| Year |
Citation |
Score |
| 2020 |
Davies RW, Fiksinski AM, Breetvelt EJ, Williams NM, Hooper SR, Monfeuga T, Bassett AS, Owen MJ, Gur RE, Morrow BE, McDonald-McGinn DM, Swillen A, Chow EWC, van den Bree M, Emanuel BS, ... ... Simon TJ, et al. Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome. Nature Medicine. PMID 33169016 DOI: 10.1038/s41591-020-1103-1 |
0.489 |
|
| 2020 |
Wigby K, Cordeiro L, Wilson R, Angkustsiri K, Simon TJ, Tartaglia N. Adaptive functioning in children and adolescents with Trisomy X: An exploratory analysis. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. PMID 32548885 DOI: 10.1002/Ajmg.C.31803 |
0.337 |
|
| 2020 |
Linton SR, Popa AM, Luck SJ, Bolden K, Carter CS, Niendam TA, Simon TJ. 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. PMID 32319730 DOI: 10.1002/Ajmg.A.61596 |
0.761 |
|
| 2020 |
Ching CRK, Gutman BA, Sun D, Villalon Reina J, Ragothaman A, Isaev D, Zavaliangos-Petropulu A, Lin A, Jonas RK, Kushan L, Pacheco-Hansen L, Vajdi A, Forsyth JK, Jalbrzikowski M, Bakker G, ... ... Simon TJ, et al. 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. PMID 32046535 DOI: 10.1176/Appi.Ajp.2019.19060583 |
0.815 |
|
| 2020 |
Cleynen I, Engchuan W, Hestand MS, Heung T, Holleman AM, Johnston HR, Monfeuga T, McDonald-McGinn DM, Gur RE, Morrow BE, Swillen A, Vorstman JAS, Bearden CE, Chow EWC, van den Bree M, ... ... Simon TJ, et al. Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Molecular Psychiatry. PMID 32015465 DOI: 10.1038/S41380-020-0654-3 |
0.743 |
|
| 2019 |
Zhao Y, Diacou A, Johnston HR, Musfee FI, McDonald-McGinn DM, McGinn D, Crowley TB, Repetto GM, Swillen A, Breckpot J, Vermeesch JR, Kates WR, Digilio MC, Unolt M, Marino B, ... ... Simon TJ, et al. 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. PMID 31870554 DOI: 10.1016/J.Ajhg.2019.11.010 |
0.594 |
|
| 2019 |
McCabe KL, Popa AM, Durdle C, Amato M, Cabaral MH, Cruz J, Wong LM, Harvey D, Tartaglia N, Simon TJ. Quantifying the resolution of spatial and temporal representation in children with 22q11.2 deletion syndrome. Journal of Neurodevelopmental Disorders. 11: 40. PMID 31861974 DOI: 10.1186/S11689-019-9301-1 |
0.813 |
|
| 2019 |
Popa AM, Cruz JR, Wong LM, Harvey DJ, Angkustsiri K, Leckliter IN, Perez-Edgar K, Simon TJ. 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. PMID 31756146 DOI: 10.1352/1944-7558-124.6.549 |
0.804 |
|
| 2019 |
Uljarević M, McCabe KL, Angkustsiri K, Simon TJ, Hardan AY. 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. PMID 31433576 DOI: 10.1002/Aur.2194 |
0.447 |
|
| 2019 |
Villalón-Reina JE, Martínez K, Qu X, Ching CRK, Nir TM, Kothapalli D, Corbin C, Sun D, Lin A, Forsyth JK, Kushan L, Vajdi A, Jalbrzikowski M, Hansen L, Jonas RK, ... ... Simon TJ, et al. Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study. Molecular Psychiatry. PMID 31358905 DOI: 10.1038/S41380-019-0450-0 |
0.801 |
|
| 2019 |
Mayo D, Bolden KA, Simon TJ, Niendam TA. Bullying and psychosis: The impact of chronic traumatic stress on psychosis risk in 22q11.2 deletion syndrome - a uniquely vulnerable population. Journal of Psychiatric Research. 114: 99-104. PMID 31054456 DOI: 10.1016/J.Jpsychires.2019.04.011 |
0.457 |
|
| 2019 |
Karcher N, Loewy R, Savill M, O’Brien K, Huber R, Simon T, Leckliter I, Sher K, Barch D. 7.1 Predictors Of Distressing Psychotic-Like Experiences In School-Age Children Schizophrenia Bulletin. 45. DOI: 10.1093/Schbul/Sbz022.023 |
0.302 |
|
| 2019 |
Villalón J, Ching C, Nir T, Jahanshad N, Kothapalli D, Sun D, Lin A, Forsyth J, Kushan L, Vajdi A, Jalbrzikowski M, van Amelsvoort T, Bakker G, Kates WR, Antshel KM, ... ... Simon T, et al. 190. Novel Diffusion MRI Measures in 22q Deletion Syndrome: Large-Scale International Studies by the ENIGMA-22q Consortium Biological Psychiatry. 85: S78-S79. DOI: 10.1016/J.Biopsych.2019.03.204 |
0.741 |
|
| 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 |
0.805 |
|
| 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 |
0.415 |
|
| 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 |
0.605 |
|
| 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 |
0.758 |
|
| 2017 |
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, ... ... Simon T, et al. Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome. The American Journal of Psychiatry. appiajp201716121417. PMID 28750581 DOI: 10.1176/Appi.Ajp.2017.16121417 |
0.61 |
|
| 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 |
0.366 |
|
| 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 |
0.577 |
|
| 2016 |
Popa A, Hunsaker N, Deng MY, Garner J, Cruz J, Cung N, Reyes D, Simon T. Cortical tissue volumes correlate to cavum septum pellucidum size in children with 22q11.2 ddeletion syndrome and typical controls F1000research. 5. DOI: 10.7490/F1000Research.1111954.1 |
0.731 |
|
| 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 |
0.782 |
|
| 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 |
0.415 |
|
| 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. Erratum: Sex differences in the corpus callosum in preschool-aged children with autism spectrum disorder. Molecular Autism. 6: 39. PMID 26097676 DOI: 10.1186/S13229-015-0030-3 |
0.334 |
|
| 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 |
0.332 |
|
| 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 |
0.561 |
|
| 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 |
0.768 |
|
| 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 |
0.778 |
|
| 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 |
0.703 |
|
| 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 |
0.464 |
|
| 2015 |
Popa A, Beaton E, Cruz J, Wong L, Cung N, Harvey D, Simon T. Adaptation to a mild stressor in initially anxious children as related to their attention to perceived threat in a dot probe experiment F1000research. 6. DOI: 10.7490/F1000Research.1098145.1 |
0.775 |
|
| 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 |
0.791 |
|
| 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 |
0.477 |
|
| 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 |
0.398 |
|
| 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 |
0.686 |
|
| 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 |
0.776 |
|
| 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 |
0.759 |
|
| 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 |
0.821 |
|
| 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 |
0.707 |
|
| 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 |
0.742 |
|
| 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 |
0.341 |
|
| 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 |
0.419 |
|
| 2014 |
Popa A, Cruz J, Angkustsiri K, Brahmbhatt K, Cung N, Leckliter I, Quintero A, Reyes D, Shapiro H, Simon T. Atypical adaptation responses to threat stimuli in children with chromosome 22q11.2 deletion syndrome F1000research. 5. DOI: 10.7490/F1000Research.1095553.1 |
0.787 |
|
| 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 |
0.357 |
|
| 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 |
0.806 |
|
| 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 |
0.536 |
|
| 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 |
0.789 |
|
| 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 |
0.455 |
|
| 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 |
0.412 |
|
| 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 |
0.54 |
|
| 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 |
0.682 |
|
| 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 |
0.344 |
|
| 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 |
0.508 |
|
| 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 |
0.321 |
|
| 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 |
0.795 |
|
| 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 |
0.38 |
|
| 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 |
0.353 |
|
| 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 |
0.765 |
|
| 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 |
0.539 |
|
| 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 |
0.47 |
|
| 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 |
0.79 |
|
| 2011 |
Shapiro HM, Simon TJ. The development of response inhibition in children with chromosome 22q11.2 deletion syndrome F1000research. 2. DOI: 10.7490/F1000Research.1223.1 |
0.669 |
|
| 2011 |
Stoddard J, Shapiro HM, Cruz J, Takarae Y, Simon TJ. Impairment in two mechanisms of cognitive control in adolescents with chromosome 22q11.2 deletion syndrome F1000research. 2. DOI: 10.7490/F1000Research.1199.1 |
0.687 |
|
| 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 |
0.442 |
|
| 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 |
0.315 |
|
| 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 |
0.404 |
|
| 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 |
0.544 |
|
| 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 |
0.429 |
|
| 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 |
0.512 |
|
| 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 |
0.673 |
|
| 2009 |
Srivastava S, Buonocore M, Simon T. Local gyrification index analysis further characterizes significant midline and fronto-parietal brain anomalies in children with chromosome 22q11.2 deletion Neuroimage. 47: S70. DOI: 10.1016/S1053-8119(09)70408-2 |
0.472 |
|
| 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: 52-8. PMID 18612330 DOI: 10.1002/Ddrr.8 |
0.527 |
|
| 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 |
0.535 |
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| 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 |
0.339 |
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| 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 |
0.309 |
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| 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 |
0.479 |
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| 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 |
0.404 |
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| 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 |
0.516 |
|
| 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 |
0.418 |
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| 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 |
0.5 |
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| 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 |
0.484 |
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| 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 |
0.681 |
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| 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 |
0.523 |
|
| 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 |
0.628 |
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| 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 |
0.621 |
|
| 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 |
0.459 |
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| 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 DOI: 10.1016/S0010-9452(08)70889-X |
0.671 |
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| 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 |
0.537 |
|
| 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 |
0.698 |
|
| 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 |
0.648 |
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| 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 |
0.523 |
|
| 2003 |
Bearden C, Simon T, Wang P, Lynch D, Jawad A, McDonald-McGinn D, Zackai E, Emanuel B. Effects of a functional COMT polymorphism on neurocognitive function in the 22Q deletion syndrome Schizophrenia Research. 60: 78-79. DOI: 10.1016/S0920-9964(03)80619-9 |
0.584 |
|
| 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 |
0.556 |
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| 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 |
0.63 |
|
| 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. DOI: 10.1207/S15516709Cog2401_3 |
0.304 |
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