Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 57,506 bioRxiv papers from 264,779 authors.

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Preprints

Integrating untargeted metabolomics, genetically informed causal inference, and pathway enrichment to define the obesity metabolome

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

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

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Widespread signatures of negative selection in the genetic architecture of human complex traits

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Deep-coverage whole genome sequences and blood lipids among 16,324 individuals

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Genome-Wide Association Study Reveals First Locus for Anorexia Nervosa and Metabolic Correlations

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Improved polygenic prediction by Bayesian multiple regression on summary statistics

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Genetic Associations with Subjective Well-Being Also Implicate Depression and Neuroticism

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Educational attainment and personality are genetically intertwined

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Genomic analysis of diet composition finds novel loci and associations with health and lifestyle

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Human loss-of-function variants suggest that partial LRRK2 inhibition is a safe therapeutic strategy for Parkinsons disease

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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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Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

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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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Constraints on eQTL fine mapping in the presence of multi-site local regulation of gene expression

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Genome-wide Association Study of Clinical Features in the Schizophrenia Psychiatric Genomics Consortium: Confirmation of Polygenic Effect on Negative Symptoms

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Functional and evolutionary impact of polymorphic inversions in the human genome

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Allele-specific expression changes dynamically during T cell activation in HLA and other autoimmune loci

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The effect of X-linked dosage compensation on complex trait variation

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PAIRUP-MS: Pathway Analysis and Imputation to Relate Unknowns in Profiles from Mass Spectrometry-based metabolite data

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Analytical strategies to include the X-chromosome in variance heterogeneity analyses: evidence for trait-specific polygenic variance structure

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