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Author: Julien Bryois

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    • genetics: 36,505 (rank: 107 out of 36,587)
    • genomics: 13,169 (rank: 979 out of 42,287)

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Preprints

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

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Genetic meta-analysis identifies 9 novel loci and functional pathways for Alzheimers disease risk

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Genome-wide Analysis of Insomnia (N=1,331,010) Identifies Novel Loci and Functional Pathways

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GWAS meta-analysis (N=279,930) identifies new genes and functional links to intelligence

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Genetic Identification of Cell Types Underlying Brain Complex Traits Yields Novel Insights Into the Etiology of Parkinson’s Disease

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Genetic Identification Of Brain Cell Types Underlying Schizophrenia

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Genetic analysis identifies molecular systems and biological pathways associated with household income

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GWAS Meta-Analysis of Neuroticism (N=449,484) Identifies Novel Genetic Loci and Pathways

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Comparative genetic architectures of schizophrenia in East Asian and European populations

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The genetics of the mood disorder spectrum: genome-wide association analyses of over 185,000 cases and 439,000 controls

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Using three-dimensional regulatory chromatin interactions from adult and fetal cortex to interpret genetic results for psychiatric disorders and cognitive traits

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Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders

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

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Evaluation Of Chromatin Accessibility In Prefrontal Cortex Of Schizophrenia Cases And Controls

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Functional consequences of genetic loci associated with intelligence in a meta-analysis of 87,740 individuals

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Building a schizophrenia genetic network: Transcription Factor 4 regulates genes involved in neuronal development and schizophrenia risk.

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Examination of the Shared Genetic Basis of Anorexia Nervosa and Obsessive-Compulsive Disorder

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Reproducible Risk Loci and Psychiatric Comorbidities in Anxiety: Results from ~200,000 Million Veteran Program Participants

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Integrative analysis of rare variants and pathway information shows convergent results between immune pathways, drug targets and epilepsy genes

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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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