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Author: Lili Milani

  • ORCiD: http://orcid.org/0000-0002-5323-3102
  • 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: 51,519 (rank: 2,306 out of 513,392)
  • Categories:
    • genetic and genomic medicine: 2,443 (rank: 211 out of 6,816)
    • genetics: 32,737 (rank: 154 out of 38,777)
    • genomics: 14,329 (rank: 935 out of 45,811)
    • pharmacology and toxicology: 936 (rank: 936 (tie) out of 6,679)
    • psychiatry and clinical psychology: 1,074 (rank: 415 (tie) out of 4,114)

Downloads per author, site-wide

Preprints

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

genetics more details view paper
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Unraveling the polygenic architecture of complex traits using blood eQTL meta-analysis

genomics more details view paper
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Genomewide association study identifies 30 loci associated with bipolar disorder

genetics more details view paper
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    • In genetics: 38 out of 5,150
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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: 160 out of 5,150
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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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    • In genetics: 225 out of 5,150
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Genome-wide association study identifies 48 common genetic variants associated with handedness

genetics more details view paper
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    • In genetics: 239 out of 5,150
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Cell specific eQTL analysis without sorting cells

genetics more details view paper
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    • In genetics: 320 out of 5,150
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Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

genetic and genomic medicine more details view paper
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    • In genetic and genomic medicine: 15 out of 495
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Human loss-of-function variants suggest that partial LRRK2 inhibition is a safe therapeutic strategy for Parkinson’s disease

genomics more details view paper
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    • In genomics: 785 out of 6,455
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    • Site-wide: 45,545 out of 119,064

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: 391 out of 5,150
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    • Site-wide: 53,196 out of 119,064

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

genomics more details view paper
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    • In genomics: 1,180 out of 6,455
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    • Site-wide: 88,142 out of 119,064

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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    • In genomics: 1,456 out of 6,455
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    • Site-wide: 68,222 out of 119,064

Lifelong genetically lowered sclerostin and risk of cardiovascular disease.

genetics more details view paper
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    • In genetics: 729 out of 5,150
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    • Site-wide: 26,900 out of 119,064
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    • Site-wide: 23,169 out of 119,064

Genome-wide association study of over 40,000 bipolar disorder cases provides novel biological insights

psychiatry and clinical psychology more details view paper
  • Downloaded 1,074 times
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    • In psychiatry and clinical psychology: 43 out of 533
  • Year to date:
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    • Site-wide: 1,773 out of 119,064

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

genetics more details view paper
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    • In genetics: 966 out of 5,150
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    • Site-wide: 64,274 out of 119,064

Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutions

pharmacology and toxicology more details view paper
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    • In pharmacology and toxicology: 100 out of 1,037
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Genome-wide association studies identify 137 loci for DNA methylation biomarkers of ageing

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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    • In genomics: 2,520 out of 6,455
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    • Site-wide: 102,268 out of 119,064

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

genetics more details view paper
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    • In genetics: 1,352 out of 5,150
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    • Site-wide: 111,428 out of 119,064

Sex-Dependent Shared and Non-Shared Genetic Architecture Across Mood and Psychotic Disorders

genetics more details view paper
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    • In genetics: 1,849 out of 5,150
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    • Site-wide: 12,871 out of 119,064

Genome-wide study identifies association between HLA-B*55:01 and penicillin allergy

genetics more details view paper
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    • In genetics: 2,173 out of 5,150
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    • Site-wide: 50,700 out of 119,064

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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    • In genetic and genomic medicine: 135 out of 495
  • Year to date:
    • Site-wide: 18,974 out of 119,064
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    • Site-wide: 6,806 out of 119,064

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

genomics more details view paper
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    • In genomics: 5,777 out of 6,455
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    • Site-wide: 39,797 out of 119,064

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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    • In genetic and genomic medicine: 441 out of 495
  • Year to date:
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    • Site-wide: 6,605 out of 119,064

Mendelian randomization study of spermine oxidase and cancer risk

genetic and genomic medicine more details view paper
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