Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 67,221 bioRxiv papers from 295,976 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 3,776
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Genomewide association study identifies 30 loci associated with bipolar disorder

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  • Site-wide: 286 out of 67,145
  • In genetics: 34 out of 3,776
• Year to date:
  • Site-wide: 317 out of 67,145
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  • Site-wide: 2,069 out of 67,145

Genetic Identification Of Brain Cell Types Underlying Schizophrenia

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  • In genomics: 239 out of 4,562
• Year to date:
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Contrasting regional architectures of schizophrenia and other complex diseases using fast variance components analysis

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  • In genetics: 111 out of 3,776
• Year to date:
  • Site-wide: 38,184 out of 67,145
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  • Site-wide: 40,213 out of 67,145

Haplotypes of common SNPs can explain missing heritability of complex diseases

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  • In genetics: 115 out of 3,776
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  • Site-wide: 36,768 out of 67,145
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  • Site-wide: 26,060 out of 67,145

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

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  • In genomics: 382 out of 4,562
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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: 300 out of 3,776
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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  • In genomics: 882 out of 4,562
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  • Site-wide: 21,573 out of 67,145
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  • Site-wide: 46,452 out of 67,145

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

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  • In genetics: 527 out of 3,776
• Year to date:
  • Site-wide: 17,188 out of 67,145
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  • Site-wide: 32,394 out of 67,145

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

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  • In genetics: 752 out of 3,776
• Year to date:
  • Site-wide: 49,059 out of 67,145
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  • Site-wide: 51,394 out of 67,145

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

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  • In genomics: 1,527 out of 4,562
• Year to date:
  • Site-wide: 23,810 out of 67,145
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  • Site-wide: 40,270 out of 67,145

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

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  • Site-wide: 13,896 out of 67,145
  • In genetics: 965 out of 3,776
• Year to date:
  • Site-wide: 12,304 out of 67,145
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  • Site-wide: 56,926 out of 67,145

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

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  • In genetics: 1,176 out of 3,776
• Year to date:
  • Site-wide: 5,057 out of 67,145
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  • Site-wide: 3,786 out of 67,145

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: 1,211 out of 3,776
• Year to date:
  • Site-wide: 37,784 out of 67,145
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  • Site-wide: 42,274 out of 67,145

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

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  • In genetics: 1,213 out of 3,776
• Year to date:
  • Site-wide: 39,206 out of 67,145
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  • Site-wide: 32,980 out of 67,145

Genetic association study of psychotic experiences in UK Biobank

• Downloaded 556 times
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  • In genetics: 1,228 out of 3,776
• Year to date:
  • Site-wide: 5,403 out of 67,145
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  • Site-wide: 19,630 out of 67,145

Using genetics to examine a general liability to childhood psychopathology

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  • Site-wide: 19,413 out of 67,145
  • In genetics: 1,291 out of 3,776
• Year to date:
  • Site-wide: 15,857 out of 67,145
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  • Site-wide: 21,564 out of 67,145

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

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  • Site-wide: 22,864 out of 67,145
  • In genetics: 1,519 out of 3,776
• Year to date:
  • Site-wide: 24,687 out of 67,145
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  • Site-wide: 20,962 out of 67,145

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

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  • Site-wide: 27,392 out of 67,145
  • In neuroscience: 4,714 out of 12,038
• Year to date:
  • Site-wide: 36,268 out of 67,145
• Since beginning of last month:
  • Site-wide: 49,263 out of 67,145

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.

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  • Site-wide: 31,742 out of 67,145
  • In genetics: 1,995 out of 3,776
• Year to date:
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  • Site-wide: 17,230 out of 67,145

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: 33,931 out of 67,145
  • In genomics: 3,219 out of 4,562
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  • Site-wide: 26,679 out of 67,145
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  • Site-wide: 45,186 out of 67,145

The role of rare copy number variants in depression

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  • Site-wide: 35,382 out of 67,145
  • In neuroscience: 6,190 out of 12,038
• Year to date:
  • Site-wide: 30,876 out of 67,145
• Since beginning of last month:
  • Site-wide: 45,443 out of 67,145

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

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  • Site-wide: 38,856 out of 67,145
  • In genetics: 2,379 out of 3,776
• Year to date:
  • Site-wide: 49,647 out of 67,145
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  • Site-wide: None out of 67,145

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

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  • Site-wide: 43,702 out of 67,145
  • In genomics: 3,718 out of 4,562
• Year to date:
  • Site-wide: 20,637 out of 67,145
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  • Site-wide: 20,661 out of 67,145

Identifying novel subtypes of irritability using a developmental genetic approach

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  • Site-wide: 44,892 out of 67,145
  • In genetics: 2,700 out of 3,776
• Year to date:
  • Site-wide: 32,527 out of 67,145
• Since beginning of last month:
  • Site-wide: 23,310 out of 67,145

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

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  • Site-wide: 53,981 out of 67,145
  • In genomics: 4,111 out of 4,562
• Year to date:
  • Site-wide: 32,566 out of 67,145
• Since beginning of last month:
  • Site-wide: 6,347 out of 67,145