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Author: Michael C. O’Donovan

  • ORCiD: http://orcid.org/0000-0001-7073-2379
  • Most recently observed institution: MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University

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    • genetics: 29,955 (rank: 150 out of 32,490)
    • genomics: 12,007 (rank: 944 out of 37,034)
    • neuroscience: 518 (rank: 25,546 (tie) out of 56,764)

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Preprints

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

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Genomewide association study identifies 30 loci associated with bipolar disorder

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

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Genetic Identification Of Brain Cell Types Underlying Schizophrenia

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Psychiatric Genomics: An Update and an Agenda

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Contrasting regional architectures of schizophrenia and other complex diseases using fast variance components analysis

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

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Using three-dimensional regulatory chromatin interactions from adult and fetal cortex to interpret genetic results for psychiatric disorders and cognitive traits

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Sex differences in gene expression in the human fetal brain

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A genetic investigation of sex bias in the prevalence of attention deficit hyperactivity disorder

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Gene expression imputation across multiple brain regions reveals schizophrenia risk throughout development.

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Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores

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Psychosis and the level of mood incongruence in Bipolar Disorder are related to genetic liability for Schizophrenia

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

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The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function.

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A Transcriptome Wide Association Study implicates specific pre- and post-synaptic abnormalities in Schizophrenia

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The role of rare copy number variants in depression

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Novel Insight into the Aetiology of Autism Spectrum Disorder Gained by Integrating Expression Data with Genome-wide Association Statistics

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

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The independent and combined influence of schizophrenia polygenic risk score and heavy cannabis use on risk for psychotic disorder: A case-control analysis from the EUGEI study.

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Identifying novel subtypes of irritability using a developmental genetic approach

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Differences in Genetic Liability for Insomnia and Hypersomnia in Bipolar Disorder Subtypes

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Meta-analysis of Scandinavian Schizophrenia Exomes

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Synaptic protein DLG2 controls neurogenic transcriptional programs disrupted in schizophrenia and related disorders

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The rate of de novo CNVs in healthy controls

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

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Genetic association of FMRP targets with psychiatric disorders

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