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Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 66,889 bioRxiv papers from 294,495 authors.

Author: George Kirov

Rankings

  • All-time downloads: 19,109 (rank: 1,473 out of 294,600)
  • Categories:
    • genetics: 10,572 (rank: 891 out of 29,418)
    • genomics: 7,845 (rank: 1,542 out of 33,528)
    • neuroscience: 692 (rank: 15,510 (tie) out of 49,377)

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Preprints

The rate of de novo CNVs in healthy controls

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No bioRxiv download data for this paper yet.

Genomewide association study identifies 30 loci associated with bipolar disorder

genetics more details view paper
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    • Site-wide: 282 out of 66,916
    • In genetics: 33 out of 3,770
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    • Site-wide: 313 out of 66,916
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    • Site-wide: 1,716 out of 66,916

Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders.

genomics more details view paper
  • Downloaded 3,231 times
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    • In genomics: 250 out of 4,551
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    • Site-wide: 206 out of 66,916
  • Since beginning of last month:
    • Site-wide: 798 out of 66,916

Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection

genomics more details view paper
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    • Site-wide: 42,019 out of 66,916
  • Since beginning of last month:
    • Site-wide: 37,273 out of 66,916

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

genetics more details view paper
  • Downloaded 1,609 times
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    • Site-wide: 51,231 out of 66,916
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

genomics more details view paper
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    • In genomics: 881 out of 4,551
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    • Site-wide: 41,223 out of 66,916

Medical consequences of pathogenic CNVs in adults: Analysis of the UK Biobank

genomics more details view paper
  • Downloaded 830 times
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    • Site-wide: 35,297 out of 66,916

Association between schizophrenia and both loss of function and missense mutations in paralog conserved sites of voltage-gated sodium channels

genetics more details view paper
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    • Site-wide: 38,790 out of 66,916

Genetic association study of psychotic experiences in UK Biobank

genetics more details view paper
  • Downloaded 556 times
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    • In genetics: 1,224 out of 3,770
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    • Site-wide: 16,196 out of 66,916

Genome-wide Association Study of Clinical Features in the Schizophrenia Psychiatric Genomics Consortium: Confirmation of Polygenic Effect on Negative Symptoms

genetics more details view paper
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    • Site-wide: 36,197 out of 66,916

Schizophrenia-associated genomic copy number variants and subcortical brain volumes in the UK Biobank

neuroscience more details view paper
  • Downloaded 384 times
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    • In neuroscience: 4,876 out of 11,996
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    • Site-wide: 46,871 out of 66,916

Analyses of rare and common alleles in parent-proband trios implicate rare missense variants in SLC6A1 in schizophrenia and confirm the involvement of loss of function intolerant and neurodevelopmental disorder genes.

genetics more details view paper
  • Downloaded 346 times
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    • In genetics: 1,992 out of 3,770
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    • Site-wide: 14,063 out of 66,916

Characterization of single gene copy number variants in schizophrenia

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  • Downloaded 319 times
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    • In genetics: 2,142 out of 3,770
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    • Site-wide: 30,700 out of 66,916

The role of rare copy number variants in depression

neuroscience more details view paper
  • Downloaded 308 times
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    • In neuroscience: 6,138 out of 11,996
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  • Since beginning of last month:
    • Site-wide: 43,001 out of 66,916

Effects of pathogenic CNVs on physical traits in participants of the UK Biobank

genetics more details view paper
  • Downloaded 275 times
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    • Site-wide: 38,583 out of 66,916
    • In genetics: 2,377 out of 3,770
  • Year to date:
    • Site-wide: 49,207 out of 66,916
  • Since beginning of last month:
    • Site-wide: None out of 66,916

Effects of pathogenic CNVs on biochemical markers: a study on the UK Biobank

genomics more details view paper
  • Downloaded 145 times
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    • Site-wide: 55,783 out of 66,916
    • In genomics: 4,188 out of 4,551
  • Year to date:
    • Site-wide: 35,243 out of 66,916
  • Since beginning of last month:
    • Site-wide: 7,836 out of 66,916

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