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Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 67,221 bioRxiv papers from 295,976 authors.

Author: Michael C O’Donovan

  • Most recently observed institution: MRC Centre for Neuropsychiatric Genetics & Genomics, Institute of Psychological Medicine and Clinical Neurosciences, Cardiff University, School of Medicine

Rankings

  • All-time downloads: 38,746 (rank: 406 out of 295,454)
  • Categories:
    • genetics: 29,400 (rank: 138 out of 29,470)
    • genomics: 8,639 (rank: 1,289 out of 33,659)
    • neuroscience: 707 (rank: 15,319 (tie) out of 49,585)

Downloads per author, site-wide

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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Genetic Identification Of Brain Cell Types Underlying Schizophrenia

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

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Haplotypes of common SNPs can explain missing heritability of complex diseases

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Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights

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

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Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders

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Medical consequences of pathogenic CNVs in adults: Analysis of the UK Biobank

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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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Conditional GWAS analysis identifies putative disorder-specific SNPs for psychiatric disorders

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

genetics more details view paper
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Genetic association study of psychotic experiences in UK Biobank

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Using genetics to examine a general liability to childhood psychopathology

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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

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

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The role of rare copy number variants in depression

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

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

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Identifying novel subtypes of irritability using a developmental genetic approach

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

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