Tony J. Simon, Ph.D. - Publications

Affiliations: 
Psychiatry University of California, Davis, Davis, CA 
Website:
http://cabil.mindinstitute.org/

88 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 Sun D, Ching CRK, Lin A, Forsyth JK, Kushan L, Vajdi A, Jalbrzikowski M, Hansen L, Villalon-Reina JE, Qu X, Jonas RK, van Amelsvoort T, Bakker G, Kates WR, Antshel KM, ... ... Simon TJ, et al. Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size. Molecular Psychiatry. PMID 29895892 DOI: 10.1038/s41380-018-0078-5  0.72
2017 Jensen M, Kooy RF, Simon TJ, Reyniers E, Girirajan S, Tassone F. A higher rare CNV burden in the genetic background potentially contributes to intellectual disability phenotypes in 22q11.2 deletion syndrome. European Journal of Medical Genetics. PMID 29191496 DOI: 10.1016/j.ejmg.2017.11.016  0.68
2017 Guo T, Repetto GM, McDonald McGinn DM, Chung JH, Nomaru H, Campbell CL, Blonska A, Bassett AS, Chow EWC, Mlynarski EE, Swillen A, Vermeesch J, Devriendt K, Gothelf D, Carmel M, ... ... Simon TJ, et al. Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3. Circulation. Cardiovascular Genetics. 10. PMID 29025761 DOI: 10.1161/CIRCGENETICS.116.001690  0.72
2017 Zhan L, Jenkins LM, Zhang A, Conte G, Forbes A, Harvey D, Angkustsiri K, Goodrich-Hunsaker NJ, Durdle C, Lee A, Schumann C, Carmichael O, Kalish K, Leow AD, Simon TJ. Baseline connectome modular abnormalities in the childhood phase of a longitudinal study on individuals with chromosome 22q11.2 deletion syndrome. Human Brain Mapping. PMID 28990258 DOI: 10.1002/hbm.23838  0.8
2017 Wang JY, Hessl D, Hagerman RJ, Simon TJ, Tassone F, Ferrer E, Rivera SM. Abnormal trajectories in cerebellum and brainstem volumes in carriers of the fragile X premutation. Neurobiology of Aging. 55: 11-19. PMID 28391068 DOI: 10.1016/j.neurobiolaging.2017.03.018  0.68
2017 Weisman O, Guri Y, Gur RE, McDonald-McGinn DM, Calkins ME, Tang SX, Emanuel B, Zackai EH, Eliez S, Schneider M, Schaer M, Kates WR, Antshel KM, Fremont W, Shashi V, ... ... Simon TJ, et al. Subthreshold Psychosis in 22q11.2 Deletion Syndrome: Multisite Naturalistic Study. Schizophrenia Bulletin. PMID 28204757 DOI: 10.1093/schbul/sbx005  0.72
2016 Mlynarski EE, Xie M, Taylor D, Sheridan MB, Guo T, Racedo SE, McDonald-McGinn DM, Chow EW, Vorstman J, Swillen A, Devriendt K, Breckpot J, Digilio MC, Marino B, Dallapiccola B, ... ... Simon TJ, et al. Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome. Human Genetics. PMID 26742502 DOI: 10.1007/s00439-015-1623-9  1
2015 Scott JA, Goodrich-Hunsaker N, Kalish K, Lee A, Hunsaker MR, Schumann CM, Carmichael OT, Simon TJ. The hippocampi of children with chromosome 22q11.2 deletion syndrome have localized anterior alterations that predict severity of anxiety. Journal of Psychiatry & Neuroscience : Jpn. 41: 140299. PMID 26599134 DOI: 10.1503/jpn.140299  1
2015 Napoli E, Tassone F, Wong S, Angkustsiri K, Simon TJ, Song G, Giulivi C. Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome. The Journal of Biological Chemistry. 290: 23240-53. PMID 26221035 DOI: 10.1074/jbc.M115.672360  1
2015 Nordahl CW, Iosif AM, Young GS, Perry LM, Dougherty R, Lee A, Li D, Buonocore MH, Simon T, Rogers S, Wandell B, Amaral DG. Sex differences in the corpus callosum in preschool-aged children with autism spectrum disorder. Molecular Autism. 6: 26. PMID 25973163 DOI: 10.1186/s13229-015-0005-4  1
2015 Mlynarski EE, Sheridan MB, Xie M, Guo T, Racedo SE, McDonald-McGinn DM, Gai X, Chow EW, Vorstman J, Swillen A, Devriendt K, Breckpot J, Digilio MC, Marino B, Dallapiccola B, ... ... Simon TJ, et al. Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome. American Journal of Human Genetics. 96: 753-64. PMID 25892112 DOI: 10.1016/j.ajhg.2015.03.007  1
2015 Deng Y, Goodrich-Hunsaker NJ, Cabaral M, Amaral DG, Buonocore MH, Harvey D, Kalish K, Carmichael OT, Schumann CM, Lee A, Dougherty RF, Perry LM, Wandell BA, Simon TJ. Disrupted fornix integrity in children with chromosome 22q11.2 deletion syndrome. Psychiatry Research. 232: 106-14. PMID 25748884 DOI: 10.1016/j.pscychresns.2015.02.002  1
2015 Vorstman JA, Breetvelt EJ, Duijff SN, Eliez S, Schneider M, Jalbrzikowski M, Armando M, Vicari S, Shashi V, Hooper SR, Chow EW, Fung WL, Butcher NJ, Young DA, McDonald-McGinn DM, ... ... Simon TJ, et al. Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome. Jama Psychiatry. 72: 377-85. PMID 25715178 DOI: 10.1001/jamapsychiatry.2014.2671  1
2015 Wong LM, Tassone F, Rivera SM, Simon TJ. Temporal dynamics of attentional selection in adult male carriers of the fragile X premutation allele and adult controls. Frontiers in Human Neuroscience. 9: 37. PMID 25698960 DOI: 10.3389/fnhum.2015.00037  1
2015 Stephenson DD, Beaton EA, Weems CF, Angkustsiri K, Simon TJ. Identifying patterns of anxiety and depression in children with chromosome 22q11.2 deletion syndrome: comorbidity predicts behavioral difficulties and impaired functional communications. Behavioural Brain Research. 276: 190-8. PMID 24906195 DOI: 10.1016/j.bbr.2014.05.056  1
2014 Wong LM, Goodrich-Hunsaker NJ, McLennan YA, Tassone F, Rivera SM, Simon TJ. A cross-sectional analysis of orienting of visuospatial attention in child and adult carriers of the fragile X premutation. Journal of Neurodevelopmental Disorders. 6: 45. PMID 25937844 DOI: 10.1186/1866-1955-6-45  1
2014 Hwang VJ, Maar D, Regan J, Angkustsiri K, Simon TJ, Tassone F. Mapping the deletion endpoints in individuals with 22q11.2 deletion syndrome by droplet digital PCR. Bmc Medical Genetics. 15: 106. PMID 25312060 DOI: 10.1186/s12881-014-0106-5  0.68
2014 Sellier C, Hwang VJ, Dandekar R, Durbin-Johnson B, Charlet-Berguerand N, Ander BP, Sharp FR, Angkustsiri K, Simon TJ, Tassone F. Decreased DGCR8 expression and miRNA dysregulation in individuals with 22q11.2 deletion syndrome. Plos One. 9: e103884. PMID 25084529 DOI: 10.1371/journal.pone.0103884  1
2014 Shapiro HM, Tassone F, Choudhary NS, Simon TJ. The development of cognitive control in children with chromosome 22q11.2 deletion syndrome. Frontiers in Psychology. 5: 566. PMID 24959159 DOI: 10.3389/fpsyg.2014.00566  1
2014 Wong LM, Goodrich-Hunsaker NJ, McLennan Y, Tassone F, Zhang M, Rivera SM, Simon TJ. Eye movements reveal impaired inhibitory control in adult male fragile X premutation carriers asymptomatic for FXTAS. Neuropsychology. 28: 571-84. PMID 24773414 DOI: 10.1037/neu0000066  1
2014 Wong LM, Riggins T, Harvey D, Cabaral M, Simon TJ. Children with chromosome 22q11.2 deletion syndrome exhibit impaired spatial working memory. American Journal On Intellectual and Developmental Disabilities. 119: 115-32. PMID 24679349 DOI: 10.1352/1944-7558-119.2.115  1
2014 Quintero AI, Beaton EA, Harvey DJ, Ross JL, Simon TJ. Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes. Journal of Neurodevelopmental Disorders. 6: 5. PMID 24628892 DOI: 10.1186/1866-1955-6-5  1
2014 Leow A, Harvey D, Goodrich-Hunsaker NJ, Gadelkarim J, Kumar A, Zhan L, Rivera SM, Simon TJ. Altered structural brain connectome in young adult fragile X premutation carriers. Human Brain Mapping. 35: 4518-30. PMID 24578183 DOI: 10.1002/hbm.22491  1
2014 Schneider M, Debbané M, Bassett AS, Chow EW, Fung WL, van den Bree M, Owen M, Murphy KC, Niarchou M, Kates WR, Antshel KM, Fremont W, McDonald-McGinn DM, Gur RE, Zackai EH, ... ... Simon TJ, et al. Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. The American Journal of Psychiatry. 171: 627-39. PMID 24577245 DOI: 10.1176/appi.ajp.2013.13070864  1
2014 Kim SY, Tassone F, Simon TJ, Rivera SM. Altered neural activity in the 'when' pathway during temporal processing in fragile X premutation carriers. Behavioural Brain Research. 261: 240-8. PMID 24398265 DOI: 10.1016/j.bbr.2013.12.044  1
2014 Angkustsiri K, Goodlin-Jones B, Deprey L, Brahmbhatt K, Harris S, Simon TJ. Social impairments in chromosome 22q11.2 deletion syndrome (22q11.2DS): autism spectrum disorder or a different endophenotype? Journal of Autism and Developmental Disorders. 44: 739-46. PMID 24045981 DOI: 10.1007/s10803-013-1920-x  1
2013 Kim SY, Hashimoto R, Tassone F, Simon TJ, Rivera SM. Altered neural activity of magnitude estimation processing in adults with the fragile X premutation. Journal of Psychiatric Research. 47: 1909-16. PMID 24045061 DOI: 10.1016/j.jpsychires.2013.08.014  1
2013 Shapiro HM, Wong LM, Simon TJ. A cross-sectional analysis of the development of response inhibition in children with chromosome 22q11.2 deletion syndrome. Frontiers in Psychiatry. 4: 81. PMID 23966958 DOI: 10.3389/fpsyt.2013.00081  1
2013 Villalon-Reina J, Jahanshad N, Beaton E, Toga AW, Thompson PM, Simon TJ. White matter microstructural abnormalities in girls with chromosome 22q11.2 deletion syndrome, Fragile X or Turner syndrome as evidenced by diffusion tensor imaging. Neuroimage. 81: 441-54. PMID 23602925 DOI: 10.1016/j.neuroimage.2013.04.028  1
2012 GadElkarim JJ, Schonfeld D, Ajilore O, Zhan L, Zhang AF, Feusner JD, Thompson PM, Simon TJ, Kumar A, Leow AD. A framework for quantifying node-level community structure group differences in brain connectivity networks. Medical Image Computing and Computer-Assisted Intervention : Miccai ... International Conference On Medical Image Computing and Computer-Assisted Intervention. 15: 196-203. PMID 23286049  1
2012 Wong LM, Goodrich-Hunsaker NJ, McLennan Y, Tassone F, Harvey D, Rivera SM, Simon TJ. Young adult male carriers of the fragile X premutation exhibit genetically modulated impairments in visuospatial tasks controlled for psychomotor speed. Journal of Neurodevelopmental Disorders. 4: 26. PMID 23148490 DOI: 10.1186/1866-1955-4-26  1
2012 Angkustsiri K, Leckliter I, Tartaglia N, Beaton EA, Enriquez J, Simon TJ. An examination of the relationship of anxiety and intelligence to adaptive functioning in children with chromosome 22q11.2 deletion syndrome. Journal of Developmental and Behavioral Pediatrics : Jdbp. 33: 713-20. PMID 23117596 DOI: 10.1097/DBP.0b013e318272dd24  1
2012 Herman SB, Guo T, McGinn DM, Blonska A, Shanske AL, Bassett AS, Chow EW, Bowser M, Sheridan M, Beemer F, Devriendt K, Swillen A, Breckpot J, Digilio MC, Marino B, ... ... Simon T, et al. Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. American Journal of Medical Genetics. Part A. 158: 2781-7. PMID 23034814 DOI: 10.1002/ajmg.a.35512  1
2012 Cabaral MH, Beaton EA, Stoddard J, Simon TJ. Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome. Journal of Neurodevelopmental Disorders. 4: 6. PMID 22958454 DOI: 10.1186/1866-1955-4-6  1
2012 Shapiro HM, Takarae Y, Harvey DJ, Cabaral MH, Simon TJ. A cross-sectional study of the development of volitional control of spatial attention in children with chromosome 22q11.2 deletion syndrome. Journal of Neurodevelopmental Disorders. 4: 5. PMID 22958432 DOI: 10.1186/1866-1955-4-5  1
2012 Stoddard J, Takarae Y, Simon TJ. A second look: no effect of the COMT Val158Met polymorphism on conflict adaptation in youth with chromosome 22q11.2 deletion syndrome. Schizophrenia Research. 135: 202-3. PMID 22245443 DOI: 10.1016/j.schres.2011.12.011  1
2012 Nordahl CW, Scholz R, Yang X, Buonocore MH, Simon T, Rogers S, Amaral DG. Increased rate of amygdala growth in children aged 2 to 4 years with autism spectrum disorders: a longitudinal study. Archives of General Psychiatry. 69: 53-61. PMID 22213789 DOI: 10.1001/archgenpsychiatry.2011.145  1
2012 Srivastava S, Buonocore MH, Simon TJ. Atypical developmental trajectory of functionally significant cortical areas in children with chromosome 22q11.2 deletion syndrome. Human Brain Mapping. 33: 213-23. PMID 21416559 DOI: 10.1002/hbm.21206  1
2011 Nordahl CW, Lange N, Li DD, Barnett LA, Lee A, Buonocore MH, Simon TJ, Rogers S, Ozonoff S, Amaral DG. Brain enlargement is associated with regression in preschool-age boys with autism spectrum disorders. Proceedings of the National Academy of Sciences of the United States of America. 108: 20195-200. PMID 22123952 DOI: 10.1073/pnas.1107560108  1
2011 Goodrich-Hunsaker NJ, Wong LM, McLennan Y, Tassone F, Harvey D, Rivera SM, Simon TJ. Adult Female Fragile X Premutation Carriers Exhibit Age- and CGG Repeat Length-Related Impairments on an Attentionally Based Enumeration Task. Frontiers in Human Neuroscience. 5: 63. PMID 21808616 DOI: 10.3389/fnhum.2011.00063  1
2011 Guo T, McDonald-McGinn D, Blonska A, Shanske A, Bassett AS, Chow E, Bowser M, Sheridan M, Beemer F, Devriendt K, Swillen A, Breckpot J, Digilio MC, Marino B, Dallapiccola B, ... ... Simon TJ, et al. Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. Human Mutation. 32: 1278-89. PMID 21796729 DOI: 10.1002/humu.21568  1
2011 Simon TJ. Clues to the foundations of numerical cognitive impairments: evidence from genetic disorders. Developmental Neuropsychology. 36: 788-805. PMID 21761998 DOI: 10.1080/87565641.2010.549879  1
2011 Goodrich-Hunsaker NJ, Wong LM, McLennan Y, Tassone F, Harvey D, Rivera SM, Simon TJ. Enhanced manual and oral motor reaction time in young adult female fragile X premutation carriers. Journal of the International Neuropsychological Society : Jins. 17: 746-50. PMID 21554789 DOI: 10.1017/S1355617711000634  1
2011 Stoddard J, Beckett L, Simon TJ. Atypical development of the executive attention network in children with chromosome 22q11.2 deletion syndrome. Journal of Neurodevelopmental Disorders. 3: 76-85. PMID 21475729 DOI: 10.1007/s11689-010-9070-3  1
2011 Beaton EA, Simon TJ. How might stress contribute to increased risk for schizophrenia in children with chromosome 22q11.2 deletion syndrome? Journal of Neurodevelopmental Disorders. 3: 68-75. PMID 21475728 DOI: 10.1007/s11689-010-9069-9  1
2011 Goodrich-Hunsaker NJ, Wong LM, McLennan Y, Srivastava S, Tassone F, Harvey D, Rivera SM, Simon TJ. Young adult female fragile X premutation carriers show age- and genetically-modulated cognitive impairments. Brain and Cognition. 75: 255-60. PMID 21295394 DOI: 10.1016/j.bandc.2011.01.001  1
2010 Karayiorgou M, Simon TJ, Gogos JA. 22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia. Nature Reviews. Neuroscience. 11: 402-16. PMID 20485365 DOI: 10.1038/nrn2841  1
2010 Simon TJ. Rewards and challenges of cognitive neuroscience studies of persons with intellectual and developmental disabilities. American Journal On Intellectual and Developmental Disabilities. 115: 79-82. PMID 20441387 DOI: 10.1352/1944-7558-115.2.79  1
2010 Beaton EA, Stoddard J, Lai S, Lackey J, Shi J, Ross JL, Simon TJ. 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: 140-56. PMID 20441384 DOI: 10.1352/1944-7558-115.2.140  1
2010 Beaton EA, Qin Y, Nguyen V, Johnson J, Pinter JD, Simon TJ. Increased incidence and size of cavum septum pellucidum in children with chromosome 22q11.2 deletion syndrome. Psychiatry Research. 181: 108-13. PMID 20074913 DOI: 10.1016/j.pscychresns.2009.10.009  1
2010 Stoddard J, Niendam T, Hendren R, Carter C, Simon TJ. Attenuated positive symptoms of psychosis in adolescents with chromosome 22q11.2 deletion syndrome. Schizophrenia Research. 118: 118-21. PMID 20056393 DOI: 10.1016/j.schres.2009.12.011  1
2009 Takarae Y, Schmidt L, Tassone F, Simon TJ. Catechol-O-methyltransferase polymorphism modulates cognitive control in children with chromosome 22q11.2 deletion syndrome. Cognitive, Affective & Behavioral Neuroscience. 9: 83-90. PMID 19246329 DOI: 10.3758/CABN.9.1.83  1
2009 Bearden CE, van Erp TG, Dutton RA, Lee AD, Simon TJ, Cannon TD, Emanuel BS, McDonald-McGinn D, Zackai EH, Thompson PM. Alterations in midline cortical thickness and gyrification patterns mapped in children with 22q11.2 deletions. Cerebral Cortex (New York, N.Y. : 1991). 19: 115-26. PMID 18483006 DOI: 10.1093/cercor/bhn064  1
2008 Simon TJ, Wu Z, Avants B, Zhang H, Gee JC, Stebbins GT. Atypical cortical connectivity and visuospatial cognitive impairments are related in children with chromosome 22q11.2 deletion syndrome. Behavioral and Brain Functions : Bbf. 4: 25. PMID 18559106 DOI: 10.1186/1744-9081-4-25  1
2008 Yushkevich PA, Zhang H, Simon TJ, Gee JC. Structure-specific statistical mapping of white matter tracts. Neuroimage. 41: 448-61. PMID 18407524 DOI: 10.1016/j.neuroimage.2008.01.013  1
2008 Nordahl CW, Simon TJ, Zierhut C, Solomon M, Rogers SJ, Amaral DG. Brief report: methods for acquiring structural MRI data in very young children with autism without the use of sedation. Journal of Autism and Developmental Disorders. 38: 1581-90. PMID 18157624 DOI: 10.1007/s10803-007-0514-x  1
2008 Simon TJ, Takarae Y, DeBoer T, McDonald-McGinn DM, Zackai EH, Ross JL. Overlapping numerical cognition impairments in children with chromosome 22q11.2 deletion or Turner syndromes. Neuropsychologia. 46: 82-94. PMID 17920087 DOI: 10.1016/j.neuropsychologia.2007.08.016  1
2008 Zhang H, Yushkevich PA, Simon TJ, Gee JC. Surface-based modeling of white matter fasciculi with orientation encoding 2008 5th Ieee International Symposium On Biomedical Imaging: From Nano to Macro, Proceedings, Isbi. 708-711. DOI: 10.1109/ISBI.2008.4541094  1
2008 Awate SP, Zhang H, Simon TJ, Gee JC. Multivariate segmentation of brain tissues by fusion of MRI and DTI data 2008 5th Ieee International Symposium On Biomedical Imaging: From Nano to Macro, Proceedings, Isbi. 213-216. DOI: 10.1109/ISBI.2008.4540970  1
2008 Simon TJ. 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. DOI: 10.1002/ddrr.8  1
2007 Sun H, Yushkevich PA, Zhang H, Cook PA, Duda JT, Simon TJ, Gee JC. Evaluation of shape-based normalization in the corpus callosum for white matter connectivity analysis. Medical Image Computing and Computer-Assisted Intervention : Miccai ... International Conference On Medical Image Computing and Computer-Assisted Intervention. 10: 777-84. PMID 18044639  1
2007 Deboer T, Wu Z, Lee A, Simon TJ. Hippocampal volume reduction in children with chromosome 22q11.2 deletion syndrome is associated with cognitive impairment. Behavioral and Brain Functions : Bbf. 3: 54. PMID 17956622 DOI: 10.1186/1744-9081-3-54  1
2007 Sun H, Yushkevich PA, Zhang H, Cook PA, Duda JT, Simon TJ, Gee JC. Shape-based normalization of the corpus callosum for DTI connectivity analysis. Ieee Transactions On Medical Imaging. 26: 1166-78. PMID 17896590 DOI: 10.1109/TMI.2007.900322  1
2007 Simon TJ. Cognitive characteristics of children with genetic syndromes. Child and Adolescent Psychiatric Clinics of North America. 16: 599-616. PMID 17562581 DOI: 10.1016/j.chc.2007.03.002  1
2007 Bish JP, Chiodo R, Mattei V, Simon TJ. Domain specific attentional impairments in children with chromosome 22q11.2 deletion syndrome. Brain and Cognition. 64: 265-73. PMID 17499412 DOI: 10.1016/j.bandc.2007.03.007  1
2007 Machado AM, Simon TJ, Nguyen V, McDonald-McGinn DM, Zackai EH, Gee JC. Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndrome. Brain Research. 1131: 197-210. PMID 17169351 DOI: 10.1016/j.brainres.2006.10.082  1
2007 Bearden CE, van Erp TG, Dutton RA, Tran H, Zimmermann L, Sun D, Geaga JA, Simon TJ, Glahn DC, Cannon TD, Emanuel BS, Toga AW, Thompson PM. Mapping cortical thickness in children with 22q11.2 deletions. Cerebral Cortex (New York, N.Y. : 1991). 17: 1889-98. PMID 17056649 DOI: 10.1093/cercor/bhl097  1
2007 Yushkevich PA, Zhang H, Simon TJ, Gee JC. Structure-specific statistical mapping of white matter tracts using the continuous medial representation Proceedings of the Ieee International Conference On Computer Vision. DOI: 10.1109/ICCV.2007.4409169  1
2006 Bish JP, Pendyal A, Ding L, Ferrante H, Nguyen V, McDonald-McGinn D, Zackai E, Simon TJ. Specific cerebellar reductions in children with chromosome 22q11.2 deletion syndrome. Neuroscience Letters. 399: 245-8. PMID 16517069 DOI: 10.1016/j.neulet.2006.02.001  1
2006 Sun H, Yushkevich PA, Zhang H, Gee JC, Simon TJ. Efficient generation of shape-based reference frames for the corpus callosum for DTI-based connectivity analysis Proceedings of the Ieee Computer Society Conference On Computer Vision and Pattern Recognition. 2006. DOI: 10.1109/CVPRW.2006.68  1
2005 Simon TJ, Bish JP, Bearden CE, Ding L, Ferrante S, Nguyen V, Gee JC, McDonald-McGinn DM, Zackai EH, Emanuel BS. A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children. Development and Psychopathology. 17: 753-84. PMID 16262991 DOI: 10.1017/S0954579405050364  1
2005 Bearden CE, Jawad AF, Lynch DR, Monterossso JR, Sokol S, McDonald-McGinn DM, Saitta SC, Harris SE, Moss E, Wang PP, Zackai E, Emanuel BS, Simon TJ. Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion Syndrome. Child Neuropsychology : a Journal On Normal and Abnormal Development in Childhood and Adolescence. 11: 109-17. PMID 15846854 DOI: 10.1080/09297040590911239  1
2005 Simon TJ, Ding L, Bish JP, McDonald-McGinn DM, Zackai EH, Gee J. Volumetric, connective, and morphologic changes in the brains of children with chromosome 22q11.2 deletion syndrome: an integrative study. Neuroimage. 25: 169-80. PMID 15734353 DOI: 10.1016/j.neuroimage.2004.11.018  1
2005 Simon TJ, Bearden CE, Mc-Ginn DM, Zackai E. Visuospatial and numerical cognitive deficits in children with chromosome 22q11.2 deletion syndrome. Cortex; a Journal Devoted to the Study of the Nervous System and Behavior. 41: 145-55. PMID 15714897  1
2005 Bish JP, Ferrante SM, McDonald-McGinn D, Zackai E, Simon TJ. Maladaptive conflict monitoring as evidence for executive dysfunction in children with chromosome 22q11.2 deletion syndrome. Developmental Science. 8: 36-43. PMID 15647065 DOI: 10.1111/j.1467-7687.2005.00391.x  1
2004 Bearden CE, van Erp TG, Monterosso JR, Simon TJ, Glahn DC, Saleh PA, Hill NM, McDonald-McGinn DM, Zackai E, Emanuel BS, Cannon TD. Regional brain abnormalities in 22q11.2 deletion syndrome: association with cognitive abilities and behavioral symptoms. Neurocase. 10: 198-206. PMID 15788257 DOI: 10.1080/13554790490495519  1
2004 Bearden CE, Jawad AF, Lynch DR, Sokol S, Kanes SJ, McDonald-McGinn DM, Saitta SC, Harris SE, Moss E, Wang PP, Zackai E, Emanuel BS, Simon TJ. Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome. The American Journal of Psychiatry. 161: 1700-2. PMID 15337663 DOI: 10.1176/appi.ajp.161.9.1700  1
2004 Bish JP, Nguyen V, Ding L, Ferrante S, Simon TJ. Thalamic reductions in children with chromosome 22q11.2 deletion syndrome. Neuroreport. 15: 1413-5. PMID 15194864 DOI: 10.1097/01.wnr.0000129855.50780.85  1
2002 Bearden CE, Wang PP, Simon TJ. Williams syndrome cognitive profile also characterizes Velocardiofacial/DiGeorge syndrome. American Journal of Medical Genetics. 114: 689-92. PMID 12210289 DOI: 10.1002/ajmg.10539  1
2002 Simon TJ, Bearden CE, Moss EM, McDonald-McGinn D, Zackai E, Wang PP. Cognitive development in VCFS Progress in Pediatric Cardiology. 15: 109-117. DOI: 10.1016/S1058-9813(02)00035-8  1
2000 Peterson SA, Simon TJ. Computational evidence for the subitizing phenomenon as an emergent property of the human cognitive architecture Cognitive Science. 24: 93-122.  1
1999 Simon TJ. The foundations of numerical thinking in a brain without numbers. Trends in Cognitive Sciences. 3: 363-365. PMID 10498924 DOI: 10.1016/S1364-6613(99)01383-2  1
1999 Sathian K, Simon TJ, Peterson S, Patel GA, Hoffman JM, Grafton ST. Neural evidence linking visual object enumeration and attention. Journal of Cognitive Neuroscience. 11: 36-51. PMID 9950713 DOI: 10.1162/089892999563238  1
1998 Simon TJ, Peterson S, Patel G, Sathian K. Do the magnocellular and parvocellular visual pathways contribute differentially to subitizing and counting? Perception & Psychophysics. 60: 451-64. PMID 9599995  1
1998 Simon TJ. Computational evidence for the foundations of numerical competence Developmental Science. 1: 71-78.  1
1997 Simon TJ. Reconceptualizing the origins of number knowledge: A "non-numerical" account Cognitive Development. 12: 349-372.  1
1996 Simon TJ, Vaishnavi S. Subitizing and counting depend on different attentional mechanisms: evidence from visual enumeration in afterimages. Perception & Psychophysics. 58: 915-26. PMID 8768186 DOI: 10.3758/BF03205493  1
1995 Simon TJ, Hespos SJ, Rochat P. Do infants understand simple arithmetic? A replication of Wynn (1992) Cognitive Development. 10: 253-269. DOI: 10.1016/0885-2014(95)90011-X  1
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