Author

Katharine Lynch-Kelly

King's College LondonORCID 0000-0003-1920-3986Unclaimed ORCID profile · follow to get notified of new preprints

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 James T.R. Walters· 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

Genetic & Genomic MedicinemedRxivPreprintAug 4, 2026

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

Cameron James Watson, Maria Rogdaki, Katharine Lynch-Kelly…·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.

DOI 10.64898/2026.08.03.26359320

humanelectronic health records

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