Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 71,071 bioRxiv papers from 310,049 authors.

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Preprints

Phenome-wide Heritability Analysis of the UK Biobank

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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: 101 out of 3,937
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The Shared Genetic Basis of Educational Attainment and Cerebral Cortical Morphology

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Comparative genetic architectures of schizophrenia in East Asian and European populations

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Widespread pleiotropy confounds causal relationships between complex traits and diseases inferred from Mendelian randomization

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Penetrance and pleiotropy of polygenic risk scores for schizophrenia in 106,160 patients across four healthcare systems

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  • In genetics: 473 out of 3,937
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Largest genome-wide association study for PTSD identifies genetic risk loci in European and African ancestries and implicates novel biological pathways

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  • In genetics: 484 out of 3,937
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Polygenic Prediction via Bayesian Regression and Continuous Shrinkage Priors

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Testing Causal Bidirectional Influences between Physical Activity and Depression using Mendelian Randomization

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Lifelong genetically lowered sclerostin and risk of cardiovascular disease.

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  • In genetics: 736 out of 3,937
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  • Site-wide: 7,554 out of 71,071
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  • Site-wide: 14,357 out of 71,071

GWAS identifies novel risk locus for erectile dysfunction and implicates hypothalamic neurobiology and diabetes in etiology

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  • In genomics: 1,639 out of 4,740
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  • Site-wide: 66,901 out of 71,071
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  • Site-wide: 66,781 out of 71,071

The genetic architecture of sporadic and recurrent miscarriage

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  • In genetics: 927 out of 3,937
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The causal role of circulating vitamin D concentrations in human complex traits and diseases: a large-scale Mendelian randomization study

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  • In genetics: 1,259 out of 3,937
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Explicit modeling of ancestry improves polygenic risk scores and BLUP prediction

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  • In genetics: 1,552 out of 3,937
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  • Site-wide: 61,736 out of 71,071

Analysis of Genetically Regulated Gene Expression identifies a trauma type specific PTSD gene, SNRNP35

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  • In genetics: 1,553 out of 3,937
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  • Site-wide: 41,994 out of 71,071

A two-stage approach to identifying and validating modifiable factors for the prevention of depression

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  • In genetics: 1,657 out of 3,937
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  • Site-wide: 17,719 out of 71,071
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  • Site-wide: 17,277 out of 71,071

GWAS meta-analysis highlights the hypothalamic-pituitary-gonadal axis (HPG axis) in the genetic regulation of menstrual cycle length

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  • Site-wide: 27,017 out of 71,071
  • In genetics: 1,748 out of 3,937
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  • Site-wide: 49,007 out of 71,071
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  • Site-wide: 42,808 out of 71,071

Genomewide Analyses of Psychological Resilience in US Army Soldiers

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  • In genetics: 1,805 out of 3,937
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Prospective Study of Polygenic Risk, Protective Factors, and Incident Depression Following Combat Deployment in US Army Soldiers

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  • In genetics: 1,941 out of 3,937
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  • Site-wide: 32,699 out of 71,071

Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cases

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  • In genetics: 1,977 out of 3,937
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  • Site-wide: 47,155 out of 71,071

The schizophrenia risk locus in SLC39A8 alters brain metal transport and plasma glycosylation

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  • In biochemistry: 1,028 out of 2,130
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  • Site-wide: 12,516 out of 71,071

Genetic validation of bipolar disorder identified by automated phenotyping using electronic health records

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  • In genetics: 2,402 out of 3,937
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  • Site-wide: 46,103 out of 71,071

Genomic Influences on Self-Reported Childhood Maltreatment

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  • In genomics: 3,935 out of 4,740
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• Since beginning of last month:
  • Site-wide: 24,715 out of 71,071