Literature DB >> 10953231

I. The neurocognitive profile of Williams Syndrome: a complex pattern of strengths and weaknesses.

U Bellugi1, L Lichtenberger, W Jones, Z Lai, M St George.   

Abstract

The rare, genetically based disorder, Williams syndrome (WMS), produces a constellation of distinctive cognitive, neuroanatomical, and electrophysiological features which we explore through the series of studies reported here. In this paper, we focus primarily on the cognitive characteristics of WMS and begin to forge links among these characteristics, the brain, and the genetic basis of the disorder. The distinctive cognitive profile of individuals with WMS includes relative strengths in language and facial processing and profound impairment in spatial cognition. The cognitive profile of abilities, including what is 'typical' for individuals with WMS is discussed, but we also highlight areas of variability across the group of individuals with WMS that we have studied. Although the overall cognitive abilities (IQs) of individuals with WMS are typically in the mild-to-moderate range of mental retardation, the peaks and valleys within different cognitive domains make this syndrome especially intriguing to study across levels. Understanding the brain basis (and ultimately the genetic basis) for higher cognitive functioning is the goal we have begun to undertake with this line of interdisciplinary research.

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Year:  2000        PMID: 10953231     DOI: 10.1162/089892900561959

Source DB:  PubMed          Journal:  J Cogn Neurosci        ISSN: 0898-929X            Impact factor:   3.225


  124 in total

1.  Molecular dissection of DNA sequences and factors involved in slow muscle-specific transcription.

Authors:  S Calvo; D Vullhorst; P Venepally; J Cheng; I Karavanova; A Buonanno
Journal:  Mol Cell Biol       Date:  2001-12       Impact factor: 4.272

2.  Induced chromosome deletion in a Williams-Beuren syndrome mouse model causes cardiovascular abnormalities.

Authors:  Craig J Goergen; Hong-Hua Li; Uta Francke; Charles A Taylor
Journal:  J Vasc Res       Date:  2010-10-07       Impact factor: 1.934

3.  An exploration of causes of non-literal language problems in individuals with Asperger Syndrome.

Authors:  Ingerith Martin; Skye McDonald
Journal:  J Autism Dev Disord       Date:  2004-06

Review 4.  Genomic copy number variation in disorders of cognitive development.

Authors:  Eric M Morrow
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  2010-11       Impact factor: 8.829

5.  Cortical Folding of the Primate Brain: An Interdisciplinary Examination of the Genetic Architecture, Modularity, and Evolvability of a Significant Neurological Trait in Pedigreed Baboons (Genus Papio).

Authors:  Elizabeth G Atkinson; Jeffrey Rogers; Michael C Mahaney; Laura A Cox; James M Cheverud
Journal:  Genetics       Date:  2015-04-14       Impact factor: 4.562

6.  Genetic mapping of brain plasticity across development in Williams syndrome: ERP markers of face and language processing.

Authors:  D L Mills; L Dai; I Fishman; A Yam; L G Appelbaum; M St George; A Galaburda; U Bellugi; J R Korenberg
Journal:  Dev Neuropsychol       Date:  2013       Impact factor: 2.253

7.  Atypical hemispheric asymmetry in the perception of negative human vocalizations in individuals with Williams syndrome.

Authors:  Anna Järvinen-Pasley; Seth D Pollak; Anna Yam; Kiley J Hill; Mark Grichanik; Debra Mills; Allan L Reiss; Julie R Korenberg; Ursula Bellugi
Journal:  Neuropsychologia       Date:  2009-12-11       Impact factor: 3.139

8.  Spatial Mechanisms within the Dorsal Visual Pathway Contribute to the Configural Processing of Faces.

Authors:  Valentinos Zachariou; Christine V Nikas; Zaid N Safiullah; Stephen J Gotts; Leslie G Ungerleider
Journal:  Cereb Cortex       Date:  2017-08-01       Impact factor: 5.357

9.  Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome.

Authors:  Timothy A Hinsley; Pamela Cunliffe; Hannah J Tipney; Andrew Brass; May Tassabehji
Journal:  Protein Sci       Date:  2004-10       Impact factor: 6.725

10.  Toddlers with Williams syndrome process upright but not inverted faces holistically.

Authors:  Cara H Cashon; Oh-Ryeong Ha; Christopher A DeNicola; Carolyn B Mervis
Journal:  J Autism Dev Disord       Date:  2013-11
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