Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 57,506 bioRxiv papers from 264,779 authors.

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Preprints

Recovery of trait heritability from whole genome sequence data

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  • Site-wide: 352 out of 57,506

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

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  • In genomics: 234 out of 4,027
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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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  • In genomics: 253 out of 4,027
• Year to date:
  • Site-wide: 10,261 out of 57,506
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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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  • In genetics: 115 out of 3,295
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  • Site-wide: 12,035 out of 57,506
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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

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  • In genetics: 261 out of 3,295
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PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

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  • In genetics: 474 out of 3,295
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  • Site-wide: 2,646 out of 57,506
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  • Site-wide: 10,190 out of 57,506

Genetic architecture of gene expression traits across diverse populations

• Downloaded 976 times
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  • In genomics: 1,101 out of 4,027
• Year to date:
  • Site-wide: 13,113 out of 57,506
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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: 651 out of 3,295
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  • Site-wide: 3,131 out of 57,506
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Identification of type 2 diabetes loci in 433,540 East Asian individuals

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  • In genetics: 765 out of 3,295
• Year to date:
  • Site-wide: 1,841 out of 57,506
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  • Site-wide: 392 out of 57,506

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: 961 out of 3,295
• Year to date:
  • Site-wide: 8,534 out of 57,506
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  • Site-wide: 18,701 out of 57,506

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

• Downloaded 577 times
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  • In genomics: 1,883 out of 4,027
• Year to date:
  • Site-wide: 36,649 out of 57,506
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  • Site-wide: 35,811 out of 57,506

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 553 times
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  • In genetics: 1,068 out of 3,295
• Year to date:
  • Site-wide: 20,663 out of 57,506
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  • Site-wide: 27,026 out of 57,506

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

• Downloaded 348 times
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  • In genomics: 2,699 out of 4,027
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  • Site-wide: 16,932 out of 57,506

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

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  • In genomics: 2,771 out of 4,027
• Year to date:
  • Site-wide: 7,002 out of 57,506
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  • Site-wide: 30,631 out of 57,506

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

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  • In physiology: 379 out of 674
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  • Site-wide: 31,257 out of 57,506
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  • Site-wide: 27,065 out of 57,506

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

• Downloaded 163 times
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  • In genetics: 2,701 out of 3,295
• Year to date:
  • Site-wide: 19,331 out of 57,506
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  • Site-wide: 1,634 out of 57,506

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

• Downloaded 157 times
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  • Site-wide: 45,250 out of 57,506
  • In genetics: 2,741 out of 3,295
• Year to date:
  • Site-wide: 42,833 out of 57,506
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  • Site-wide: 49,654 out of 57,506

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

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  • In genetics: 2,787 out of 3,295
• Year to date:
  • Site-wide: 41,242 out of 57,506
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  • Site-wide: 43,994 out of 57,506

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

• Downloaded 145 times
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  • In genetics: 2,809 out of 3,295
• Year to date:
  • Site-wide: 22,204 out of 57,506
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  • Site-wide: 20,265 out of 57,506

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

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  • Site-wide: 47,851 out of 57,506
  • In genetics: 2,869 out of 3,295
• Year to date:
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  • Site-wide: 25,197 out of 57,506

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

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  • In epidemiology: 1,162 out of 1,556
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  • Site-wide: 43,645 out of 57,506