Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 67,594 bioRxiv papers from 298,144 authors.

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Preprints

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

• Downloaded 1,609 times
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  • Site-wide: 3,548 out of 67,594
  • In genetics: 302 out of 3,799
• Year to date:
  • Site-wide: 53,150 out of 67,594
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  • Site-wide: 61,517 out of 67,594

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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  • Site-wide: 5,077 out of 67,594
  • In genomics: 889 out of 4,581
• Year to date:
  • Site-wide: 22,173 out of 67,594
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  • Site-wide: 55,104 out of 67,594

Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores

• Downloaded 681 times
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  • Site-wide: 14,033 out of 67,594
  • In genetics: 976 out of 3,799
• Year to date:
  • Site-wide: 12,682 out of 67,594
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  • Site-wide: 61,705 out of 67,594

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

• Downloaded 555 times
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  • Site-wide: 18,700 out of 67,594
  • In genetics: 1,242 out of 3,799
• Year to date:
  • Site-wide: 35,639 out of 67,594
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  • Site-wide: 49,322 out of 67,594

Allele-specific open chromatin in human iPSC neurons elucidates functional non-coding disease variants

• Downloaded 176 times
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  • Site-wide: 52,205 out of 67,594
  • In genetics: 3,077 out of 3,799
• Year to date:
  • Site-wide: 30,176 out of 67,594
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  • Site-wide: 1,383 out of 67,594