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Author: Roel A. Ophoff

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    • genomics: 6,694 (rank: 2,393 out of 40,588)
    • neuroscience: 2,006 (rank: 7,497 (tie) out of 63,839)

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Preprints

Gene expression imputation provides insight into the genetic architecture of frontotemporal dementia

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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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Comprehensive analysis of RNA-sequencing to find the source of 1 trillion reads across diverse adult human tissues

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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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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Dynamics of Brain Structure and its Genetic Architecture over the Lifespan

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Complement component 4 genes contribute sex-specific vulnerability in diverse illnesses

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Shared vulnerability for connectome alterations across psychiatric and neurological brain disorders

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

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

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Planar cell polarity pathway and development of the human visual cortex

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

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Integrative analysis of Dupuytren's disease identifies novel risk locus and reveals a shared genetic etiology with BMI

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Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates

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Functionally distinct ERAP1 and ERAP2 are a hallmark of HLA-A29-(Birdshot) Uveitis.

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Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies

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Whole blood transcriptome analysis in bipolar disorder reveals strong lithium effect

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Structural brain alterations in youth with psychosis and bipolar spectrum symptoms

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

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Transient patterns of functional dysconnectivity in youth with psychosis spectrum symptoms

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