Rxivist logo

Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 73,081 bioRxiv papers from 318,132 authors.

Author: Harrison Brand

  • Most recently observed institution: Department of Neurology, Massachusetts General Hospital and Harvard Medical School

Rankings

  • All-time downloads: 48,819 (rank: 344 out of 318,152)
  • Categories:
    • bioinformatics: 2,076 (rank: 4,113 (tie) out of 27,611)
    • genetics: 8,488 (rank: 1,441 (tie) out of 31,250)
    • genomics: 38,255 (rank: 151 out of 35,572)

Downloads per author, site-wide

Preprints

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 73,076
    • In genomics: 10 out of 4,853
  • Year to date:
    • Site-wide: 71 out of 73,076
  • Since beginning of last month:
    • Site-wide: 71 out of 73,076

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 73,076
    • In genomics: 51 out of 4,853
  • Year to date:
    • Site-wide: 252 out of 73,076
  • Since beginning of last month:
    • Site-wide: 252 out of 73,076

Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

genetics more details view paper
  • Downloaded 8,078 times
  • Download rankings, all-time:
    • Site-wide: 211 out of 73,076
    • In genetics: 22 out of 4,015
  • Year to date:
    • Site-wide: 145 out of 73,076
  • Since beginning of last month:
    • Site-wide: 145 out of 73,076

Multi-platform discovery of haplotype-resolved structural variation in human genomes

genomics more details view paper
  • Downloaded 8,030 times
  • Download rankings, all-time:
    • Site-wide: 214 out of 73,076
    • In genomics: 56 out of 4,853
  • Year to date:
    • Site-wide: 14,013 out of 73,076
  • Since beginning of last month:
    • Site-wide: 14,013 out of 73,076

Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families

genomics more details view paper
  • Downloaded 2,361 times
  • Download rankings, all-time:
    • Site-wide: 2,019 out of 73,076
    • In genomics: 428 out of 4,853
  • Year to date:
    • Site-wide: 50,732 out of 73,076
  • Since beginning of last month:
    • Site-wide: 50,732 out of 73,076

CNView: a visualization and annotation tool for copy number variation from whole-genome sequencing

bioinformatics more details view paper
  • Downloaded 2,076 times
  • Download rankings, all-time:
    • Site-wide: 2,515 out of 73,076
    • In bioinformatics: 500 out of 7,134
  • Year to date:
    • Site-wide: 11,676 out of 73,076
  • Since beginning of last month:
    • Site-wide: 11,676 out of 73,076

Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly

genomics more details view paper
  • Downloaded 1,097 times
  • Download rankings, all-time:
    • Site-wide: 7,418 out of 73,076
    • In genomics: 1,176 out of 4,853
  • Year to date:
    • Site-wide: 35,314 out of 73,076
  • Since beginning of last month:
    • Site-wide: 35,314 out of 73,076

Functional annotation of rare structural variation in the human brain

genomics more details view paper
  • Downloaded 715 times
  • Download rankings, all-time:
    • Site-wide: 14,499 out of 73,076
    • In genomics: 1,906 out of 4,853
  • Year to date:
    • Site-wide: 4,350 out of 73,076
  • Since beginning of last month:
    • Site-wide: 4,350 out of 73,076

Structural disruption of genomic regions containing ultraconserved elements is associated with neurodevelopmental phenotypes

genomics more details view paper
  • Downloaded 589 times
  • Download rankings, all-time:
    • Site-wide: 19,191 out of 73,076
    • In genomics: 2,283 out of 4,853
  • Year to date:
    • Site-wide: 45,187 out of 73,076
  • Since beginning of last month:
    • Site-wide: 45,187 out of 73,076

Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathy

genetics more details view paper
  • Downloaded 410 times
  • Download rankings, all-time:
    • Site-wide: 30,014 out of 73,076
    • In genetics: 1,899 out of 4,015
  • Year to date:
    • Site-wide: 50,814 out of 73,076
  • Since beginning of last month:
    • Site-wide: 50,814 out of 73,076

PanLingua

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


News