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Author: Andres Metspalu

  • ORCiD: http://orcid.org/0000-0002-3718-796X
  • Most recently observed institution: Estonian Genome Center, University of Tartu, Tartu, Estonia, Institute of Molecular and Cell Biology, University of Tartu

Rankings

  • All-time downloads: 62,665 (rank: 1,899 out of 510,946)
  • Categories:
    • bioinformatics: 687 (rank: 17,406 (tie) out of 36,842)
    • epidemiology: 323 (rank: 15,610 (tie) out of 23,897)
    • genetic and genomic medicine: 1,609 (rank: 559 out of 6,821)
    • genetics: 48,997 (rank: 72 out of 38,712)
    • genomics: 10,283 (rank: 1,587 out of 45,704)
    • hiv aids: 766 (rank: 59 (tie) out of 933)

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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Genomewide association study identifies 30 loci associated with bipolar disorder

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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.

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Improved polygenic prediction by Bayesian multiple regression on summary statistics

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

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Genome-wide association study identifies 48 common genetic variants associated with handedness

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

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

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Cell specific eQTL analysis without sorting cells

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

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

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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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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The genetic architecture of sporadic and recurrent miscarriage

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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)

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Personalized Risk Prediction for Type 2 Diabetes: the Potential of Genetic Risk Scores

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Identifying tissues implicated in Anorexia Nervosa using Transcriptomic Imputation

genetics more details view paper
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A high-resolution HLA reference panel capturing global population diversity enables multi-ethnic fine-mapping in HIV host response

hiv aids more details view paper
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Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms

genetics more details view paper
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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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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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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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Trans-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

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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 Trans-Ancestral Genomic Architecture of Glycaemic Traits

genetics more details view paper
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Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies

genetics more details view paper
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Advantages of genotype imputation with ethnically matched reference panel for rare variant association analyses

genomics more details view paper
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The effect of X-linked dosage compensation on complex trait variation

genetics more details view paper
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Genome-wide study identifies association between HLA-B*55:01 and penicillin allergy

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

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Genomic and phenomic insights from an atlas of genetic effects on DNA methylation

genetic and genomic medicine 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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Search for early pancreatic cancer blood biomarkers in five European prospective population biobanks using metabolomics

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

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Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome

genetic and genomic medicine more details view paper
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Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

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The landscape of autosomal-recessive pathogenic variants in European populations reveals phenotype-specific effects

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Genotype-first approach to the detection of hereditary breast and ovarian cancer risk, and effects of risk disclosure to biobank participants

genetic and genomic medicine more details view paper
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Mendelian randomization identifies the potential causal impact of dietary patterns on circulating blood metabolites

genomics more details view paper
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Genome-wide Screen of Otosclerosis in Population Biobanks: 18 Loci and Shared Heritability with Skeletal Structure

genetic and genomic medicine more details view paper
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