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Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 62,482 bioRxiv papers from 277,419 authors.

Author: Namrata Gupta

  • Most recently observed institution: Center for Genomic Medicine, Massachusetts General Hospital

Rankings

  • All-time downloads: 47,925 (rank: 281 out of 277,419)
  • Categories:
    • genetics: 5,375 (rank: 2,581 out of 27,685)
    • genomics: 42,550 (rank: 122 out of 31,917)

Downloads per author, site-wide

Preprints

Analysis of protein-coding genetic variation in 60,706 humans

genomics more details view paper
  • Downloaded 21,430 times
  • Download rankings, all-time:
    • Site-wide: 24 out of 62,482
    • In genomics: 6 out of 4,297
  • Year to date:
    • Site-wide: 3,393 out of 62,482
  • Since beginning of last month:
    • Site-wide: 4,837 out of 62,482

Variation across 141,456 human exomes and genomes reveals the spectrum of loss-of-function intolerance across human protein-coding genes

genomics more details view paper
  • Downloaded 12,643 times
  • Download rankings, all-time:
    • Site-wide: 69 out of 62,482
    • In genomics: 20 out of 4,297
  • Year to date:
    • Site-wide: 9 out of 62,482
  • Since beginning of last month:
    • Site-wide: 26 out of 62,482

An open resource of structural variation for medical and population genetics

genomics more details view paper
  • Downloaded 6,715 times
  • Download rankings, all-time:
    • Site-wide: 239 out of 62,482
    • In genomics: 68 out of 4,297
  • Year to date:
    • Site-wide: 44 out of 62,482
  • Since beginning of last month:
    • Site-wide: 238 out of 62,482

Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum

genetics more details view paper
  • Downloaded 1,854 times
  • Download rankings, all-time:
    • Site-wide: 2,542 out of 62,482
    • In genetics: 236 out of 3,548
  • Year to date:
    • Site-wide: 27,144 out of 62,482
  • Since beginning of last month:
    • Site-wide: 19,755 out of 62,482

A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease

genomics more details view paper
  • Downloaded 1,425 times
  • Download rankings, all-time:
    • Site-wide: 3,961 out of 62,482
    • In genomics: 732 out of 4,297
  • Year to date:
    • Site-wide: 766 out of 62,482
  • Since beginning of last month:
    • Site-wide: 4,309 out of 62,482

Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals

genetics more details view paper
  • Downloaded 1,414 times
  • Download rankings, all-time:
    • Site-wide: 4,016 out of 62,482
    • In genetics: 349 out of 3,548
  • Year to date:
    • Site-wide: 776 out of 62,482
  • Since beginning of last month:
    • Site-wide: 6,384 out of 62,482

The Genetic Landscape of Diamond-Blackfan Anemia

genetics more details view paper
  • Downloaded 934 times
  • Download rankings, all-time:
    • Site-wide: 7,861 out of 62,482
    • In genetics: 613 out of 3,548
  • Year to date:
    • Site-wide: 18,277 out of 62,482
  • Since beginning of last month:
    • Site-wide: 34,148 out of 62,482

Case-control analysis identifies shared properties of rare germline variation in cancer predisposing genes

genetics more details view paper
  • Downloaded 554 times
  • Download rankings, all-time:
    • Site-wide: 16,738 out of 62,482
    • In genetics: 1,137 out of 3,548
  • Year to date:
    • Site-wide: 32,252 out of 62,482
  • Since beginning of last month:
    • Site-wide: 58,393 out of 62,482

Quality Control and Integration of Genotypes from Two Calling Pipelines for Whole Genome Sequence Data in the Alzheimer's Disease Sequencing Project

genetics more details view paper
  • Downloaded 479 times
  • Download rankings, all-time:
    • Site-wide: 20,125 out of 62,482
    • In genetics: 1,347 out of 3,548
  • Year to date:
    • Site-wide: 13,855 out of 62,482
  • Since beginning of last month:
    • Site-wide: 13,989 out of 62,482

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

genomics more details view paper
  • Downloaded 337 times
  • Download rankings, all-time:
    • Site-wide: 29,421 out of 62,482
    • In genomics: 2,927 out of 4,297
  • Year to date:
    • Site-wide: 9,310 out of 62,482
  • Since beginning of last month:
    • Site-wide: 6,545 out of 62,482

Heterozygous ATP-binding Cassette Transporter G5 Gene Deficiency and Risk of Coronary Artery Disease

genetics more details view paper
  • Downloaded 140 times
  • Download rankings, all-time:
    • Site-wide: 51,926 out of 62,482
    • In genetics: 3,057 out of 3,548
  • Year to date:
    • Site-wide: 29,744 out of 62,482
  • Since beginning of last month:
    • Site-wide: 1,808 out of 62,482

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