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 |
777 | Lessard et al; An erythroid-specific ATP2B4 enhancer mediates red blood cell hydration and malaria susceptibility; Journal of Clinical Investigation 2017 |
3065 | Nave et al; Are Bigger Brains Smarter? Evidence From a Large-Scale Preregistered Study; Psychological Science (2018) |
2881 | Thompson et al; Association of maternal circulating 25(OH)D and calcium with birth weight: A mendelian randomisation analysis; PLoS Medicine (2019) |
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 |
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) |
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 |
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) |
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) |
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 |
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) |
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 |
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) |
2898 | Timmers et al; Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances; eLife (2018) |
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 |
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 |
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) |
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) |
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 |
263 | Joshi, et al.; Variants near CHRNA3/5 and APOE have age- and sex-related effects on human lifespan.; Nature Communications 2016 |