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Author: Heiko Runz

Rankings

  • All-time downloads: 21,183 (rank: 8,347 (tie) )
  • Categories:
    • genetic and genomic medicine: 2,071 (rank: 784 (tie) )
    • genetics: 8,647 (rank: 2,061 )
    • genomics: 9,460 (rank: 2,048 )
    • neurology: 1,005 (rank: 863 (tie) )

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Preprints

Whole exome sequencing in the UK Biobank reveals risk gene SLC2A1 and biological insights for major depressive disorder

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Consequences Of Natural Perturbations In The Human Plasma Proteome

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  • Downloaded 4,262 times
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    • Site-wide: 2,603
    • In genomics: 283
  • Year to date:
    • Site-wide: 94,819
  • Since beginning of last month:
    • Site-wide: 93,591

Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases

genetics more details view paper
  • Downloaded 3,884 times
  • Download rankings, all-time:
    • Site-wide: 2,981
    • In genetics: 112
  • Year to date:
    • Site-wide: 10,001
  • Since beginning of last month:
    • Site-wide: 14,271

Phenome-wide association studies (PheWAS) across large "real-world data" population cohorts support drug target validation

genetics more details view paper
  • Downloaded 3,531 times
  • Download rankings, all-time:
    • Site-wide: 3,429
    • In genetics: 128
  • Year to date:
    • Site-wide: 42,065
  • Since beginning of last month:
    • Site-wide: 30,619

Phenotype-specific information improves prediction of functional impact for noncoding variants

genomics more details view paper
  • Downloaded 2,727 times
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    • Site-wide: 4,937
    • In genomics: 539
  • Year to date:
    • Site-wide: 87,015
  • Since beginning of last month:
    • Site-wide: 77,159

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

genetic and genomic medicine more details view paper
  • Downloaded 2,071 times
  • Download rankings, all-time:
    • Site-wide: 7,388
    • In genetic and genomic medicine: 25
  • Year to date:
    • Site-wide: 1,699
  • Since beginning of last month:
    • Site-wide: 3,556

New genetic signals for lung function highlight pathways and pleiotropy, and chronic obstructive pulmonary disease associations across multiple ancestries

genomics more details view paper
  • Downloaded 1,596 times
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    • Site-wide: 10,896
    • In genomics: 1,169
  • Year to date:
    • Site-wide: 68,158
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    • Site-wide: 50,744

The burden of rare protein-truncating genetic variants on human lifespan

genetics more details view paper
  • Downloaded 993 times
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    • Site-wide: 22,015
    • In genetics: 1,043
  • Year to date:
    • Site-wide: 37,131
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    • Site-wide: 51,406

Brain expression quantitative trait locus and network analysis reveals downstream effects and putative drivers for brain-related diseases

genomics more details view paper
  • Downloaded 875 times
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    • Site-wide: 26,427
    • In genomics: 2,464
  • Year to date:
    • Site-wide: 1,909
  • Since beginning of last month:
    • Site-wide: 1,849

Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

neurology more details view paper
  • Downloaded 825 times
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    • Site-wide: 28,692
    • In neurology: 52
  • Year to date:
    • Site-wide: 2,096
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    • Site-wide: 3,363

Pairwise genetic interactions modulate lipid plasma levels and cellular uptake

genetics more details view paper
  • Downloaded 239 times
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    • Site-wide: 101,704
    • In genetics: 4,491
  • Year to date:
    • Site-wide: 71,200
  • Since beginning of last month:
    • Site-wide: 100,439

Genome-wide study of DNA methylation in Amyotrophic Lateral Sclerosis identifies differentially methylated loci and implicates metabolic, inflammatory and cholesterol pathways

neurology more details view paper
  • Downloaded 180 times
  • Download rankings, all-time:
    • Site-wide: 115,130
    • In neurology: 409
  • Year to date:
    • Site-wide: 17,714
  • Since beginning of last month:
    • Site-wide: 10,869

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