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Is the Autism Treatment Evaluation Checklist a useful tool for monitoring progress in children with autism spectrum disorders?Self-injury and aggression in tuberous sclerosis complex: cross syndrome comparison and associated risk markers.Face scanning and spontaneous emotion preference in Cornelia de Lange syndrome and Rubinstein-Taybi syndrome.A national survey of Rett syndrome: behavioural characteristicsVisual preference for social stimuli in individuals with autism or neurodevelopmental disorders: an eye-tracking study.Persistence of self-injurious behaviour in autism spectrum disorder over 3 years: a prospective cohort study of risk markersPrevalence of autism spectrum disorder phenomenology in genetic disorders: a systematic review and meta-analysis.Executive functioning in Cornelia de Lange syndrome: domain asynchrony and age-related performance.An experimental study of executive function and social impairment in Cornelia de Lange syndrome.Prevalence of autism spectrum phenomenology in Cornelia de Lange and Cri du Chat syndromes.Prevalence of autism spectrum disorder symptomatology and related behavioural characteristics in individuals with Down syndrome.Prospective study of autism phenomenology and the behavioural phenotype of Phelan-McDermid syndrome: comparison to fragile X syndrome, Down syndrome and idiopathic autism spectrum disorder.Associations between behaviours that challenge in adults with intellectual disability, parental perceptions and parental mental health.Self-injury and aggression in adults with tuberous sclerosis complex: Frequency, associated person characteristics, and implications for assessment.Self-injurious behaviour in individuals with autism spectrum disorder and intellectual disability.The association between repetitive behaviours, impulsivity and hyperactivity in people with intellectual disability.The association between environmental events and self-injurious behaviour in Cornelia de Lange syndrome.Differential effects of anxiety and autism on social scene scanning in males with fragile X syndrome.The behavioural phenotype of Potocki-Lupski syndrome: a cross-syndrome comparison.Implicit Discrimination of Basic Facial Expressions of Positive/Negative Emotion in Fragile X Syndrome and Autism Spectrum Disorder.A longitudinal follow-up study of affect in children and adults with Cornelia de Lange syndrome.Brief Report: Repetitive Behaviour Profiles in Williams syndrome: Cross Syndrome Comparisons with Prader-Willi and Down syndromes.Profiles of children with Down syndrome who meet screening criteria for autism spectrum disorder (ASD): a comparison with children diagnosed with ASD attending specialist schools.Persistence of self-injury, aggression and property destruction in children and adults with tuberous sclerosis complex.A Comparative Study of Sociability in Angelman, Cornelia de Lange, Fragile X, Down and Rubinstein Taybi Syndromes and Autism Spectrum Disorder.Delineation of behavioral phenotypes in genetic syndromes: characteristics of autism spectrum disorder, affect and hyperactivity.Autism spectrum disorder and attention-deficit-hyperactivity disorder in Down syndrome.Repetitive behavior in Rubinstein-Taybi syndrome: parallels with autism spectrum phenomenology.Autism characteristics and behavioural disturbances in ~ 500 children with Down's syndrome in England and Wales.Contrasting age related changes in autism spectrum disorder phenomenology in Cornelia de Lange, Fragile X, and Cri du Chat syndromes: Results from a 2.5 year follow-up.Stability of the autism diagnostic interview-revised from pre-school to elementary school age in children with autism spectrum disorders.The prevalence and phenomenology of repetitive behavior in genetic syndromes.Facial expression of affect in children with Cornelia de Lange syndrome.Phenotypes and genotypes in individuals with SMC1A variants.Behavioral characteristics associated with 19p13.2 microdeletions.Genotype-phenotype correlations in Cornelia de Lange syndrome: Behavioral characteristics and changes with age.Mental Health and Well-Being in Mothers of Children With Rare Genetic Syndromes Showing Chronic Challenging Behavior: A Cross-Sectional and Longitudinal Study.Attenuated behaviour in Cornelia de Lange and fragile X syndromes.Development, behaviour and autism in individuals with SMC1A variantsAre Angelman and Prader-Willi syndromes more similar than we thought? Food-related behavior problems in Angelman, Cornelia de Lange, Fragile X, Prader-Willi and 1p36 deletion syndromes
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description
researcher
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wetenschapper
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հետազոտող
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name
J Moss
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J Moss
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J Moss
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J Moss
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type
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J Moss
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J Moss
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J Moss
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J Moss
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J Moss
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J Moss
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J Moss
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J Moss
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P106
P31
P496
0000-0002-7676-933X