Tony Simon

image of Tony Simon

Assoc Professor

Departments

Psychiatry-Medicine

Offices and Labs

MIND Bldg/UCDMC
+1 916 703 0407

Degrees

1985 PhD Developmental Psychology University of Sheffield, UK

Department and Center Affiliations

M.I.N.D. Institute and Department of Psychiatry & Behavioral Sciences

ProfessionalSocieties

Society for Neuroscience, Cognitive Neuroscience Society, Organization for Human Brain Mapping, Society for Research in Child Development, Society for Study of Behavioral Phenotypes

CBS Grad Group Affiliations

Neuroscience

Labs

Tracy DeBoer Ph.D.
  • Postdoctoral Scientist
Yukari Takarae Ph.D.
  • Postdoctoral Scientist
Zhongle Wu Ph.D.
  • Postdoctoral Scientist

Field Sites

M.I.N.D. Institute, UCDMC Campus, Sacramento website
M.I.N.D. Institute Computational Neuroimaging Lab, TB171, Davis Campus

Publications

5/21/2010 9:26:34 AM
  • Simon, T.J., Bearden, C.E., McDonald-McGinn, D., & Zackai, E. (2005) Visuospatial and numerical cognitive deficits in children with Chromosome 22q11.2 Deletion Syndrome. Cortex, 41: 131-141. Simon, T.J., Ding, L., Bish, J.P., McDonald-McGinn, D., Zackai, E.H., & Gee, J. (2005) Volumetric, connective and morphologic changes in the brains of children with chromosome 22q11.2 deletion syndrome: An integrative study. NeuroImage, 25: 169-180. Simon, T.J., Bish, J.P., Bearden, C.E., Ferrante, S., Ding, L., Nguyen, V., Gee, J., McDonald-McGinn, D., Zackai, E.H., & Emanuel, B. (2005) A multi-level analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children. Development and Psychopathology. 17, 753-784. Bish, J.P., Ferrante, S., McDonald-McGinn, D., Zackai, E.H., & Simon, T.J. (2005) Maladaptive conflict monitoring as evidence for executive dysfunction in children with chromosome 22q11.2 deletion syndrome. Developmental Science, 8: 36-43. Bish, J.P., Nguyen, V., Ding, L., Ferrante, S., & Simon, T.J. (2004) Thalamic reductions in children with chromosome 22q11.2 deletion syndrome. NeuroReport, 15, 1413-1415. Bish, J.P., Pendyal, A., Ding, L., Ferrante, H., Nguyen, V., McDonald-McGinn, D.M., Zackai, E.H., & Simon, T.J. (2006) Specific cerebellar reductions in children with chromosome 22q11.2 deletion syndrome. Neuroscience Letters. 399, 245-248. Bearden, C.E., Jawad, A.F., Lynch, D.R., Sokol, S., Kanes, S.J., McDonald-McGinn, D., Saitta, S., Harris, S., Moss, E.M., Wang, P.P., Zackai, E., Emanuel, B.S., & Simon, T.J. (2004) Effects of function COMT polymorphism on prefrontal cognitive function in the 22q11.2 deletion syndrome. American Journal of Psychiatry, 161, 1700-1702. Bearden, C.E., Jawad, A.F., Lynch, D.R., Monterosso, J.R., Sokol, S., McDonald-McGinn, D., Saitta, S., Harris, S., Moss, E.M., Wang, P.P., Zackai, E., Emanuel, B.S., & Simon, T.J. (2005) Effects of COMT genotype on behavioral symptomatology in the 22q11.2 deletion syndrome. Child Neuropsychology, 11(1), 109-117.