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Author: Suganthi Balasubramanian

Rankings

  • All-time downloads: 26,892 (rank: 10,063 )
  • Categories:
    • bioinformatics: 1,312 (rank: 14,692 (tie) )
    • genetic and genomic medicine: 8,000 (rank: 197 )
    • genomics: 16,662 (rank: 1,071 (tie) )

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Preprints

Whole exome sequencing and characterization of coding variation in 49,960 individuals in the UK Biobank

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    • Site-wide: 796
    • In genomics: 34
  • Year to date:
    • Site-wide: 8,552
  • Since beginning of last month:
    • Site-wide: 7,961

Genome-wide analysis in 756,646 individuals provides first genetic evidence that ACE2 expression influences COVID-19 risk and yields genetic risk scores predictive of severe disease

genetic and genomic medicine more details view paper
  • Downloaded 4,478 times
  • Download rankings, all-time:
    • Site-wide: 3,677
    • In genetic and genomic medicine: 16
  • Year to date:
    • Site-wide: 2,933
  • Since beginning of last month:
    • Site-wide: 3,086

Advancing Human Genetics Research and Drug Discovery through Exome Sequencing of the UK Biobank

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  • Downloaded 3,374 times
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    • Site-wide: 5,507
    • In genetic and genomic medicine: 27
  • Year to date:
    • Site-wide: 8,459
  • Since beginning of last month:
    • Site-wide: 11,931

Determining the impact of putative loss-of-function variants in protein-coding genes

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    • Site-wide: 19,892
    • In genomics: 1,705
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    • Site-wide: 177,798
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Enhanced Transcriptome Maps from Multiple Mouse Tissues Reveal Evolutionary Constraint in Gene Expression for Thousands of Genes

bioinformatics more details view paper
  • Downloaded 1,043 times
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    • Site-wide: 32,001
    • In bioinformatics: 3,246
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    • Site-wide: 161,046
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    • Site-wide: 142,070

Profiling and leveraging relatedness in a precision medicine cohort of 92,455 exomes

genomics more details view paper
  • Downloaded 980 times
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    • Site-wide: 35,159
    • In genomics: 2,745
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    • Site-wide: 150,506
  • Since beginning of last month:
    • Site-wide: 134,851

Population-scale analysis of common and rare genetic variation associated with hearing loss in adults

genetic and genomic medicine more details view paper
  • Downloaded 754 times
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    • Site-wide: 51,655
    • In genetic and genomic medicine: 314
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    • Site-wide: 18,646
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    • Site-wide: 24,293

Validating gene-phenotype associations using relationships in the UMLS

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  • Downloaded 335 times
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    • Site-wide: 128,213
    • In bioinformatics: 10,369
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