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Ocular Oncology and Pathology|April 2, 2021
A Case Series of "Solitary Idiopathic Choroiditis" and Proposal of a Nomenclature Change to "Idiopathic Scleroma"Emma Duignan, Roderick O'Day, Thomas Moloney, et al.
Case Reports in Ophthalmology|March 12, 2015
Ophthalmic manifestations of vitamin A and D deficiency in two autistic teenagers: case reports and a review of the literatureEmma Duignan, Paul Kenna, Rosemarie Watson, et al.
Retinal Cases & Brief Reports|June 17, 2020
MONOZYGOTIC TWINS DISCORDANT FOR ASYMMETRIC PIGMENTED PARAVENOUS CHORIORETINAL ATROPHYNaomi Fischer, Emma Duignan, Anthony G Robson, et al.
The British Journal of Ophthalmology|October 17, 2015
A novel homozygous truncating GNAT1 mutation implicated in retinal degenerationMatthew Carrigan, Emma Duignan, Pete Humphries, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|July 29, 2010
Should cardiac surgery be delayed among carriers of methicillin-resistant Staphylococcus aureus to reduce methicillin-resistant Staphylococcus aureus-related morbidity by preoperative decolonisation?David G Healy, Emma Duignan, Michael Tolan, et al.
Scientific Reports|September 15, 2016
Panel-Based Population Next-Generation Sequencing for Inherited Retinal DegenerationsMatthew Carrigan, Emma Duignan, Conor P G Malone, et al.
Genes|June 26, 2026
First Exonic Cryptic Branchpoint Variant in an Inherited Retinal Degeneration Detected in an Irish RPGR Pedigree with X-Linked Retinitis PigmentosaElla Kopčić, Laura Whelan, Ciara Shortall, et al.
Investigative Ophthalmology & Visual Science|January 14, 2026
Dynamic Inner Blood Retina Barrier Disruption in Retinitis PigmentosaKieva Byrne, Natalie Hudson, Jeffrey O'Callaghan, et al.
Genes|January 25, 2025
Novel Splice-Altering Variants in the CHM and CACNA1F Genes Causative of X-Linked Choroideremia and Cone DystrophyAnna R Ridgeway, Ciara Shortall, Laura K Finnegan, et al.
Scientific Reports|June 9, 2023
Detailed analysis of an enriched deep intronic ABCA4 variant in Irish Stargardt disease patientsLaura Whelan, Adrian Dockery, Kirk A J Stephenson, et al.
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