Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 67,594 bioRxiv papers from 298,144 authors.

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Preprints

Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

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  • In genetics: 23 out of 3,799
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  • Site-wide: 99 out of 67,591
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  • Site-wide: 205 out of 67,591

Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation

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  • In genetics: 25 out of 3,799
• Year to date:
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De novo Variants In Neurodevelopmental Disorders With Epilepsy

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  • In genetics: 321 out of 3,799
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Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals

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  • In genetics: 333 out of 3,799
• Year to date:
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  • Site-wide: 7,129 out of 67,591

ASD and ADHD have a similar burden of rare protein-truncating variants

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  • Site-wide: 4,770 out of 67,591

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

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  • In genomics: 1,382 out of 4,581
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  • Site-wide: 59,614 out of 67,591

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

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Contribution of Retrotransposition to Developmental Disorders

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• Year to date:
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  • Site-wide: 31,217 out of 67,591

Schizophrenia risk conferred by protein-coding de novo mutations

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  • In genetics: 1,099 out of 3,799
• Year to date:
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  • Site-wide: 28,630 out of 67,591

Meta-analysis of Scandinavian Schizophrenia Exomes

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  • Site-wide: 53,498 out of 67,591
  • In genetics: 3,132 out of 3,799
• Year to date:
  • Site-wide: 31,855 out of 67,591
• Since beginning of last month:
  • Site-wide: 1,460 out of 67,591