Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 72,916 bioRxiv papers from 317,499 authors.

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Preprints

Genetic Identification Of Brain Cell Types Underlying Schizophrenia

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

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  • Site-wide: 29,043 out of 72,916
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Using three-dimensional regulatory chromatin interactions from adult and fetal cortex to interpret genetic results for psychiatric disorders and cognitive traits

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  • In genetics: 413 out of 4,008
• Year to date:
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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  • In genomics: 916 out of 4,843
• Year to date:
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Common Variant Associations with Fragile X Syndrome

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  • In genetics: 804 out of 4,008
• Year to date:
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Examination of the Shared Genetic Basis of Anorexia Nervosa and Obsessive-Compulsive Disorder

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  • In genetics: 902 out of 4,008
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Instability of the pseudoautosomal boundary in house mice

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Cross-disorder GWAS meta-analysis for Attention Deficit/Hyperactivity Disorder, Autism Spectrum Disorder, Obsessive Compulsive Disorder, and Tourette Syndrome

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• Year to date:
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Characterization of single gene copy number variants in schizophrenia

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  • In genetics: 2,137 out of 4,008
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Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies

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  • In genetics: 2,380 out of 4,008
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  • Site-wide: 17,943 out of 72,916

Antipsychotic behavioral phenotypes in the mouse Collaborative Cross recombinant inbred inter-crosses (RIX)

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  • Site-wide: 67,521 out of 72,916
  • In systems biology: 1,917 out of 1,998
• Year to date:
  • Site-wide: 29,195 out of 72,916
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  • Site-wide: 29,195 out of 72,916