Article

Robust candidates for language development and evolution are significantly dysregulated in the blood of people with Williams syndrome

2018-12-06

Abstract excerpt

Williams syndrome (WS) is a clinical condition entailing cognitive deficits and with an uneven language profile, which has been object of intense inquiry over the last decades. Although WS results from the hemideletion of around two dozens of genes in chromosome 7, no gene has been yet probed to account for, or contribute significantly to, the language problems exhibited by the affected people. In this paper we sh...

Topics

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

Identifiers and source

Literature Corpus work: e549740a-2cd6-5547-96f7-062dcad0cc46
DOI: 10.1101/488155

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Robust candidates for language development and evolution are significantly dysregulated in the blood of people with Williams syndromeDOI 10.1101/488155Read

Genes and their role in human brain development -- current knowledge and future perspectivesSemantic proximity Read

Genetic changes shaping the human brain.Semantic proximity Read

Autism and Williams syndrome: dissimilar socio-cognitive profiles with similar patterns of abnormal gene expression in the bloodSemantic proximity Read

VI. Genome structure and cognitive map of Williams syndrome.Semantic proximity Read

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

Whole Genome Sequencing Illuminates the Developmental Signatures of Human Language AbilitySemantic proximity Read

Williams syndrome: a relationship between genetics, brain morphology and behaviour.Semantic proximity Read

Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior.Semantic proximity Read

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

Genetic insights into the functional elements of language.Semantic proximity Read

Williams Syndrome-Specific Neuroarchitectural Profile and Its Associations with Cognitive FeaturesSemantic proximity Read

Williams syndrome, human self-domestication, and language evolutionSemantic proximity Read