SPECIAL ISSUE ON COGNITIVE NEUROSCIENCE APPROACHES TO THE STUDY OF INTELLECTUAL AND DEVELOPMENTAL DISABILITIESSIMON, Tony J.American journal on intellectual and developmental disabilities (Print). 2010, Vol 115, Num 2, issn 1944-7515, 114 p.Serial Issue

Clues to the Foundations of Numerical Cognitive Impairments: Evidence From Genetic DisordersSIMON, Tony J.Developmental neuropsychology. 2011, Vol 36, Num 6, pp 788-805, issn 8756-5641, 18 p.Article

Molecular and Cellular Mechanisms Elucidating Neurocognitive Basis of Functional Impairments Associated With Intellectual Disability in Down SyndromeRACHIDI, Mohammed; LOPES, Carmela.American journal on intellectual and developmental disabilities (Print). 2010, Vol 115, Num 2, issn 1944-7515, 83-112, 190 [31 p.]Article

22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophreniaKARAYIORGOU, Maria; SIMON, Tony J; GOGOS, Joseph A et al.Nature reviews. Neuroscience (Print). 2010, Vol 11, Num 6, pp 402-416, issn 1471-003X, 15 p.Article

Atypical Developmental Trajectory of Functionally Significant Cortical Areas in Children with Chromosome 22q II.2 Deletion SyndromeSRIVASTAVA, Siddharth; BUONOCORE, Michael H; SIMON, Tony J et al.Human brain mapping. 2012, Vol 33, Num 1, pp 213-223, issn 1065-9471, 11 p.Article

A second look: No effect of the COMT Val158Met polymorphism on conflict adaptation in youth with chromosome 22q11.2 deletion syndromeSTODDARD, Joel; TAKARAE, Yukari; SIMON, Tony J et al.Schizophrenia research. 2012, Vol 135, Num 1-3, pp 202-203, issn 0920-9964, 2 p.Article

Atypical Functional Brain Activation During a Multiple Object Tracking Task in Girls With Turner Syndrome: Neurocorrelates of Reduced Spatiotemporal ResolutionBEATON, Elliott A; STODDARD, Joel; SONG LAI et al.American journal on intellectual and developmental disabilities (Print). 2010, Vol 115, Num 2, issn 1944-7515, 140-156, 191 [18 p.]Article

Catechol-O-methyltransferase polymorphism modulates cognitive control in children with chromosome 22qll.2 deletion syndromeTAKARAE, Yukari; SCHMIDT, Linda; TASSONE, Flora et al.Cognitive, affective & behavioral neuroscience (Print). 2009, Vol 9, Num 1, pp 83-90, issn 1530-7026, 8 p.Article

Domain specific attentional impairments in children with chromosome 22qll.2 deletion syndromeBISH, Joel P; CHIODO, Renee; MATTEI, Victoria et al.Brain and cognition (Print). 2007, Vol 64, Num 3, pp 265-273, issn 0278-2626, 9 p.Article

Discovering Structure in Auditory Input: Evidence From Williams SyndromeELSABBAGH, Mayada; COHEN, Henri; KARMILOFF-SMITH, Annette et al.American journal on intellectual and developmental disabilities (Print). 2010, Vol 115, Num 2, issn 1944-7515, 128-139, 190 [13 p.]Article

A NEW ACCOUNT OF THE NEUROCOGNITIVE FOUNDATIONS OF IMPAIRMENTS IN SPACE, TIME, AND NUMBER PROCESSING IN CHILDREN WITH CHROMOSOME 22Q11.2 DELETION SYNDROMESIMON, Tony J.Developmental disabilities research reviews. 2008, Vol 14, Num 1, pp 52-58, 7 p.Article

Identifying patterns of anxiety and depression in children with chromosome 22q11.2 deletion syndrome: Comorbidity predicts behavioral difficulties and impaired functional communicationsSTEPHENSON, David D; BEATON, Elliott A; WEEMS, Carl F et al.Behavioural brain research. 2015, Vol 276, pp 190-198, issn 0166-4328, 9 p.Article

Altered Structural Brain Connectome in Young Adult Fragile X Premutation CarriersLEOW, Alex; HARVEY, Danielle; GOODRICH-HUNSAKER, Naomi J et al.Human brain mapping. 2014, Vol 35, Num 9, pp 4518-4530, issn 1065-9471, 13 p.Article

Altered neural activity in the 'when' pathway during temporal processing in fragile X premutation carriersKIM, So-Yeon; TASSONE, Flora; SIMON, Tony J et al.Behavioural brain research. 2014, Vol 261, pp 240-248, issn 0166-4328, 9 p.Article

Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndromeMACHADO, Alexei M. C; SIMON, Tony J; NGUYEN, Vy et al.Brain research. 2007, Vol 1131, pp 197-210, issn 0006-8993, 14 p.Article

Thalamic reductions in children with chromosome 22qII.2 deletion syndromeBISH, Joel P; VY NGUYEN; LIJUN DING et al.Neuroreport (Oxford). 2004, Vol 15, Num 9, pp 1413-1415, issn 0959-4965, 3 p.Article

An Examination of the Relationship of Anxiety and Intelligence to Adaptive Functioning in Children with Chromosome 22q11.2 Deletion SyndromeANGKUSTSIRI, Kathleen; LECKLITER, Ingrid; TARTAGLIA, Nicole et al.Journal of developmental and behavioral pediatrics. 2012, Vol 33, Num 9, pp 713-720, issn 0196-206X, 8 p.Article

Children With Chromosome 22q11.2 Deletion Syndrome Exhibit Impaired Spatial Working MemoryWONG, Ling M; RIGGINS, Tracy; HARVEY, Danielle et al.American journal on intellectual and developmental disabilities (Print). 2014, Vol 119, Num 2, issn 1944-7515, 115-132, 199, 201 [20 p.]Article

Social Impairments in Chromosome 22q11.2 Deletion Syndrome (22q11.2DS): Autism Spectrum Disorder or a Different Endophenotype?ANGKUSTSIRI, Kathleen; GOODLIN-JONES, Beth; DEPREY, Lesley et al.Journal of autism and developmental disorders. 2014, Vol 44, Num 4, pp 739-746, issn 0162-3257, 8 p.Article

Auditory Attraction: Activation of Visual Cortex by Music and Sound in Williams SyndromeTHORNTON-WELLS, Tricia A; CANNISTRACI, Christopher J; ANDERSON, Adam W et al.American journal on intellectual and developmental disabilities (Print). 2010, Vol 115, Num 2, issn 1944-7515, 172-189, 191 [19 p.]Article

White matter microstructural abnormalities in girls with chromosome 22q11.2 deletion syndrome, Fragile X or Turner syndrome as evidenced by diffusion tensor imagingVILLALON-REINA, Julio; JAHANSHAD, Neda; BEATON, Elliott et al.NeuroImage (Orlando, Fla.). 2013, Vol 81, pp 441-454, issn 1053-8119, 14 p.Article

Neural Mechanisms Underlying Action Observation in Adults With Down SyndromeVIRJI-BABUL, Naznin; MOISEEV, Alexander; CHEUNG, Teresa et al.American journal on intellectual and developmental disabilities (Print). 2010, Vol 115, Num 2, issn 1944-7515, 113-127, 190 [16 p.]Article

Performance in Temporal Discounting Tasks by People With Intellectual Disabilities Reveals Difficulties in Decision-Making and Impulse ControlWILLNER, Paul; BAILEY, Rebecca; PARRY, Rhonwen et al.American journal on intellectual and developmental disabilities (Print). 2010, Vol 115, Num 2, issn 1944-7515, 157-171, 191 [16 p.]Article

Increased incidence and size of cavum septum pellucidum in children with chromosome 22q11.2 deletion syndromeBEATONA, Elliott A; YUFENG QIN; NGUYENA, Vy et al.Psychiatry research. Neuroimaging. 2010, Vol 181, Num 2, pp 108-113, issn 0925-4927, 6 p.Article

Specific cerebellar reductions in children with chromosome 22q11l.2 deletion syndromeBISH, Joel P; PENDYAL, Akshay; LIJUN DING et al.Neuroscience letters. 2006, Vol 399, Num 3, pp 245-248, issn 0304-3940, 4 p.Article