Rxivist logo

Author: Mariza de Andrade

  • Most recently observed institution: Mayo Clinic

Rankings

  • All-time downloads: 18,558 (rank: 2,834 out of 361,589)
  • Categories:
    • genetics: 10,735 (rank: 1,101 out of 33,914)
    • genomics: 7,823 (rank: 1,878 out of 39,078)

Downloads per author, site-wide

Preprints

Recovery of trait heritability from whole genome sequence data

genetics more details view paper
  • Downloaded 9,496 times
  • Download rankings, all-time:
    • Site-wide: 243 out of 83,960
    • In genetics: 16 out of 4,413
  • Year to date:
    • Site-wide: 856 out of 83,960
  • Since beginning of last month:
    • Site-wide: 1,297 out of 83,960

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

genomics more details view paper
  • Downloaded 5,670 times
  • Download rankings, all-time:
    • Site-wide: 544 out of 83,960
    • In genomics: 112 out of 5,420
  • Year to date:
    • Site-wide: 599 out of 83,960
  • Since beginning of last month:
    • Site-wide: 596 out of 83,960

Inherited Causes of Clonal Hematopoiesis of Indeterminate Potential in TOPMed Whole Genomes

genomics more details view paper
  • Downloaded 1,702 times
  • Download rankings, all-time:
    • Site-wide: 4,415 out of 83,960
    • In genomics: 754 out of 5,420
  • Year to date:
    • Site-wide: 1,622 out of 83,960
  • Since beginning of last month:
    • Site-wide: 2,140 out of 83,960

Novel genetic determinants of telomere length from a multi-ethnic analysis of 75,000 whole genome sequences in TOPMed

genetics more details view paper
  • Downloaded 743 times
  • Download rankings, all-time:
    • Site-wide: 16,868 out of 83,960
    • In genetics: 1,102 out of 4,413
  • Year to date:
    • Site-wide: 6,089 out of 83,960
  • Since beginning of last month:
    • Site-wide: 8,170 out of 83,960

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

genetics more details view paper
  • Downloaded 496 times
  • Download rankings, all-time:
    • Site-wide: 29,418 out of 83,960
    • In genetics: 1,804 out of 4,413
  • Year to date:
    • Site-wide: 59,289 out of 83,960
  • Since beginning of last month:
    • Site-wide: 75,418 out of 83,960

Atlas-CNV: a validated approach to call Single-Exon CNVs in the eMERGESeq gene panel

genomics more details view paper
  • Downloaded 451 times
  • Download rankings, all-time:
    • Site-wide: 32,952 out of 83,960
    • In genomics: 3,249 out of 5,420
  • Year to date:
    • Site-wide: 60,846 out of 83,960
  • Since beginning of last month:
    • Site-wide: 53,044 out of 83,960

PanLingua

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


News