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Autistic Disorder in Patients with Williams-Beuren Syndrome: A Reconsideration of the Williams-Beuren Syndrome Phenotype

Overview of attention for article published in PLOS ONE, March 2012
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Title
Autistic Disorder in Patients with Williams-Beuren Syndrome: A Reconsideration of the Williams-Beuren Syndrome Phenotype
Published in
PLOS ONE, March 2012
DOI 10.1371/journal.pone.0030778
Pubmed ID
Authors

Sylvie Tordjman, George M. Anderson, Michel Botbol, Annick Toutain, Pierre Sarda, Michèle Carlier, Pascale Saugier-Veber, Clarisse Baumann, David Cohen, Céline Lagneaux, Anne-Claude Tabet, Alain Verloes

Abstract

Williams-Beuren syndrome (WBS), a rare developmental disorder caused by deletion of contiguous genes at 7q11.23, has been characterized by strengths in socialization (overfriendliness) and communication (excessive talkativeness). WBS has been often considered as the polar opposite behavioral phenotype to autism. Our objective was to better understand the range of phenotypic expression in WBS and the relationship between WBS and autistic disorder.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 153 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
France 1 <1%
Austria 1 <1%
South Africa 1 <1%
United Kingdom 1 <1%
United States 1 <1%
Unknown 148 97%

Demographic breakdown

Readers by professional status Count As %
Student > Master 27 18%
Student > Ph. D. Student 20 13%
Researcher 18 12%
Student > Bachelor 15 10%
Student > Postgraduate 13 8%
Other 35 23%
Unknown 25 16%
Readers by discipline Count As %
Psychology 31 20%
Medicine and Dentistry 23 15%
Agricultural and Biological Sciences 14 9%
Biochemistry, Genetics and Molecular Biology 12 8%
Social Sciences 9 6%
Other 32 21%
Unknown 32 21%