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Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 53,027 bioRxiv papers from 245,564 authors.

Author: Andres Metspalu

Rankings

  • All-time downloads: 40,492 (rank: 308 out of 245,564)
  • Categories:
    • bioinformatics: 289 (rank: 15,757 (tie) out of 21,725)
    • epidemiology: 154 (rank: 5,402 (tie) out of 9,248)
    • genetics: 29,989 (rank: 107 out of 23,769)
    • genomics: 10,060 (rank: 852 out of 28,414)

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Preprints

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

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Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

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

genetics more details view paper
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Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

genetics more details view paper
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Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

genetics more details view paper
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Widespread signatures of negative selection in the genetic architecture of human complex traits

genetics more details view paper
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Genome-Wide Association Study Reveals First Locus for Anorexia Nervosa and Metabolic Correlations

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Cell specific eQTL analysis without sorting cells

genetics more details view paper
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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

genetics more details view paper
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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

genetics more details view paper
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Genome-wide association analyses in >119,000 individuals identifies thirteen morningness and two sleep duration loci

genetics more details view paper
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Improved polygenic prediction by Bayesian multiple regression on summary statistics

genetics more details view paper
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

genomics more details view paper
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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

genomics more details view paper
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Haplotype sharing provides insights into fine-scale population history and disease in Finland

genetics more details view paper
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    • In genetics: 554 out of 3,086
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Mega-analysis of 31,396 individuals from 6 countries uncovers strong gene-environment interaction for human fertility

genomics more details view paper
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An epigenome-wide association study of educational attainment (n = 10,767)

genetics more details view paper
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    • In genetics: 659 out of 3,086
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Personalized Risk Prediction for Type 2 Diabetes: the Potential of Genetic Risk Scores

genetics more details view paper
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    • In genetics: 801 out of 3,086
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An interaction map of circulating metabolites, immune gene networks and their genetic regulation

genomics more details view paper
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    • In genomics: 1,584 out of 3,782
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Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms

genetics more details view paper
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    • In genetics: 871 out of 3,086
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Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

genomics more details view paper
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Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

genomics more details view paper
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    • In genomics: 1,794 out of 3,782
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Constraints on eQTL fine mapping in the presence of multi-site local regulation of gene expression

genetics more details view paper
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The genetic architecture of sporadic and recurrent miscarriage

genetics more details view paper
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Polygenic prediction of breast cancer: comparison of genetic predictors and implications for screening

genetics more details view paper
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    • In genetics: 1,549 out of 3,086
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The effect of X-linked dosage compensation on complex trait variation

genetics more details view paper
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Multi-ancestry analysis of gene-sleep interactions in 126,926 individuals identifies multiple novel blood lipid loci that contribute to our understanding of sleep-associated adverse blood lipid profile

genomics more details view paper
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PAIRUP-MS: Pathway Analysis and Imputation to Relate Unknowns in Profiles from Mass Spectrometry-based metabolite data

bioinformatics more details view paper
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    • Site-wide: 39,908 out of 53,027

Advantages of genotype imputation with ethnically matched reference panel for rare variant association analyses

genomics more details view paper
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    • In genomics: 2,805 out of 3,782
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    • Site-wide: 10,333 out of 53,027

Search for early pancreatic cancer blood biomarkers in five European prospective population biobanks using metabolomics

epidemiology more details view paper
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