Giles Atton
University Hospital Southampton NHS Foundation Trust(GB)
Publications by Year
Research Areas
Lymphatic System and Diseases, Hippo pathway signaling and YAP/TAZ, RNA and protein synthesis mechanisms, Wnt/β-catenin signaling in development and cancer, Blood properties and coagulation
Most-Cited Works
- → Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis(2015)316 cited
- → EPHB4 kinase–inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis(2016)103 cited
- → The lymphatic phenotype in Turner syndrome: an evaluation of nineteen patients and literature review(2015)73 cited
- → Mutations in the small nuclear RNA gene RNU2-2 cause a severe neurodevelopmental disorder with prominent epilepsy(2025)28 cited
- → Extending the phenotypes associated with TRIO gene variants in a cohort of 25 patients and review of the literature(2023)13 cited
- → Janus-faced EPHB4-associated disorders: novel pathogenic variants and unreported intrafamilial overlapping phenotypes(2021)13 cited
- → Mutations in the U2 snRNA gene RNU2-2P cause a severe neurodevelopmental disorder with prominent epilepsy(2024)6 cited
- → Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis(2019)5 cited
- → 57 Exploring the functions of an E-prescribing system to reduce prescribing errors and improve inpatient medication record keeping(2019)1 cited
- → Correction: Janus-faced EPHB4-associated disorders: novel pathogenic variants and unreported intrafamilial overlapping phenotypes(2021)