Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

In vivo evidence of microstructural hypo-connectivity of brain white matter in 22q11.2 deletion syndrome

26 Jul 2023

Abstract excerpt

22q11.2 deletion syndrome, or 22q11.2DS, is a genetic syndrome associated with high rates of schizophrenia and autism spectrum disorders, in addition to widespread structural and functional abnormalities throughout the brain. Experimental animal models have identified neuronal connectivity deficits, e.g., decreased axonal length and complexity of axonal branching, as a primary mechanism underlying atypical brain...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Congenital heart defects research
Share to Congenital Heart Disease Studies
Share to Coronary Artery Anomalies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 37495890
DOI: 10.1038/s41380-023-02178-w

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

In vivo evidence of microstructural hypo-connectivity of brain white matter in 22q11.2 deletion syndromePMID 37495890Read ↗

In vivo evidence of microstructural hypo-connectivity of brain white matter in 22q11.2 deletion syndromeSemantic proximity Read ↗

Aberrant White Matter Microstructure in Children with 16p11.2 DeletionsSemantic proximity Read ↗

Charting Brain Structure in 22q11.2 Deletion Syndrome with Clinical NeuroimagingSemantic proximity Read ↗

White matter abnormalities in 22q11.2 deletion syndrome: preliminary associations with the Nogo-66 receptor gene and symptoms of psychosis.Semantic proximity Read ↗

The Hidden Architecture of Brain Structural Variability in 22q11.2 Deletion Syndrome: A Multi-site StudySemantic proximity Read ↗

Machine-learning classification of 22q11.2 deletion syndrome: A diffusion tensor imaging studySemantic proximity Read ↗

Longitudinal development of the human white matter structural connectome and its association with brain transcriptomic and cellular architectureSemantic proximity Read ↗

Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion sizeSemantic proximity Read ↗

Neuroanatomical Correlates of Cognitive Dysfunction in 22q11.2 Deletion SyndromeSemantic proximity Read ↗

Neuroanatomical phenotypes in a mouse model of the 22q11.2 microdeletion.Semantic proximity Read ↗

Synaptic-dependent developmental dysconnectivity in 22q11.2 deletion syndromeSemantic proximity Read ↗

Longitudinal trajectories of cortical development in 22q11.2 copy number variants and typically developing controlsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.