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 298,341 authors.

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Preprints

Partitioning heritability by functional category using GWAS summary statistics

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Haplotypes of common SNPs can explain missing heritability of complex diseases

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GWAS in 446,118 European adults identifies 78 genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates

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Biological and clinical insights from genetics of insomnia symptoms

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Subtle stratification confounds estimates of heritability from rare variants

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Gene expression imputation across multiple brain regions reveals schizophrenia risk throughout development.

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Genome-wide association analysis of excessive daytime sleepiness identifies 42 loci that suggest phenotypic subgroups

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Characterization of single gene copy number variants in schizophrenia

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Whole-Genome Association Analyses of Sleep-disordered Breathing Phenotypes in the NHLBI TOPMed Program

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Epigenome-wide association analysis of daytime sleepiness in the Multi-Ethnic Study of Atherosclerosis reveals African-American specific associations

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