Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 67,594 bioRxiv papers from 298,341 authors.

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Preprints

Recovery of trait heritability from whole genome sequence data

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  • Site-wide: 658 out of 67,594

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

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

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  • In genetics: 131 out of 3,799
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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

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PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

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Genetic architecture of gene expression traits across diverse populations

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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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Identification of type 2 diabetes loci in 433,540 East Asian individuals

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  • Site-wide: 11,376 out of 67,594

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

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  • In genomics: 1,414 out of 4,581
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  • Site-wide: 2,439 out of 67,594
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  • Site-wide: 1,173 out of 67,594

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: 1,032 out of 3,799
• Year to date:
  • Site-wide: 12,990 out of 67,594
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  • Site-wide: 43,716 out of 67,594

Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes

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  • In genetics: 1,096 out of 3,799
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  • Site-wide: 26,783 out of 67,594
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  • Site-wide: 26,943 out of 67,594

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

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  • In genomics: 2,070 out of 4,581
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  • Site-wide: 48,118 out of 67,594

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

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  • In genetics: 1,138 out of 3,799
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  • Site-wide: 37,798 out of 67,594

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

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  • In genomics: 2,529 out of 4,581
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  • Site-wide: 13,253 out of 67,594

Novel genetic determinants of telomere length from a multi-ethnic analysis of 75,000 whole genome sequences in TOPMed

• Downloaded 424 times
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  • In genetics: 1,687 out of 3,799
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  • Site-wide: 5,380 out of 67,594

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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  • Site-wide: 24,792 out of 67,594

Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

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  • In genetics: 1,982 out of 3,799
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  • Site-wide: 3,938 out of 67,594

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

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  • In genetics: 2,105 out of 3,799
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  • Site-wide: 15,227 out of 67,594

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

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  • In genetics: 2,748 out of 3,799
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  • Site-wide: 28,197 out of 67,594

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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  • In genetics: 2,753 out of 3,799
• Year to date:
  • Site-wide: 22,656 out of 67,594
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  • Site-wide: 21,633 out of 67,594

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

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  • Site-wide: 46,449 out of 67,594
  • In physiology: 400 out of 853
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  • Site-wide: 49,947 out of 67,594

Multi-ethnic genome-wide association study of decomposed cardioelectric phenotypes illustrates strategies to identify and characterize evidence of shared genetic effects for complex traits

• Downloaded 197 times
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  • Site-wide: 49,234 out of 67,594
  • In epidemiology: 970 out of 1,556
• Year to date:
  • Site-wide: 26,457 out of 67,594
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  • Site-wide: 37,768 out of 67,594

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

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  • In genetics: 3,053 out of 3,799
• Year to date:
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  • Site-wide: 42,488 out of 67,594

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

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  • In epidemiology: 1,238 out of 1,556
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  • Site-wide: 49,034 out of 67,594