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Author: Peter A Holmans

  • ORCiD: http://orcid.org/0000-0003-0870-9412
  • Most recently observed institution: Medical Research Council (MRC) Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurology, School of Medicine, Cardiff University

Rankings

  • All-time downloads: 19,689 (rank: 2,809 (tie) out of 380,039)
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    • genetics: 13,673 (rank: 811 out of 35,084)
    • genomics: 5,026 (rank: 3,540 out of 40,563)
    • neuroscience: 990 (rank: 16,189 (tie) out of 63,800)

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Preprints

Genomewide association study identifies 30 loci associated with bipolar disorder

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Huntington's disease onset is determined by length of uninterrupted CAG, not encoded polyglutamine, and is modified by DNA maintenance mechanisms

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

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

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Genotype-phenotype relationships in children with Copy Number Variants associated with high neuropsychiatric risk: Findings from the case-control IMAGINE-ID cohort in the United Kingdom

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Genetic association study of psychotic experiences in UK Biobank

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Genetic risk underlying psychiatric and cognitive symptoms in Huntington’s Disease

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

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Dynamic expression of risk genes for schizophrenia and bipolar disorder across development

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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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Genetic association of FMRP targets with psychiatric disorders

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The onset and prevalence of motor and psychiatric symptoms in Huntington's disease

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Monocyte-specific changes in gene expression implicate LACTB2 and PLIN2 in Alzheimer's disease.

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