Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 62,725 bioRxiv papers from 278,303 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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Genomewide association study identifies 30 loci associated with bipolar disorder

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Genetic Identification Of Brain Cell Types Underlying Schizophrenia

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  • In genomics: 227 out of 4,314
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Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection

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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: 286 out of 3,562
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

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Causal Analyses, Statistical Efficiency And Phenotypic Precision Through Recall-By-Genotype Study Design

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  • In genetics: 637 out of 3,562
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Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders

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

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  • Site-wide: 36,440 out of 62,725

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

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  • In genetics: 931 out of 3,562
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Association between schizophrenia and both loss of function and missense mutations in paralog conserved sites of voltage-gated sodium channels

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  • Site-wide: 55,240 out of 62,725

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

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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: 38,196 out of 62,725

Genetic association study of psychotic experiences in UK Biobank

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  • Site-wide: 8,311 out of 62,725

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

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  • In genetics: 1,400 out of 3,562
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A Transcriptome Wide Association Study implicates specific pre- and post-synaptic abnormalities in Schizophrenia

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  • In genetics: 1,507 out of 3,562
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  • Site-wide: 15,292 out of 62,725

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

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  • In neuroscience: 4,371 out of 11,204
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  • Site-wide: 31,775 out of 62,725
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  • Site-wide: 50,973 out of 62,725

Cyfip1 haploinsufficiency is associated with white matter changes, myelin thinning, reduction of mature oligodendrocytes and behavioural inflexibility

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  • In neuroscience: 5,104 out of 11,204
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  • Site-wide: 42,707 out of 62,725

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

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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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  • In genetics: 2,050 out of 3,562
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  • Site-wide: 21,259 out of 62,725

The role of rare copy number variants in depression

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  • In neuroscience: 5,779 out of 11,204
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  • Site-wide: 37,357 out of 62,725

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

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  • In genetics: 2,254 out of 3,562
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  • Site-wide: 54,904 out of 62,725

Haploinsufficiency of the schizophrenia risk gene Cyfip1 causes abnormal postnatal hippocampal neurogenesis through a novel microglia dependent mechanism

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  • In neuroscience: 6,445 out of 11,204
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  • Site-wide: 35,769 out of 62,725
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  • Site-wide: 39,476 out of 62,725

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

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  • In genomics: 3,646 out of 4,314
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  • Site-wide: 21,012 out of 62,725

Coordination difficulties, IQ and psychopathology in children with high-risk Copy Number Variants

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  • In genetics: 3,211 out of 3,562
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  • Site-wide: 40,525 out of 62,725

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

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  • In genomics: 4,116 out of 4,314
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  • Site-wide: 19,438 out of 62,725

Electrophysiological network alterations in adults with copy number variants associated with high neurodevelopmental risk

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  • In neuroscience: 10,469 out of 11,204
• Year to date:
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  • Site-wide: 4,842 out of 62,725

Manipulating immune pathways differentially impact emotionality: dissociable effects of complement C3 and C3aR on learned fear and innate anxiety

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  • In neuroscience: 10,736 out of 11,204
• Year to date:
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  • Site-wide: None out of 62,725