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Author: Tõnu Esko

  • Most recently observed institution: Program in Medical and Population Genetics, Broad Institute

Rankings

  • All-time downloads: 35,459 (rank: 1,101 out of 379,082)
  • Categories:
    • genetics: 24,489 (rank: 215 out of 35,032)
    • genomics: 10,970 (rank: 1,280 out of 40,497)

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Preprints

Unraveling the polygenic architecture of complex traits using blood eQTL meta-analysis

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Genomewide association study identifies 30 loci associated with bipolar disorder

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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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Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

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Cell specific eQTL analysis without sorting cells

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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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Trans-ethnic and ancestry-specific blood-cell genetics in 746,667 individuals from 5 global populations

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

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Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure

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

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    • In genetics: 741 out of 4,590
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Mega-analysis of 31,396 individuals from 6 countries uncovers strong gene-environment interaction for human fertility

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

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    • In genetics: 858 out of 4,590
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Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms

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    • In genetics: 1,189 out of 4,590
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Functional and evolutionary impact of polymorphic inversions in the human genome

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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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Polygenic prediction of breast cancer: comparison of genetic predictors and implications for screening

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Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies

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    • Site-wide: 36,598 out of 88,402

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 456 times
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    • In genomics: 3,359 out of 5,641
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    • Site-wide: 58,068 out of 88,402

Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

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    • In genomics: 5,369 out of 5,641
  • Year to date:
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  • Since beginning of last month:
    • Site-wide: 7,337 out of 88,402

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