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Tony J Simon

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InstitutionUniversity of California Davis
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
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    1. 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, Fremont W, Campbell LE, McCabe KL, Daly E, Gudbrandsen M, Murphy CM, Murphy D, Craig M, Vorstman J, Fiksinski A, Koops S, Ruparel K, Roalf DR, Gur RE, Schmitt JE, Simon T, Goodrich-Hunsaker NJ, Durdle CA, Bassett AS, Chow EWC, Butcher NJ, Vila-Rodriguez F, Doherty J, Cunningham A, van den Bree MBM, Linden DEJ, Moss H, Owen MJ, Murphy KC, McDonald-McGinn DM, Emanuel B, van Erp TGM, Turner JA, Thompson PM, Bearden CE. Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size. Mol Psychiatry. 2018 Jun 13. PMID: 29895892.
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    2. Karcher NR, Barch DM, Avenevoli S, Savill M, Huber RS, Simon T, Leckliter IN, Sher KJ, Loewy RL. Assessment of the Prodromal Questionnaire-Brief Child Version for Measurement of Self-reported Psychoticlike Experiences in Childhood. JAMA Psychiatry. 2018 Jun 06. PMID: 29874361.
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    3. Jensen M, Kooy RF, Simon T, 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. Eur J Med Genet. 2018 Apr; 61(4):209-212. PMID: 29191496.
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    4. 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 T. Baseline connectome modular abnormalities in the childhood phase of a longitudinal study on individuals with chromosome 22q11.2 deletion syndrome. Hum Brain Mapp. 2018 Jan; 39(1):232-248. PMID: 28990258.
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    5. 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, Michaelovsky E, Schneider M, Eliez S, Antonarakis SE, Coleman K, Tomita-Mitchell A, Mitchell ME, Digilio MC, Dallapiccola B, Marino B, Philip N, Busa T, Kushan-Wells L, Bearden CE, Piotrowicz M, Hawula W, Roberts AE, Tassone F, Simon T, van Duin EDA, van Amelsvoort TA, Kates WR, Zackai E, Johnston HR, Cutler DJ, Agopian AJ, Goldmuntz E, Mitchell LE, Wang T, Emanuel BS, Morrow BE. 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. Circ Cardiovasc Genet. 2017 Oct; 10(5). PMID: 29025761.
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    6. 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, Hooper SR, Armando M, Vicari S, Pontillo M, Kushan L, Jalbrzikowski M, Bearden CE, Cubells JF, Ousley OY, Walker EF, Simon T, Stoddard J, Niendam TA, van den Bree MBM, Gothelf D. Subthreshold Psychosis in 22q11.2 Deletion Syndrome: Multisite Naturalistic Study. Schizophr Bull. 2017 Sep 01; 43(5):1079-1089. PMID: 28204757.
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    7. Bassett AS, Lowther C, Merico D, Costain G, Chow EWC, van Amelsvoort T, McDonald-McGinn D, Gur RE, Swillen A, Van den Bree M, Murphy K, Gothelf D, Bearden CE, Eliez S, Kates W, Philip N, Sashi V, Campbell L, Vorstman J, Cubells J, Repetto GM, Simon T, Boot E, Heung T, Evers R, Vingerhoets C, van Duin E, Zackai E, Vergaelen E, Devriendt K, Vermeesch JR, Owen M, Murphy C, Michaelovosky E, Kushan L, Schneider M, Fremont W, Busa T, Hooper S, McCabe K, Duijff S, Isaev K, Pellecchia G, Wei J, Gazzellone MJ, Scherer SW, Emanuel BS, Guo T, Morrow BE, Marshall CR. Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome. Am J Psychiatry. 2017 11 01; 174(11):1054-1063. PMID: 28750581.
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    8. Wang JY, Hessl D, Hagerman RJ, Simon T, Tassone F, Ferrer E, Rivera SM. Abnormal trajectories in cerebellum and brainstem volumes in carriers of the fragile X premutation. Neurobiol Aging. 2017 Jul; 55:11-19. PMID: 28391068.
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    9. Scott JA, Goodrich-Hunsaker N, Kalish K, Lee A, Hunsaker MR, Schumann CM, Carmichael OT, Simon T. The hippocampi of children with chromosome 22q11.2 deletion syndrome have localized anterior alterations that predict severity of anxiety. J Psychiatry Neurosci. 2016 04; 41(3):203-13. PMID: 26599134.
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    10. 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, Philip N, Simon T, Roberts AE, Piotrowicz M, Bearden CE, Eliez S, Gothelf D, Coleman K, Kates WR, Devoto M, Zackai E, Heine-Suñer D, Goldmuntz E, Bassett AS, Morrow BE, Emanuel BS. Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome. Hum Genet. 2016 Mar; 135(3):273-85. PMID: 26742502; PMCID: PMC4896312.
    11. Napoli E, Tassone F, Wong S, Angkustsiri K, Simon T, Song G, Giulivi C. Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome. J Biol Chem. 2015 Sep 18; 290(38):23240-53. PMID: 26221035; PMCID: PMC4645608.
    12. Nordahl CW, Iosif AM, Young GS, Perry LM, Dougherty R, Lee A, Li D, Buonocore MH, Simon T, Rogers S, Wandell B, Amaral DG. Erratum: Sex differences in the corpus callosum in preschool-aged children with autism spectrum disorder. Mol Autism. 2015; 6:39. PMID: 26097676; PMCID: PMC4475327.
    13. 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. Mol Autism. 2015; 6:26. PMID: 25973163; PMCID: PMC4429319.
    14. 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, Philip N, Simon T, Roberts AE, Piotrowicz M, Bearden CE, Eliez S, Gothelf D, Coleman K, Kates WR, Devoto M, Zackai E, Heine-Suñer D, Shaikh TH, Bassett AS, Goldmuntz E, Morrow BE, Emanuel BS. Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome. Am J Hum Genet. 2015 May 07; 96(5):753-64. PMID: 25892112; PMCID: PMC4570279.
    15. 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, Vogels A, van Amelsvoort T, Gothelf D, Weinberger R, Weizman A, Klaassen PW, Koops S, Kates WR, Antshel KM, Simon T, Ousley OY, Swillen A, Gur RE, Bearden CE, Kahn RS, Bassett AS. Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome. JAMA Psychiatry. 2015 Apr; 72(4):377-85. PMID: 25715178.
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    16. 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 T. Disrupted fornix integrity in children with chromosome 22q11.2 deletion syndrome. Psychiatry Res. 2015 Apr 30; 232(1):106-14. PMID: 25748884; PMCID: PMC4404209.
    17. Wong LM, Tassone F, Rivera SM, Simon T. Temporal dynamics of attentional selection in adult male carriers of the fragile X premutation allele and adult controls. Front Hum Neurosci. 2015; 9:37. PMID: 25698960; PMCID: PMC4318336.
    18. Wong LM, Goodrich-Hunsaker NJ, McLennan YA, Tassone F, Rivera SM, Simon T. A cross-sectional analysis of orienting of visuospatial attention in child and adult carriers of the fragile X premutation. J Neurodev Disord. 2014; 6(1):45. PMID: 25937844; PMCID: PMC4416306.
    19. Hwang VJ, Maar D, Regan J, Angkustsiri K, Simon T, Tassone F. Mapping the deletion endpoints in individuals with 22q11.2 deletion syndrome by droplet digital PCR. BMC Med Genet. 2014 Oct 14; 15:106. PMID: 25312060; PMCID: PMC4258952.
    20. Sellier C, Hwang VJ, Dandekar R, Durbin-Johnson B, Charlet-Berguerand N, Ander BP, Sharp FR, Angkustsiri K, Simon T, Tassone F. Decreased DGCR8 expression and miRNA dysregulation in individuals with 22q11.2 deletion syndrome. PLoS One. 2014; 9(8):e103884. PMID: 25084529; PMCID: PMC4118991.
    21. Shapiro HM, Tassone F, Choudhary NS, Simon T. The development of cognitive control in children with chromosome 22q11.2 deletion syndrome. Front Psychol. 2014; 5:566. PMID: 24959159; PMCID: PMC4050531.
    22. Stephenson DD, Beaton EA, Weems CF, Angkustsiri K, Simon T. Identifying patterns of anxiety and depression in children with chromosome 22q11.2 deletion syndrome: comorbidity predicts behavioral difficulties and impaired functional communications. Behav Brain Res. 2015 Jan 01; 276:190-8. PMID: 24906195; PMCID: PMC4254311.
    23. 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, Vorstman J, Duijff SN, Klaassen PW, Swillen A, Gothelf D, Green T, Weizman A, Van Amelsvoort T, Evers L, Boot E, Shashi V, Hooper SR, Bearden CE, Jalbrzikowski M, Armando M, Vicari S, Murphy DG, Ousley O, Campbell LE, Simon T, Eliez S. 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. Am J Psychiatry. 2014 Jun; 171(6):627-39. PMID: 24577245; PMCID: PMC4285461.
    24. Wong LM, Goodrich-Hunsaker NJ, McLennan Y, Tassone F, Zhang M, Rivera SM, Simon T. Eye movements reveal impaired inhibitory control in adult male fragile X premutation carriers asymptomatic for FXTAS. Neuropsychology. 2014 Jul; 28(4):571-84. PMID: 24773414; PMCID: PMC4172343.
    25. Angkustsiri K, Goodlin-Jones B, Deprey L, Brahmbhatt K, Harris S, Simon T. Social impairments in chromosome 22q11.2 deletion syndrome (22q11.2DS): autism spectrum disorder or a different endophenotype? J Autism Dev Disord. 2014 Apr; 44(4):739-46. PMID: 24045981; PMCID: PMC4327991.
    26. Quintero AI, Beaton EA, Harvey DJ, Ross JL, Simon T. Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes. J Neurodev Disord. 2014 Mar 14; 6(1):5. PMID: 24628892; PMCID: PMC3995552.
    27. Wong LM, Riggins T, Harvey D, Cabaral M, Simon T. Children with chromosome 22q11.2 deletion syndrome exhibit impaired spatial working memory. Am J Intellect Dev Disabil. 2014 Mar; 119(2):115-32. PMID: 24679349; PMCID: PMC4036086.
    28. Leow A, Harvey D, Goodrich-Hunsaker NJ, Gadelkarim J, Kumar A, Zhan L, Rivera SM, Simon T. Altered structural brain connectome in young adult fragile X premutation carriers. Hum Brain Mapp. 2014 Sep; 35(9):4518-30. PMID: 24578183; PMCID: PMC4106982.
    29. Kim SY, Tassone F, Simon T, Rivera SM. Altered neural activity in the 'when' pathway during temporal processing in fragile X premutation carriers. Behav Brain Res. 2014 Mar 15; 261:240-8. PMID: 24398265; PMCID: PMC4867552.
    30. Kim SY, Hashimoto R, Tassone F, Simon T, Rivera SM. Altered neural activity of magnitude estimation processing in adults with the fragile X premutation. J Psychiatr Res. 2013 Dec; 47(12):1909-16. PMID: 24045061; PMCID: PMC3880247.
    31. Shapiro HM, Wong LM, Simon T. A cross-sectional analysis of the development of response inhibition in children with chromosome 22q11.2 deletion syndrome. Front Psychiatry. 2013; 4:81. PMID: 23966958; PMCID: PMC3736116.
    32. Villalon-Reina J, Jahanshad N, Beaton E, Toga AW, Thompson PM, Simon T. White matter microstructural abnormalities in girls with chromosome 22q11.2 deletion syndrome, Fragile X or Turner syndrome as evidenced by diffusion tensor imaging. Neuroimage. 2013 Nov 01; 81:441-54. PMID: 23602925; PMCID: PMC3947617.
    33. Wong LM, Goodrich-Hunsaker NJ, McLennan Y, Tassone F, Harvey D, Rivera SM, Simon T. Young adult male carriers of the fragile X premutation exhibit genetically modulated impairments in visuospatial tasks controlled for psychomotor speed. J Neurodev Disord. 2012 Nov 13; 4(1):26. PMID: 23148490; PMCID: PMC3506571.
    34. Angkustsiri K, Leckliter I, Tartaglia N, Beaton EA, Enriquez J, Simon T. An examination of the relationship of anxiety and intelligence to adaptive functioning in children with chromosome 22q11.2 deletion syndrome. J Dev Behav Pediatr. 2012 Nov-Dec; 33(9):713-20. PMID: 23117596; PMCID: PMC3523689.
    35. 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, Dallapiccola B, Carpenter C, Zheng X, Johnson J, Chung J, Higgins AM, Philip N, Simon T, Coleman K, Heine-Suner D, Rosell J, Kates W, Devoto M, Zackai E, Wang T, Shprintzen R, Emanuel BS, Morrow BE. Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. Am J Med Genet A. 2012 Nov; 158A(11):2781-7. PMID: 23034814; PMCID: PMC3477281.
    36. Cabaral MH, Beaton EA, Stoddard J, Simon T. Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome. J Neurodev Disord. 2012 Apr 12; 4(1):6. PMID: 22958454; PMCID: PMC3374294.
    37. Shapiro HM, Takarae Y, Harvey DJ, Cabaral MH, Simon T. A cross-sectional study of the development of volitional control of spatial attention in children with chromosome 22q11.2 deletion syndrome. J Neurodev Disord. 2012 Feb 15; 4(1):5. PMID: 22958432; PMCID: PMC3374293.
    38. Stoddard J, Takarae Y, Simon T. A second look: no effect of the COMT Val158Met polymorphism on conflict adaptation in youth with chromosome 22q11.2 deletion syndrome. Schizophr Res. 2012 Mar; 135(1-3):202-3. PMID: 22245443; PMCID: PMC4331111.
    39. 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. Arch Gen Psychiatry. 2012 Jan; 69(1):53-61. PMID: 22213789; PMCID: PMC3632313.
    40. Nordahl CW, Lange N, Li DD, Barnett LA, Lee A, Buonocore MH, Simon T, Rogers S, Ozonoff S, Amaral DG. Brain enlargement is associated with regression in preschool-age boys with autism spectrum disorders. Proc Natl Acad Sci U S A. 2011 Dec 13; 108(50):20195-200. PMID: 22123952; PMCID: PMC3250128.
    41. 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, Carpenter C, Zheng X, Johnson J, Chung J, Higgins AM, Philip N, Simon T, Coleman K, Heine-Suner D, Rosell J, Kates W, Devoto M, Goldmuntz E, Zackai E, Wang T, Shprintzen R, Emanuel B, Morrow B. Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. Hum Mutat. 2011 Nov; 32(11):1278-89. PMID: 21796729; PMCID: PMC3196824.
    42. Goodrich-Hunsaker NJ, Wong LM, McLennan Y, Tassone F, Harvey D, Rivera SM, Simon T. Adult Female Fragile X Premutation Carriers Exhibit Age- and CGG Repeat Length-Related Impairments on an Attentionally Based Enumeration Task. Front Hum Neurosci. 2011; 5:63. PMID: 21808616; PMCID: PMC3139190.
    43. Goodrich-Hunsaker NJ, Wong LM, McLennan Y, Tassone F, Harvey D, Rivera SM, Simon T. Enhanced manual and oral motor reaction time in young adult female fragile X premutation carriers. J Int Neuropsychol Soc. 2011 Jul; 17(4):746-50. PMID: 21554789; PMCID: PMC3210929.
    44. Srivastava S, Buonocore MH, Simon T. Atypical developmental trajectory of functionally significant cortical areas in children with chromosome 22q11.2 deletion syndrome. Hum Brain Mapp. 2012 Jan; 33(1):213-23. PMID: 21416559; PMCID: PMC3212617.
    45. Goodrich-Hunsaker NJ, Wong LM, McLennan Y, Srivastava S, Tassone F, Harvey D, Rivera SM, Simon T. Young adult female fragile X premutation carriers show age- and genetically-modulated cognitive impairments. Brain Cogn. 2011 Apr; 75(3):255-60. PMID: 21295394; PMCID: PMC3050049.
    46. Simon T. Clues to the foundations of numerical cognitive impairments: evidence from genetic disorders. Dev Neuropsychol. 2011; 36(6):788-805. PMID: 21761998; PMCID: PMC3152315.
    47. Stoddard J, Beckett L, Simon T. Atypical development of the executive attention network in children with chromosome 22q11.2 deletion syndrome. J Neurodev Disord. 2011 Mar; 3(1):76-85. PMID: 21475729; PMCID: PMC3056994.
    48. Beaton EA, Simon T. How might stress contribute to increased risk for schizophrenia in children with chromosome 22q11.2 deletion syndrome? J Neurodev Disord. 2011 Mar; 3(1):68-75. PMID: 21475728; PMCID: PMC3056992.
    49. Karayiorgou M, Simon T, Gogos JA. 22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia. Nat Rev Neurosci. 2010 Jun; 11(6):402-16. PMID: 20485365; PMCID: PMC2977984.
    50. Beaton EA, Stoddard J, Lai S, Lackey J, Shi J, Ross JL, Simon T. Atypical functional brain activation during a multiple object tracking task in girls with Turner syndrome: neurocorrelates of reduced spatiotemporal resolution. Am J Intellect Dev Disabil. 2010 Mar; 115(2):140-56. PMID: 20441384; PMCID: PMC2967304.
    51. Simon T. Rewards and challenges of cognitive neuroscience studies of persons with intellectual and developmental disabilities. Am J Intellect Dev Disabil. 2010 Mar; 115(2):79-82. PMID: 20441387.
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    52. Beaton EA, Qin Y, Nguyen V, Johnson J, Pinter JD, Simon T. Increased incidence and size of cavum septum pellucidum in children with chromosome 22q11.2 deletion syndrome. Psychiatry Res. 2010 Feb 28; 181(2):108-13. PMID: 20074913; PMCID: PMC2904971.
    53. Stoddard J, Niendam T, Hendren R, Carter C, Simon T. Attenuated positive symptoms of psychosis in adolescents with chromosome 22q11.2 deletion syndrome. Schizophr Res. 2010 May; 118(1-3):118-21. PMID: 20056393; PMCID: PMC2856801.
    54. Takarae Y, Schmidt L, Tassone F, Simon T. Catechol-O-methyltransferase polymorphism modulates cognitive control in children with chromosome 22q11.2 deletion syndrome. Cogn Affect Behav Neurosci. 2009 Mar; 9(1):83-90. PMID: 19246329; PMCID: PMC2730497.
    55. Simon T, 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. Behav Brain Funct. 2008 Jun 17; 4:25. PMID: 18559106; PMCID: PMC2443161.
    56. Bearden CE, van Erp TG, Dutton RA, Lee AD, Simon T, 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. Cereb Cortex. 2009 Jan; 19(1):115-26. PMID: 18483006; PMCID: PMC2733329.
    57. Yushkevich PA, Zhang H, Simon T, Gee JC. Structure-specific statistical mapping of white matter tracts. Neuroimage. 2008 Jun; 41(2):448-61. PMID: 18407524; PMCID: PMC2519052.
    58. Simon T. A new account of the neurocognitive foundations of impairments in space, time and number processing in children with chromosome 22q11.2 deletion syndrome. Dev Disabil Res Rev. 2008; 14(1):52-8. PMID: 18612330; PMCID: PMC2442464.
    59. Nordahl CW, Simon T, 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. J Autism Dev Disord. 2008 Sep; 38(8):1581-90. PMID: 18157624; PMCID: PMC4864596.
    60. Deboer T, Wu Z, Lee A, Simon T. Hippocampal volume reduction in children with chromosome 22q11.2 deletion syndrome is associated with cognitive impairment. Behav Brain Funct. 2007 Oct 23; 3:54. PMID: 17956622; PMCID: PMC2173902.
    61. Sun H, Yushkevich PA, Zhang H, Cook PA, Duda JT, Simon T, Gee JC. Shape-based normalization of the corpus callosum for DTI connectivity analysis. IEEE Trans Med Imaging. 2007 Sep; 26(9):1166-78. PMID: 17896590.
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    62. Simon T. Cognitive characteristics of children with genetic syndromes. Child Adolesc Psychiatr Clin N Am. 2007 Jul; 16(3):599-616. PMID: 17562581; PMCID: PMC2435488.
    63. Bish JP, Chiodo R, Mattei V, Simon T. Domain specific attentional impairments in children with chromosome 22q11.2 deletion syndrome. Brain Cogn. 2007 Aug; 64(3):265-73. PMID: 17499412; PMCID: PMC2727671.
    64. Sun H, Yushkevich PA, Zhang H, Cook PA, Duda JT, Simon T, Gee JC. Evaluation of shape-based normalization in the corpus callosum for white matter connectivity analysis. Med Image Comput Comput Assist Interv. 2007; 10(Pt 2):777-84. PMID: 18044639.
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    65. Machado AM, Simon T, Nguyen V, McDonald-McGinn DM, Zackai EH, Gee JC. Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndrome. Brain Res. 2007 Feb 02; 1131(1):197-210. PMID: 17169351; PMCID: PMC1802103.
    66. Bearden CE, van Erp TG, Dutton RA, Tran H, Zimmermann L, Sun D, Geaga JA, Simon T, Glahn DC, Cannon TD, Emanuel BS, Toga AW, Thompson PM. Mapping cortical thickness in children with 22q11.2 deletions. Cereb Cortex. 2007 Aug; 17(8):1889-98. PMID: 17056649; PMCID: PMC2819929.
    67. Bish JP, Pendyal A, Ding L, Ferrante H, Nguyen V, McDonald-McGinn D, Zackai E, Simon T. Specific cerebellar reductions in children with chromosome 22q11.2 deletion syndrome. Neurosci Lett. 2006 May 22; 399(3):245-8. PMID: 16517069.
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    68. Simon T, Bearden CE, Mc-Ginn DM, Zackai E. Visuospatial and numerical cognitive deficits in children with chromosome 22q11.2 deletion syndrome. Cortex. 2005 Apr; 41(2):145-55. PMID: 15714897.
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    69. 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 T. Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion Syndrome. Child Neuropsychol. 2005 Feb; 11(1):109-17. PMID: 15846854; PMCID: PMC2810976.
    70. Simon T, 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. 2005 Mar; 25(1):169-80. PMID: 15734353.
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    71. Simon T, 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. Dev Psychopathol. 2005; 17(3):753-84. PMID: 16262991; PMCID: PMC1360281.
    72. Bish JP, Ferrante SM, McDonald-McGinn D, Zackai E, Simon T. Maladaptive conflict monitoring as evidence for executive dysfunction in children with chromosome 22q11.2 deletion syndrome. Dev Sci. 2005 Jan; 8(1):36-43. PMID: 15647065.
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    73. 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 T. Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome. Am J Psychiatry. 2004 Sep; 161(9):1700-2. PMID: 15337663.
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    74. Bish JP, Nguyen V, Ding L, Ferrante S, Simon T. Thalamic reductions in children with chromosome 22q11.2 deletion syndrome. Neuroreport. 2004 Jun 28; 15(9):1413-5. PMID: 15194864.
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    75. Bearden CE, van Erp TG, Monterosso JR, Simon T, 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. 2004 Jun; 10(3):198-206. PMID: 15788257.
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    76. Bearden CE, Wang PP, Simon T. Williams syndrome cognitive profile also characterizes Velocardiofacial/DiGeorge syndrome. Am J Med Genet. 2002 Aug 08; 114(6):689-92. PMID: 12210289.
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