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Times Cited: 1865
Times Cited
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The UK Biobank resource with deep phenotyping and genomic data.
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A framework for the investigation of pleiotropy in two-sample summary data Mendelian randomization.
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Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure.
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Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA.
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An atlas of genetic correlations across human diseases and traits.
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Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.
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Mendelian randomization: genetic anchors for causal inference in epidemiological studies.
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Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes.
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Andrew P Morris, Benjamin F Voight, Tanya M Teslovich, Teresa Ferreira, Ayellet V Segrè, Valgerdur Steinthorsdottir, Rona J Strawbridge, Hassan Khan, Harald Grallert, Anubha Mahajan,[...]. Nat Genet 2012
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Bias due to participant overlap in two-sample Mendelian randomization.
Stephen Burgess, Neil M Davies, Simon G Thompson. Genet Epidemiol 2016
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Newly identified loci that influence lipid concentrations and risk of coronary artery disease.
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Orienting the causal relationship between imprecisely measured traits using GWAS summary data.
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Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry.
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Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.