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Author: Shaun M. Purcell

Rankings

  • All-time downloads: 40,664 (rank: 3,565 )
  • Categories:
    • bioinformatics: 81 (rank: 39,968 (tie) )
    • genetics: 30,692 (rank: 188 )
    • genomics: 9,891 (rank: 1,890 (tie) )

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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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Regulatory variants explain much more heritability than coding variants across 11 common diseases

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    • Site-wide: 2,330
    • In genetics: 87
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Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

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Gene Expression Elucidates Functional Impact of Polygenic Risk for Schizophrenia

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Biological and clinical insights from genetics of insomnia symptoms

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    • In genomics: 826
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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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GWAS in 446,118 European adults identifies 78 genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates

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Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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    • In genomics: 1,296
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Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits

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    • Site-wide: 13,037
    • In genetics: 638
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Gene expression imputation across multiple brain regions reveals schizophrenia risk throughout development.

genetics more details view paper
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    • In genetics: 861
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Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

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    • In genomics: 2,033
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Integrative analysis of rare variants and pathway information shows convergent results between immune pathways, drug targets and epilepsy genes

genomics more details view paper
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    • Site-wide: 30,743
    • In genomics: 2,762
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Genome-wide association analysis of excessive daytime sleepiness identifies 42 loci that suggest phenotypic subgroups

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    • Site-wide: 44,973
    • In genomics: 3,615
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Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cases

genetics more details view paper
  • Downloaded 522 times
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    • Site-wide: 50,180
    • In genetics: 2,341
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Characterization of single gene copy number variants in schizophrenia

genetics more details view paper
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    • Site-wide: 58,035
    • In genetics: 2,699
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Whole-Genome Association Analyses of Sleep-disordered Breathing Phenotypes in the NHLBI TOPMed Program

genetics more details view paper
  • Downloaded 437 times
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    • Site-wide: 61,179
    • In genetics: 2,842
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mTADA: a framework for analyzing de novo mutations in multiple traits

genomics more details view paper
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    • In genomics: 5,256
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    • Site-wide: 116,600
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Epigenome-wide association analysis of daytime sleepiness in the Multi-Ethnic Study of Atherosclerosis reveals African-American specific associations

genomics more details view paper
  • Downloaded 323 times
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    • Site-wide: 80,622
    • In genomics: 5,276
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    • Site-wide: 115,559
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A group refactorization procedure for sleep electroencephalography

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    • In bioinformatics: 10,273
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