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Author: Peter R. Schofield

  • ORCiD: http://orcid.org/0000-0003-2967-9662
  • Most recently observed institution: Neuroscience Research Australia, Sydney, NSW, AU, School of Medical Sciences, University of New South Wales, Sydney, NSW, AU

Rankings

  • All-time downloads: 32,017 (rank: 3,785 out of 512,356)
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    • genetics: 25,524 (rank: 233 out of 38,759)
    • genomics: 2,934 (rank: 7,325 out of 45,764)
    • neuroscience: 2,485 (rank: 7,196 (tie) out of 73,730)
    • psychiatry and clinical psychology: 1,074 (rank: 415 (tie) out of 4,114)

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Preprints

The genetic architecture of the human cerebral cortex

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Genomewide association study identifies 30 loci associated with bipolar disorder

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Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360)

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Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

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Dynamics of Brain Structure and its Genetic Architecture over the Lifespan

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Brain Aging in Major Depressive Disorder: Results from the ENIGMA Major Depressive Disorder working group

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Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium

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Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

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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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Epigenome-wide meta-analysis of blood DNA methylation and its association with subcortical volumes: findings from the ENIGMA Epigenetics Working Group

genomics more details view paper
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Polygenic scores for major depressive disorder and depressive symptoms predict response to lithium in patients with bipolar disorder

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Planar cell polarity pathway and development of the human visual cortex

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Sex-Dependent Shared and Non-Shared Genetic Architecture Across Mood and Psychotic Disorders

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High genetic loading for schizophrenia predicts poor response to lithium in patients with bipolar disorder: A polygenic score and cross-trait genetic analysis

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Common genetic variation indicates separate etiologies for periventricular and deep white matter hyperintensities

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Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders.

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Genetic and environmental determinants of variation in the plasma lipidome of older Australian twins

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