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Crawford, Hayley; Moss, Joanna; Groves, Laura; Dowlen, Robyn; Nelson, Lisa; Reid, Donna; Oliver, Chris – Journal of Autism and Developmental Disorders, 2020
Unique socio-behavioural phenotypes are reported for individuals with different neurodevelopmental disorders. Here, the effects of adult familiarity and nature of interaction on social anxiety and social motivation were investigated in individuals with fragile X (FXS; n = 20), Cornelia de Lange (CdLS; n = 20) and Rubinstein-Taybi (RTS; n = 20)…
Descriptors: Genetic Disorders, Intellectual Disability, Anxiety, Motivation
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Wilde, Lucy; Mitchell, Anna; Oliver, Chris – Journal of Autism and Developmental Disorders, 2016
Social excesses, characterised by heightened social motivation, are important for describing social functioning. Smith-Magenis syndrome (SMS) is a potential exemplar of a disorder where heightened social motivation is associated with negative behavioural outcomes. In Down syndrome (DS) strong social motivation is described, but less commonly…
Descriptors: Intellectual Disability, Down Syndrome, Motivation, Interpersonal Competence
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Wilde, Lucy; Oliver, Chris – Journal of Autism and Developmental Disorders, 2017
Everyday executive function (EF) was examined in Smith-Magenis syndrome (SMS), associated with high risk of behaviour disorder, and Down syndrome (DS), associated with relatively low risk of behaviour disorder. Caregivers of 13 children with SMS and 17 with DS rated everyday EF using the Behavioral Rating Inventory of Executive…
Descriptors: Down Syndrome, Executive Function, Behavior Disorders, Behavior Rating Scales
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Waite, Jane; Moss, Joanna; Beck, Sarah R.; Richards, Caroline; Nelson, Lisa; Arron, Kate; Burbidge, Cheryl; Berg, Katy; Oliver, Chris – Journal of Autism and Developmental Disorders, 2015
Syndrome specific repetitive behavior profiles have been described previously. A detailed profile is absent for Rubinstein-Taybi syndrome (RTS). The Repetitive Behaviour Questionnaire and Social Communication Questionnaire were completed for children and adults with RTS (N = 87), Fragile-X (N = 196) and Down (N = 132) syndromes, and individuals…
Descriptors: Genetic Disorders, Repetition, Behavior Problems, Down Syndrome
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Oliver, Chris; Kalsy, Sunny; McQuillan, Sharna; Hall, Scott – Journal of Applied Research in Intellectual Disabilities, 2011
Background: Informant-based assessment of behavioural change and difference in dementia in Down syndrome can aid diagnosis and inform service delivery. To date few studies have examined the impact of different types of behavioural change. Methods: The Assessment for Adults with Developmental Disabilities (AADS), developed for this study, assesses…
Descriptors: Dementia, Down Syndrome, Adults, Behavior Change
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Moss, Jo; Richards, Caroline; Nelson, Lisa; Oliver, Chris – Autism: The International Journal of Research and Practice, 2013
We evaluated the proportion of individuals with Down syndrome (DS: N = 108) who met criteria for autism spectrum disorder (ASD) on the Social Communication Questionnaire and the severity of ASD-related symptomatology in this group. The proportions of individuals with DS meeting the cut-off for ASD and autism in this sample were 19% and 8%,…
Descriptors: Autism, Pervasive Developmental Disorders, Down Syndrome, Incidence
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Kalsy, Sunny; Heath, Rebecca; Adams, Dawn; Oliver, Chris – Journal of Applied Research in Intellectual Disabilities, 2007
Background: Whereas there is a knowledge base on staff attributions of challenging behaviour, there has been little research on the effects of training, type of behaviour and biological context on staff attributions of controllability in the context of people with intellectual disabilities and dementia. Methods: A mixed design was used to…
Descriptors: Mental Retardation, Dementia, Down Syndrome, Behavior Problems
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Oliver, Chris; Holland, Tony; Hall, Scott; Crayton, Lissa – American Journal on Mental Retardation, 2005
The effect of increasing the number of stimuli to be recalled was investigated to evaluate whether sensitivity for memory impairment was enhanced in adults with Down syndrome when using higher task load. Three levels of load were compared across three groups of adults: those with cognitive deterioration, no cognitive deterioration over age 40, and…
Descriptors: Dementia, Memory, Down Syndrome, Adults