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Author: Peter Holmans

Rankings

  • All-time downloads: 24,535 (rank: 6,315 )
  • Categories:
    • genetics: 17,609 (rank: 766 )
    • genomics: 4,475 (rank: 5,138 )
    • neuroscience: 894 (rank: 24,325 (tie) )
    • psychiatry and clinical psychology: 1,557 (rank: 368 (tie) )

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Preprints

Modest changes in Spi1 dosage reveal the potential for altered microglial function as seen in Alzheimers disease

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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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Comparative genetic architectures of schizophrenia in East Asian and European populations

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Genome-wide association study of over 40,000 bipolar disorder cases provides novel biological insights

psychiatry and clinical psychology more details view paper
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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 risk underlying psychiatric and cognitive symptoms in Huntington’s Disease

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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

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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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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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Genetic association of FMRP targets with psychiatric disorders

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

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

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Developmental profile of psychiatric risk associated with voltage-gated cation channel activity

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