22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia
暂无分享,去创建一个
[1] J. Waddington,et al. Phenotypic characterization of cognition and social behavior in mice with heterozygous versus homozygous deletion of catechol-O-methyltransferase , 2008, Neuroscience.
[2] Steven W. Flavell,et al. Mef2-mediated transcription of the miR379–410 cluster regulates activity-dependent dendritogenesis by fine-tuning Pumilio2 protein levels , 2009, The EMBO journal.
[3] M. Karayiorgou,et al. The molecular genetics of the 22q11-associated schizophrenia. , 2004, Brain research. Molecular brain research.
[4] A. Meyer-Lindenberg,et al. Prefrontal-Hippocampal Coupling During Memory Processing Is Modulated by COMT Val158Met Genotype , 2006, Biological Psychiatry.
[5] A. Reiss,et al. Psychiatric disorders and behavioral problems in children with velocardiofacial syndrome: usefulness as phenotypic indicators of schizophrenia risk , 2002, Biological Psychiatry.
[6] Robert T. Schultz,et al. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes , 2009, Nature.
[7] Stephan Eliez,et al. A quantitative MRI study of posterior fossa development in velocardiofacial syndrome , 2001, Biological Psychiatry.
[8] E. Zackai,et al. Communication issues in 22q11.2 deletion syndrome: Children at risk , 2001, Genetics in Medicine.
[9] Paul J. Harrison,et al. The met(158) allele of catechol-O-methyltransferase (COMT) is associated with obsessive-compulsive disorder in men: case-control study and meta-analysis. , 2007, Molecular psychiatry.
[10] J. Ford,et al. Reduced communication between frontal and temporal lobes during talking in schizophrenia , 2002, Biological Psychiatry.
[11] C. Adams,et al. Mismatch negativity and frequency representational width in children with specific language impairment , 2008, Developmental medicine and child neurology.
[12] C. Feinstein,et al. Psychotic symptoms in children and adolescents with 22q11.2 deletion syndrome: Neuropsychological and behavioral implications , 2006, Schizophrenia Research.
[13] Bruce D. McCandliss,et al. Testing the Efficiency and Independence of Attentional Networks , 2002, Journal of Cognitive Neuroscience.
[14] Scott T. Grafton,et al. Neural Evidence Linking Visual Object Enumeration and Attention , 1999, Journal of Cognitive Neuroscience.
[15] Tyrone D. Cannon,et al. The Neurocognitive Phenotype of the 22Q11.2 Deletion Syndrome: Selective Deficit in Visual-Spatial Memory , 2001, Journal of clinical and experimental neuropsychology.
[16] M. Cooper,et al. A new concept of the cellular basis of immunity , 1965 .
[17] D. Pfaff,et al. Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[18] M. Posner. The Cognitive Neuroscience of Attention , 2020 .
[19] E. Donchin,et al. Optimizing the use of information: strategic control of activation of responses. , 1992, Journal of experimental psychology. General.
[20] J. Gogos,et al. Modeling Madness in Mice: One Piece at a Time , 2006, Neuron.
[21] James C. Gee,et al. Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndrome , 2007, Brain Research.
[22] E. Zackai,et al. Communication disorders in the 22Q11.2 microdeletion syndrome. , 2000, Journal of communication disorders.
[23] Eileen Daly,et al. Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study. , 2004, Archives of general psychiatry.
[24] Roland Bammer,et al. Arithmetic ability and parietal alterations: a diffusion tensor imaging study in velocardiofacial syndrome. , 2005, Brain research. Cognitive brain research.
[25] Y. Eto,et al. Morphometry of the head of the caudate nucleus in patients with velocardiofacial syndrome (del 22qll.2) , 2000, Acta paediatrica.
[26] A. Pulver,et al. Hyperprolinaemia in patients with deletion (22)(q11.2) syndrome , 2000, Journal of Inherited Metabolic Disease.
[27] Joseph A. Gogos,et al. Strong association of de novo copy number mutations with sporadic schizophrenia , 2008, Nature Genetics.
[28] S. Eliez,et al. Temporal perception in velo-cardio-facial syndrome , 2005, Neuropsychologia.
[29] Andrew M. Poulos,et al. The neuroscience of mammalian associative learning. , 2005, Annual review of psychology.
[30] B. Moghaddam,et al. Distinct contributions of glutamate and dopamine receptors to temporal aspects of rodent working memory using a clinically relevant task , 2001, Psychopharmacology.
[31] Marco Zorzi,et al. The spatial representation of numerical and non-numerical sequences: Evidence from neglect , 2006, Neuropsychologia.
[32] Allan L. Reiss,et al. Functional brain imaging study of mathematical reasoning abilities in velocardiofacial syndrome , 2001 .
[33] Fumiko Hoeft,et al. Abnormal cortical activation during response inhibition in 22q11.2 deletion syndrome , 2007, Human brain mapping.
[34] J. Potter. One piece at a time. , 1993, Journal of the American Optometric Association.
[35] R. Weksberg,et al. 22q11 deletion syndrome in adults with schizophrenia. , 1998, American journal of medical genetics.
[36] Inah Lee,et al. Time-Dependent Relationship between the Dorsal Hippocampus and the Prefrontal Cortex in Spatial Memory , 2003, The Journal of Neuroscience.
[37] Joel P. Bish,et al. A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children , 2005, Development and Psychopathology.
[38] Hanna Mandel,et al. A mutation in SNAP29, coding for a SNARE protein involved in intracellular trafficking, causes a novel neurocutaneous syndrome characterized by cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma. , 2005, American journal of human genetics.
[39] Raymond Klein,et al. Inhibition of return , 2000, Trends in Cognitive Sciences.
[40] Christina Sobin,et al. Networks of Attention in Children With the 22q11 Deletion Syndrome , 2004, Developmental neuropsychology.
[41] Z. Pylyshyn,et al. Why are small and large numbers enumerated differently? A limited-capacity preattentive stage in vision. , 1994, Psychological review.
[42] J. Engelberg. On integrative study , 1991 .
[43] James C. Gee,et al. Volumetric, connective, and morphologic changes in the brains of children with chromosome 22q11.2 deletion syndrome: an integrative study , 2005, NeuroImage.
[44] K. Sullivan,et al. Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes , 2007, The Lancet.
[45] B. Morrow,et al. Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome. , 1999, American journal of human genetics.
[46] J. Lieberman,et al. A comprehensive analysis of 22q11 gene expression in the developing and adult brain , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[47] Karl J. Friston,et al. Reduced frontotemporal functional connectivity in schizophrenia associated with auditory hallucinations , 2002, Biological Psychiatry.
[48] Klaus P. Ebmeier,et al. Meta-analysis of magnetic resonance imaging studies in chromosome 22q11.2 deletion syndrome (velocardiofacial syndrome) , 2009, Schizophrenia Research.
[49] J. Ott,et al. Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[50] K. Kosik. The neuronal microRNA system , 2006, Nature Reviews Neuroscience.
[51] D. Campion,et al. Hyperprolinemia is a risk factor for schizoaffective disorder , 2005, Molecular Psychiatry.
[52] Godfrey D Pearlson,et al. Regional cortical white matter reductions in velocardiofacial syndrome: a volumetric MRI analysis , 2001, Biological Psychiatry.
[53] Thomas W. Mühleisen,et al. Large recurrent microdeletions associated with schizophrenia , 2008, Nature.
[54] Tony J. Simon,et al. Visuospatial and Numerical Cognitive Deficits in Children with Chromosome 22Q11.2 Deletion Syndrome , 2005, Cortex.
[55] R. Näätänen,et al. Mismatch negativity (MMN): perspectives for application. , 2000, International journal of psychophysiology : official journal of the International Organization of Psychophysiology.
[56] Agatha D. Lee,et al. Alterations in midline cortical thickness and gyrification patterns mapped in children with 22q11.2 deletions. , 2009, Cerebral cortex.
[57] D. Housman,et al. Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives. , 1994, The Journal of nervous and mental disease.
[58] D. Rujescu,et al. Strong evidence that GNB1L is associated with schizophrenia. , 2008, Human molecular genetics.
[59] Jurg Ott,et al. Family-based association studies support a sexually dimorphic effect of COMT and MAOA on genetic susceptibility to obsessive-compulsive disorder , 1999, Biological Psychiatry.
[60] M. Karayiorgou,et al. Lower prepulse inhibition in children with the 22q11 deletion syndrome. , 2005, The American journal of psychiatry.
[61] D. Maurer,et al. Developmental changes in attention: the effects of endogenous cueing and of distractors , 2001 .
[62] A. Green,et al. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. , 1997, Journal of medical genetics.
[63] A. Baldini,et al. Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments. , 2001, Human molecular genetics.
[64] E. Bigler,et al. Memory and Learning in Children with 22q11.2 Deletion Syndrome: Evidence for Ventral and Dorsal Stream Disruption? , 2005, Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence.
[65] Joel P. Bish,et al. Domain specific attentional impairments in children with chromosome 22q11.2 deletion syndrome , 2007, Brain and Cognition.
[66] E. Zackai,et al. Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion , 2001, Genetics in Medicine.
[67] M. Posner,et al. The attention system of the human brain. , 1990, Annual review of neuroscience.
[68] D. Goldstein. Common genetic variation and human traits. , 2009, The New England journal of medicine.
[69] T. Sejnowski,et al. [Letters to nature] , 1996, Nature.
[70] P. Zamore,et al. MicroRNA Biogenesis: Drosha Can't Cut It without a Partner , 2005, Current Biology.
[71] M. Karayiorgou,et al. d-Amphetamine responses in catechol-O-methyltransferase (COMT) disrupted mice , 2004, Psychopharmacology.
[72] M M Mesulam,et al. Report of IFCN Committee on Basic Mechanisms. Basic mechanisms of cerebral rhythmic activities. , 1990, Electroencephalography and clinical neurophysiology.
[73] M. Morishima,et al. Genetic factors are major determinants of phenotypic variability in a mouse model of the DiGeorge/del22q11 syndromes , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[74] Nuria Y. AbdulSabur,et al. Autistic Spectrum Disorders in Velo-cardio Facial Syndrome (22q11.2 Deletion) , 2007, Journal of autism and developmental disorders.
[75] Martin Radetzki,et al. CONCEPTUAL AND METHODOLOGICAL ISSUES , 2021, Handbook on Austerity, Populism and the Welfare State.
[76] Wanda Fremont,et al. ADHD, major depressive disorder, and simple phobias are prevalent psychiatric conditions in youth with velocardiofacial syndrome. , 2006, Journal of the American Academy of Child and Adolescent Psychiatry.
[77] R. Deschenes,et al. Thematic review series: Lipid Posttranslational Modifications. Protein palmitoylation by a family of DHHC protein S-acyltransferases Published, JLR Papers in Press, April 1, 2006. , 2006, Journal of Lipid Research.
[78] R. Shprintzen,et al. Defining the clinical spectrum of deletion 22q11.2. , 2005, The Journal of pediatrics.
[79] P. Visscher,et al. Rare chromosomal deletions and duplications increase risk of schizophrenia , 2008, Nature.
[80] Godfrey D. Pearlson,et al. Frontal and Caudate Alterations in Velocardiofacial Syndrome (Deletion at Chromosome 22q11.2) , 2004, Journal of child neurology.
[81] D. Bredt,et al. Protein palmitoylation: a regulator of neuronal development and function , 2002, Nature Reviews Neuroscience.
[82] P. Scambler,et al. Velo-Cardio-Facial Syndrome: A Model for Understanding Microdeletion Disorders , 2005 .
[83] Fei Xu,et al. Linking Visual Attention and Number Processing in the Brain: The Role of the Temporo-parietal Junction in Small and Large Symbolic and Nonsymbolic Number Comparison , 2007, Journal of Cognitive Neuroscience.
[84] D. Skuse,et al. COMT Val108/158Met Modifies Mismatch Negativity and Cognitive Function in 22q11 Deletion Syndrome , 2005, Biological Psychiatry.
[85] B. Turetsky,et al. Proline Affects Brain Function in 22q11DS Children with the Low Activity COMT158 Allele , 2009, Neuropsychopharmacology.
[86] S Eliez,et al. Children and adolescents with velocardiofacial syndrome: a volumetric MRI study. , 2000, The American journal of psychiatry.
[87] Z. Sheng,et al. SNAP-29: A general SNARE protein that inhibits SNARE disassembly and is implicated in synaptic transmission , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[88] Lu-Yang Wang,et al. Superfluous Role of Mammalian Septins 3 and 5 in Neuronal Development and Synaptic Transmission , 2008, Molecular and Cellular Biology.
[89] Joseph A. Gogos,et al. Palmitoylation-dependent neurodevelopmental deficits in a mouse model of the 22q11 microdeletion , 2008, Nature Neuroscience.
[90] A. Kihara,et al. Intracellular localization and tissue-specific distribution of human and yeast DHHC cysteine-rich domain-containing proteins. , 2006, Biochimica et biophysica acta.
[91] M. Owen,et al. Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: Implications for 22q11 deletion syndrome , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[92] E. Zackai,et al. Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion. , 1999, American journal of medical genetics.
[93] Douglas C. Noll,et al. Activation of Prefrontal Cortex in Children during a Nonspatial Working Memory Task with Functional MRI , 1995, NeuroImage.
[94] Andrew L. Lemire,et al. Altered expression of hippocampal dentate granule neuron genes in a mouse model of human 22q11 deletion syndrome , 2006, Schizophrenia Research.
[95] S. Cichon,et al. Neural Mechanisms of a Genome-Wide Supported Psychosis Variant , 2009, Science.
[96] Edward Moss,et al. Research on behavioural phenotypes: velocardiofacial syndrome (deletion 22q11.2) , 2000 .
[97] Edwin H. Cook,et al. Copy-number variations associated with neuropsychiatric conditions , 2008, Nature.
[98] High Rates of Schizophrenia in Adults With Velo-Cardio-Facial Syndrome , 1999 .
[99] Anthony-Samuel LaMantia,et al. Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome , 2009, Proceedings of the National Academy of Sciences.
[100] N. Kanwisher,et al. Numerical Magnitude in the Human Parietal Lobe Tests of Representational Generality and Domain Specificity , 2004, Neuron.
[101] Stephan Eliez,et al. COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome , 2005, Nature Neuroscience.
[102] Hui Zhang,et al. Atypical cortical connectivity and visuospatial cognitive impairments are related in children with chromosome 22q11.2 deletion syndrome , 2008, Behavioral and Brain Functions.
[103] Joel P. Bish,et al. Specific cerebellar reductions in children with chromosome 22q11.2 deletion syndrome , 2006, Neuroscience Letters.
[104] Stephan Eliez,et al. Increased basal ganglia volumes in velo-cardio-facial syndrome (deletion 22q11.2) , 2002, Biological Psychiatry.
[105] C. Ogilvie,et al. Chromosome 22q11 deletions are not found in autistic patients identified using strict diagnostic criteria. IMGSAC. International Molecular Genetics Study of Autism Consortium. , 2000, American journal of medical genetics.
[106] M. Corbetta,et al. Control of goal-directed and stimulus-driven attention in the brain , 2002, Nature Reviews Neuroscience.
[107] G. Wagner,et al. P.1.e.028 Increase of whole brain volume and gray and white matter tissue in OCD: a volumetric and voxel-based morphometry MRI study , 2010, European Neuropsychopharmacology.
[108] G. Abecasis,et al. Nogo Receptor 1 (RTN4R) as a Candidate Gene for Schizophrenia: Analysis Using Human and Mouse Genetic Approaches , 2007, PloS one.
[109] J. Gogos,et al. Cognition in mouse models of schizophrenia susceptibility genes. , 2010, Schizophrenia bulletin.
[110] P. Scambler,et al. Deletion of 150 kb in the minimal DiGeorge/velocardiofacial syndrome critical region in mouse. , 1999, Human molecular genetics.
[111] F. J. Friedrich,et al. Effects of parietal injury on covert orienting of attention , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[112] S. Benzer,et al. The sluggish-A gene of Drosophila melanogaster is expressed in the nervous system and encodes proline oxidase, a mitochondrial enzyme involved in glutamate biosynthesis. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[113] V. Ambros. The functions of animal microRNAs , 2004, Nature.
[114] Donna McDonald-McGinn,et al. Maladaptive conflict monitoring as evidence for executive dysfunction in children with chromosome 22q11.2 deletion syndrome. , 2005, Developmental science.
[115] D. V. van Essen,et al. Symmetry of Cortical Folding Abnormalities in Williams Syndrome Revealed by Surface-Based Analyses , 2006, The Journal of Neuroscience.
[116] L. Campbell,et al. Velo-Cardio-Facial Syndrome: The cognitive spectrum in velo-cardio-facial syndrome , 2005 .
[117] Paul J. Harrison,et al. The met158 allele of catechol-O-methyltransferase (COMT) is associated with obsessive-compulsive disorder in men: case–control study and meta-analysis , 2007, Molecular Psychiatry.
[118] S. Eliez. Autism in children with 22q11.2 deletion syndrome. , 2007, Journal of the American Academy of Child and Adolescent Psychiatry.
[119] M. Karayiorgou,et al. Brain catecholamine metabolism in catechol‐O‐methyltransferase (COMT)‐deficient mice , 2002, The European journal of neuroscience.
[120] Meritxell Bach Cuadra,et al. Congenital heart disease affects local gyrification in 22q11.2 deletion syndrome , 2009, Developmental medicine and child neurology.
[121] B. De Smedt,et al. Mathematical disabilities in children with velo-cardio-facial syndrome , 2007, Neuropsychologia.
[122] A. M. Smith,et al. A century after cajal. , 1993, Science.
[123] Eileen Daly,et al. Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study. , 2006, Brain : a journal of neurology.
[124] M. Tervaniemi,et al. The first neurophysiological evidence for cognitive brain dysfunctions in children with CATCH , 1997, Neuroreport.
[125] K. Devriendt,et al. Neuropsychological, learning and psychosocial profile of primary school aged children with the velo-cardio-facial syndrome (22q11 deletion): evidence for a nonverbal learning disability? , 1999, Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence.
[126] A. Meyer-Lindenberg,et al. Regionally specific disturbance of dorsolateral prefrontal-hippocampal functional connectivity in schizophrenia. , 2005, Archives of general psychiatry.
[127] Stephan Eliez,et al. Functional brain imaging study of mathematical reasoning abilities in velocardiofacial syndrome (del22q11.2) , 2001, Genetics in Medicine.
[128] M. Owen,et al. Cognitive deficits associated with schizophrenia in velo-cardio-facial syndrome , 2004, Schizophrenia Research.
[129] Daniel Ansari,et al. Atypical trajectories of number development: a neuroconstructivist perspective , 2002, Trends in Cognitive Sciences.
[130] S. Dehaene,et al. Functional and Structural Alterations of the Intraparietal Sulcus in a Developmental Dyscalculia of Genetic Origin , 2003, Neuron.
[131] Stephan Eliez,et al. Psychiatric disorders and intellectual functioning throughout development in velocardiofacial (22q11.2 deletion) syndrome. , 2009, Journal of the American Academy of Child and Adolescent Psychiatry.
[132] J. Lieberman,et al. Mitochondrial localization and function of a subset of 22q11 deletion syndrome candidate genes , 2008, Molecular and Cellular Neuroscience.
[133] Stephan Eliez,et al. Investigation of white matter structure in velocardiofacial syndrome: a diffusion tensor imaging study. , 2003, The American journal of psychiatry.
[134] M. Karayiorgou,et al. The gene encoding proline dehydrogenase modulates sensorimotor gating in mice , 1999, Nature Genetics.
[135] D. Klahr,et al. Span and rate of apprehension in children and adults. , 1975, Journal of experimental child psychology.
[136] R. Shprintzen,et al. Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[137] A. Üçok,et al. Mismatch negativity at acute and post-acute phases of first-episode schizophrenia , 2008, European Archives of Psychiatry and Clinical Neuroscience.
[138] Wolf Singer,et al. Neuronal Synchrony: A Versatile Code for the Definition of Relations? , 1999, Neuron.
[139] Alexander Eckehart Urban,et al. High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[140] Noam Shomron,et al. Canalization of development by microRNAs , 2006, Nature Genetics.
[141] K. Sullivan. The clinical, immunological, and molecular spectrum of chromosome 22q11.2 deletion syndrome and DiGeorge syndrome , 2004, Current opinion in allergy and clinical immunology.
[142] Joseph A. Gogos,et al. Site-Specific Role of Catechol-O-Methyltransferase in Dopamine Overflow within Prefrontal Cortex and Dorsal Striatum , 2007, The Journal of Neuroscience.
[143] T. Curran,et al. Crk and Crk-Like Play Essential Overlapping Roles Downstream of Disabled-1 in the Reelin Pathway , 2008, The Journal of Neuroscience.
[144] C. Carter,et al. The anterior cingulate as a conflict monitor: fMRI and ERP studies , 2002, Physiology & Behavior.
[145] J. Flint,et al. Behavioral phenotypes: conceptual and methodological issues. , 1998, American journal of medical genetics.
[146] Stephan Eliez,et al. Abnormal patterns of cortical gyrification in velo-cardio-facial syndrome (deletion 22q11.2): An MRI study , 2006, Psychiatry Research: Neuroimaging.
[147] A. Bassett,et al. Neurocognitive profile in 22q11 deletion syndrome and schizophrenia , 2006, Schizophrenia Research.
[148] T. van Amelsvoort,et al. Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome. , 2007, Human molecular genetics.
[149] F. L. D. Silva,et al. Basic mechanisms of cerebral rhythmic activities , 1990 .
[150] D. Campion,et al. PRODH mutations and hyperprolinemia in a subset of schizophrenic patients. , 2002, Human molecular genetics.
[151] E. Ornitz,et al. Maturation of startle modulation. , 1986, Psychophysiology.
[152] S. Dehaene,et al. Single-trial classification of parallel pre-attentive and serial attentive processes using functional magnetic resonance imaging , 2003, Proceedings of the Royal Society of London. Series B: Biological Sciences.
[153] Jin Fan,et al. Response inhibition in adolescents diagnosed with attention deficit hyperactivity disorder during childhood: an event-related FMRI study. , 2004, The American journal of psychiatry.
[154] Chris Moore,et al. Inhibition of return in children and adolescents. , 2003, Journal of experimental child psychology.
[155] J. Mukai,et al. Palmitoylation-dependent neurodevelopmental deficits in a mouse model of 22q11 microdeletion , 2009, Neuroscience Research.
[156] D. Weinberger,et al. Genetic Dissection of the Role of Catechol-O-Methyltransferase in Cognition and Stress Reactivity in Mice , 2008, The Journal of Neuroscience.
[157] T. Goldberg,et al. Cognitive impairment in schizophrenia is the core of the disorder. , 2000, Critical reviews in neurobiology.
[158] Lorenzo D Botto,et al. A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population. , 2003, Pediatrics.
[159] D. Campion,et al. The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene , 2003, Journal of medical genetics.
[160] Paul Pavlidis,et al. Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model , 2008, Nature Genetics.
[161] G. Abecasis,et al. Genetic variation in the 22q11 locus and susceptibility to schizophrenia , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[162] Shifting visual attention between objects and locations: evidence from normal and parietal lesion subjects. , 1994 .
[163] Wendy R. Kates,et al. The neural correlates of non-spatial working memory in velocardiofacial syndrome (22q11.2 deletion syndrome) , 2007, Neuropsychologia.
[164] David J Mikulis,et al. Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome , 2002, Biological Psychiatry.
[165] Arthur W Toga,et al. Cerebral Cortex Advance Access published October 20, 2006 Mapping Cortical Thickness in Children with 22q11.2 Deletions , 2022 .
[166] Ellen M Wijsman,et al. Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[167] R. Kahn,et al. The 22q11.2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms. , 2006, Journal of the American Academy of Child and Adolescent Psychiatry.
[168] R. Kucherlapati,et al. Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients. , 1997, American journal of human genetics.
[169] K. Devriendt,et al. Velo-Cardio-Facial Syndrome a model for understanding microdeletion disorders , 2005 .
[170] Wanda Fremont,et al. Velo-cardio-facial syndrome , 2005, Current opinion in pediatrics.
[171] T. Arinami,et al. Analyses of the associations between the genes of 22q11 deletion syndrome and schizophrenia , 2006, Journal of Human Genetics.
[172] M. Wilson,et al. Theta Rhythms Coordinate Hippocampal–Prefrontal Interactions in a Spatial Memory Task , 2005, PLoS biology.
[173] Y. Takarae,et al. Catechol-O-methyltransferase polymorphism modulates cognitive control in children with chromosome 22q11.2 deletion syndrome , 2009, Cognitive, affective & behavioral neuroscience.
[174] R. Rafal,et al. Shifting visual attention between objects and locations: evidence from normal and parietal lesion subjects. , 1994, Journal of experimental psychology. General.
[175] D. Campion,et al. APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy , 2006, Nature Genetics.
[176] J. Kalbfleisch,et al. Early speech and language development in children with velocardiofacial syndrome. , 1999, American journal of medical genetics.
[177] Geraldine Sadoway. Children at Risk , 2002 .
[178] Hillel Adesnik,et al. Identification of PSD-95 Palmitoylating Enzymes , 2004, Neuron.
[179] E. Moss,et al. Research on behavioral phenotypes: velocardiofacial syndrome (deletion 22q11.2) , 2000, Developmental medicine and child neurology.
[180] J. Gordon,et al. Impaired hippocampal–prefrontal synchrony in a genetic mouse model of schizophrenia , 2010, Nature.
[181] Bruce D. McCandliss,et al. Development of attentional networks in childhood , 2004, Neuropsychologia.
[182] Steven P. Wise,et al. Forward frontal fields: phylogeny and fundamental function , 2008, Trends in Neurosciences.
[183] Mark H Johnson,et al. Neuroimaging of typical and atypical development: A perspective from multiple levels of analysis , 2002, Development and Psychopathology.
[184] W. Bodmer,et al. Common and rare variants in multifactorial susceptibility to common diseases , 2008, Nature Genetics.
[185] Maria Karayiorgou,et al. Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia , 2004, Nature Genetics.
[186] Rosanna Weksberg,et al. The schizophrenia phenotype in 22q11 deletion syndrome. , 2003, The American journal of psychiatry.
[187] T J Simon,et al. Subitizing and counting depend on different attentional mechanisms: Evidence from visual enumeration in afterimages , 1996, Perception & psychophysics.
[188] S. Tsukita,et al. Size-selective loosening of the blood-brain barrier in claudin-5–deficient mice , 2003, The Journal of cell biology.
[189] D. Tank,et al. Dendritic Integration in Mammalian Neurons, a Century after Cajal , 1996, Neuron.
[190] R. Kucherlapati,et al. Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome , 2006, Neurogenetics.
[191] Stephan Eliez,et al. Risk factors for the emergence of psychotic disorders in adolescents with 22q11.2 deletion syndrome. , 2007, The American journal of psychiatry.
[192] E. Zackai,et al. Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern. , 1999, The Journal of pediatrics.
[193] T. DeBoer,et al. Overlapping numerical cognition impairments in children with chromosome 22q11.2 deletion or Turner syndromes , 2008, Neuropsychologia.
[194] John R. Yates,et al. Neural Palmitoyl-Proteomics Reveals Dynamic Synaptic Palmitoylation , 2008, Nature.
[195] B. Roe,et al. Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis. , 2000, Human molecular genetics.
[196] William P. Hetrick,et al. Temporal processing dysfunction in schizophrenia , 2008, Brain and Cognition.
[197] M. Karayiorgou,et al. NEUROPSYCHOLOGICAL CHARACTERISTICS OF CHILDREN WITH THE 22Q11 DELETION SYNDROME: A DESCRIPTIVE ANALYSIS , 2005, Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence.
[198] Jie Qin,et al. Transcriptional and behavioral interaction between 22q11.2 orthologs modulates schizophrenia-related phenotypes in mice , 2005, Nature Neuroscience.
[199] R. Shprintzen,et al. A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome. , 1978, The Cleft palate journal.
[200] Michael E. Greenberg,et al. A brain-specific microRNA regulates dendritic spine development , 2006, Nature.
[201] C. Cytrynbaum,et al. Velo-cardio-facial syndrome: Implications of microdeletion 22q11 for schizophrenia and mood disorders. , 2001, American journal of medical genetics.
[202] B. J. Casey,et al. The Effect of Preceding Context on Inhibition: An Event-Related fMRI Study , 2002, NeuroImage.