Rxivist logo

Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 73,249 bioRxiv papers from 318,847 authors.

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: 55,294 (rank: 292 out of 318,928)
  • Categories:
    • genetics: 5,916 (rank: 2,643 out of 31,247)
    • genomics: 49,378 (rank: 115 out of 35,528)

Downloads per author, site-wide

Preprints

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

genomics more details view paper
  • Downloaded 21,590 times
  • Download rankings, all-time:
    • Site-wide: 33 out of 73,279
    • In genomics: 7 out of 4,867
  • Year to date:
    • Site-wide: 22,050 out of 73,279
  • Since beginning of last month:
    • Site-wide: 22,050 out of 73,279

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 16,691 times
  • Download rankings, all-time:
    • Site-wide: 48 out of 73,279
    • In genomics: 10 out of 4,867
  • Year to date:
    • Site-wide: 75 out of 73,279
  • Since beginning of last month:
    • Site-wide: 75 out of 73,279

An open resource of structural variation for medical and population genetics

genomics more details view paper
  • Downloaded 8,772 times
  • Download rankings, all-time:
    • Site-wide: 183 out of 73,279
    • In genomics: 51 out of 4,867
  • Year to date:
    • Site-wide: 279 out of 73,279
  • Since beginning of last month:
    • Site-wide: 279 out of 73,279

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

genetics more details view paper
  • Downloaded 1,898 times
  • Download rankings, all-time:
    • Site-wide: 2,954 out of 73,279
    • In genetics: 257 out of 4,026
  • Year to date:
    • Site-wide: 44,753 out of 73,279
  • Since beginning of last month:
    • Site-wide: 44,753 out of 73,279

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

genomics more details view paper
  • Downloaded 1,835 times
  • Download rankings, all-time:
    • Site-wide: 3,127 out of 73,279
    • In genomics: 608 out of 4,867
  • Year to date:
    • Site-wide: 2,694 out of 73,279
  • Since beginning of last month:
    • Site-wide: 2,694 out of 73,279

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

genetics more details view paper
  • Downloaded 1,674 times
  • Download rankings, all-time:
    • Site-wide: 3,660 out of 73,279
    • In genetics: 303 out of 4,026
  • Year to date:
    • Site-wide: 4,741 out of 73,279
  • Since beginning of last month:
    • Site-wide: 4,741 out of 73,279

The Genetic Landscape of Diamond-Blackfan Anemia

genetics more details view paper
  • Downloaded 986 times
  • Download rankings, all-time:
    • Site-wide: 8,866 out of 73,279
    • In genetics: 658 out of 4,026
  • Year to date:
    • Site-wide: 32,389 out of 73,279
  • Since beginning of last month:
    • Site-wide: 32,389 out of 73,279

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

genetics more details view paper
  • Downloaded 593 times
  • Download rankings, all-time:
    • Site-wide: 19,083 out of 73,279
    • In genetics: 1,264 out of 4,026
  • Year to date:
    • Site-wide: 50,849 out of 73,279
  • Since beginning of last month:
    • Site-wide: 50,849 out of 73,279

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 532 times
  • Download rankings, all-time:
    • Site-wide: 22,031 out of 73,279
    • In genetics: 1,462 out of 4,026
  • Year to date:
    • Site-wide: 34,599 out of 73,279
  • Since beginning of last month:
    • Site-wide: 34,599 out of 73,279

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 490 times
  • Download rankings, all-time:
    • Site-wide: 24,446 out of 73,279
    • In genomics: 2,642 out of 4,867
  • Year to date:
    • Site-wide: 13,426 out of 73,279
  • Since beginning of last month:
    • Site-wide: 13,426 out of 73,279

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

genetics more details view paper
  • Downloaded 233 times
  • Download rankings, all-time:
    • Site-wide: 49,526 out of 73,279
    • In genetics: 2,933 out of 4,026
  • Year to date:
    • Site-wide: 24,037 out of 73,279
  • Since beginning of last month:
    • Site-wide: 24,037 out of 73,279

PanLingua

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


News