Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 62,102 bioRxiv papers from 275,834 authors.

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Preprints

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: 261 out of 4,270
• Year to date:
  • Site-wide: 10,163 out of 62,183
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  • Site-wide: 9,482 out of 62,183

Human pancreatic islet 3D chromatin architecture provides insights into the genetics of type 2 diabetes

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  • In genomics: 410 out of 4,270
• Year to date:
  • Site-wide: 1,411 out of 62,183
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  • Site-wide: 11,813 out of 62,183

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

• Downloaded 1,654 times
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  • In genetics: 268 out of 3,530
• Year to date:
  • Site-wide: 21,997 out of 62,183
• Since beginning of last month:
  • Site-wide: 28,507 out of 62,183

Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries

• Downloaded 1,381 times
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  • Site-wide: 4,105 out of 62,183
  • In genetics: 354 out of 3,530
• Year to date:
  • Site-wide: 3,253 out of 62,183
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  • Site-wide: 15,341 out of 62,183

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

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  • In genetics: 479 out of 3,530
• Year to date:
  • Site-wide: 3,152 out of 62,183
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  • Site-wide: 9,983 out of 62,183

A Comprehensive Reanalysis Of Publicly Available GWAS Datasets Reveals An X Chromosome Rare Regulatory Variant Associated With High Risk For Type 2 Diabetes.

• Downloaded 1,091 times
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  • In genetics: 489 out of 3,530
• Year to date:
  • Site-wide: 24,942 out of 62,183
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  • Site-wide: 20,688 out of 62,183

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

• Downloaded 988 times
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  • Site-wide: 7,084 out of 62,183
  • In genetics: 557 out of 3,530
• Year to date:
  • Site-wide: 2,527 out of 62,183
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  • Site-wide: 12,103 out of 62,183

Selection on the FADS region in Europeans

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  • In genetics: 690 out of 3,530
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  • Site-wide: 42,769 out of 62,183
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A common allele in FGF21 associated with preference for sugar consumption lowers body fat in the lower body and increases blood pressure

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  • In genetics: 822 out of 3,530
• Year to date:
  • Site-wide: 26,340 out of 62,183
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  • Site-wide: 21,475 out of 62,183

Extreme distribution of deleterious variation in a historically small and isolated population-insights from the Greenlandic Inuit

• Downloaded 684 times
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  • In genetics: 874 out of 3,530
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  • Site-wide: 43,126 out of 62,183
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  • Site-wide: 31,837 out of 62,183

Estimating narrow-sense heritability from genome-wide data in admixed populations

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  • In genetics: 1,601 out of 3,530
• Year to date:
  • Site-wide: 6,668 out of 62,183
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  • Site-wide: None out of 62,183

Meta-analysis of exome array data identifies six novel genetic loci for lung function

• Downloaded 374 times
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  • Site-wide: 26,143 out of 62,183
  • In genetics: 1,711 out of 3,530
• Year to date:
  • Site-wide: 55,681 out of 62,183
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  • Site-wide: 38,013 out of 62,183

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

• Downloaded 374 times
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  • Site-wide: 26,093 out of 62,183
  • In genetics: 1,709 out of 3,530
• Year to date:
  • Site-wide: 34,383 out of 62,183
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  • Site-wide: 50,774 out of 62,183

Exome-wide association study on Albuminuria identifies a novel rare variant in CUBN and additional genes, in 33,985 Europeans with and without diabetes

• Downloaded 156 times
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  • Site-wide: 49,015 out of 62,183
  • In genetics: 2,921 out of 3,530
• Year to date:
  • Site-wide: 54,011 out of 62,183
• Since beginning of last month:
  • Site-wide: None out of 62,183