Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 60,161 bioRxiv papers from 267,433 authors.

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Preprints

Heart Rate Variability with Photoplethysmography in 8 Million Individuals: Results and Scaling Relations with Age, Gender, and Time of Day

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Analysis of protein-coding genetic variation in 60,706 humans

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  • In genomics: 5 out of 4,168
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Genome-wide polygenic score to identify a monogenic risk-equivalent for coronary disease

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  • In genomics: 138 out of 4,168
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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

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Human knockouts in a cohort with a high rate of consanguinity

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  • In genomics: 364 out of 4,168
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Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

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  • In genetics: 180 out of 3,431
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A statistical framework for cross-tissue transcriptome-wide association analysis

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  • In genetics: 194 out of 3,431
• Year to date:
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Deep-coverage whole genome sequences and blood lipids among 16,324 individuals

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  • In genomics: 474 out of 4,168
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Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms

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  • In genetics: 942 out of 3,431
• Year to date:
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  • Site-wide: 57,504 out of 60,161

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

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  • In genomics: 1,851 out of 4,168
• Year to date:
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  • Site-wide: 55,784 out of 60,161

Loss-of-function genomic variants with impact on liver-related blood traits highlight potential therapeutic targets for cardiovascular disease

• Downloaded 376 times
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  • In genomics: 2,658 out of 4,168
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  • Site-wide: 16,394 out of 60,161

Genetic Association of Arterial Stiffness Index with Blood Pressure and Coronary Artery Disease

• Downloaded 348 times
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  • Site-wide: 27,375 out of 60,161
  • In bioinformatics: 3,699 out of 6,077
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