Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 62,660 bioRxiv papers from 278,042 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: 13 out of 3,561
• Year to date:
  • Site-wide: 2,278 out of 62,660
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  • Site-wide: 8,698 out of 62,660

Genomewide association study identifies 30 loci associated with bipolar disorder

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  • Site-wide: 282 out of 62,660
  • In genetics: 32 out of 3,561
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  • Site-wide: 289 out of 62,660
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  • Site-wide: 2,018 out of 62,660

Genetic Identification Of Brain Cell Types Underlying Schizophrenia

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  • In genomics: 227 out of 4,312
• Year to date:
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  • Site-wide: 18,046 out of 62,660

Contrasting regional architectures of schizophrenia and other complex diseases using fast variance components analysis

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  • In genetics: 104 out of 3,561
• Year to date:
  • Site-wide: 35,887 out of 62,660
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  • Site-wide: 39,530 out of 62,660

Haplotypes of common SNPs can explain missing heritability of complex diseases

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  • In genetics: 105 out of 3,561
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  • Site-wide: 35,825 out of 62,660
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  • Site-wide: 31,149 out of 62,660

Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights

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  • In genomics: 364 out of 4,312
• Year to date:
  • Site-wide: 22,895 out of 62,660
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  • Site-wide: None out of 62,660

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

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  • In genetics: 286 out of 3,561
• Year to date:
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  • Site-wide: 46,547 out of 62,660

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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  • In genomics: 836 out of 4,312
• Year to date:
  • Site-wide: 19,179 out of 62,660
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  • Site-wide: 35,489 out of 62,660

A genetic investigation of sex bias in the prevalence of attention deficit hyperactivity disorder

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  • In genetics: 517 out of 3,561
• Year to date:
  • Site-wide: 15,341 out of 62,660
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  • Site-wide: 21,438 out of 62,660

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

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  • In genetics: 715 out of 3,561
• Year to date:
  • Site-wide: 45,873 out of 62,660
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  • Site-wide: 50,279 out of 62,660

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

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  • Site-wide: 9,831 out of 62,660
  • In genomics: 1,449 out of 4,312
• Year to date:
  • Site-wide: 20,978 out of 62,660
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  • Site-wide: 35,727 out of 62,660

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

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  • Site-wide: 13,193 out of 62,660
  • In genetics: 931 out of 3,561
• Year to date:
  • Site-wide: 10,324 out of 62,660
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  • Site-wide: 27,659 out of 62,660

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

• Downloaded 546 times
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  • Site-wide: 17,125 out of 62,660
  • In genetics: 1,160 out of 3,561
• Year to date:
  • Site-wide: 34,460 out of 62,660
• Since beginning of last month:
  • Site-wide: 52,292 out of 62,660

Psychosis and the level of mood incongruence in Bipolar Disorder are related to genetic liability for Schizophrenia

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  • Site-wide: 17,462 out of 62,660
  • In genetics: 1,181 out of 3,561
• Year to date:
  • Site-wide: 37,721 out of 62,660
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  • Site-wide: 50,360 out of 62,660

Genetic association study of psychotic experiences in UK Biobank

• Downloaded 522 times
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  • In genetics: 1,216 out of 3,561
• Year to date:
  • Site-wide: 4,522 out of 62,660
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  • Site-wide: 8,157 out of 62,660

Using genetics to examine a general liability to childhood psychopathology

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  • In genetics: 1,317 out of 3,561
• Year to date:
  • Site-wide: 15,514 out of 62,660
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  • Site-wide: 33,150 out of 62,660

Conditional GWAS analysis identifies putative disorder-specific SNPs for psychiatric disorders

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  • Site-wide: 20,916 out of 62,660
  • In genetics: 1,399 out of 3,561
• Year to date:
  • Site-wide: 5,501 out of 62,660
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  • Site-wide: 6,422 out of 62,660

A Transcriptome Wide Association Study implicates specific pre- and post-synaptic abnormalities in Schizophrenia

• Downloaded 433 times
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  • Site-wide: 22,705 out of 62,660
  • In genetics: 1,506 out of 3,561
• Year to date:
  • Site-wide: 24,386 out of 62,660
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  • Site-wide: 15,019 out of 62,660

Dynamic expression of risk genes for schizophrenia and bipolar disorder across development

• Downloaded 387 times
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  • Site-wide: 25,654 out of 62,660
  • In neuroscience: 4,370 out of 11,193
• Year to date:
  • Site-wide: 31,694 out of 62,660
• Since beginning of last month:
  • Site-wide: 50,307 out of 62,660

Novel Insight into the Aetiology of Autism Spectrum Disorder Gained by Integrating Expression Data with Genome-wide Association Statistics

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  • Site-wide: 31,583 out of 62,660
  • In genomics: 3,060 out of 4,312
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  • Site-wide: 22,440 out of 62,660
• Since beginning of last month:
  • Site-wide: 41,827 out of 62,660

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 303 times
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  • Site-wide: 32,561 out of 62,660
  • In genetics: 2,054 out of 3,561
• Year to date:
  • Site-wide: 11,063 out of 62,660
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  • Site-wide: 20,859 out of 62,660

The role of rare copy number variants in depression

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  • Site-wide: 33,397 out of 62,660
  • In neuroscience: 5,770 out of 11,193
• Year to date:
  • Site-wide: 27,015 out of 62,660
• Since beginning of last month:
  • Site-wide: 35,973 out of 62,660

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

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  • Site-wide: 36,135 out of 62,660
  • In genetics: 2,253 out of 3,561
• Year to date:
  • Site-wide: 43,623 out of 62,660
• Since beginning of last month:
  • Site-wide: 53,720 out of 62,660

Differences in Genetic Liability for Insomnia and Hypersomnia in Bipolar Disorder Subtypes

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  • Site-wide: 43,877 out of 62,660
  • In genomics: 3,643 out of 4,312
• Year to date:
  • Site-wide: 19,801 out of 62,660
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  • Site-wide: 20,619 out of 62,660

Identifying novel subtypes of irritability using a developmental genetic approach

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  • Site-wide: 44,431 out of 62,660
  • In genetics: 2,689 out of 3,561
• Year to date:
  • Site-wide: 31,902 out of 62,660
• Since beginning of last month:
  • Site-wide: 24,199 out of 62,660

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

• Downloaded 102 times
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  • Site-wide: 56,664 out of 62,660
  • In genomics: 4,117 out of 4,312
• Year to date:
  • Site-wide: 39,402 out of 62,660
• Since beginning of last month:
  • Site-wide: 18,696 out of 62,660