Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 62,963 bioRxiv papers from 279,321 authors.

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Preprints

Junction-skipping regulation in complex disease

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Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

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Common risk variants identified in autism spectrum disorder

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Rewiring of the cellular and inter-cellular landscape of the human colon during ulcerative colitis

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Association mapping of inflammatory bowel disease loci to single variant resolution

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Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

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

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Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

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Comparative genetic architectures of schizophrenia in East Asian and European populations

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Whole Genome Sequencing in Psychiatric Disorders: the WGSPD Consortium

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Integrative genetic and epigenetic analysis uncovers regulatory mechanisms of autoimmune disease

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Bootstrat: Population Informed Bootstrapping for Rare Variant Tests

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The Cancer Epitope Trees of 23 Early Cervical Cancers in Chinese Women

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RICOPILI: Rapid Imputation for COnsortias PIpeLIne

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Fine-mapping of genetic loci driving spontaneous clearance of hepatitis C virus infection

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