Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 57,910 bioRxiv papers from 266,458 authors.

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Preprints

Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders.

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  • In genomics: 302 out of 4,058
• Year to date:
  • Site-wide: 173 out of 57,910
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  • Site-wide: 1,287 out of 57,910

Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection

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  • In genomics: 368 out of 4,058
• Year to date:
  • Site-wide: 39,455 out of 57,910
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  • Site-wide: 39,653 out of 57,910

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

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  • Site-wide: 3,044 out of 57,910
  • In genetics: 277 out of 3,319
• Year to date:
  • Site-wide: 41,337 out of 57,910
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  • Site-wide: 33,078 out of 57,910

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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  • In genomics: 799 out of 4,058
• Year to date:
  • Site-wide: 16,617 out of 57,910
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  • Site-wide: 34,157 out of 57,910

Medical consequences of pathogenic CNVs in adults: Analysis of the UK Biobank

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  • In genomics: 1,415 out of 4,058
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  • Site-wide: 19,091 out of 57,910
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  • Site-wide: 33,360 out of 57,910

Association between schizophrenia and both loss of function and missense mutations in paralog conserved sites of voltage-gated sodium channels

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  • In genetics: 1,114 out of 3,319
• Year to date:
  • Site-wide: 29,755 out of 57,910
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  • Site-wide: 35,666 out of 57,910

Genome-wide Association Study of Clinical Features in the Schizophrenia Psychiatric Genomics Consortium: Confirmation of Polygenic Effect on Negative Symptoms

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  • In genetics: 1,169 out of 3,319
• Year to date:
  • Site-wide: 28,873 out of 57,910
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  • Site-wide: 34,687 out of 57,910

Genetic association study of psychotic experiences in UK Biobank

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  • In genetics: 1,354 out of 3,319
• Year to date:
  • Site-wide: 4,338 out of 57,910
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  • Site-wide: 6,863 out of 57,910

Schizophrenia-associated genomic copy number variants and subcortical brain volumes in the UK Biobank

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  • Site-wide: 26,286 out of 57,910
  • In neuroscience: 4,440 out of 10,204
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  • Site-wide: 24,880 out of 57,910
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  • Site-wide: 40,828 out of 57,910

The role of rare copy number variants in depression

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  • Site-wide: 32,095 out of 57,910
  • In neuroscience: 5,492 out of 10,204
• Year to date:
  • Site-wide: 24,036 out of 57,910
• Since beginning of last month:
  • Site-wide: 36,421 out of 57,910

Analyses of rare and common alleles in parent-proband trios implicate rare missense variants in SLC6A1 in schizophrenia and confirm the involvement of loss of function intolerant and neurodevelopmental disorder genes.

• Downloaded 274 times
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  • In genetics: 2,074 out of 3,319
• Year to date:
  • Site-wide: 9,803 out of 57,910
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  • Site-wide: 26,885 out of 57,910

Characterization of single gene copy number variants in schizophrenia

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  • Site-wide: 34,149 out of 57,910
  • In genetics: 2,160 out of 3,319
• Year to date:
  • Site-wide: 10,837 out of 57,910
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  • Site-wide: 26,065 out of 57,910

Effects of pathogenic CNVs on physical traits in participants of the UK Biobank

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  • Site-wide: 34,167 out of 57,910
  • In genetics: 2,164 out of 3,319
• Year to date:
  • Site-wide: 39,300 out of 57,910
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  • Site-wide: 36,648 out of 57,910

Effects of pathogenic CNVs on biochemical markers: a study on the UK Biobank

• Downloaded 66 times
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  • Site-wide: 55,363 out of 57,910
  • In genomics: 3,975 out of 4,058
• Year to date:
  • Site-wide: 44,408 out of 57,910
• Since beginning of last month:
  • Site-wide: 7,855 out of 57,910