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Author: Claire Churchhouse

  • ORCiD: http://orcid.org/0000-0003-3140-6452
  • Most recently observed institution: Program in Medical and Population Genetics, Broad Institute of MIT and Harvard; Analytical and Translational Genetics Unit, Massachusetts General Hospital and Harvard Medical School; Stanley Center, Broad Institute of MIT and Harvard.

Rankings

  • All-time downloads: 45,221 (rank: 3,886 )
  • Categories:
    • bioinformatics: 402 (rank: 31,100 (tie) )
    • genetic and genomic medicine: 8,863 (rank: 104 (tie) )
    • genetics: 34,726 (rank: 162 )
    • genomics: 1,230 (rank: 20,227 (tie) )

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Preprints

Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

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    • In genetics: 18
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Common risk variants identified in autism spectrum disorder

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  • Downloaded 8,485 times
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    • Site-wide: 1,189
    • In genetics: 30
  • Year to date:
    • Site-wide: 2,809
  • Since beginning of last month:
    • Site-wide: 25,845

Genomewide association study identifies 30 loci associated with bipolar disorder

genetics more details view paper
  • Downloaded 7,478 times
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    • Site-wide: 1,388
    • In genetics: 39
  • Year to date:
    • Site-wide: 19,728
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Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

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  • Downloaded 4,806 times
  • Download rankings, all-time:
    • Site-wide: 2,517
    • In genetic and genomic medicine: 11
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Systematic single-variant and gene-based association testing of 3,700 phenotypes in 281,850 UK Biobank exomes

genetic and genomic medicine more details view paper
  • Downloaded 3,306 times
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    • Site-wide: 4,271
    • In genetic and genomic medicine: 17
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    • Site-wide: 221

Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum

genetics more details view paper
  • Downloaded 2,582 times
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    • Site-wide: 6,058
    • In genetics: 256
  • Year to date:
    • Site-wide: 24,690
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Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals

genetics more details view paper
  • Downloaded 2,070 times
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    • Site-wide: 8,371
    • In genetics: 366
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Genetic predisposition to myeloproliferative neoplasms implicates hematopoietic stem cell biology

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  • Downloaded 1,345 times
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    • In genetics: 732
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    • Site-wide: 7,526

Enrichment of rare protein truncating variants in amyotrophic lateral sclerosis patients

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  • Downloaded 1,230 times
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    • In genomics: 1,765
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Schizophrenia risk conferred by protein-coding de novo mutations

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    • In genetics: 1,366
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Exome sequencing in bipolar disorder reveals shared risk gene AKAP11 with schizophrenia

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  • Downloaded 751 times
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    • Site-wide: 37,032
    • In genetic and genomic medicine: 145
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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
  • Downloaded 402 times
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    • Site-wide: 77,613
    • In bioinformatics: 7,177
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    • Site-wide: 144,998
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    • Site-wide: None

A data harmonization pipeline to leverage external controls and boost power in GWAS

genetics more details view paper
  • Downloaded 264 times
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    • Site-wide: 107,500
    • In genetics: 4,554
  • Year to date:
    • Site-wide: 42,751
  • Since beginning of last month:
    • Site-wide: 27,362

Analysis of genetic dominance in the UK Biobank

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  • Downloaded 3 times
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    • Site-wide: 154,696
    • In genetics: 5,954
  • Year to date:
    • Site-wide: 154,682
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    • Site-wide: 65,912

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