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Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 65,428 bioRxiv papers from 289,803 authors.

Author: Michael E. Talkowski

  • Most recently observed institution: Stanley Center for Psychiatric Research, Broad Institute of Harvard and M.I.T.

Rankings

  • All-time downloads: 38,385 (rank: 401 out of 289,803)
  • Categories:
    • bioinformatics: 1,997 (rank: 3,868 (tie) out of 25,231)
    • genetics: 7,434 (rank: 1,602 out of 28,741)
    • genomics: 28,954 (rank: 196 out of 32,966)

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 13,728 times
  • Download rankings, all-time:
    • Site-wide: 59 out of 65,428
    • In genomics: 16 out of 4,463
  • Year to date:
    • Site-wide: 9 out of 65,428
  • Since beginning of last month:
    • Site-wide: 41 out of 65,428

An open resource of structural variation for medical and population genetics

genomics more details view paper
  • Downloaded 7,504 times
  • Download rankings, all-time:
    • Site-wide: 200 out of 65,428
    • In genomics: 59 out of 4,463
  • Year to date:
    • Site-wide: 43 out of 65,428
  • Since beginning of last month:
    • Site-wide: 106 out of 65,428

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

genetics more details view paper
  • Downloaded 6,637 times
  • Download rankings, all-time:
    • Site-wide: 257 out of 65,428
    • In genetics: 28 out of 3,699
  • Year to date:
    • Site-wide: 108 out of 65,428
  • Since beginning of last month:
    • Site-wide: 274 out of 65,428

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 2,324 times
  • Download rankings, all-time:
    • Site-wide: 1,799 out of 65,428
    • In genomics: 397 out of 4,463
  • Year to date:
    • Site-wide: 25,956 out of 65,428
  • Since beginning of last month:
    • Site-wide: 25,182 out of 65,428

Mapping And Phasing Of Structural Variation In Patient Genomes Using Nanopore Sequencing

genomics more details view paper
  • Downloaded 2,320 times
  • Download rankings, all-time:
    • Site-wide: 1,810 out of 65,428
    • In genomics: 399 out of 4,463
  • Year to date:
    • Site-wide: 39,686 out of 65,428
  • Since beginning of last month:
    • Site-wide: 49,285 out of 65,428

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

bioinformatics more details view paper
  • Downloaded 1,997 times
  • Download rankings, all-time:
    • Site-wide: 2,375 out of 65,428
    • In bioinformatics: 487 out of 6,484
  • Year to date:
    • Site-wide: 11,456 out of 65,428
  • Since beginning of last month:
    • Site-wide: 11,631 out of 65,428

Indexcov: fast coverage quality control for whole-genome sequencing

genomics more details view paper
  • Downloaded 1,456 times
  • Download rankings, all-time:
    • Site-wide: 4,028 out of 65,428
    • In genomics: 743 out of 4,463
  • Year to date:
    • Site-wide: 24,739 out of 65,428
  • Since beginning of last month:
    • Site-wide: 33,682 out of 65,428

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

genomics more details view paper
  • Downloaded 1,064 times
  • Download rankings, all-time:
    • Site-wide: 6,795 out of 65,428
    • In genomics: 1,100 out of 4,463
  • Year to date:
    • Site-wide: 22,401 out of 65,428
  • Since beginning of last month:
    • Site-wide: 37,347 out of 65,428

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

genomics more details view paper
  • Downloaded 558 times
  • Download rankings, all-time:
    • Site-wide: 17,693 out of 65,428
    • In genomics: 2,157 out of 4,463
  • Year to date:
    • Site-wide: 36,394 out of 65,428
  • Since beginning of last month:
    • Site-wide: 36,238 out of 65,428

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

genetics more details view paper
  • Downloaded 378 times
  • Download rankings, all-time:
    • Site-wide: 27,976 out of 65,428
    • In genetics: 1,807 out of 3,699
  • Year to date:
    • Site-wide: 27,711 out of 65,428
  • Since beginning of last month:
    • Site-wide: 23,575 out of 65,428

SYCP2 translocation-mediated dysregulation and frameshift variants cause human male infertility

genetics more details view paper
  • Downloaded 287 times
  • Download rankings, all-time:
    • Site-wide: 36,187 out of 65,428
    • In genetics: 2,259 out of 3,699
  • Year to date:
    • Site-wide: 14,205 out of 65,428
  • Since beginning of last month:
    • Site-wide: 14,375 out of 65,428

Hypomorphic mutation of the mouse Huntington’s disease gene orthologue

genetics more details view paper
  • Downloaded 132 times
  • Download rankings, all-time:
    • Site-wide: 55,966 out of 65,428
    • In genetics: 3,272 out of 3,699
  • Year to date:
    • Site-wide: 49,764 out of 65,428
  • Since beginning of last month:
    • Site-wide: 40,271 out of 65,428

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