Author

Patricia A. Foley

Oxford Centre for Genomic Medicine;

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

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Genetic & Genomic Medicine· 1

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Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1

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Andres RamosiD· 1 shared Cristina DiasiD· 1 shared Ingrid M. WentzenseniD· 1 shared Mary-Alice Abbott· 1 shared Rebecca Igbokwe· 1 shared Tim HubbardiD· 1 shared Yaroslav KainoviD· 1 shared

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2026-2026 · peak 1/yr

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7 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Andres RamosORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintNov 10, 2026

Inactivating mutations in polyadenylation factor CSTF2 disrupt intronic polyadenylation patterns and are associated with intellectual disability.

Yaroslav Kainov, Patricia A. Foley, Rebecca Igbokwe…·Cristina Dias

This study identifies inactivating CSTF2 variants in males with intellectual disability and shows they disrupt intronic polyadenylation patterns, linking CSTF2 to neurodevelopmental disorders.

DOI 10.64898/2026.11.10.26367664

humanbulk RNA-seq