Publications by authors named "Samuel Chawner"

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Inequalities of the Waiting Time for Education Health and Care Plan Provision for Pupils With Intellectual Developmental Disabilities: A Brief Report.
Irene O Lee, Jeanne Wolstencroft, Harriet Housby, Marianne B M van den Bree, Samuel J R A Chawner

J Intellect Disabil Res· November 2025

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Eating behaviour and eating disorders in individuals with rare neurodevelopmental variants: current knowledge and future research directions.
Samuel J R A Chawner

Front Psychiatry· November 2025

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Prevalence, Characteristics, and Genetic Architecture of Avoidant/Restrictive Food Intake Phenotypes.
Ludvig Daae Bjørndal, Elizabeth C Corfield, Laurie J Hannigan, Ziada Ayorech, Cynthia M Bulik, Samuel J R A Chawner

JAMA Pediatr· November 2025

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Pica in Childhood: Concurrent and Sequential Psychiatric Comorbidity.
Laura G Rubino, Cynthia M Bulik, Samuel J R A Chawner, Nadia Micali

Int J Eat Disord· October 2025

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Genome-wide copy number variation association study in anorexia nervosa.
Alicia Walker, Robert Karlsson, Jin P Szatkiewicz, Laura M Thornton, Zeynep Yilmaz, Samuel J R A Chawner

Mol Psychiatry· May 2025

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Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications.
Ruben C Gur, Carrie E Bearden, Sebastien Jacquemont, Ann Swillen, Therese van Amelsvoort, Samuel J R A Chawner

Mol Psychiatry· February 2025

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Comparison of autism domains across thirty rare variant genotypes.
Nabila M H Ali, Samuel J R A Chawner, Leila Kushan-Wells, Carrie E Bearden, Jennifer Gladys Mulle

EBioMedicine· February 2025

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Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs).
Jessica H Hall, Samuel J R A Chawner, , Jeanne Wolstencroft, David Skuse

Transl Psychiatry· June 2024

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Prevalence and recurrence of pica behaviors in early childhood within the ALSPAC birth cohort.
Natalie M Papini, Cynthia M Bulik, Samuel J R A Chawner, Nadia Micali

Int J Eat Disord· February 2024

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Atypical cortical networks in children at high-genetic risk of psychiatric and neurodevelopmental disorders.
Joanne L Doherty, Adam C Cunningham, Samuel J R A Chawner, Hayley M Moss, Diana C Dima

Neuropsychopharmacology· January 2024

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Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs).
Jessica H Hall, Samuel J R A Chawner, , Jeanne Wolstencroft, David Skuse

medRxiv· December 2023

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Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications.
Ruben Gur, Carrie Bearden, Sébastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Samuel Chawner

Res Sq· December 2023

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Psychopathology in mothers of children with pathogenic Copy Number Variants.
Maria Niarchou, Adam C Cunningham, Samuel J R A Chawner, Hayley Moulding, Matthew Sopp

J Med Genet· July 2023

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Prevalence and Recurrence of Pica Behaviors in Early Childhood: Findings from the ALSPAC Birth Cohort.
Natalie M Papini, Cynthia M Bulik, Samuel Jra Chawner, Nadia Micali

medRxiv· June 2023

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Neurodevelopmental dimensional assessment of young children at high genomic risk of neuropsychiatric conditions.
Samuel J R A Chawner, Amy L Paine, Matt J Dunn, Alice Walsh, Poppy Sloane

JCPP Adv· June 2023

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Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach.
Nicholas Donnelly, Adam Cunningham, Sergio Marco Salas, Matthew Bracher-Smith, Samuel Chawner

Mol Autism· May 2023

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DRAGON-Data: a platform and protocol for integrating genomic and phenotypic data across large psychiatric cohorts.
Amy J Lynham, Sarah Knott, Jack F G Underwood, Leon Hubbard, Sharifah S Agha, Samuel J R A Chawner

BJPsych Open· February 2023

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Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions.
Samuel J R A Chawner, Alexandra Evans, , Nigel Williams, Michael J Owen

Transl Psychiatry· January 2023

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Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE, a UK national cohort study.
Jeanne Wolstencroft, Francesca Wicks, Ramya Srinivasan, Sarah Wynn, Tamsin Ford, Samuel J R A Chawner

Lancet Psychiatry· September 2022

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Autism: A model of neurodevelopmental diversity informed by genomics.
Samuel J R A Chawner, Michael J Owen

Front Psychiatry· September 2022

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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.
Sébastien Jacquemont, Guillaume Huguet, Marieke Klein, Samuel J R A Chawner, Kirsten A Donald

Am J Psychiatry· March 2022

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Clinical evaluation of patients with a neuropsychiatric risk copy number variant.
Samuel Jra Chawner, Cameron J Watson, Michael J Owen

Curr Opin Genet Dev· June 2021

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Correction: The psychiatric phenotypes of 1q21 distal deletion and duplication.
Stefanie C Linden, Cameron J Watson, Jacqueline Smith, Samuel J R A Chawner, Thomas M Lancaster

Transl Psychiatry· June 2021

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The psychiatric phenotypes of 1q21 distal deletion and duplication.
Stefanie C Linden, Cameron J Watson, Jacqueline Smith, Samuel J R A Chawner, Thomas M Lancaster

Transl Psychiatry· February 2021

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Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome.
Ania M Fiksinski, Maude Schneider, Janneke Zinkstok, Danielle Baribeau, Samuel J R A Chawner

Curr Psychiatry Rep· February 2021

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