Published in Neuroreport on June 28, 2004
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) 1.20
The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders. Int J Dev Neurosci (2010) 1.16
A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children. Dev Psychopathol (2005) 1.13
The 22q11.2 deletion syndrome as a window into complex neuropsychiatric disorders over the lifespan. Biol Psychiatry (2013) 1.11
Hippocampal malrotation is associated with chromosome 22q11.2 microdeletion. Can J Neurol Sci (2013) 0.99
Domain specific attentional impairments in children with chromosome 22q11.2 deletion syndrome. Brain Cogn (2007) 0.92
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) 0.91
Increased incidence and size of cavum septum pellucidum in children with chromosome 22q11.2 deletion syndrome. Psychiatry Res (2010) 0.85
Regional cortical volumes and congenital heart disease: a MRI study in 22q11.2 deletion syndrome. J Neurodev Disord (2010) 0.83
Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes. Neuroimage (2010) 0.81
Neural phenotypes of common and rare genetic variants. Biol Psychol (2008) 0.81
Clues to the foundations of numerical cognitive impairments: evidence from genetic disorders. Dev Neuropsychol (2011) 0.80
Disrupted fornix integrity in children with chromosome 22q11.2 deletion syndrome. Psychiatry Res (2015) 0.77
Longitudinal study of cerebral surface morphology in youth with 22q11.2 deletion syndrome, and association with positive symptoms of psychosis. J Child Psychol Psychiatry (2016) 0.75
What's in a name: voxel-based morphometric analyses of MRI and naming difficulty in Alzheimer's disease, frontotemporal dementia and corticobasal degeneration. Brain (2004) 2.90
22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia. Nat Rev Neurosci (2010) 2.54
Structure-specific statistical mapping of white matter tracts. Neuroimage (2008) 2.28
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) 2.15
Pharmacological inhibition of the Wnt acyltransferase PORCN prevents growth of WNT-driven mammary cancer. Cancer Res (2012) 1.89
Brain enlargement is associated with regression in preschool-age boys with autism spectrum disorders. Proc Natl Acad Sci U S A (2011) 1.73
Volumetric, connective, and morphologic changes in the brains of children with chromosome 22q11.2 deletion syndrome: an integrative study. Neuroimage (2005) 1.55
Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome. Am J Psychiatry (2004) 1.43
Mapping cortical thickness in children with 22q11.2 deletions. Cereb Cortex (2006) 1.30
Brief report: methods for acquiring structural MRI data in very young children with autism without the use of sedation. J Autism Dev Disord (2007) 1.20
Alterations in midline cortical thickness and gyrification patterns mapped in children with 22q11.2 deletions. Cereb Cortex (2008) 1.15
A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children. Dev Psychopathol (2005) 1.13
Alzheimer's disease and frontotemporal dementia exhibit distinct atrophy-behavior correlates: a computer-assisted imaging study. Acad Radiol (2003) 1.13
Young adult female fragile X premutation carriers show age- and genetically-modulated cognitive impairments. Brain Cogn (2011) 1.12
Attenuated positive symptoms of psychosis in adolescents with chromosome 22q11.2 deletion syndrome. Schizophr Res (2010) 1.11
Maladaptive conflict monitoring as evidence for executive dysfunction in children with chromosome 22q11.2 deletion syndrome. Dev Sci (2005) 1.10
Adult Female Fragile X Premutation Carriers Exhibit Age- and CGG Repeat Length-Related Impairments on an Attentionally Based Enumeration Task. Front Hum Neurosci (2011) 1.06
Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. Hum Mutat (2011) 1.05
Shape-based normalization of the corpus callosum for DTI connectivity analysis. IEEE Trans Med Imaging (2007) 1.03
Glucose and endoplasmic reticulum calcium channels regulate HIF-1beta via presenilin in pancreatic beta-cells. J Biol Chem (2008) 1.02
Enhanced manual and oral motor reaction time in young adult female fragile X premutation carriers. J Int Neuropsychol Soc (2011) 1.00
A framework for quantifying node-level community structure group differences in brain connectivity networks. Med Image Comput Comput Assist Interv (2012) 0.99
Social impairments in chromosome 22q11.2 deletion syndrome (22q11.2DS): autism spectrum disorder or a different endophenotype? J Autism Dev Disord (2014) 0.98
Specific cerebellar reductions in children with chromosome 22q11.2 deletion syndrome. Neurosci Lett (2006) 0.95
Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndrome. Brain Res (2006) 0.95
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) 0.94
Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion Syndrome. Child Neuropsychol (2005) 0.94
Catechol-O-methyltransferase polymorphism modulates cognitive control in children with chromosome 22q11.2 deletion syndrome. Cogn Affect Behav Neurosci (2009) 0.94
Regional brain abnormalities in 22q11.2 deletion syndrome: association with cognitive abilities and behavioral symptoms. Neurocase (2004) 0.93
Hippocampal volume reduction in children with chromosome 22q11.2 deletion syndrome is associated with cognitive impairment. Behav Brain Funct (2007) 0.93
Domain specific attentional impairments in children with chromosome 22q11.2 deletion syndrome. Brain Cogn (2007) 0.92
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) 0.91
MicroRNA-181a suppresses mouse granulosa cell proliferation by targeting activin receptor IIA. PLoS One (2013) 0.91
How might stress contribute to increased risk for schizophrenia in children with chromosome 22q11.2 deletion syndrome? J Neurodev Disord (2010) 0.91
Williams syndrome cognitive profile also characterizes Velocardiofacial/DiGeorge syndrome. Am J Med Genet (2002) 0.90
MicroRNA-133b stimulates ovarian estradiol synthesis by targeting Foxl2. FEBS Lett (2013) 0.89
Atypical development of the executive attention network in children with chromosome 22q11.2 deletion syndrome. J Neurodev Disord (2010) 0.88
Mapping the deletion endpoints in individuals with 22q11.2 deletion syndrome by droplet digital PCR. BMC Med Genet (2014) 0.87
Hesperidin suppressed proliferations of both human breast cancer and androgen-dependent prostate cancer cells. Phytother Res (2010) 0.87
Polycystin-1 regulates actin cytoskeleton organization and directional cell migration through a novel PC1-Pacsin 2-N-Wasp complex. Hum Mol Genet (2014) 0.86
Atypical developmental trajectory of functionally significant cortical areas in children with chromosome 22q11.2 deletion syndrome. Hum Brain Mapp (2011) 0.85
Increased incidence and size of cavum septum pellucidum in children with chromosome 22q11.2 deletion syndrome. Psychiatry Res (2010) 0.85
A cross-sectional analysis of the development of response inhibition in children with chromosome 22q11.2 deletion syndrome. Front Psychiatry (2013) 0.84
Young adult male carriers of the fragile X premutation exhibit genetically modulated impairments in visuospatial tasks controlled for psychomotor speed. J Neurodev Disord (2012) 0.83
Orphan nuclear receptor Nur77 regulates androgen receptor gene expression in mouse ovary. PLoS One (2012) 0.83
Assessment of cell viability. Curr Protoc Cytom (2013) 0.82
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) 0.82
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) 0.82
Altered neural activity of magnitude estimation processing in adults with the fragile X premutation. J Psychiatr Res (2013) 0.81
Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome. J Neurodev Disord (2012) 0.80
Regeneration of uterine horns in rats using collagen scaffolds loaded with human embryonic stem cell-derived endometrium-like cells. Tissue Eng Part A (2014) 0.79
CYR61 modulates the vascular endothelial growth factor C expression of decidual NK cells via PI3K/AKT pathway. Am J Reprod Immunol (2011) 0.78
Incremental value and clinical impact of neck sonography for primary hyperparathyroidism: a risk-adjusted analysis. Can J Surg (2013) 0.78
Children with chromosome 22q11.2 deletion syndrome exhibit impaired spatial working memory. Am J Intellect Dev Disabil (2014) 0.78
Rewards and challenges of cognitive neuroscience studies of persons with intellectual and developmental disabilities. Am J Intellect Dev Disabil (2010) 0.76
Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes. J Neurodev Disord (2014) 0.76
Altered structural brain connectome in young adult fragile X premutation carriers. Hum Brain Mapp (2014) 0.76
A second look: no effect of the COMT Val158Met polymorphism on conflict adaptation in youth with chromosome 22q11.2 deletion syndrome. Schizophr Res (2012) 0.75
[Diagnostic value of contrast-enhanced ultrasonography in preoperative Borrmann classification of gastric cancer]. Zhonghua Wei Chang Wai Ke Za Zhi (2014) 0.75
Erratum. Blood and Islet Phenotypes Indicate Immunological Heterogeneity in Type 1 Diabetes. Diabetes 2014;63:3835-3845. Diabetes (2015) 0.75
Embryo Selection for Single Embryo Transfer on Day 3 Based on Combination of Cleavage Patterns and Timing Parameters in in Vitro Fertilization Patients. J Reprod Med (2016) 0.75
Evaluation of shape-based normalization in the corpus callosum for white matter connectivity analysis. Med Image Comput Comput Assist Interv (2007) 0.75
Yeast dynamin and Ypt6 function in parallel for the endosome-to-Golgi retrieval of Snc1. Cell Biol Int (2019) 0.75