Author

Samuel J. R. A. Chawner

Cardiff UniversityORCID 0000-0002-2590-2874Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2

Frequent Co-Authors

David SkuseiD· 2 shared Frances Lucy RaymondiD· 2 shared Jérémy HalliD· 2 shared Marianne B. M. van den BreeiD· 2 shared Michael John OweniD· 2 shared Peter HolmansiD· 2 shared Danielle Le Roux· 1 shared Harriet HousbyiD· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

David SkuseORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineTranslational PsychiatryPeer-reviewedJun 18, 2024

Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs)

Jessica H. Hall, Samuel J. R. A. Chawner, Harriet Housby…·Shreeya Sivakumar

This study examines irritability in young people with neurodevelopmental copy number variants (ND-CNVs) and finds it is more common than in controls, independent of psychiatric diagnoses or IQ.

3 citations

humanstatistical model

GenomicsThe Lancet PsychiatryPeer-reviewedMay 2, 2019

Genotype-phenotype relationships in children with Copy Number Variants associated with high neuropsychiatric risk: Findings from the case-control IMAGINE-ID cohort in the United Kingdom

Samuel J. R. A. Chawner, Michael John Owen, Peter Holmans…·Marianne B. M. van den Bree

This study examines genotype-phenotype relationships in children with copy number variants (CNVs) associated with high neuropsychiatric risk, finding similar adverse effects across different CNVs with some qualitative differences.

124 citationstop 1%

humanstatistical model