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.

Downloads per author, site-wide

Preprints

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

• Downloaded 2,170 times
• Download rankings, all-time:
  • Site-wide: 1,760 out of 57,381
  • In genetics: 175 out of 3,275
• Year to date:
  • Site-wide: 39,349 out of 57,381
• Since beginning of last month:
  • Site-wide: 34,062 out of 57,381

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

• 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
• Since beginning of last month:
  • Site-wide: 36,801 out of 57,381

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

• 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

• Downloaded 890 times
• Download rankings, all-time:
  • Site-wide: 7,765 out of 57,381
  • 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

• Downloaded 808 times
• Download rankings, all-time:
  • Site-wide: 9,038 out of 57,381
  • In genetics: 679 out of 3,275
• Year to date:
  • Site-wide: 40,932 out of 57,381
• 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

• Downloaded 455 times
• Download rankings, all-time:
  • Site-wide: 19,508 out of 57,381
  • In genetics: 1,336 out of 3,275
• Year to date:
  • 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

• Downloaded 311 times
• Download rankings, all-time:
  • Site-wide: 28,841 out of 57,381
  • In genomics: 2,859 out of 4,011
• Year to date:
  • 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

• Downloaded 292 times
• Download rankings, all-time:
  • Site-wide: 30,454 out of 57,381
  • 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

• 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