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Author: George Kirov

  • ORCiD: http://orcid.org/0000-0002-3427-3950
  • 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: 25,756 (rank: 2,204 out of 425,964)
  • Categories:
    • genetics: 14,472 (rank: 886 out of 37,998)
    • genomics: 9,915 (rank: 1,605 out of 44,631)
    • neuroscience: 1,369 (rank: 13,518 (tie) out of 72,361)

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Preprints

Genomewide association study identifies 30 loci associated with bipolar disorder

genetics more details view paper
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Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders.

genomics more details view paper
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    • In genomics: 215 out of 6,253
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Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection

genomics more details view paper
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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

genetics more details view paper
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

genomics more details view paper
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Sex-biased reduction in reproductive success drives selective constraint on human genes

genetics 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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Genetic association study of psychotic experiences in UK Biobank

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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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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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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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Sex-Dependent Shared and Non-Shared Genetic Architecture Across Mood and Psychotic Disorders

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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    • In neuroscience: 6,220 out of 17,975
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Characterization of single gene copy number variants in schizophrenia

genetics more details view paper
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Genetic association of FMRP targets with psychiatric disorders

neuroscience 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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Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations

genetics more details view paper
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The rate of de novo CNVs in healthy controls

genomics 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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Analysis of diffusion tensor imaging data from UK Biobank confirms dosage effect of 15q11.2 copy-number variation on white matter and shows association with cognition

neuroscience more details view paper
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    • Site-wide: 98,287 out of 100,845
    • In neuroscience: 17,487 out of 17,975
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    • Site-wide: 98,043 out of 100,845
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    • Site-wide: 20,487 out of 100,845
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