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Author: F. Kyle Satterstrom

  • ORCiD: http://orcid.org/0000-0001-6187-7680
  • Most recently observed institution: Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital, Boston, MA 02114, USA; Program in Medical and Populati

Rankings

  • All-time downloads: 34,893 (rank: 6,435 )
  • Categories:
    • genetic and genomic medicine: 7,429 (rank: 209 )
    • genetics: 22,247 (rank: 493 )
    • genomics: 4,007 (rank: 7,264 (tie) )
    • neurology: 925 (rank: 2,068 (tie) )
    • psychiatry and clinical psychology: 285 (rank: 5,631 (tie) )

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Preprints

Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

genetics more details view paper
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    • Site-wide: 1,085
    • In genetics: 23
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    • Site-wide: 14,239
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    • Site-wide: 15,727

Common risk variants identified in autism spectrum disorder

genetics more details view paper
  • Downloaded 9,031 times
  • Download rankings, all-time:
    • Site-wide: 1,306
    • In genetics: 27
  • Year to date:
    • Site-wide: 8,105
  • Since beginning of last month:
    • Site-wide: 5,484

Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

genetic and genomic medicine more details view paper
  • Downloaded 6,338 times
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    • Site-wide: 2,066
    • In genetic and genomic medicine: 10
  • Year to date:
    • Site-wide: 840
  • Since beginning of last month:
    • Site-wide: 1,438

Transcript expression-aware annotation improves rare variant discovery and interpretation

genomics more details view paper
  • Downloaded 4,007 times
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    • Site-wide: 3,840
    • In genomics: 370
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ASD and ADHD have a similar burden of rare protein-truncating variants

genetics more details view paper
  • Downloaded 1,947 times
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    • Site-wide: 10,903
    • In genetics: 442
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The female protective effect against autism spectrum disorder

genetic and genomic medicine more details view paper
  • Downloaded 1,091 times
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    • Site-wide: 26,235
    • In genetic and genomic medicine: 135
  • Year to date:
    • Site-wide: 8,293
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Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

neurology more details view paper
  • Downloaded 925 times
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    • In neurology: 90
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Meta-analysis of Scandinavian Schizophrenia Exomes

genetics more details view paper
  • Downloaded 632 times
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    • Site-wide: 57,344
    • In genetics: 2,401
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    • Site-wide: 100,754
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    • Site-wide: 61,036

Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention deficit hyperactivity disorder

psychiatry and clinical psychology more details view paper
  • Downloaded 285 times
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    • In psychiatry and clinical psychology: 627
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