Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 66,889 bioRxiv papers from 294,495 authors.

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Preprints

The rate of de novo CNVs in healthy controls

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Genomewide association study identifies 30 loci associated with bipolar disorder

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Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders.

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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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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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

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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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Genetic association study of psychotic experiences in UK Biobank

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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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Schizophrenia-associated genomic copy number variants and subcortical brain volumes in the UK Biobank

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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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Characterization of single gene copy number variants in schizophrenia

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The role of rare copy number variants in depression

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

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

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