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.

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Preprints

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

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  • In genetics: 197 out of 3,773
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  • Site-wide: 47,823 out of 67,039
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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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  • In genetics: 298 out of 3,773
• Year to date:
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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  • In genomics: 881 out of 4,557
• Year to date:
  • Site-wide: 21,262 out of 67,039
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Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

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  • In genomics: 1,364 out of 4,557
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  • Site-wide: 52,439 out of 67,039

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

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  • In genetics: 748 out of 3,773
• Year to date:
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Contribution of rare and common variants to intellectual disability in a high-risk population sub-isolate of Northern Finland

• Downloaded 476 times
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  • In genetics: 1,485 out of 3,773
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Advantages of genotype imputation with ethnically matched reference panel for rare variant association analyses

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  • In genomics: 2,963 out of 4,557
• Year to date:
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  • 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

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  • In genetics: 2,194 out of 3,773
• Year to date:
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  • Site-wide: 62,976 out of 67,039

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

• Downloaded 238 times
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  • 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