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Times Cited: 1186
Times Cited: 1186
Times Cited
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PLINK: a tool set for whole-genome association and population-based linkage analyses.
Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
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Second-generation PLINK: rising to the challenge of larger and richer datasets.
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A reference panel of 64,976 haplotypes for genotype imputation.
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Reference-based phasing using the Haplotype Reference Consortium panel.
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A global reference for human genetic variation.
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Principal components analysis corrects for stratification in genome-wide association studies.
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LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.
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Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing.
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Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.
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Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk.
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Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.
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PRSice-2: Polygenic Risk Score software for biobank-scale data.
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Tutorial: a guide to performing polygenic risk score analyses.
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The personal and clinical utility of polygenic risk scores.
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Fast and accurate long-range phasing in a UK Biobank cohort.
Po-Ru Loh, Pier Francesco Palamara, Alkes L Price. Nat Genet 2016
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Genotype imputation for genome-wide association studies.
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A new multipoint method for genome-wide association studies by imputation of genotypes.
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LocusZoom: regional visualization of genome-wide association scan results.
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The UK Biobank resource with deep phenotyping and genomic data.
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Genetic effects on gene expression across human tissues.
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Polygenic prediction via Bayesian regression and continuous shrinkage priors.
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Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.
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Partitioning heritability by functional annotation using genome-wide association summary statistics.
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The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019.
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Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering.
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Improved whole-chromosome phasing for disease and population genetic studies.
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Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders.
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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.