Developmental trajectories of brain structure in adolescents with 22q11.2 deletion syndrome: a longitudinal study
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Converging levels of analysis on a genomic hotspot for psychosis: insights from 22q11.2 deletion syndromeDysregulation of presynaptic calcium and synaptic plasticity in a mouse model of 22q11 deletion syndrome.The Danish 22q11 research initiativePre-pulse inhibition and antisaccade performance indicate impaired attention modulation of cognitive inhibition in 22q11.2 deletion syndrome (22q11DS).The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders.Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.Neuroanatomic predictors to prodromal psychosis in velocardiofacial syndrome (22q11.2 deletion syndrome): a longitudinal studySchizophrenia and 22q11.2 deletion syndrome.Velo-Cardio-Facial Syndrome.The development of cognitive control in children with chromosome 22q11.2 deletion syndromeA Synaptic Function Approach to Investigating Complex Psychiatric Diseases.Adaptive strategy for the statistical analysis of connectomes.22q11 deletion syndrome: a review of the neuropsychiatric features and their neurobiological basis.Developmental changes in multivariate neuroanatomical patterns that predict risk for psychosis in 22q11.2 deletion syndromeGenotype-phenotype correlation in 22q11.2 deletion syndrome.White matter microstructural abnormalities of the cingulum bundle in youths with 22q11.2 deletion syndrome: associations with medication, neuropsychological function, and prodromal symptoms of psychosisMapping cortical morphology in youth with velocardiofacial (22q11.2 deletion) syndrome.Long-term intellectual outcome after temporal lobe surgery in childhood.Atypical developmental trajectory of functionally significant cortical areas in children with chromosome 22q11.2 deletion syndromeAssociation of schizophrenia in 22q11.2 deletion syndrome and gray matter volumetric deficits in the superior temporal gyrus.Structural and functional connectivity in the default mode network in 22q11.2 deletion syndrome.Genomic sister-disorders of neurodevelopment: an evolutionary approachIncreased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms.Reduced fractional anisotropy and axial diffusivity in white matter in 22q11.2 deletion syndrome: a pilot study.The hippocampi of children with chromosome 22q11.2 deletion syndrome have localized anterior alterations that predict severity of anxiety.Action simulation in hallucination-prone adolescents.Social cognition in 22q11.2 microdeletion syndrome: relevance to psychosis?A cross-sectional analysis of the development of response inhibition in children with chromosome 22q11.2 deletion syndromeGenetic contributions to changes of fiber tracts of ventral visual stream in 22q11.2 deletion syndrome.Alterations in midline cortical thickness and gyrification patterns mapped in children with 22q11.2 deletions.White matter microstructural abnormalities in girls with chromosome 22q11.2 deletion syndrome, Fragile X or Turner syndrome as evidenced by diffusion tensor imaging.Long-range dysconnectivity in frontal and midline structures is associated to psychosis in 22q11.2 deletion syndrome.Facial emotion perception by intensity in children and adolescents with 22q11.2 deletion syndrome.Adolescence is the starting point of sex-dichotomous COMT genetic effects.Childhood cognitive development in 22q11.2 deletion syndrome: case-control study.Structural abnormalities in cortical volume, thickness, and surface area in 22q11.2 microdeletion syndrome: Relationship with psychotic symptoms.Multimodal investigation of triple network connectivity in patients with 22q11DS and association with executive functions.Longitudinal study of cerebral surface morphology in youth with 22q11.2 deletion syndrome, and association with positive symptoms of psychosis.Quantifying indices of short- and long-range white matter connectivity at each cortical vertex.Neuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson's disease.
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Developmental trajectories of brain structure in adolescents with 22q11.2 deletion syndrome: a longitudinal study
description
article científic
@ca
article scientifique
@fr
articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 04 September 2007
@en
vedecký článok
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vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Developmental trajectories of ...... syndrome: a longitudinal study
@en
Developmental trajectories of ...... yndrome: a longitudinal study.
@nl
type
label
Developmental trajectories of ...... syndrome: a longitudinal study
@en
Developmental trajectories of ...... yndrome: a longitudinal study.
@nl
prefLabel
Developmental trajectories of ...... syndrome: a longitudinal study
@en
Developmental trajectories of ...... yndrome: a longitudinal study.
@nl
P2093
P2860
P50
P1476
Developmental trajectories of ...... syndrome: a longitudinal study
@en
P2093
Doron Gothelf
Lauren Penniman
Stephan Eliez
P2860
P356
10.1016/J.SCHRES.2007.07.021
P407
P577
2007-09-04T00:00:00Z