Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 70,903 bioRxiv papers from 309,378 authors.

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Preprints

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

• Downloaded 21,578 times
• Download rankings, all-time:
  • Site-wide: 31 out of 70,927
  • In genomics: 7 out of 4,728
• Year to date:
  • Site-wide: 14,282 out of 70,927
• Since beginning of last month:
  • Site-wide: 18,453 out of 70,927

Genome-wide polygenic score to identify a monogenic risk-equivalent for coronary disease

• Downloaded 4,458 times
• Download rankings, all-time:
  • Site-wide: 588 out of 70,927
  • In genomics: 153 out of 4,728
• Year to date:
  • Site-wide: 5,995 out of 70,927
• Since beginning of last month:
  • Site-wide: 5,291 out of 70,927

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

• Downloaded 4,382 times
• Download rankings, all-time:
  • Site-wide: 608 out of 70,927
  • In genomics: 155 out of 4,728
• Year to date:
  • Site-wide: 1,125 out of 70,927
• Since beginning of last month:
  • Site-wide: 1,276 out of 70,927

Human knockouts in a cohort with a high rate of consanguinity

• Downloaded 2,399 times
• Download rankings, all-time:
  • Site-wide: 1,878 out of 70,927
  • In genomics: 409 out of 4,728
• Year to date:
  • Site-wide: 30,191 out of 70,927
• Since beginning of last month:
  • Site-wide: 43,367 out of 70,927

A statistical framework for cross-tissue transcriptome-wide association analysis

• Downloaded 2,344 times
• Download rankings, all-time:
  • Site-wide: 1,970 out of 70,927
  • In genetics: 180 out of 3,928
• Year to date:
  • Site-wide: 11,443 out of 70,927
• Since beginning of last month:
  • Site-wide: 4,441 out of 70,927

Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

• Downloaded 2,207 times
• Download rankings, all-time:
  • Site-wide: 2,178 out of 70,927
  • In genetics: 201 out of 3,928
• Year to date:
  • Site-wide: 36,098 out of 70,927
• Since beginning of last month:
  • Site-wide: 62,339 out of 70,927

Deep-coverage whole genome sequences and blood lipids among 16,324 individuals

• Downloaded 1,999 times
• Download rankings, all-time:
  • Site-wide: 2,590 out of 70,927
  • In genomics: 530 out of 4,728
• Year to date:
  • Site-wide: 65,140 out of 70,927
• Since beginning of last month:
  • Site-wide: 44,582 out of 70,927

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

• Downloaded 1,052 times
• Download rankings, all-time:
  • Site-wide: 7,639 out of 70,927
  • In genomics: 1,217 out of 4,728
• Year to date:
  • Site-wide: 3,293 out of 70,927
• Since beginning of last month:
  • Site-wide: 1,426 out of 70,927

Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores

• Downloaded 972 times
• Download rankings, all-time:
  • Site-wide: 8,705 out of 70,927
  • In genomics: 1,337 out of 4,728
• Year to date:
  • Site-wide: 6,714 out of 70,927
• Since beginning of last month:
  • Site-wide: 6,609 out of 70,927

Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms

• Downloaded 675 times
• Download rankings, all-time:
  • Site-wide: 15,141 out of 70,927
  • In genetics: 1,035 out of 3,928
• Year to date:
  • Site-wide: 67,828 out of 70,927
• Since beginning of last month:
  • Site-wide: 34,829 out of 70,927

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

• Downloaded 645 times
• Download rankings, all-time:
  • Site-wide: 16,176 out of 70,927
  • In genomics: 2,046 out of 4,728
• Year to date:
  • Site-wide: 60,681 out of 70,927
• Since beginning of last month:
  • Site-wide: 65,192 out of 70,927

Genetic predisposition to myeloproliferative neoplasms implicates hematopoietic stem cell biology

• Downloaded 528 times
• Download rankings, all-time:
  • Site-wide: 21,290 out of 70,927
  • In genetics: 1,419 out of 3,928
• Year to date:
  • Site-wide: 7,571 out of 70,927
• Since beginning of last month:
  • Site-wide: 4,952 out of 70,927

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

• Downloaded 510 times
• Download rankings, all-time:
  • Site-wide: 22,240 out of 70,927
  • In genomics: 2,500 out of 4,728
• Year to date:
  • Site-wide: 8,237 out of 70,927
• Since beginning of last month:
  • Site-wide: 17,212 out of 70,927

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

• Downloaded 383 times
• Download rankings, all-time:
  • Site-wide: 30,965 out of 70,927
  • In bioinformatics: 4,010 out of 6,940
• Year to date:
  • Site-wide: 40,217 out of 70,927
• Since beginning of last month:
  • Site-wide: 50,541 out of 70,927

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

• Downloaded 338 times
• Download rankings, all-time:
  • Site-wide: 35,134 out of 70,927
  • In physiology: 233 out of 909
• Year to date:
  • Site-wide: 8,253 out of 70,927
• Since beginning of last month:
  • Site-wide: 8,765 out of 70,927

Heterozygous ATP-binding Cassette Transporter G5 Gene Deficiency and Risk of Coronary Artery Disease

• Downloaded 215 times
• Download rankings, all-time:
  • Site-wide: 49,864 out of 70,927
  • In genetics: 2,968 out of 3,928
• Year to date:
  • Site-wide: 31,705 out of 70,927
• Since beginning of last month:
  • Site-wide: 17,991 out of 70,927