Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 62,719 bioRxiv papers from 278,291 authors.

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Preprints

Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes

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  • In genetics: 1,070 out of 3,561
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  • Site-wide: 25,321 out of 62,719
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Genetic determinants of risk and survival in pulmonary arterial hypertension

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  • In genetics: 1,241 out of 3,561
• Year to date:
  • Site-wide: 33,343 out of 62,719
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Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity

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  • In genetics: 1,403 out of 3,561
• Year to date:
  • Site-wide: 43,700 out of 62,719
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Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

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  • In genetics: 1,635 out of 3,561
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Mutations in RPL3L and MYZAP increase risk of atrial fibrillation

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  • In genetics: 1,974 out of 3,561
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  • Site-wide: 55,446 out of 62,719
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  • Site-wide: 50,342 out of 62,719

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

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  • Site-wide: 36,556 out of 62,719
  • In genetics: 2,265 out of 3,561
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A Bayesian method using sparse data to estimate penetrance of disease-associated genetic variants

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  • In genetics: 2,479 out of 3,561
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  • Site-wide: 28,078 out of 62,719

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

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  • In genetics: 2,534 out of 3,561
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  • Site-wide: 27,938 out of 62,719

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

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  • In genetics: 2,732 out of 3,561
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  • Site-wide: 32,762 out of 62,719