Alcohol Use Disorders Identification Test (AUDIT) in Two Population-Based Cohorts; Am J Psychiatry (2018) |
| 3428 | Han Y. et al; Genome-wide analysis highlights contribution of immune system pathways to the genetic architecture of asthma; Nature Communications (2020) |
| 3431 | Hartiala et al; Genome-wide analysis identifies novel susceptibility loci for myocardial infarction; European Heart Journal (2021) |
| 739 | Wain et al; Genome-wide association analyses for lung funtion and chronic obstructive pulmonary disease identify new loci and potnential druggable targets; Nature Genetics 2017 |
| 1862 | Samuel E. Jones et al.; Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms; Nature Communications 2019 |
| 2159 | Karlsson Linner, R. et al; Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences; Nature Genetics. 2019 |
| 745 | Lane et al; Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits; Nature Genetics 2016 |
| 584 | Warren et al.; Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk; Nature Genetics 2017 |
| 2886 | Savage et al; Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence; Nature Genetics (2018) |
| 723 | Sniekers et al; Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence; Nature Genetics 2017 |
| 3393 | Revez, J. et al; Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration; Nature Communications. 2020 |
| 3547 | Revez et al.,; Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration; Nature Communications (2020) |
| 749 | Clarke et al; Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=122117); Molecular Psychiatry 2017 |
| 1878 | Howard, D. M et al; Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways.; Nature Communications (2018) 9, 1470 |
| 1848 | Robin N. Beaumont et al; Genome-wide association study of offspring birth weight in 86577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics; Human Molecular Genetics (2018) |
| 744 | Lane et al; Genome-wide association study reveals ten loci associated with chronotype in the UKBiobank.; Nature Communications 2016 |
| 752 | McCarthy et al; Genome-wide associations for birth weight and correlations with adult disease; Nature 2016 |
| 2710 | Jansen et al; Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk; Nature Genetics (2019) |
| 3049 | Howard et al; Genome-wide meta-analysis of depression in 807,553 individuals identifies 102 independent variants with replication in a further 1,507,153 individuals; Nature Neuroscience (2019) |
| 3459 | Lello et al; Genomic Prediction of 16 Complex Disease Risks Including Heart Attack, Diabetes, Breast and Prostate Cancer; Scientific Reports (2019) |
| 2898 | Timmers et al; Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances; eLife (2018) |
| 3301 | Wang, H. et al; Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank; Science Advances. 2019 |
| 1491 | Adewoye, A.B. et al.; Human CCL3L1 copy number variation, gene expression, and the role of the CCL3L1-CCR5 axis in lung function; Wellcome Open Research. 2018 |
| 1827 | Zenin et al; Identification of 12 genetic loci associated with human healthspan; Communications Biology 2019 |
| 3630 | Nalls et al; Identification of novel risk loci, causal insights, and heritable risk for Parkinson”s disease: a meta-analysis of genome-wide association studies; Lancet Neurology (2019) |
| 2883 | Mostafavi et al; Identifying genetic variants that affect viability in large cohorts; PLOS Biology (2017) |
| 1623 | Atkins et al; Impact of Low Cardiovascular Risk Profiles on Geriatric Outcomes: Evidence From 421,000 Participants in Two Cohorts; Journal of Gerontology: Medical Sciences. 2018 |
| 2245 | Canela-Xandri, O. et al; Improved Genetic Profiling of Anthropometric Traits Using a Big Data Approach; PLoS ONE. 2016. |
| 3255 | Lloyd-Jones, L.R. et al; Improved polygenic prediction by Bayesian multiple regression on summary statistics; Nature Communications. 2019 |
| 2154 | Border et al; Imputation of behavioral candidate gene repeat variants in 486,551 publicly-available UK Biobank individuals; European Journal of Human Genetics (2019) |
| 3202 | Nagel et al; Item-level Analyses Reveal Genetic Heterogeneity in Neuroticism; Nature Communications (2018) |
| 726 | Gazal et al; Linkage disequilibrium - dependent architecture of human complex traits shows action of negative selection; Nature Genetics 2017 |
| 2880 | Warrington et al.; Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors; Nature Genetics (2019) |
| 3444 | Brcic et al; Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank; Journal of Medical Genetics (2020) |
| 1701 | Crawford, K. et al; Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank; Journal of Medical Genetics. 2019. |
| 1969 | Nagel, M. et al; Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways; Nature Genetics. 2018 |
| 736 | Loh et al; Mixed model association for biobank-scale data sets.; BioRxiv 2018 |
| 2887 | Turley et al; Multi-trait analysis of genome-wide association summary statistics using MTAG; Nature Genetics (2018) |
| 542 | Young et al; Multiple novel gene-by-environment interactions modify the effect of FTO variants on body mass index; Nature Communications 2016 |
| 1943 | Shrine, N. et al; New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries; Nature Genetics. 2019 |
| 2893 | Vetter et al; Night Shift Work, Genetic Risk, and Type 2 Diabetes in the UK Biobank; Diabetes Care (2018) |
| 1782 | Van Kippersluis, H. & Rietveld, C.A.; Pleiotropy-robust Mendelian Randomization; International Journal of Epidemiology. 2017 |
| 3107 | Yao et al; Quantifying genetic effects on disease mediated by assayed gene expression levels; Nature Genetics (2020) |
| 776 | Mousas et al; Rare coding variants pinpoint genes that control human hematological traits; PLoS Genetics 2017 |
| 2818 | NA; Raw fluorescent probe data; NA |
| 735 | Pilling et al; Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers; PLos One 2017 |
| 3586 | Becker, J. et al; Resource Profile and User Guide of the Polygenic Index Repository; Nature Human Behavior. 2021 |
| 3662 | Flynn et al.,; Sex-specific genetic effects across biomarkers; European Journal of Human Genetics (2021) |
| 3461 | Lello et al; Sibling validation of polygenic risk scores and complex trait prediction; Scientific Reports (2020) |
| 3447 | Sidorenko et al.; The effect of X-linked dosage compensation on complex trait variation; Nature Communications (2019) |
| 263 | Joshi, et al.; Variants near CHRNA3/5 and APOE have age- and sex-related effects on human lifespan.; Nature Communications 2016 |
| 3123 | Le Guen Y. et al; eQTL of KCNK2 regionally influences the brain sulcal widening: evidence from 15,597 UK Biobank participants with neuroimaging data; Brain Structure and Function. 2019 |