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

Neuroanatomical Correlates of Cognitive Dysfunction in 22q11.2 Deletion Syndrome

30 Mar 2024

Abstract excerpt

22q11.2 Deletion Syndrome (22q11.2DS), the most common chromosomal microdeletion, presents as a heterogeneous phenotype characterized by an array of anatomical, behavioral, and cognitive abnormalities. Individuals with 22q11.2DS exhibit extensive cognitive deficits, both in overall intellectual capacity and focal challenges in executive functioning, attentional control, perceptual abilities, motor skills, verbal...

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 Coronary Artery Anomalies

Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 38674375
DOI: 10.3390/genes15040440

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 20 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Neuroanatomical Correlates of Cognitive Dysfunction in 22q11.2 Deletion SyndromePMID 38674375Read ↗

22q11.2 deletion syndrome: genetics, neuroanatomy and cognitive/behavioral features keywords.Semantic proximity Read ↗

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

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

Atypical cortical connectivity and visuospatial cognitive impairments are related in children with chromosome 22q11.2 deletion syndromeSemantic proximity Read ↗

[22q11.2 microdeletion].Semantic proximity Read ↗

Subtypes in 22q11.2 deletion syndrome associated with behaviour and neurofacial morphology.Semantic proximity Read ↗

[Neurocognitive and psychiatric management of the 22q11.2 deletion syndrome].Semantic proximity Read ↗

Variability in Neuropsychological Phenotypes in Patients with 22Q11.2 Deletion Syndrome: Case Series.Semantic proximity Read ↗

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

Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndrome.Semantic proximity Read ↗

Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms.Semantic proximity Read ↗

Mapping Cortical Thickness in Children with 22q11.2 DeletionsSemantic proximity Read ↗

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