Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 67,354 bioRxiv papers from 296,559 authors.

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Preprints

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

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  • In genetics: 14 out of 3,786
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  • Site-wide: 5,949 out of 67,354

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

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  • In genetics: 300 out of 3,786
• Year to date:
  • Site-wide: 52,235 out of 67,354
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  • Site-wide: 61,265 out of 67,354

Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

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  • Site-wide: 3,531 out of 67,354
  • In genetics: 301 out of 3,786
• Year to date:
  • Site-wide: 4,961 out of 67,354
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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  • Site-wide: 5,047 out of 67,354
  • In genomics: 884 out of 4,574
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  • Site-wide: 21,833 out of 67,354
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  • Site-wide: 49,425 out of 67,354

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

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  • In genetics: 968 out of 3,786
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  • Site-wide: 60,422 out of 67,354

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

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  • Site-wide: 18,577 out of 67,354
  • In genetics: 1,232 out of 3,786
• Year to date:
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  • Site-wide: 44,877 out of 67,354

FIQT: a simple, powerful method to accurately estimate effect sizes in genome scans

• Downloaded 369 times
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  • In genetics: 1,894 out of 3,786
• Year to date:
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  • Site-wide: 49,086 out of 67,354