Literature DB >> 16968140

Environmental influences on the behavioral phenotype of Angelman syndrome.

Kate Horsler1, Chris Oliver.   

Abstract

Using observational methods, we examined the social influences on laughing and smiling behavior in children with Angelman syndrome by systematically manipulating aspects of social interaction. Seven boys and 4 girls who were between 4 and 11 years of age and who had a confirmed maternal deletion of chromosome 15q11-q13 completed the study. Each child was observed while repeatedly exposed to three conditions in which parameters of social interaction were manipulated. Laughing and smiling behavior varied across all children and was significantly heightened in a condition involving adult speech, touch, smiling, laughing, and eye contact. The findings highlight the importance of examining environmental and social influences on purported phenotypic behavior in genetic syndromes.

Entities:  

Mesh:

Year:  2006        PMID: 16968140     DOI: 10.1352/0895-8017(2006)111[311:EIOTBP]2.0.CO;2

Source DB:  PubMed          Journal:  Am J Ment Retard        ISSN: 0895-8017


  13 in total

1.  Brief Report: A Longitudinal Study of Excessive Smiling and Laughing in Children with Angelman Syndrome.

Authors:  Dawn Adams; Kate Horsler; Rebecca Mount; Chris Oliver
Journal:  J Autism Dev Disord       Date:  2015-08

2.  Validating and Applying the CSBS-ITC in Neurogenetic Syndromes.

Authors:  Lisa R Hamrick; Bridgette L Tonnsen
Journal:  Am J Intellect Dev Disabil       Date:  2019-05

3.  Delineation of behavioral phenotypes in genetic syndromes: characteristics of autism spectrum disorder, affect and hyperactivity.

Authors:  Chris Oliver; Katy Berg; Jo Moss; Kate Arron; Cheryl Burbidge
Journal:  J Autism Dev Disord       Date:  2011-08

4.  Molecular and Clinical Aspects of Angelman Syndrome.

Authors:  A Dagli; K Buiting; C A Williams
Journal:  Mol Syndromol       Date:  2011-07-28

5.  A Behavioural Assessment of Social Anxiety and Social Motivation in Fragile X, Cornelia de Lange and Rubinstein-Taybi Syndromes.

Authors:  Hayley Crawford; Joanna Moss; Laura Groves; Robyn Dowlen; Lisa Nelson; Donna Reid; Chris Oliver
Journal:  J Autism Dev Disord       Date:  2020-01

6.  Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3.

Authors:  Yong-Hui Jiang; Yanzhen Pan; Li Zhu; Luis Landa; Jong Yoo; Corinne Spencer; Isabel Lorenzo; Murray Brilliant; Jeffrey Noebels; Arthur L Beaudet
Journal:  PLoS One       Date:  2010-08-20       Impact factor: 3.240

7.  An experimental study of executive function and social impairment in Cornelia de Lange syndrome.

Authors:  Lisa Nelson; Hayley Crawford; Donna Reid; Joanna Moss; Chris Oliver
Journal:  J Neurodev Disord       Date:  2017-09-11       Impact factor: 4.025

8.  Normal social seeking behavior, hypoactivity and reduced exploratory range in a mouse model of Angelman syndrome.

Authors:  Melody Allensworth; Anand Saha; Lawrence T Reiter; Detlef H Heck
Journal:  BMC Genet       Date:  2011-01-14       Impact factor: 2.797

9.  Evaluation of autism traits in Angelman syndrome: a resource to unfold autism genes.

Authors:  Maria Teresa Bonati; Silvia Russo; Palma Finelli; Maria Rosa Valsecchi; Francesca Cogliati; Florinda Cavalleri; Wendy Roberts; Maurizio Elia; Lidia Larizza
Journal:  Neurogenetics       Date:  2007-04-06       Impact factor: 3.017

10.  Behavior and neuropsychiatric manifestations in Angelman syndrome.

Authors:  Karine Pelc; Guy Cheron; Bernard Dan
Journal:  Neuropsychiatr Dis Treat       Date:  2008-06       Impact factor: 2.570

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.