Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 63,016 bioRxiv papers from 279,490 authors.

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Preprints

Characterisation of an inflammation-related epigenetic score and its association with cognitive ability

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

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Genomic analysis of family data reveals additional genetic effects on intelligence and personality

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Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360)

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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection

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Genetic analysis identifies molecular systems and biological pathways associated with household income

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Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112,117).

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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

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Genome-wide association analyses in >119,000 individuals identifies thirteen morningness and two sleep duration loci

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New genetic signals for lung function highlight pathways and pleiotropy, and chronic obstructive pulmonary disease associations across multiple ancestries

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Genome-wide association study of suicide death and polygenic prediction of clinical antecedents

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PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

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Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility

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Genome-wide association and functional studies identify 46 novel loci for alcohol consumption and suggest common genetic mechanisms with neuropsychiatric disorders

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Genome-wide Meta-analysis of 158,000 Individuals of European Ancestry Identifies Three Loci Associated with Chronic Back Pain

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Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank

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Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder

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Proteome-by-phenome Mendelian Randomisation detects 38 proteins with causal roles in human diseases and traits

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Do Regional Brain Volumes and Major Depressive Disorder Share Genetic Architecture: a study in Generation Scotland (n=19,762), UK Biobank (n=24,048) and the English Longitudinal Study of Ageing (n=5,766)

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Genome-Wide Meta-Analyses Of Stratified Depression In Generation Scotland And UK Biobank

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Quantifying the extent to which index event biases influence large genetic association studies

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Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes

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Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

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Psychosis and the level of mood incongruence in Bipolar Disorder are related to genetic liability for Schizophrenia

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Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity

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Electronic Health Record and Genome-wide Genetic Data in Generation Scotland Participants

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A validation of the diathesis-stress model for depression in Generation Scotland.

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Novel Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk Of Coronary Artery Disease

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Meta-analysis of exome array data identifies six novel genetic loci for lung function

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Low-frequency variation in TP53 has large effects on head circumference and intracranial volume

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A meta-analysis of genome-wide association studies of epigenetic age acceleration

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Global variability of the human IgG glycome

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Genetic and environmental determinants of stressful life events and their overlap with depression and neuroticism

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Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

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The influence of X chromosome variants on trait neuroticism.

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Insight into the genetic aetiology of retinal detachment by combining small clinical and large population-based datasets

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Genome-wide by environment interaction studies (GWEIS) of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland.

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Genetic and shared couple environmental contributions to smoking and alcohol use in the UK population

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Shared genetics and couple-associated environment are major contributors to the risk of both clinical and self-declared depression

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A strategy to incorporate prior knowledge into correlation network cutoff selection

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Distinguishing pedigree relationships using multi-way identical by descent sharing and sex-specific genetic maps

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Associations of ‘Relative corticosterone deficiency’ with genetic variation in CYP17A1 and metabolic syndrome features

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