Jennifer K. Forsyth

Psychology University of California, Los Angeles, Los Angeles, CA 
schizophrenia, cognitive neuroscience, clinical high risk, EEG, fMRI
"Jennifer Forsyth"
Mean distance: 15.72 (cluster 50)
Cross-listing: PsychTree

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Ge R, Ching CRK, Bassett AS, et al. (2024) Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome. Human Brain Mapping. 45: e26553
Forsyth JK, Bearden CE. (2023) Rethinking the First Episode of Schizophrenia: Identifying Convergent Mechanisms During Development and Moving Toward Prediction. The American Journal of Psychiatry. 180: 792-804
Jalbrzikowski M, Lin A, Vajdi A, et al. (2022) Longitudinal trajectories of cortical development in 22q11.2 copy number variants and typically developing controls. Molecular Psychiatry
Lin A, Forsyth JK, Hoftman GD, et al. (2021) Transcriptomic profiling of whole blood in 22q11.2 reciprocal copy number variants reveals that cell proportion highly impacts gene expression. Brain, Behavior, & Immunity - Health. 18: 100386
Cao H, Chen OY, McEwen SC, et al. (2020) Cross-paradigm connectivity: reliability, stability, and utility. Brain Imaging and Behavior
Ching CRK, Gutman BA, Sun D, et al. (2020) Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness. The American Journal of Psychiatry. appiajp201919060583
Forsyth JK, Asarnow RF. (2020) Genetics of Childhood-onset Schizophrenia 2019 Update. Child and Adolescent Psychiatric Clinics of North America. 29: 157-170
Hoftman G, Forsyth J, Mennigen E, et al. (2020) Association of Human Supragranular Enriched Gene Expression With Cortical Thickness Patterns in 22q11.2 Deletion Syndrome Biological Psychiatry. 87: S366
Forsyth JK, Nachun D, Gandal MJ, et al. (2019) Synaptic and Gene Regulatory Mechanisms in Schizophrenia, Autism, and 22q11.2 Copy Number Variant-Mediated Risk for Neuropsychiatric Disorders. Biological Psychiatry
Villalón-Reina JE, Martínez K, Qu X, et al. (2019) Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study. Molecular Psychiatry
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