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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 63,046 bioRxiv papers from 279,617 authors.

Author: Andres Metspalu

Rankings

  • All-time downloads: 47,789 (rank: 284 out of 279,617)
  • Categories:
    • bioinformatics: 450 (rank: 14,471 (tie) out of 24,467)
    • epidemiology: 210 (rank: 5,585 (tie) out of 9,536)
    • genetics: 38,348 (rank: 88 out of 27,857)
    • genomics: 8,781 (rank: 1,156 out of 32,025)

Downloads per author, site-wide

Preprints

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

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    • In genetics: 14 out of 3,574
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Genomewide association study identifies 30 loci associated with bipolar disorder

genetics more details view paper
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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

genomics more details view paper
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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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    • In genetics: 121 out of 3,574
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    • Site-wide: 13,528 out of 63,046
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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
  • Downloaded 2,184 times
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    • In genetics: 184 out of 3,574
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Improved polygenic prediction by Bayesian multiple regression on summary statistics

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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    • In genetics: 208 out of 3,574
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    • Site-wide: 36,188 out of 63,046
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    • Site-wide: 39,523 out of 63,046

Cell specific eQTL analysis without sorting cells

genetics more details view paper
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    • In genetics: 256 out of 3,574
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    • Site-wide: 15,230 out of 63,046

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

genetics more details view paper
  • Downloaded 1,659 times
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    • In genetics: 272 out of 3,574
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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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    • In genetics: 288 out of 3,574
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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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    • In genetics: 328 out of 3,574
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

genomics more details view paper
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    • In genomics: 840 out of 4,328
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    • Site-wide: 36,697 out of 63,046

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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  • Year to date:
    • Site-wide: 40,705 out of 63,046
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    • Site-wide: 38,558 out of 63,046

Haplotype sharing provides insights into fine-scale population history and disease in Finland

genetics more details view paper
  • Downloaded 938 times
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    • In genetics: 613 out of 3,574
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    • Site-wide: 37,913 out of 63,046
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    • Site-wide: 45,627 out of 63,046

Mega-analysis of 31,396 individuals from 6 countries uncovers strong gene-environment interaction for human fertility

genomics more details view paper
  • Downloaded 858 times
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    • Site-wide: 44,866 out of 63,046

An epigenome-wide association study of educational attainment (n = 10,767)

genetics more details view paper
  • Downloaded 836 times
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    • In genetics: 698 out of 3,574
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Personalized Risk Prediction for Type 2 Diabetes: the Potential of Genetic Risk Scores

genetics more details view paper
  • Downloaded 691 times
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    • In genetics: 878 out of 3,574
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    • Site-wide: 55,562 out of 63,046
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    • Site-wide: 49,967 out of 63,046

An interaction map of circulating metabolites, immune gene networks and their genetic regulation

genomics more details view paper
  • Downloaded 666 times
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    • In genomics: 1,776 out of 4,328
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    • Site-wide: 46,497 out of 63,046

Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms

genetics more details view paper
  • Downloaded 652 times
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    • In genetics: 952 out of 3,574
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The genetic architecture of sporadic and recurrent miscarriage

genetics more details view paper
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    • In genetics: 983 out of 3,574
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    • Site-wide: 8,454 out of 63,046

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

genomics more details view paper
  • Downloaded 616 times
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    • In genomics: 1,905 out of 4,328
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  • Since beginning of last month:
    • Site-wide: 61,272 out of 63,046

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

genomics more details view paper
  • Downloaded 589 times
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    • In genomics: 1,970 out of 4,328
  • Year to date:
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Identifying tissues implicated in Anorexia Nervosa using Transcriptomic Imputation

genetics more details view paper
  • Downloaded 568 times
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    • In genetics: 1,114 out of 3,574
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    • Site-wide: 30,002 out of 63,046

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

genetics more details view paper
  • Downloaded 560 times
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    • In genetics: 1,131 out of 3,574
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    • Site-wide: 60,511 out of 63,046

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

genetics more details view paper
  • Downloaded 396 times
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    • In genetics: 1,651 out of 3,574
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Polygenic prediction of breast cancer: comparison of genetic predictors and implications for screening

genetics more details view paper
  • Downloaded 383 times
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    • In genetics: 1,699 out of 3,574
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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
  • Downloaded 363 times
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    • In genomics: 2,811 out of 4,328
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  • Since beginning of last month:
    • Site-wide: 21,365 out of 63,046

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

genomics more details view paper
  • Downloaded 346 times
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    • In genomics: 2,896 out of 4,328
  • Year to date:
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  • Since beginning of last month:
    • Site-wide: 22,759 out of 63,046

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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  • Since beginning of last month:
    • Site-wide: 58,343 out of 63,046

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

epidemiology more details view paper
  • Downloaded 210 times
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    • In epidemiology: 791 out of 1,556
  • Year to date:
    • Site-wide: 18,886 out of 63,046
  • Since beginning of last month:
    • Site-wide: 31,714 out of 63,046

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

bioinformatics more details view paper
  • Downloaded 142 times
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    • Site-wide: 51,849 out of 63,046
    • In bioinformatics: 5,619 out of 6,269
  • Year to date:
    • Site-wide: 29,613 out of 63,046
  • Since beginning of last month:
    • Site-wide: 16,693 out of 63,046

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