Literature DB >> 10501552

Towards the neural basis for hypersociability in a genetic syndrome.

U Bellugi1, R Adolphs, C Cassady, M Chiles.   

Abstract

Williams syndrome (WMS), a rare disorder with a distinctive profile of medical, psychological, neurophysiological and neuroanatomical characteristics, results from hemizygous deletion of about 20 genes. The phenotype exhibits specific dissociations in higher cognitive functions: general cognitive deficits but spared linguistic abilities; extreme spatial cognitive deficits, but intact face processing. Of special interest is an unusual social phenotype in WMS: an overly friendly, engaging personality and excessive sociability with strangers. In this first experimental study of social behavior in WMS, we report that WMS subjects show an abnormal positive bias in their social judgments of unfamiliar individuals, consistent with their behavior in real life. Our findings contribute to an understanding of the neural and genetic bases of human social behavior.

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Year:  1999        PMID: 10501552     DOI: 10.1097/00001756-199906030-00006

Source DB:  PubMed          Journal:  Neuroreport        ISSN: 0959-4965            Impact factor:   1.837


  53 in total

1.  Preliminary evidence of abnormal white matter related to the fusiform gyrus in Williams syndrome: a diffusion tensor imaging tractography study.

Authors:  B W Haas; F Hoeft; N Barnea-Goraly; G Golarai; U Bellugi; A L Reiss
Journal:  Genes Brain Behav       Date:  2011-10-19       Impact factor: 3.449

2.  White matter integrity deficits in prefrontal-amygdala pathways in Williams syndrome.

Authors:  Suzanne N Avery; Tricia A Thornton-Wells; Adam W Anderson; Jennifer Urbano Blackford
Journal:  Neuroimage       Date:  2011-10-08       Impact factor: 6.556

Review 3.  Language phenotypes and intervention planning: bridging research and practice.

Authors:  Deborah J Fidler; Amy Philofsky; Susan L Hepburn
Journal:  Ment Retard Dev Disabil Res Rev       Date:  2007

4.  Model syndromes for investigating social cognitive and affective neuroscience: a comparison of Autism and Williams syndrome.

Authors:  Helen Tager-Flusberg; Daniela Plesa Skwerer; Robert M Joseph
Journal:  Soc Cogn Affect Neurosci       Date:  2006-12       Impact factor: 3.436

Review 5.  Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.

Authors:  Daniel Paul Eisenberg; Mbemba Jabbi; Karen Faith Berman
Journal:  Neuroimage       Date:  2010-03-03       Impact factor: 6.556

6.  Exploratory analysis of social cognition and neurocognition in individuals at clinical high risk for psychosis.

Authors:  Emma Yong; Mariapaola Barbato; David L Penn; Richard S E Keefe; Scott W Woods; Diana O Perkins; Jean Addington
Journal:  Psychiatry Res       Date:  2014-04-12       Impact factor: 3.222

7.  Genetic influences on sociability: heightened amygdala reactivity and event-related responses to positive social stimuli in Williams syndrome.

Authors:  Brian W Haas; Debra Mills; Anna Yam; Fumiko Hoeft; Ursula Bellugi; Allan Reiss
Journal:  J Neurosci       Date:  2009-01-28       Impact factor: 6.167

8.  Abnormalities in neural processing of emotional stimuli in Williams syndrome vary according to social vs. non-social content.

Authors:  Karen E Muñoz; Andreas Meyer-Lindenberg; Ahmad R Hariri; Carolyn B Mervis; Venkata S Mattay; Colleen A Morris; Karen Faith Berman
Journal:  Neuroimage       Date:  2009-12-11       Impact factor: 6.556

9.  Enhanced prefrontal serotonin 5-HT(1A) currents in a mouse model of Williams-Beuren syndrome with low innate anxiety.

Authors:  Eliane Proulx; Edwin J Young; Lucy R Osborne; Evelyn K Lambe
Journal:  J Neurodev Disord       Date:  2010-03-19       Impact factor: 4.025

10.  Autonomic responses to dynamic displays of facial expressions in adolescents and adults with Williams syndrome.

Authors:  D Plesa Skwerer; L Borum; A Verbalis; C Schofield; N Crawford; L Ciciolla; H Tager-Flusberg
Journal:  Soc Cogn Affect Neurosci       Date:  2008-11-30       Impact factor: 3.436

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