Author

James T.R. Walters

Cardiff University

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:benchmarking· 1 Assay:electronic health records· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Cameron James WatsoniD· 1 shared Danish HafeeziD· 1 shared David E.J. LindeniD· 1 shared Evangelos VassosiD· 1 shared Katharine Lynch-KellyiD· 1 shared Maria RogdakiiD· 1 shared Mark John EdwardsiD· 1 shared Talia EiloniD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

9 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Cameron James WatsonORCID

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1 paper

Recent·Most cited

The Neuropsychiatry of 22q11.2 Deletion Syndrome: An Electronic Health Records Study.

Cameron James Watson, Maria Rogdaki, Katharine Lynch-Kelly, Danish Hafeez, Talia Eilon, David E.J. Linden, James T.R. Walters, Evangelos Vassos, Mark John Edwards, Thomas Arthur Pollak

This study uses electronic health records to analyze the neuropsychiatric phenotype of 22q11.2 deletion syndrome at scale, revealing high prevalence of neurodevelopmental and psychiatric disorders.

medRxiv · Aug 4, 2026 · PreprintGenetic & Genomic Medicine