Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 52,985 bioRxiv papers from 245,402 authors.

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Preprints

Recovery of trait heritability from whole genome sequence data

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  • Site-wide: 42 out of 52,985

Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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  • In genetics: 113 out of 3,086
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  • Site-wide: 12,061 out of 52,985
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  • Site-wide: 9,318 out of 52,985

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

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  • In genomics: 277 out of 3,779
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  • Site-wide: 226 out of 52,985

Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

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  • In genetics: 246 out of 3,086
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PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

• Downloaded 973 times
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  • In genetics: 504 out of 3,086
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  • Site-wide: 2,337 out of 52,985
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  • Site-wide: 3,977 out of 52,985

Genetic architecture of gene expression traits across diverse populations

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  • In genomics: 1,079 out of 3,779
• Year to date:
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  • Site-wide: 21,286 out of 52,985

Genome-wide association and functional studies identify 46 novel loci for alcohol consumption and suggest common genetic mechanisms with neuropsychiatric disorders

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  • In genetics: 711 out of 3,086
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  • Site-wide: 3,119 out of 52,985
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  • Site-wide: 7,762 out of 52,985

Efficient variant set mixed model association tests for continuous and binary traits in large-scale whole genome sequencing studies

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  • In genetics: 959 out of 3,086
• Year to date:
  • Site-wide: 7,250 out of 52,985
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  • Site-wide: 15,404 out of 52,985

Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

• Downloaded 555 times
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  • In genomics: 1,790 out of 3,779
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  • Site-wide: 31,954 out of 52,985
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  • Site-wide: 25,507 out of 52,985

Trans-ethnic genome-wide association study provides insight into effector genes and molecular mechanisms for kidney function and highlights a causal effect on kidney-specific disease aetiologies

• Downloaded 519 times
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  • In genetics: 1,044 out of 3,086
• Year to date:
  • Site-wide: 18,295 out of 52,985
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  • Site-wide: 16,168 out of 52,985

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

• Downloaded 296 times
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  • In genomics: 2,692 out of 3,779
• Year to date:
  • Site-wide: 5,294 out of 52,985
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  • Site-wide: 4,596 out of 52,985

Multi-ancestry analysis of gene-sleep interactions in 126,926 individuals identifies multiple novel blood lipid loci that contribute to our understanding of sleep-associated adverse blood lipid profile

• Downloaded 295 times
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  • In genomics: 2,696 out of 3,779
• Year to date:
  • Site-wide: 5,333 out of 52,985
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  • Site-wide: 16,387 out of 52,985

GWAS of QRS Duration Identifies New Loci Specific to Hispanic/Latino Populations

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  • In genetics: 2,572 out of 3,086
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  • Site-wide: 36,669 out of 52,985

Adiposity-Independent Effects of Aging on Insulin Sensitivity and Clearance in Humans and Mice

• Downloaded 136 times
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  • Site-wide: 42,953 out of 52,985
  • In physiology: 375 out of 602
• Year to date:
  • Site-wide: 28,734 out of 52,985
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  • Site-wide: 23,376 out of 52,985

Evaluation of the causal effect of fibrinogen on incident coronary heart disease via Mendelian randomization

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  • In genetics: 2,682 out of 3,086
• Year to date:
  • Site-wide: 35,560 out of 52,985
• Since beginning of last month:
  • Site-wide: 42,774 out of 52,985

Whole-Genome Association Analyses of Sleep-disordered Breathing Phenotypes in the NHLBI TOPMed Program

• Downloaded 106 times
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  • In genetics: 2,799 out of 3,086
• Year to date:
  • Site-wide: 20,988 out of 52,985
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  • Site-wide: 3,938 out of 52,985

Role of Rare and Low Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels

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  • In epidemiology: 1,096 out of 1,543
• Year to date:
  • Site-wide: 22,246 out of 52,985
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  • Site-wide: 22,035 out of 52,985

Impact of rare and common genetic variants on diabetes diagnosis by hemoglobin A1c in multi-ancestry cohorts: The Trans-Omics for Precision Medicine Program.

• Downloaded 98 times
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  • Site-wide: 47,434 out of 52,985
  • In genetics: 2,843 out of 3,086
• Year to date:
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• Since beginning of last month:
  • Site-wide: 4,459 out of 52,985