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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: 63,295 (rank: 565 out of 383,431)
  • Categories:
    • genetics: 6,568 (rank: 2,673 out of 35,367)
    • genomics: 56,727 (rank: 113 out of 40,807)

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Preprints

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

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    • In genomics: 8 out of 5,699
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    • Site-wide: 136 out of 89,473
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    • Site-wide: 312 out of 89,473

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

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  • Downloaded 21,746 times
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    • In genomics: 9 out of 5,699
  • Year to date:
    • Site-wide: 18,213 out of 89,473
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    • Site-wide: 31,119 out of 89,473

An open resource of structural variation for medical and population genetics

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  • Downloaded 10,276 times
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    • Site-wide: 228 out of 89,473
    • In genomics: 46 out of 5,699
  • Year to date:
    • Site-wide: 529 out of 89,473
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    • Site-wide: 1,434 out of 89,473

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

genomics more details view paper
  • Downloaded 2,171 times
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    • Site-wide: 3,191 out of 89,473
    • In genomics: 593 out of 5,699
  • Year to date:
    • Site-wide: 4,302 out of 89,473
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    • Site-wide: 17,757 out of 89,473

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

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  • Downloaded 2,093 times
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    • In genetics: 261 out of 4,625
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    • Site-wide: 15,086 out of 89,473
  • Since beginning of last month:
    • Site-wide: 10,761 out of 89,473

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

genetics more details view paper
  • Downloaded 1,833 times
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    • Site-wide: 4,220 out of 89,473
    • In genetics: 311 out of 4,625
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    • Site-wide: 11,251 out of 89,473
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    • Site-wide: 28,344 out of 89,473

The Genetic Landscape of Diamond-Blackfan Anemia

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  • Downloaded 1,050 times
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    • In genetics: 718 out of 4,625
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    • Site-wide: 47,630 out of 89,473

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 650 times
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    • In genetics: 1,397 out of 4,625
  • Year to date:
    • Site-wide: 26,769 out of 89,473
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    • Site-wide: 29,537 out of 89,473

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

genetics more details view paper
  • Downloaded 639 times
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    • Site-wide: 22,725 out of 89,473
    • In genetics: 1,430 out of 4,625
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    • Site-wide: 67,632 out of 89,473

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 580 times
  • Download rankings, all-time:
    • Site-wide: 26,044 out of 89,473
    • In genomics: 2,802 out of 5,699
  • Year to date:
    • Site-wide: 28,264 out of 89,473
  • Since beginning of last month:
    • Site-wide: 43,229 out of 89,473

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

genetics more details view paper
  • Downloaded 303 times
  • Download rankings, all-time:
    • Site-wide: 52,862 out of 89,473
    • In genetics: 2,984 out of 4,625
  • Year to date:
    • Site-wide: 41,017 out of 89,473
  • Since beginning of last month:
    • Site-wide: 31,087 out of 89,473

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