Rxivist logo

Author: Namrata Gupta

  • Most recently observed institution: Program in Medical and Population Genetics, Broad Institute of Massachusetts Institute of Technology (M.I.T.) and Harvard

Rankings

  • All-time downloads: 64,197 (rank: 608 out of 423,771)
  • Categories:
    • genetics: 6,762 (rank: 2,721 out of 37,726)
    • genomics: 57,435 (rank: 112 out of 44,222)

Downloads per author, site-wide

Preprints

The mutational constraint spectrum quantified from variation in 141,456 humans

genomics more details view paper
  • Downloaded 22,459 times
  • Download rankings, all-time:
    • Site-wide: 69 out of 100,306
    • In genomics: 9 out of 6,221
  • Year to date:
    • Site-wide: 157 out of 100,306
  • Since beginning of last month:
    • Site-wide: None out of 100,306

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

genomics more details view paper
  • Downloaded 21,775 times
  • Download rankings, all-time:
    • Site-wide: 73 out of 100,306
    • In genomics: 10 out of 6,221
  • Year to date:
    • Site-wide: 21,214 out of 100,306
  • Since beginning of last month:
    • Site-wide: None out of 100,306

An open resource of structural variation for medical and population genetics

genomics more details view paper
  • Downloaded 10,408 times
  • Download rankings, all-time:
    • Site-wide: 244 out of 100,306
    • In genomics: 50 out of 6,221
  • Year to date:
    • Site-wide: 656 out of 100,306
  • Since beginning of last month:
    • Site-wide: None out of 100,306

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

genomics more details view paper
  • Downloaded 2,201 times
  • Download rankings, all-time:
    • Site-wide: 3,388 out of 100,306
    • In genomics: 606 out of 6,221
  • Year to date:
    • Site-wide: 5,844 out of 100,306
  • Since beginning of last month:
    • Site-wide: None out of 100,306

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

genetics more details view paper
  • Downloaded 2,168 times
  • Download rankings, all-time:
    • Site-wide: 3,480 out of 100,306
    • In genetics: 255 out of 4,997
  • Year to date:
    • Site-wide: 14,035 out of 100,306
  • Since beginning of last month:
    • Site-wide: None out of 100,306

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

genetics more details view paper
  • Downloaded 1,868 times
  • Download rankings, all-time:
    • Site-wide: 4,425 out of 100,306
    • In genetics: 317 out of 4,997
  • Year to date:
    • Site-wide: 13,623 out of 100,306
  • Since beginning of last month:
    • Site-wide: None out of 100,306

The Genetic Landscape of Diamond-Blackfan Anemia

genetics more details view paper
  • Downloaded 1,066 times
  • Download rankings, all-time:
    • Site-wide: 11,271 out of 100,306
    • In genetics: 747 out of 4,997
  • Year to date:
    • Site-wide: 51,954 out of 100,306
  • Since beginning of last month:
    • Site-wide: None out of 100,306

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 693 times
  • Download rankings, all-time:
    • Site-wide: 21,925 out of 100,306
    • In genetics: 1,367 out of 4,997
  • Year to date:
    • Site-wide: 26,501 out of 100,306
  • Since beginning of last month:
    • Site-wide: None out of 100,306

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

genetics more details view paper
  • Downloaded 651 times
  • Download rankings, all-time:
    • Site-wide: 24,045 out of 100,306
    • In genetics: 1,475 out of 4,997
  • Year to date:
    • Site-wide: 70,603 out of 100,306
  • Since beginning of last month:
    • Site-wide: None out of 100,306

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 592 times
  • Download rankings, all-time:
    • Site-wide: 27,505 out of 100,306
    • In genomics: 2,892 out of 6,221
  • Year to date:
    • Site-wide: 35,204 out of 100,306
  • Since beginning of last month:
    • Site-wide: None out of 100,306

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

genetics more details view paper
  • Downloaded 316 times
  • Download rankings, all-time:
    • Site-wide: 55,193 out of 100,306
    • In genetics: 3,055 out of 4,997
  • Year to date:
    • Site-wide: 47,651 out of 100,306
  • Since beginning of last month:
    • Site-wide: None out of 100,306

PanLingua

Sign up for the Rxivist weekly newsletter! (Click here for more details.)


News

  • 20 Oct 2020: Support for sorting preprints using Twitter activity has been removed, at least temporarily, until a new source of social media activity data becomes available.
  • 18 Dec 2019: We're pleased to announce PanLingua, a new tool that enables you to search for machine-translated bioRxiv preprints using more than 100 different languages.
  • 21 May 2019: PLOS Biology has published a community page about Rxivist.org and its design.
  • 10 May 2019: The paper analyzing the Rxivist dataset has been published at eLife.
  • 1 Mar 2019: We now have summary statistics about bioRxiv downloads and submissions.
  • 8 Feb 2019: Data from Altmetric is now available on the Rxivist details page for every preprint. Look for the "donut" under the download metrics.
  • 30 Jan 2019: preLights has featured the Rxivist preprint and written about our findings.
  • 22 Jan 2019: Nature just published an article about Rxivist and our data.
  • 13 Jan 2019: The Rxivist preprint is live!