Back to search

Article

Alterations in resting-state activity and functional connectivity in children with 22q11.2 deletion syndrome

2021-09-22

Abstract excerpt

<h4>Background</h4> While genetic risk factors for psychiatric and neurodevelopmental disorders have been identified, the neurobiological route from genetic risk to neuropsychiatric outcome remains unclear. 22q11.2 deletion syndrome (22q11.2DS) is a copy number variant (CNV) syndrome associated with high rates of neurodevelopmental and psychiatric disorders including autism spectrum disorder (ASD), attention defic...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
f4f29ccb-170b-5f70-a554-a4ec36a68bbb
DOI
10.1101/2021.09.14.21263530
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Alterations in resting-state activity and functional connectivity in children with 22q11.2 deletion syndromeDOI 10.1101/2021.09.14.21263530
Reciprocal Disruptions in Thalamic and Hippocampal Resting-State Functional Connectivity in Youth with 22q11.2 DeletionsSemantic proximity
Sleep EEG in young people with 22q11.2 deletion syndrome: a cross-sectional study of slow-waves, spindles and correlations with memory and neurodevelopmental symptomsSemantic proximity
Mutations associated with neuropsychiatric conditions delineate functional brain connectivity dimensions contributing to autism and schizophrenia.Semantic proximity
Genetic modulation of brain dynamics in neurodevelopmental disorders: the impact of copy number variations on resting-state EEGSemantic proximity
Electrophysiological network alterations in adults with copy number variants associated with high neurodevelopmental risk.Semantic proximity
Spontaneous neural activity relates to psychiatric traits in 16p11.2 CNV carriers: An analysis of EEG spectral power and multiscale entropy.Semantic proximity
Aberrant Developmental Patterns of Gamma-Band Response and Long-Range Communication Disruption in Youths With 22q11.2 Deletion SyndromeSemantic proximity
Intrinsic Connectivity Network-Based Classification and Detection of Psychotic Symptoms in Youth With 22q11.2 DeletionsSemantic proximity
Neuroanatomical underpinnings of autism symptomatology in carriers and non-carriers of the 22q11.2 microdeletionSemantic proximity
Longitudinal development of thalamocortical functional connectivity in 22q11.2 deletion syndromeSemantic proximity
Neuroanatomical underpinnings of autism symptomatology in carriers and non-carriers of the 22q11.2 microdeletion.Semantic proximity
Adaptive and Behavioral Phenotype in Pediatric 22q11.2 Deletion Syndrome: Characterizing a High-Risk Neurogenetic Copy Number Variant.Semantic proximity
Select a neighboring publication to make it the new centre.