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Times Cited: 585
Times Cited: 585
Times Cited
Times Co-cited
Similarity
Next-generation genotype imputation service and methods.
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A reference panel of 64,976 haplotypes for genotype imputation.
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A global reference for human genetic variation.
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The UK Biobank resource with deep phenotyping and genomic data.
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LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.
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An atlas of genetic correlations across human diseases and traits.
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MAGMA: generalized gene-set analysis of GWAS data.
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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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Annotation of functional variation in personal genomes using RegulomeDB.
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Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.
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The mutational constraint spectrum quantified from variation in 141,456 humans.
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Clinical use of current polygenic risk scores may exacerbate health disparities.
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Genetic effects on gene expression across human tissues.
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Integrating common and rare genetic variation in diverse human populations.
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The Sequence Alignment/Map format and SAMtools.
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minimac2: faster genotype imputation.
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Fast and accurate short read alignment with Burrows-Wheeler transform.
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The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
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Common SNPs explain a large proportion of the heritability for human height.
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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.