Jennifer K. Forsyth
Affiliations: | Psychology | University of California, Los Angeles, Los Angeles, CA |
Area:
schizophrenia, cognitive neuroscience, clinical high risk, EEG, fMRIGoogle:
"Jennifer Forsyth"Mean distance: 15.72 (cluster 50) | S | N | B | C | P |
Cross-listing: PsychTree
Parents
Sign in to add mentor| Richard J. Beninger | research assistant | Queens University | |
| William Paul Hetrick | research assistant | Indiana University Bloomington | |
| Brian F. O'Donnell | research assistant | Indiana University Bloomington | |
| Robert Asarnow | grad student | UCLA | |
| Tyrone D. Cannon | grad student | UCLA |
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Publications
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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 |