Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 53,026 bioRxiv papers from 245,564 authors.

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Preprints

The genomic architecture of blood metabolites based on a decade of genome-wide analyses

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Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

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Genome-wide association analysis of lifetime cannabis use (N=184,765) identifies new risk loci, genetic overlap with mental health, and a causal influence of schizophrenia on cannabis use

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  • In genetics: 16 out of 3,086
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Genetic Consequences of Social Stratification in Great Britain

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Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences

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  • In genetics: 97 out of 3,086
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Multivariate Genome-wide and integrated transcriptome and epigenome-wide analyses of the Well-being spectrum.

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  • In genetics: 318 out of 3,086
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A high-quality reference panel reveals the complexity and distribution of structural genome changes in a human population

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  • In genetics: 434 out of 3,086
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Stratified Linkage Disequilibrium Score Regression reveals enrichment of eQTL effects on complex traits is not tissue specific

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  • In genomics: 928 out of 3,782
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Phenome-wide investigation of health outcomes associated with genetic predisposition to loneliness

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  • In genetics: 1,066 out of 3,086
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Genetic overlap between schizophrenia and developmental psychopathology: a longitudinal approach applied to common childhood disorders between age 7 and 15 years

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  • In genetics: 1,360 out of 3,086
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Genetic risk for major depressive disorder and loneliness in gender-specific associations with coronary artery disease

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