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Author: Jaana Suvisaari

Rankings

  • All-time downloads: 22,561 (rank: 13,304 )
  • Categories:
    • genetic and genomic medicine: 8,813 (rank: 231 (tie) )
    • genetics: 7,375 (rank: 3,350 (tie) )
    • genomics: 3,486 (rank: 9,153 )
    • neuroscience: 1,210 (rank: 31,021 (tie) )
    • psychiatry and clinical psychology: 489 (rank: 4,949 (tie) )

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Preprints

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

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    • Site-wide: 1,555
    • In genetic and genomic medicine: 9
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    • Site-wide: 694
  • Since beginning of last month:
    • Site-wide: 758

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

genetics more details view paper
  • Downloaded 2,453 times
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    • Site-wide: 9,537
    • In genetics: 362
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    • Site-wide: 131,959
  • Since beginning of last month:
    • Site-wide: 109,717

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

genetics more details view paper
  • Downloaded 1,956 times
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    • Site-wide: 13,451
    • In genetics: 504
  • Year to date:
    • Site-wide: 166,173
  • Since beginning of last month:
    • Site-wide: 203,583

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

genomics more details view paper
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    • Site-wide: 18,203
    • In genomics: 1,618
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Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders

genetics more details view paper
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    • Site-wide: 29,963
    • In genetics: 1,204
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Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

genomics more details view paper
  • Downloaded 1,146 times
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    • Site-wide: 31,080
    • In genomics: 2,528
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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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    • Site-wide: 52,254
    • In genomics: 3,777
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Patient iPSC-astrocytes show transcriptional and functional dysregulation in schizophrenia

neuroscience more details view paper
  • Downloaded 759 times
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    • In neuroscience: 8,296
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Variants in regulatory elements of PDE4D associate with Major Mental Illness in the Finnish population

genetics more details view paper
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    • In genetics: 2,545
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Contribution of rare and common variants to intellectual disability in a high-risk population sub-isolate of Northern Finland

genetics more details view paper
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    • Site-wide: 66,265
    • In genetics: 2,512
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Implementation of CYP2D6 copy-number imputation panel and frequency of key pharmacogenetic variants in Finnish individuals with a psychotic disorder

genetic and genomic medicine more details view paper
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    • Site-wide: 73,453
    • In genetic and genomic medicine: 443
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    • Site-wide: 110,385
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    • Site-wide: 98,226

The NDE1 genomic locus can affect treatment of psychiatric illness through gene expression changes related to MicroRNA-484

genetics more details view paper
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    • Site-wide: 89,007
    • In genetics: 3,440
  • Year to date:
    • Site-wide: 120,218
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Molecular signaling pathways underlying schizophrenia

neuroscience more details view paper
  • Downloaded 527 times
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    • Site-wide: 93,964
    • In neuroscience: 13,557
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    • Site-wide: 120,772
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Circulating lipids associate with future weight gain in individuals with an at-risk mental state and in first-episode psychosis

psychiatry and clinical psychology more details view paper
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    • In psychiatry and clinical psychology: 472
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    • Site-wide: 132,676
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    • Site-wide: 183,830

Functional characterization of six SLCO1B1 (OATP1B1) variants observed in Finnish individuals with a psychotic disorder

genetic and genomic medicine more details view paper
  • Downloaded 87 times
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    • Site-wide: 202,675
    • In genetic and genomic medicine: None
  • Year to date:
    • Site-wide: 105,652
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    • Site-wide: 132,521

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