Tony J. Simon, Ph.D.
Affiliations: | Psychiatry | University of California, Davis, Davis, CA |
Website:
http://cabil.mindinstitute.org/Google:
"Tony Simon"Mean distance: 16.04 (cluster 38)
Parents
Sign in to add mentor| David Klahr | post-doc | 1988-1991 | ||
| Allen Newell | post-doc | 1988-1991 | Carnegie Mellon / Univ. of Pittsburgh | |
| (Joint Computer Science & Psychology (w/David Klahr)) | ||||
Children
Sign in to add trainee| Andrea I. Quintero | grad student | 2011- | UC Davis |
| Abbie M. Popa | grad student | 2013- | UC Davis |
| Heather M. Shapiro | grad student | 2013 | UC Davis |
| Ling M. Wong | grad student | 2008-2013 | |
| Tracy DeBoer Riggins | post-doc | University of Maryland | |
| Naomi J. Goodrich-Hunsaker | post-doc | University of California, Davis Medical Center | |
| Carrie E. Bearden | post-doc | 2003-2004 |
BETA: Related publications
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Publications
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| Supekar K, de Los Angeles C, Ryali S, et al. (2024) Robust and replicable functional brain signatures of 22q11.2 deletion syndrome and associated psychosis: a deep neural network-based multi-cohort study. Molecular Psychiatry |
| Davies RW, Fiksinski AM, Breetvelt EJ, et al. (2020) Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome. Nature Medicine |
| Wigby K, Cordeiro L, Wilson R, et al. (2020) Adaptive functioning in children and adolescents with Trisomy X: An exploratory analysis. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics |
| Linton SR, Popa AM, Luck SJ, et al. (2020) Neural and behavioral measures suggest that cognitive and affective functioning interactions mediate risk for psychosis-proneness symptoms in youth with chromosome 22q11.2 deletion syndrome. American Journal of Medical Genetics. Part A |
| 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 |
| Cleynen I, Engchuan W, Hestand MS, et al. (2020) Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Molecular Psychiatry |
| Zhao Y, Diacou A, Johnston HR, et al. (2019) Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects. American Journal of Human Genetics |
| McCabe KL, Popa AM, Durdle C, et al. (2019) Quantifying the resolution of spatial and temporal representation in children with 22q11.2 deletion syndrome. Journal of Neurodevelopmental Disorders. 11: 40 |
| Popa AM, Cruz JR, Wong LM, et al. (2019) Seeing Eye to Eye With Threat: Atypical Threat Bias in Children With 22q11.2 Deletion Syndrome. American Journal On Intellectual and Developmental Disabilities. 124: 549-567 |
| Uljarević M, McCabe KL, Angkustsiri K, et al. (2019) Interrelationship Between Cognitive Control, Anxiety, and Restricted and Repetitive Behaviors in Children with 22q11.2 Deletion Syndrome. Autism Research : Official Journal of the International Society For Autism Research |