Jennifer K. Forsyth
Affiliations: | Psychology | University of California, Los Angeles, Los Angeles, CA |
Area:
schizophrenia, cognitive neuroscience, clinical high risk, EEG, fMRIGoogle:
"Jennifer Forsyth"Cross-listing: Neurotree
Parents
Sign in to add mentor| Richard J. Beninger | research assistant | Queens University (Neurotree) | |
| William Paul Hetrick | research assistant | Indiana University (Neurotree) | |
| Brian F. O'Donnell | research assistant | Indiana University (Neurotree) | |
| Robert Asarnow | grad student | UCLA (Neurotree) | |
| Tyrone D. Cannon | grad student | UCLA (Neurotree) |
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Publications
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| 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 |
| Gokhale A, Hartwig C, Freeman AAH, et al. (2019) Systems Analysis of the 22q11.2 Microdeletion Syndrome Converges on a Mitochondrial Interactome Necessary for Synapse Function and Behavior. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience |
| Forsyth J, Nachun D, Gandal M, et al. (2019) T55SYNAPTIC AND GENE REGULATORY MECHANISMS IN SCHIZOPHRENIA, AUTISM, AND 22Q11.2 CNV MEDIATED RISK FOR NEUROPSYCHIATRIC DISORDERS European Neuropsychopharmacology. 29: S244-S245 |