Author: Tõnu Esko

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Preprints

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

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  • Site-wide: 792
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  • Site-wide: None
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  • Site-wide: 4,603

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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  • Site-wide: 2,916
  • In genetics: 122
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  • Site-wide: 23,634
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  • Site-wide: 22,664

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

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  • Site-wide: 5,388
  • In genetics: 267
• Year to date:
  • Site-wide: 106,677
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Trans-ethnic and ancestry-specific blood-cell genetics in 746,667 individuals from 5 global populations

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  • Site-wide: 6,116
  • In genetics: 309
• Year to date:
  • Site-wide: 5,702
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  • Site-wide: 11,156

Cell specific eQTL analysis without sorting cells

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  • Site-wide: 6,569
  • In genetics: 332
• Year to date:
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  • Site-wide: 78,016

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

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  • Site-wide: 7,892
  • In genetics: 396
• Year to date:
  • Site-wide: 13,586
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PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

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  • Site-wide: 8,888
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Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure

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  • Site-wide: 10,467
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  • Site-wide: 64,757

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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  • Site-wide: 13,630
  • In genomics: 1,489
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  • Site-wide: 93,564

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

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  • Site-wide: 16,267
  • In genetics: 843
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  • Site-wide: 51,587
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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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  • Site-wide: 18,002
  • In genomics: 1,899
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  • Site-wide: 35,578
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  • Site-wide: 71,788

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

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  • Site-wide: 19,446
  • In genetics: 985
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  • Site-wide: 39,064
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  • Site-wide: 117,281

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

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  • In genetics: 1,411
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  • Site-wide: 108,031
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  • Site-wide: 110,537

Functional and evolutionary impact of polymorphic inversions in the human genome

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  • Site-wide: 29,002
  • In genomics: 2,687
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  • Site-wide: 40,105
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  • Site-wide: 93,724

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

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  • Site-wide: 31,296
  • In genetics: 1,578
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  • Site-wide: 96,566

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

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  • In genetics: 2,000
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  • Site-wide: 32,001
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Polygenic prediction of breast cancer: comparison of genetic predictors and implications for screening

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  • Site-wide: 46,766
  • In genetics: 2,279
• Year to date:
  • Site-wide: 46,186
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  • Site-wide: 99,972

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

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  • Site-wide: 47,172
  • In genomics: 3,798
• Year to date:
  • Site-wide: 75,412
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  • Site-wide: 108,299

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

• Downloaded 193 times
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  • Site-wide: 98,621
  • In genomics: 5,906
• Year to date:
  • Site-wide: 72,748
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  • Site-wide: 68,404