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Autism spectrum disorder and attention‐deficit–hyperactivity disorder in Down syndrome

Developmental medicine and child neurology, 2017-03, Vol.59 (3), p.240-240

Moss, Joanna F

2017

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Age-related Behavioural Change in Cornelia de Lange and Cri du Chat Syndromes: A Seven Year Follow-up Study

Journal of autism and developmental disorders, 2019-06, Vol.49 (6), p.2476-2487

2019

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ATG8-dependent LMX1B-autophagy crosstalk shapes human midbrain dopaminergic neuronal resilience

The Journal of cell biology, 2023-05, Vol.222 (5), p.1

2023

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Differential effects of anxiety and autism on social scene scanning in males with fragile X syndrome

Journal of neurodevelopmental disorders, 2017-09, Vol.9 (1), p.9-9, Article 9

2017

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The behavioural phenotype of SATB2-associated syndrome: a within-group and cross-syndrome analysis

Journal of neurodevelopmental disorders, 2022-03, Vol.14 (1), p.25-25, Article 25

2022

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Profiles of autism characteristics in thirteen genetic syndromes: a machine learning approach

Molecular autism, 2023-01, Vol.14 (1), p.3-14, Article 3

2023

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The Prevalence and Phenomenology of Repetitive Behavior in Genetic Syndromes

Journal of autism and developmental disorders, 2009-04, Vol.39 (4), p.572-588

2009

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

Journal of autism and developmental disorders, 2020, Vol.50 (1), p.127-144

2020

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Autism Characteristics and Behavioural Disturbances in ∼ 500 Children with Down's Syndrome in England and Wales

Autism research, 2014-08, Vol.7 (4), p.433-441

2014

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A Comparative Study of Sociability in Angelman, Cornelia de Lange, Fragile X, Down and Rubinstein Taybi Syndromes and Autism Spectrum Disorder

American journal on intellectual and developmental disabilities, 2016-11, Vol.121 (6), p.465-486

2016

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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

American journal of medical genetics. Part C, Seminars in medical genetics, 2015-06, Vol.169C (2), p.188-197

2015

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Delineating the Profile of Autism Spectrum Disorder Characteristics in Cornelia de Lange and Fragile X Syndromes

American journal on intellectual and developmental disabilities, 2013-01, Vol.118 (1), p.55-73

2013

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The behavioral characteristics of Sotos syndrome

American journal of medical genetics. Part A, 2015-12, Vol.167A (12), p.2945-2956

2015

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Repetitive Behavior in Rubinstein–Taybi Syndrome: Parallels with Autism Spectrum Phenomenology

Journal of autism and developmental disorders, 2015-05, Vol.45 (5), p.1238-1253

2015

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Visual preference for social stimuli in individuals with autism or neurodevelopmental disorders: an eye-tracking study

Molecular autism, 2016-04, Vol.7 (24), p.24-24, Article 24

2016

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Genotype–phenotype correlations in Cornelia de Lange syndrome: Behavioral characteristics and changes with age

American journal of medical genetics. Part A, 2017-06, Vol.173 (6), p.1566-1574

2017

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Implicit Discrimination of Basic Facial Expressions of Positive/Negative Emotion in Fragile X Syndrome and Autism Spectrum Disorder

American journal on intellectual and developmental disabilities, 2015-07, Vol.120 (4), p.328-345

2015

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Social Behavior and Characteristics of Autism Spectrum Disorder in Angelman, Cornelia de Lange, and Cri du Chat Syndromes

American journal on intellectual and developmental disabilities, 2013-07, Vol.118 (4), p.262-283

2013

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Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement

Nature reviews. Genetics, 2018-10, Vol.19 (10), p.649-666

2018

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Behavioral characteristics associated with 19p13.2 microdeletions

American journal of medical genetics. Part A, 2015-10, Vol.167A (10), p.2334-2343

2015

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Are 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

American journal of medical genetics. Part A, 2015-03, Vol.167A (3), p.572-578

2015

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Prevalence of Autism Spectrum Phenomenology in Cornelia de Lange and Cri du Chat Syndromes

American journal of mental retardation, 2008-07, Vol.113 (4), p.278

2008

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“You Have to Sit and Explain it All, and Explain Yourself.” Mothers’ Experiences of Support Services for Their Offspring with a Rare Genetic Intellectual Disability Syndrome

Journal of genetic counseling, 2011-04, Vol.20 (2), p.165-177

2011

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Cornelia de Lange syndrome: Extending the physical and psychological phenotype

American journal of medical genetics. Part A, 2010-05, Vol.152A (5), p.1127-1135

2010

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The effectiveness of cognitive behavioural therapy and third‐wave cognitive behavioural interventions on diabetes‐related distress: A systematic review and meta‐analysis

Diabetic medicine, 2022-11, Vol.39 (11), p.e14948-n/a

2022

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Autism spectrum disorder and attention‐deficit–hyperactivity disorder in Down syndrome

Age-related Behavioural Change in Cornelia de Lange and Cri du Chat Syndromes: A Seven Year Follow-up Study

ATG8-dependent LMX1B-autophagy crosstalk shapes human midbrain dopaminergic neuronal resilience

Differential effects of anxiety and autism on social scene scanning in males with fragile X syndrome

The behavioural phenotype of SATB2-associated syndrome: a within-group and cross-syndrome analysis

Profiles of autism characteristics in thirteen genetic syndromes: a machine learning approach

The Prevalence and Phenomenology of Repetitive Behavior in Genetic Syndromes

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

Autism Characteristics and Behavioural Disturbances in ∼ 500 Children with Down's Syndrome in England and Wales

A Comparative Study of Sociability in Angelman, Cornelia de Lange, Fragile X, Down and Rubinstein Taybi Syndromes and Autism Spectrum Disorder

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

Delineating the Profile of Autism Spectrum Disorder Characteristics in Cornelia de Lange and Fragile X Syndromes

The behavioral characteristics of Sotos syndrome

Repetitive Behavior in Rubinstein–Taybi Syndrome: Parallels with Autism Spectrum Phenomenology

Visual preference for social stimuli in individuals with autism or neurodevelopmental disorders: an eye-tracking study

Genotype–phenotype correlations in Cornelia de Lange syndrome: Behavioral characteristics and changes with age

Implicit Discrimination of Basic Facial Expressions of Positive/Negative Emotion in Fragile X Syndrome and Autism Spectrum Disorder

Social Behavior and Characteristics of Autism Spectrum Disorder in Angelman, Cornelia de Lange, and Cri du Chat Syndromes

Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement

Behavioral characteristics associated with 19p13.2 microdeletions

Are 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

Prevalence of Autism Spectrum Phenomenology in Cornelia de Lange and Cri du Chat Syndromes

“You Have to Sit and Explain it All, and Explain Yourself.” Mothers’ Experiences of Support Services for Their Offspring with a Rare Genetic Intellectual Disability Syndrome

Cornelia de Lange syndrome: Extending the physical and psychological phenotype

The effectiveness of cognitive behavioural therapy and third‐wave cognitive behavioural interventions on diabetes‐related distress: A systematic review and meta‐analysis

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