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Samuel J. R. A. Chawner

Cardiff University

13

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28

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Clinical evaluation of patients with a neuropsychiatric risk copy number variant.

2021 Current Opinion in Genetics & Development
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Alterations in resting-state activity and functional connectivity in children with 22q11.2 deletion syndrome

2021 medRxiv
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INVESTIGATING THE SPECIFICITY OF GENOTYPE-PHENOTYPE RELATIONSHIPS IN CHILDREN WITH NEUROPSYCHIATRIC RISK COPY VARIANTS

2021 European Neuropsychopharmacology
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Genes To Mental Health (G2MH): A framework to map the combined effects of rare and common variants on dimensions of cognition and psychopathology

2021
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Correction: The psychiatric phenotypes of 1q21 distal deletion and duplication

2021 Translational Psychiatry
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Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome

2021 Current Psychiatry Reports
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Pan-european landscape of research into neurodevelopmental copy number variants: a survey by the MINDDS consortium.

2020 European Journal of Medical Genetics
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Psychopathology in mothers of children with pathogenic Copy Number Variants

2020 medRxiv
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A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants

2020 medRxiv
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SA118LONGITUDINAL COGNITIVE DEVELOPMENT AND ASSOCIATION WITH PRODROMAL PSYCHOTIC SYMPTOMS IN ADOLESCENTS WITH 22Q11.2 DELETION SYNDROME

2019 European Neuropsychopharmacology
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