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UC Davis MIND Institute

UC Davis MIND Institute

CABIL Publications

  • Quintero, A. I., Beaton, E. A. & Harvey, D. J. Common and specific impairments in attention functioning in girls with chromosome 22q11. 2 deletion, fragile X or Turner syndromes. Journal of … (2014) Article (PDF)

 

  • Wong, L. M., Riggins, T., Harvey, D., Cabaral, M. & Simon, T. J. Children With Chromosome 22q11.2 Deletion Syndrome Exhibit Impaired Spatial Working Memory. Am J Intellect Dev Disabil 119, 115–132 (2014)  Article (PDF)

 

  • Leow, A., Harvey, D. & Hunsaker, N. G. Altered structural brain connectome in young adult fragile X premutation carriers. Human brain … (2014). doi:10.1002/hbm.22491 Article (PDF)

 

  • Angkustsiri, K. et al. Social Impairments in Chromosome 22q11.2 Deletion Syndrome (22q11.2DS): Autism Spectrum Disorder or a Different Endophenotype? J Autism Dev Disord (2013). doi:10.1007/s10803-013-1920-x.  Article (PDF)

 

  • Shapiro, H., et al. A cross-sectional analysis of the development of response inhibition in children with Chromosome 22q11.2 Deletion Syndrome. Frontiers in Child and Neurodevelopmental Psychiatry, 4, 81 (2013).   Article (PDF)

 

  • Wong, L. M. et al. Young adult male carriers of the fragile X premutation exhibit genetically modulated impairments in visuospatial tasks controlled for psychomotor speed. J Neurodevelop Disord 4, 26 (2012).  Article (PDF)

 

  • Angkustsiri, K. et al. An examination of the relationship of anxiety and intelligence to adaptive functioning in children with chromosome 22q11.2 deletion syndrome. J Dev Behav Pediatr 33, 713–720 (2012).  Article (PDF)

 

  • Stoddard, J., Takarae, Y. & Simon, T. J. A second look: no effect of the COMT Val158Met polymorphism on conflict adaptation in youth with chromosome 22q11.2 deletion syndrome. Schizophr Res 135, 202–203 (2012).  Article (PDF)

 

  • Shapiro, H. M., Takarae, Y., Harvey, D. J., Cabaral, M. H. & Simon, T. J. A cross-sectional study of the development of volitional control of spatial attention in children with chromosome 22q11.2 deletion syndrome. J Neurodevelop Disord 4, 5 (2012).  Article (PDF)

 

  • Cabaral, M. H., Beaton, E. A., Stoddard, J. & Simon, T. J. Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome. J Neurodevelop Disord 4, 6 (2012).  Article (PDF)

 

  • Goodrich-Hunsaker, N.J. et al. (2011) Enhanced Manual and Oral Motor Reaction Time in Young Adult Female Fragile X Premutation Carriers. J. Inter. Neuropsych. Soc. 1–5 doi:10.1017/S1355617711000634.  Article (PDF)

     

  • Srivastava, S., Buonocore, M.H. & Simon, T.J. (2011) Atypical developmental trajectory of functionally significant cortical areas in children with chromosome 22q11.2 deletion syndrome. Human Brain Mapping doi:10.1002/hbm.21206.  Article (PDF)

     

  • Goodrich-Hunsaker, N.J., Wong, L.M., Mclennan, Y., Srivastava, S., Tassone, F., Harvey, D., Rivera, S., Simon, T.J. (2011) Young adult female fragile X premutation carriers show age- and genetically-modulated cognitive impairments. Brain and Cognition. doi:10.3389/fnhum.2011.00063/abstract 75, 255–260.  Article (PDF)

     

  • Goodrich-Hunsaker, N.J., Wong, L., McLennan, Y., Tassone, F., Harvey, D., Rivera, S., Simon, T.J. (2011) Adult female fragile X premutation carriers exhibit age- and CGG repeat length-related impairments on an attentionally based enumeration task. 1–7.  Frontiers in Human Neuroscience Article (PDF)

     

  • Beaton, E.A. & Simon, T.J. (2011) How might stress contribute to increased risk for schizophrenia in children with chromosome 22q11.2 deletion syndrome? Journal of Neurodevelopmental Disorders. 3, 68-75.  Article (PDF)

     

  • Stoddard, J., Beckett, L., Simon, T.J. (2011) Atypical Development of the Executive Attention Network in Children with Chromosome 22q11.2 Deletion Syndrome. Journal of Neurodevelopmental Disorders. 3, 76-85.  Article (PDF)

     

  • Beaton, E. A. et al. (2010) Increased incidence and size of cavum septum pellucidum in children with chromosome 22q11.2 deletion syndrome. Psychiatry Res 181, 108–113.   Article (PDF)

     

  • Karayiorgou, M., Simon, T.J., Gogos, J.A. (2010). 22q11.2 microdeletions: Linking DNA structural variation to brain dysfunction and schizophrenia. Nature Reviews Neuroscience. 11, 402-16.  Article (PDF)

     

  • Beaton, E. A., Stoddard, J., Lai, S., Lackney, J., Shi, J., Ross, J.L., Simon, T.J. (2010). Atypical functional brain activation during a multiple object tracking task in girls with Turner syndrome: Neurocorrelates of reduced spatiotemporal resolution. American Journal on Intellectual and Developmental Disabilities 115, 2: 140-156. Article (PDF)

     

  • Stoddard, J., Niendam, T., Hendren, R., Carter, C., Simon, T.J. (2010). Attenuated positive symptoms of psychosis in adolescents with chromosome 22q11.2 deletion syndrome. Schizophrenia Research. 2010 Jan 5. [Epub ahead of print]  Article (PDF)

     

  • Takarae, Y., Schmidt, L., Tassone, F., Simon, T.J. (2009) Catechol-O-methyltransferase polymorphism modulates cognitive control in children with chromosome 22q11.2 deletion syndrome. Cognitive and Behavioral Neuroscience 9, 83-90.  Article (PDF)

     

  • Simon, T.J., Wu, Z., Avants, B., Zhang, H., Gee, J.C., Stebbins, G.T. (2008) Atypical Cortical Connectivity and Visuospatial Cognitive Impairments are Related in Children with Chromosome 22q11.2 Deletion Syndrome. Behavioral and Brain Functions, 4: 25.  Article (PDF)

     

  • Simon, T.J., (2008) A New Account of the Neurocognitive Foundations of Impairments in Space, Time and Number Processing in Children with Chromosome 22q11.2 Deletion Syndrome. Developmental Disabilities Research Reviews. 14, 52-58.  Article (PDF)

     

  • Simon, T.J., Takarae, Y., DeBoer, T.L., McDonald-McGinn, D.M., Zackai, E.H., Ross, J.L. (2008) Overlapping Numerical Cognition Impairments In Children With Chromosome 22q11.2 Deletion Or Turner Syndromes. Neuropsychologia, 46, 82-94.  Article (PDF)

     

  • DeBoer, T., Wu, Z., Lee., A., Simon, T.J. (2007) Hippocampal volume reduction in children with chromosome 22q11.2 deletion syndrome is associated with cognitive impairment. Behavioral and Brain Functions, 3:54 (23 Oct 2007) .  Article (PDF)

     

  • Cutler-Landsman, D., Simon, T.J., & Kates, W.R. (2007) Introduction to education and the neurocognitive profile. In Cutler-Landsman, D. (Ed). Practical Handbook for Educating Children with Velo-Cardio-Facial Syndrome and Other Developmental Disabilities. Plural Publishing, San Diego, CA.

     

  • Bish, J.P., Chiodo, R., Mattei, V., Simon, T.J. (2007) Domain specific attentional impairments in children with chromosome 22q11.2 deletion syndrome. Brain and Cognition.  Article (PDF)

     

  • Simon, T.J., Burg-Malki, M., & Gothelf, D. (2007) Cognitive and behavioral characteristics of children with chromosome 22q11.2 deletion. (in press) In M.M.M. Mazzocco & J.L. Ross (Eds.) Neurogenetic Developmental Disorders: Manifestation and Identification in Childhood. Cambridge, MA: The MIT Press.  Article (PDF)

     

  • Machado, A.M.C., Simon, T.J., Nguyen, V., McDonald-McGinn, D.M., Zackai, E.H., Gee, J.C. Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndrome. (2007) Brain Research.   Article (PDF)

     

  • Bearden C.E., van Erp, T.G., Dutton, R.A., Tran, H., Zimmerman, L., Sun, D., Geaga, J., Simon, T.J., Glahn, D.C., Emanuel, B.S., Cannon, T.D., Toga, A.W., & Thompson, P.W. (2006) Mapping cortical thickness in children with 22q11.2 deletions.  Cerebral Cortex.   Article (PDF)

     

  • 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.  Article (PDF)

     

  • Simon T.J., Bish JP, Bearden CE, Ding L, Ferrante S, Nguyen V, Gee JC, McDonald-McGinn DM, Zackai EH, Emanuel BS. (2005) A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children. Dev Psychopathol. 2005 Summer;17(3):753-84.  Article (PDF)

     

  • 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 22q1 1.2 deletion syndrome: An, integrative study. NeuroImage 25: 1 69-1 80.  Article (PDF)

     

  • 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

 

  • Bearden, CE., Jawad, A.F., Lynch, D.R., Monterosso, J.R., Sokol, S., McDonald-McGinn, D., Saitta, S., Harris, S., Moss, E.M., Wang, PP., Zackai, E., Emanuel, B.S., & Simon, T.J. (2005) Effects of COMT genotype on behavioral symptomatology in the 22q1 1 .2 deletion syndrome. Child Neuropsychology, 11, 109-117.  Article (PDF) 
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  • 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.  Article (PDF)

     

  • 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.

 

  • 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.  Article (PDF)

     

  • Simon, T.J., Bearden, C.E., Moss, E.M., McGinn, D.M., Zackai, E, & Wang, P.P. (2002) Cognitive development in VCFS. Progress in Pediatric Cardiology, 15,109-117.  Article (PDF)

     

  • Bearden, C.E., Wang, P.P., & Simon, T.J. (2002) Williams Syndrome cognitive profile also characterizes Velocardiofacial/DiGeorge Syndrome. American Journal of Medical Genetics (Neuropsychiatric G enetics), 114, 689-692.  Article (PDF)

 

  • Sathian, K., Simon, T.J., Peterson, S., Patel, G., Hoffman, J.M., & Grafton, S.T. (1999) Neural evidence linking object enumeration and visual attention. Journal of Cognitive Neuroscience 11, 36-51.  Article (PDF)
  • Simon, T.J., & Vaishnavi, S. (1996) Subitizing and counting depend on different attentional mechanisms. Evidence from visual enumeration in afterimages. Perception & Psychophysics, 58,915-926.

 

  • Simon, T.J. (1997) Reconceptualizing the origins of number knowledge: A "non-numerical" account. Cognitive Development, 12, 349-372.  Article (PDF)