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Article

VI. Genome structure and cognitive map of Williams syndrome.

Journal of cognitive neuroscience - 1 Jan 2000

Korenberg J R, Chen X N, Hirota H, Lai Z, Bellugi U, Burian D, Roe B, Matsuoka R

Abstract excerpt

Williams syndrome (WMS) is a most compelling model of human cognition, of human genome organization, and of evolution. Due to a deletion in chromosome band 7q11.23, subjects have cardiovascular, connective tissue, and neurodevelopmental deficits. Given the striking peaks and valleys in neurocognition including deficits in visual-spatial and global processing, preserved language and face processing,...

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Source

Identifiers

PMID: 10953236
DOI: 10.1162/089892900562002

Genes

FZD9
LIMK1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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VI. Genome structure and cognitive map of Williams syndrome.PMID 10953236Read ↗

Neuropsychological Genotype-Phenotype in Patients with Williams Syndrome with Atypical Deletions: A Systematic Review.Semantic proximity Read ↗

Genetic contributions to visuospatial cognition in Williams syndrome: insights from two contrasting partial deletion patientsSemantic proximity Read ↗

Integrated DNA methylation analysis reveals a potential role for ANKRD30B in Williams syndrome.Semantic proximity Read ↗

Williams-Beuren syndrome: a challenge for genotype-phenotype correlations.Semantic proximity Read ↗

Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.Semantic proximity Read ↗

Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice.Semantic proximity Read ↗

Robust candidates for language development and evolution are significantly dysregulated in the blood of people with Williams syndromeSemantic proximity Read ↗

The behavioral phenotype of Williams syndrome: A recognizable pattern of neurodevelopment.Semantic proximity Read ↗

Severe expressive-language delay related to duplication of the Williams-Beuren locus.Semantic proximity Read ↗

Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndrome.Semantic proximity Read ↗

Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23.Semantic proximity Read ↗

Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture.Semantic proximity Read ↗

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