Author: Hyejung Won

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Preprints

Schizophrenia-linked protein tSNARE1 regulates endolysosomal trafficking in cortical neurons

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Chromatin architecture in addiction circuitry elucidates biological mechanisms underlying cigarette smoking and alcohol use traits.

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Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

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Common risk variants identified in autism spectrum disorder

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Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders.

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De novo mutations in regulatory elements cause neurodevelopmental disorders

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Widespread allelic heterogeneity in complex traits

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A genome-wide association study for shared risk across major psychiatric disorders in a nation-wide birth cohort implicates fetal neurodevelopment as a key mediator

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Neuronal and glial 3D chromatin architecture illustrates cellular etiology of brain disorders

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Integrative genomics identifies a convergent molecular subtype that links epigenomic with transcriptomic differences in autism

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Connecting gene regulatory relationships to neurobiological mechanisms of brain disorders

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Social and non-social autism symptom and trait domains are genetically dissociable

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Common genetic risk variants identified in the SPARK cohort implicate DDHD2 as a novel autism risk gene

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Expanding the Genetic Architecture of Nicotine Dependence and its Shared Genetics with Multiple Traits: Findings from the Nicotine Dependence GenOmics (iNDiGO) Consortium

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FIREcaller: Detecting Frequently Interacting Regions from Hi-C Data

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A response to Yurko et al: H-MAGMA, inheriting a shaky statistical foundation, yields excess false positives

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