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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 67,039 bioRxiv papers from 295,099 authors.

Author: Jaana Suvisaari

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

Rankings

  • All-time downloads: 8,244 (rank: 5,847 (tie) out of 295,099)
  • Categories:
    • genetics: 5,661 (rank: 2,588 (tie) out of 29,443)
    • genomics: 2,583 (rank: 5,666 out of 33,595)

Downloads per author, site-wide

Preprints

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

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  • Downloaded 2,195 times
  • Download rankings, all-time:
    • Site-wide: 2,061 out of 67,039
    • In genetics: 197 out of 3,773
  • Year to date:
    • Site-wide: 47,823 out of 67,039
  • Since beginning of last month:
    • Site-wide: 56,442 out of 67,039

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

genetics more details view paper
  • Downloaded 1,609 times
  • Download rankings, all-time:
    • Site-wide: 3,489 out of 67,039
    • In genetics: 298 out of 3,773
  • Year to date:
    • Site-wide: 51,447 out of 67,039
  • Since beginning of last month:
    • Site-wide: 52,764 out of 67,039

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

genomics more details view paper
  • Downloaded 1,298 times
  • Download rankings, all-time:
    • Site-wide: 5,000 out of 67,039
    • In genomics: 881 out of 4,557
  • Year to date:
    • Site-wide: 21,262 out of 67,039
  • Since beginning of last month:
    • Site-wide: 41,880 out of 67,039

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

genomics more details view paper
  • Downloaded 912 times
  • Download rankings, all-time:
    • Site-wide: 8,935 out of 67,039
    • In genomics: 1,364 out of 4,557
  • Year to date:
    • Site-wide: 46,074 out of 67,039
  • Since beginning of last month:
    • Site-wide: 52,439 out of 67,039

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

genetics more details view paper
  • Downloaded 835 times
  • Download rankings, all-time:
    • Site-wide: 10,228 out of 67,039
    • In genetics: 748 out of 3,773
  • Year to date:
    • Site-wide: 48,557 out of 67,039
  • Since beginning of last month:
    • Site-wide: 46,045 out of 67,039

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 476 times
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    • Site-wide: 22,270 out of 67,039
    • In genetics: 1,485 out of 3,773
  • Year to date:
    • Site-wide: 49,545 out of 67,039
  • Since beginning of last month:
    • Site-wide: 56,472 out of 67,039

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

genomics more details view paper
  • Downloaded 373 times
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    • Site-wide: 29,202 out of 67,039
    • In genomics: 2,963 out of 4,557
  • Year to date:
    • Site-wide: 10,300 out of 67,039
  • Since beginning of last month:
    • Site-wide: 18,496 out of 67,039

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

genetics more details view paper
  • Downloaded 308 times
  • Download rankings, all-time:
    • Site-wide: 35,147 out of 67,039
    • In genetics: 2,194 out of 3,773
  • Year to date:
    • Site-wide: 58,811 out of 67,039
  • Since beginning of last month:
    • Site-wide: 62,976 out of 67,039

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

genetics more details view paper
  • Downloaded 238 times
  • Download rankings, all-time:
    • Site-wide: 43,077 out of 67,039
    • In genetics: 2,611 out of 3,773
  • Year to date:
    • Site-wide: 36,262 out of 67,039
  • Since beginning of last month:
    • Site-wide: 49,746 out of 67,039

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