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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 57,381 bioRxiv papers from 264,204 authors.

Author: Jaana Suvisaari

  • Most recently observed institution: National Institute for Health and Welfare, Helsinki, Finland

Rankings

  • All-time downloads: 7,981 (rank: 4,844 (tie) out of 264,204)
  • Categories:
    • genetics: 5,520 (rank: 2,220 out of 25,187)
    • genomics: 2,461 (rank: 5,424 (tie) out of 30,209)

Downloads per author, site-wide

Preprints

Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

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  • Downloaded 2,170 times
  • Download rankings, all-time:
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    • In genetics: 175 out of 3,275
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    • Site-wide: 39,349 out of 57,381
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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

genetics more details view paper
  • Downloaded 1,588 times
  • Download rankings, all-time:
    • Site-wide: 3,025 out of 57,381
    • In genetics: 274 out of 3,275
  • Year to date:
    • Site-wide: 41,546 out of 57,381
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    • Site-wide: 36,801 out of 57,381

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

genomics more details view paper
  • Downloaded 1,260 times
  • Download rankings, all-time:
    • Site-wide: 4,414 out of 57,381
    • In genomics: 794 out of 4,011
  • Year to date:
    • Site-wide: 16,035 out of 57,381
  • Since beginning of last month:
    • Site-wide: 29,558 out of 57,381

Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

genomics more details view paper
  • Downloaded 890 times
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    • In genomics: 1,215 out of 4,011
  • Year to date:
    • Site-wide: 36,325 out of 57,381
  • Since beginning of last month:
    • Site-wide: 37,407 out of 57,381

Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders

genetics more details view paper
  • Downloaded 808 times
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    • In genetics: 679 out of 3,275
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  • Since beginning of last month:
    • Site-wide: 44,550 out of 57,381

Contribution of rare and common variants to intellectual disability in a high-risk population sub-isolate of Northern Finland

genetics more details view paper
  • Downloaded 455 times
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    • In genetics: 1,336 out of 3,275
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    • Site-wide: 39,861 out of 57,381
  • Since beginning of last month:
    • Site-wide: 39,733 out of 57,381

Advantages of genotype imputation with ethnically matched reference panel for rare variant association analyses

genomics more details view paper
  • Downloaded 311 times
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    • Site-wide: 28,841 out of 57,381
    • In genomics: 2,859 out of 4,011
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    • Site-wide: 7,676 out of 57,381
  • Since beginning of last month:
    • Site-wide: 19,392 out of 57,381

The NDE1 genomic locus can affect treatment of psychiatric illness through gene expression changes related to MicroRNA-484

genetics more details view paper
  • Downloaded 292 times
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    • In genetics: 1,952 out of 3,275
  • Year to date:
    • Site-wide: 48,023 out of 57,381
  • Since beginning of last month:
    • Site-wide: 26,787 out of 57,381

Variants in regulatory elements of PDE4D associate with Major Mental Illness in the Finnish population

genetics more details view paper
  • Downloaded 207 times
  • Download rankings, all-time:
    • Site-wide: 39,099 out of 57,381
    • In genetics: 2,427 out of 3,275
  • Year to date:
    • Site-wide: 29,406 out of 57,381
  • Since beginning of last month:
    • Site-wide: 25,410 out of 57,381

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