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Author: Roel A. Ophoff

  • ORCiD: http://orcid.org/0000-0002-8287-6457
  • Most recently observed institution: University Medical Center Utrecht, Department of Psychiatry, Rudolf Magnus Institute of Neuroscience

Rankings

  • All-time downloads: 41,343 (rank: 1,043 out of 426,789)
  • Categories:
    • genetics: 28,433 (rank: 193 out of 38,052)
    • genomics: 6,911 (rank: 2,654 out of 44,673)
    • microbiology: 3,848 (rank: 2,581 (tie) out of 50,831)
    • neuroscience: 2,151 (rank: 8,133 (tie) out of 72,420)

Downloads per author, site-wide

Preprints

The genetic architecture of the human cerebral cortex

genetics more details view paper
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Genomewide association study identifies 30 loci associated with bipolar disorder

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Transcriptome analysis in whole blood reveals increased microbial diversity in schizophrenia

microbiology more details view paper
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Comprehensive analysis of RNA-sequencing to find the source of 1 trillion reads across diverse adult human tissues

genomics more details view paper
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Genome-wide association study identifies 48 common genetic variants associated with handedness

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

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

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Whole Genome Sequencing in Psychiatric Disorders: the WGSPD Consortium

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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

genomics more details view paper
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Complement component 4 genes contribute sex-specific vulnerability in diverse illnesses

genetics more details view paper
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Shared vulnerability for connectome alterations across psychiatric and neurological brain disorders

neuroscience more details view paper
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Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores

genetics 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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A longitudinal model of human neuronal differentiation for functional investigation of schizophrenia polygenic risk

genetics more details view paper
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Planar cell polarity pathway and development of the human visual cortex

neuroscience more details view paper
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Genome-wide Association Study of Clinical Features in the Schizophrenia Psychiatric Genomics Consortium: Confirmation of Polygenic Effect on Negative Symptoms

genetics more details view paper
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Integrative analysis of Dupuytren's disease identifies novel risk locus and reveals a shared genetic etiology with BMI

genetics more details view paper
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Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates

genetics more details view paper
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Sex-Dependent Shared and Non-Shared Genetic Architecture Across Mood and Psychotic Disorders

genetics more details view paper
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Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies

genetics more details view paper
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Functionally distinct ERAP1 and ERAP2 are a hallmark of HLA-A29-(Birdshot) Uveitis.

genetics more details view paper
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Whole blood transcriptome analysis in bipolar disorder reveals strong lithium effect

genomics more details view paper
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Structural brain alterations in youth with psychosis and bipolar spectrum symptoms

neuroscience more details view paper
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Genetic and clinical analyses of psychosis spectrum symptoms in a large multi-ethnic youth cohort reveal significant link with ADHD.

genetics more details view paper
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Transient patterns of functional dysconnectivity in youth with psychosis spectrum symptoms

neuroscience more details view paper
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    • In neuroscience: 14,139 out of 18,003
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Gene expression imputation provides insight into the genetic architecture of frontotemporal dementia

genetics more details view paper
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