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Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 73,307 bioRxiv papers from 319,075 authors.

Author: Dan M. Roden

Rankings

  • All-time downloads: 5,586 (rank: 11,600 (tie) out of 319,209)
  • Categories:
    • genetics: 4,412 (rank: 3,309 (tie) out of 31,247)
    • genomics: 1,174 (rank: 12,554 (tie) out of 35,528)

Downloads per author, site-wide

Preprints

High-throughput discovery of trafficking-deficient variants in the cardiac potassium channel KCNH2

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No bioRxiv download data for this paper yet.

Inherited Causes of Clonal Hematopoiesis of Indeterminate Potential in TOPMed Whole Genomes

genomics more details view paper
  • Downloaded 1,174 times
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    • Site-wide: 6,654 out of 73,343
    • In genomics: 1,076 out of 4,869
  • Year to date:
    • Site-wide: 1,987 out of 73,343
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    • Site-wide: 1,987 out of 73,343

Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes

genetics more details view paper
  • Downloaded 656 times
  • Download rankings, all-time:
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    • In genetics: 1,113 out of 4,027
  • Year to date:
    • Site-wide: 31,777 out of 73,343
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    • Site-wide: 31,777 out of 73,343

Genetic determinants of risk and survival in pulmonary arterial hypertension

genetics more details view paper
  • Downloaded 561 times
  • Download rankings, all-time:
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    • In genetics: 1,355 out of 4,027
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    • Site-wide: 46,556 out of 73,343

Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity

genetics more details view paper
  • Downloaded 488 times
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    • In genetics: 1,602 out of 4,027
  • Year to date:
    • Site-wide: 61,536 out of 73,343
  • Since beginning of last month:
    • Site-wide: 61,536 out of 73,343

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

genetics more details view paper
  • Downloaded 464 times
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    • In genetics: 1,685 out of 4,027
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    • Site-wide: 39,415 out of 73,343
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    • Site-wide: 39,415 out of 73,343

Deep Mutational Scan of a cardiac sodium channel voltage sensor

genetics more details view paper
  • Downloaded 396 times
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    • In genetics: 1,953 out of 4,027
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    • Site-wide: 7,684 out of 73,343

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

genetics more details view paper
  • Downloaded 389 times
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    • Site-wide: 15,067 out of 73,343
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    • Site-wide: 15,067 out of 73,343

Mutations in RPL3L and MYZAP increase risk of atrial fibrillation

genetics more details view paper
  • Downloaded 359 times
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    • In genetics: 2,135 out of 4,027
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    • Site-wide: 63,567 out of 73,343
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    • Site-wide: 63,567 out of 73,343

High-throughput reclassification of SCN5A variants

genetics more details view paper
  • Downloaded 288 times
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    • In genetics: 2,529 out of 4,027
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    • Site-wide: 9,554 out of 73,343

A rare variant on a common risk haplotype of HFE causes increased risk of hereditary hemochromatosis

genetics more details view paper
  • Downloaded 284 times
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    • In genetics: 2,552 out of 4,027
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  • Since beginning of last month:
    • Site-wide: 31,096 out of 73,343

A Bayesian method using sparse data to estimate penetrance of disease-associated genetic variants

genetics more details view paper
  • Downloaded 282 times
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    • Site-wide: 43,095 out of 73,343
    • In genetics: 2,570 out of 4,027
  • Year to date:
    • Site-wide: 40,110 out of 73,343
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    • Site-wide: 40,110 out of 73,343

Temporal changes in genetic admixture are linked to heterozygosity and health diagnoses in humans

genetics more details view paper
  • Downloaded 245 times
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    • Site-wide: 47,970 out of 73,343
    • In genetics: 2,844 out of 4,027
  • Year to date:
    • Site-wide: 32,393 out of 73,343
  • Since beginning of last month:
    • Site-wide: 32,393 out of 73,343

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