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Article

The emerging fragile X premutation phenotype: evidence from the domain of social cognition.

Brain and cognition - 1 Feb 2005

Cornish Kim, Kogan Cary, Turk Jeremy, Manly Tom, James Nicole, Mills Andrea, Dalton Ann

Abstract excerpt

Fragile X syndrome is a neurodevelopmental disorder that is caused by large methylated expansions of a CGG repeat (>200) region upstream of the FMR1 gene that results in the lack of expression of the fragile X mental retardation protein (FMRP). Affected individuals display a neurobehavioral phenotype that includes a significant impairment in social cognition alongside deficits in attentional control, inhibition...

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Source

Identifiers

PMID: 15629215
DOI: 10.1016/j.bandc.2004.08.020

Genes

FMR1

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

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

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The fragile X continuum: new advances and perspectives.Semantic proximity Read ↗

Neurobehavioural evidence for the involvement of the FMR1 gene in female carriers of fragile X syndrome.Semantic proximity Read ↗

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