Author

Talia Eilon

King's College LondonORCID 0000-0001-5250-0806Unclaimed 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 Katharine Lynch-KellyiD· 1 shared Maria RogdakiiD· 1 shared Mark John EdwardsiD· 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

Mutual co-authors in cluster

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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