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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 73,401 bioRxiv papers from 319,519 authors.

Author: Elliott Rees

  • ORCiD: http://orcid.org/0000-0002-6168-9222
  • Most recently observed institution: MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University

Rankings

  • All-time downloads: 9,749 (rank: 5,311 out of 319,524)
  • Categories:
    • genetics: 4,355 (rank: 3,360 out of 31,252)
    • genomics: 4,341 (rank: 3,519 out of 35,586)
    • neuroscience: 1,053 (rank: 11,905 (tie) out of 53,880)

Downloads per author, site-wide

Preprints

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

genomics more details view paper
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Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

genomics more details view paper
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Medical consequences of pathogenic CNVs in adults: Analysis of the UK Biobank

genomics more details view paper
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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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Rare copy number variants in NRXN1 and CNTN6 increase risk for Tourette syndrome

genetics more details view paper
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Genetic association study of psychotic experiences in UK Biobank

genetics more details view paper
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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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Schizophrenia-associated genomic copy number variants and subcortical brain volumes in the UK Biobank

neuroscience more details view paper
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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
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Characterization of single gene copy number variants in schizophrenia

genetics more details view paper
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The role of rare copy number variants in depression

neuroscience more details view paper
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Effects of pathogenic CNVs on physical traits in participants of the UK Biobank

genetics more details view paper
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Genetic risk for schizophrenia and developmental delay is associated with shape and microstructure of midline white matter structures

neuroscience more details view paper
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Meta-analysis of Scandinavian Schizophrenia Exomes

genetics more details view paper
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Effects of pathogenic CNVs on biochemical markers: a study on the UK Biobank

genomics more details view paper
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Synaptic protein DLG2 controls neurogenic transcriptional programs disrupted in schizophrenia and related disorders

genetics more details view paper
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