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Prevalence of autism spectrum disorder phenomenology in genetic disorders: a systematic review and meta-analysis

The Lancet. Psychiatry, 2015-10, Vol.2 (10), p.909-916

2015

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Advancing Health Equity Through Issue Spotting in Primary Care: A Case for Medical-legal Partnerships

Journal of pediatric health care, 2024-03, Vol.38 (2), p.279-284

2024

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The development of early social cognitive skills in neurogenetic syndromes associated with autism: Cornelia de Lange, fragile X and Rubinstein-Taybi syndromes

Orphanet journal of rare diseases, 2021-11, Vol.16 (1), p.488-488, Article 488

2021

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Persistence and predictors of self-injurious behaviour in autism: a ten-year prospective cohort study

Molecular autism, 2020-01, Vol.11 (1), p.8-8, Article 8

2020

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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

Journal of neurodevelopmental disorders, 2017-11, Vol.9 (1), p.37-37, Article 37

2017

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Executive functioning in Cornelia de Lange syndrome: domain asynchrony and age-related performance

Journal of neurodevelopmental disorders, 2017-08, Vol.9 (1), p.29-29, Article 29

2017

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The behavioural phenotype of Potocki-Lupski syndrome: a cross-syndrome comparison

Journal of neurodevelopmental disorders, 2018-01, Vol.10 (1), p.2-2, Article 2

2018

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Using Bayesian methodology to explore the profile of mental health and well-being in 646 mothers of children with 13 rare genetic syndromes in relation to mothers of children with autism

Orphanet journal of rare diseases, 2018-10, Vol.13 (1), p.185-185, Article 185

2018

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Behavioural and psychological characteristics in Pitt-Hopkins syndrome: a comparison with Angelman and Cornelia de Lange syndromes

Journal of neurodevelopmental disorders, 2019-10, Vol.11 (1), p.24-24, Article 24

2019

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Social Anxiety in Cornelia de Lange Syndrome

Journal of autism and developmental disorders, 2009-08, Vol.39 (8), p.1155-1162

2009

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Cornelia de Lange syndrome and molecular implications of the cohesin complex: Abstracts from the 7th biennial scientific and educational symposium 2016

American journal of medical genetics. Part A, 2017-05, Vol.173 (5), p.1172-1185

2017

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Prevalence and Risk-Markers of Self-Harm in Autistic Children and Adults

Journal of autism and developmental disorders, 2020-10, Vol.50 (10), p.3561-3574

2020

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Visual attention patterns during a gaze following task in neurogenetic syndromes associated with unique profiles of autistic traits: Fragile X and Cornelia de Lange syndromes

Cortex, 2024-05, Vol.174, p.110-124

2024

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Delineation of Behavioral Phenotypes in Genetic Syndromes: Characteristics of Autism Spectrum Disorder, Affect and Hyperactivity

Journal of autism and developmental disorders, 2011-08, Vol.41 (8), p.1019-1032

2011

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An Observational Study of Social Interaction Skills and Behaviors in Cornelia de Lange, Fragile X and Rubinstein-Taybi Syndromes

Journal of autism and developmental disorders, 2020-11, Vol.50 (11), p.4001-4010

2020

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Prevalence of autism spectrum disorder symptomatology and related behavioural characteristics in individuals with Down syndrome

Autism : the international journal of research and practice, 2013-07, Vol.17 (4), p.390-404

2013

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Characteristics of autism spectrum disorder in Cornelia de Lange syndrome

Journal of child psychology and psychiatry, 2012-08, Vol.53 (8), p.883-891

2012

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Persistence of self-injurious behaviour in autism spectrum disorder over 3 years: a prospective cohort study of risk markers

Journal of neurodevelopmental disorders, 2016-05, Vol.8 (20), p.21-21, Article 21

2016

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The prevalence and profile of autism in Sturge–Weber syndrome

Journal of autism and developmental disorders, 2022-05, Vol.52 (5), p.1942-1955

2022

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A Longitudinal Follow-Up Study of Affect in Children and Adults with Cornelia de Lange Syndrome

American journal on intellectual and developmental disabilities, 2014-05, Vol.119 (3), p.235

2014

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Mental Health and Well-Being in Mothers of Children with Rare Genetic Syndromes Showing Chronic Challenging Behavior: A Cross-Sectional and Longitudinal Study

American journal on intellectual and developmental disabilities, 2018-05, Vol.123 (3), p.241-303

2018

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Executive function, repetitive behaviour and restricted interests in neurodevelopmental disorders

Research in developmental disabilities, 2022-03, Vol.122, p.104166-104166, Article 104166

2022

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Self-injury and aggression in adults with tuberous sclerosis complex: Frequency, associated person characteristics, and implications for assessment

Research in developmental disabilities, 2017-05, Vol.64, p.119-130

2017

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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

Journal of intellectual disability research, 2017-01, Vol.61 (1), p.75-82

2017

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Associations between behaviours that challenge in adults with intellectual disability, parental perceptions and parental mental health

British journal of clinical psychology, 2017-11, Vol.56 (4), p.408-430

2017

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Prevalence of autism spectrum disorder phenomenology in genetic disorders: a systematic review and meta-analysis

Advancing Health Equity Through Issue Spotting in Primary Care: A Case for Medical-legal Partnerships

The development of early social cognitive skills in neurogenetic syndromes associated with autism: Cornelia de Lange, fragile X and Rubinstein-Taybi syndromes

Persistence and predictors of self-injurious behaviour in autism: a ten-year prospective cohort study

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

Executive functioning in Cornelia de Lange syndrome: domain asynchrony and age-related performance

The behavioural phenotype of Potocki-Lupski syndrome: a cross-syndrome comparison

Using Bayesian methodology to explore the profile of mental health and well-being in 646 mothers of children with 13 rare genetic syndromes in relation to mothers of children with autism

Behavioural and psychological characteristics in Pitt-Hopkins syndrome: a comparison with Angelman and Cornelia de Lange syndromes

Social Anxiety in Cornelia de Lange Syndrome

Cornelia de Lange syndrome and molecular implications of the cohesin complex: Abstracts from the 7th biennial scientific and educational symposium 2016

Prevalence and Risk-Markers of Self-Harm in Autistic Children and Adults

Visual attention patterns during a gaze following task in neurogenetic syndromes associated with unique profiles of autistic traits: Fragile X and Cornelia de Lange syndromes

Delineation of Behavioral Phenotypes in Genetic Syndromes: Characteristics of Autism Spectrum Disorder, Affect and Hyperactivity

An Observational Study of Social Interaction Skills and Behaviors in Cornelia de Lange, Fragile X and Rubinstein-Taybi Syndromes

Prevalence of autism spectrum disorder symptomatology and related behavioural characteristics in individuals with Down syndrome

Characteristics of autism spectrum disorder in Cornelia de Lange syndrome

Persistence of self-injurious behaviour in autism spectrum disorder over 3 years: a prospective cohort study of risk markers

The prevalence and profile of autism in Sturge–Weber syndrome

A Longitudinal Follow-Up Study of Affect in Children and Adults with Cornelia de Lange Syndrome

Mental Health and Well-Being in Mothers of Children with Rare Genetic Syndromes Showing Chronic Challenging Behavior: A Cross-Sectional and Longitudinal Study

Executive function, repetitive behaviour and restricted interests in neurodevelopmental disorders

Self-injury and aggression in adults with tuberous sclerosis complex: Frequency, associated person characteristics, and implications for assessment

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

Associations between behaviours that challenge in adults with intellectual disability, parental perceptions and parental mental health

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