Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 62,709 bioRxiv papers from 278,266 authors.

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Preprints

Recovery of trait heritability from whole genome sequence data

• Downloaded 7,755 times
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  • In genetics: 19 out of 3,561
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  • Site-wide: 28 out of 62,709
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  • Site-wide: 374 out of 62,709

A reference panel of 64,976 haplotypes for genotype imputation

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  • Site-wide: 505 out of 62,709
  • In genetics: 54 out of 3,561
• Year to date:
  • Site-wide: 38,666 out of 62,709
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  • Site-wide: 36,506 out of 62,709

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

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  • In genomics: 190 out of 4,312
• Year to date:
  • Site-wide: 122 out of 62,709
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  • Site-wide: 332 out of 62,709

The PAGE Study: How Genetic Diversity Improves Our Understanding of the Architecture of Complex Traits

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  • In genetics: 137 out of 3,561
• Year to date:
  • Site-wide: 1,880 out of 62,709
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  • Site-wide: 7,264 out of 62,709

Narrow-sense heritability estimation of complex traits using identity-by-descent information.

• Downloaded 887 times
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  • In genetics: 639 out of 3,561
• Year to date:
  • Site-wide: 15,767 out of 62,709
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  • Site-wide: 28,799 out of 62,709

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

• Downloaded 628 times
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  • In genetics: 990 out of 3,561
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  • Site-wide: 10,610 out of 62,709
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  • Site-wide: 37,627 out of 62,709

Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes

• Downloaded 590 times
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  • In genetics: 1,072 out of 3,561
• Year to date:
  • Site-wide: 25,328 out of 62,709
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  • Site-wide: 24,642 out of 62,709

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 578 times
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  • In genetics: 1,089 out of 3,561
• Year to date:
  • Site-wide: 22,764 out of 62,709
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  • Site-wide: 26,598 out of 62,709

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

• Downloaded 526 times
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  • In genomics: 2,167 out of 4,312
• Year to date:
  • Site-wide: 4,486 out of 62,709
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  • Site-wide: 158 out of 62,709

Exome chip meta-analysis elucidates the genetic architecture of rare coding variants in smoking and drinking behavior

• Downloaded 473 times
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  • In genetics: 1,373 out of 3,561
• Year to date:
  • Site-wide: 43,566 out of 62,709
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  • Site-wide: 44,574 out of 62,709

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

• Downloaded 399 times
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  • Site-wide: 24,830 out of 62,709
  • In genomics: 2,642 out of 4,312
• Year to date:
  • Site-wide: 7,064 out of 62,709
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  • Site-wide: 13,205 out of 62,709

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 363 times
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  • Site-wide: 27,416 out of 62,709
  • In genomics: 2,802 out of 4,312
• Year to date:
  • Site-wide: 8,285 out of 62,709
• Since beginning of last month:
  • Site-wide: 19,611 out of 62,709

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

• Downloaded 337 times
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  • Site-wide: 29,497 out of 62,709
  • In genomics: 2,932 out of 4,312
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  • Site-wide: 9,366 out of 62,709
• Since beginning of last month:
  • Site-wide: 6,851 out of 62,709

Threshold trait architecture of Hsp90-buffered variation

• Downloaded 318 times
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  • Site-wide: 31,198 out of 62,709
  • In genetics: 1,976 out of 3,561
• Year to date:
  • Site-wide: 54,453 out of 62,709
• Since beginning of last month:
  • Site-wide: 44,617 out of 62,709

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

• Downloaded 264 times
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  • Site-wide: 36,559 out of 62,709
  • In genetics: 2,265 out of 3,561
• Year to date:
  • Site-wide: 13,688 out of 62,709
• Since beginning of last month:
  • Site-wide: 10,094 out of 62,709

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 184 times
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  • Site-wide: 46,038 out of 62,709
  • In genetics: 2,764 out of 3,561
• Year to date:
  • Site-wide: 22,088 out of 62,709
• Since beginning of last month:
  • Site-wide: 15,016 out of 62,709

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 172 times
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  • Site-wide: 47,657 out of 62,709
  • In epidemiology: 963 out of 1,556
• Year to date:
  • Site-wide: 23,884 out of 62,709
• Since beginning of last month:
  • Site-wide: 49,940 out of 62,709

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

• Downloaded 166 times
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  • Site-wide: 48,334 out of 62,709
  • In genetics: 2,879 out of 3,561
• Year to date:
  • Site-wide: 47,784 out of 62,709
• Since beginning of last month:
  • Site-wide: 52,144 out of 62,709

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

• Downloaded 131 times
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  • Site-wide: 53,221 out of 62,709
  • In epidemiology: 1,188 out of 1,556
• Year to date:
  • Site-wide: 31,868 out of 62,709
• Since beginning of last month:
  • Site-wide: 41,875 out of 62,709