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Journal of Autism and Developmental Disorders|May 27, 2021
The prevalence and profile of autism in Sturge-Weber syndromeJenny Sloneem, Jo Moss, Sebastian Powell, et al.American Journal on Intellectual and Developmental Disabilities|April 20, 2018
Mental Health and Well-Being in Mothers of Children With Rare Genetic Syndromes Showing Chronic Challenging Behavior: A Cross-Sectional and Longitudinal StudyDawn Adams, Samantha Clarke, Gemma Griffith, et al.Journal of Neurodevelopmental Disorders|March 10, 2015
A national survey of Rett syndrome: behavioural characteristicsRina Cianfaglione, Angus Clarke, Michael Kerr, et al.Journal of Neurodevelopmental Disorders|October 7, 2019
Behavioural and psychological characteristics in Pitt-Hopkins syndrome: a comparison with Angelman and Cornelia de Lange syndromesAlice Watkins, Stacey Bissell, Jo Moss, et al.Oxford Open Neuroscience|November 28, 2025
Evidence of spontaneous mentalizing in children with Cornelia de Lange and fragile X syndromes, but not autistic childrenKatherine Ellis, Jo Moss, Malwina Dziwisz, et al.Research in Developmental Disabilities|January 11, 2022
Executive function, repetitive behaviour and restricted interests in neurodevelopmental disordersVictoria Perry, Katherine Ellis, Jo Moss, et al.Journal of Child Psychology and Psychiatry, and Allied Disciplines|October 9, 2018
Development, behaviour and autism in individuals with SMC1A variantsPaul A Mulder, Sylvia Huisman, Annemiek M Landlust, et al.Orphanet Journal of Rare Diseases|October 26, 2018
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 autismDawn Adams, Richard P Hastings, Clair Alston-Knox, et al.American Journal of Medical Genetics. Part A|February 13, 2017
Cornelia de Lange syndrome and molecular implications of the cohesin complex: Abstracts from the 7th biennial scientific and educational symposium 2016Antonie D Kline, Ian D Krantz, Matthew A Deardorff, et al.American Journal of Medical Genetics. Part A|May 27, 2017
Phenotypes and genotypes in individuals with SMC1A variantsSylvia Huisman, Paul A Mulder, Egbert Redeker, et al.Pageof 3