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Author: Peter 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: 10,946 (rank: 3,885 out of 298,132)
  • Categories:
    • genetics: 6,956 (rank: 2,132 out of 29,770)
    • genomics: 3,990 (rank: 3,717 (tie) out of 33,991)

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Preprints

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

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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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Comparative genetic architectures of schizophrenia in East Asian and European populations

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Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

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

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Gene based Analysis in HRC Imputed Genome Wide Association Data Identifies Three Novel Genes for Alzheimer's Disease

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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

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