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Plos Genetics|December 26, 2024
Inhibitory KIRs decrease HLA class II-mediated protection in Type 1 DiabetesLaura Mora-Bitria, Bisrat J Debebe, Kelly L Miners, et al.
American Journal of Ophthalmology|October 8, 2023
RBP3-Retinopathy-Inherited High Myopia and Retinal Dystrophy: Genetic Characterization, Natural History, and Deep PhenotypingMichalis Georgiou, Kaoru Fujinami, Anthony G Robson, et al.
JAMA Ophthalmology|May 9, 2024
Pegcetacoplan Treatment and Consensus Features of Geographic Atrophy Over 24 MonthsDun Jack Fu, Pallavi Bagga, Gunjan Naik, et al.
BMJ Open|March 17, 2022
AlzEye: longitudinal record-level linkage of ophthalmic imaging and hospital admissions of 353 157 patients in London, UKSiegfried Karl Wagner, Fintan Hughes, Mario Cortina-Borja, et al.
American Journal of Human Genetics|March 3, 2018
Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 4Petra Liskova, Lubica Dudakova, Cerys J Evans, et al.
Translational Vision Science & Technology|June 6, 2025
Current Applications of Artificial Intelligence for Fuchs Endothelial Corneal Dystrophy: A Systematic ReviewSiyin Liu, Lynn Kandakji, Aleksander Stupnicki, et al.
The Lancet. Digital Health|December 16, 2020
Automated deep learning design for medical image classification by health-care professionals with no coding experience: a feasibility studyLivia Faes, Siegfried K Wagner, Dun Jack Fu, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|August 22, 2020
Clinical and genetic characteristics of 10 Japanese patients with PROM1-associated retinal disorder: A report of the phenotype spectrum and a literature review in the Japanese populationKaoru Fujinami, Akio Oishi, Lizhu Yang, et al.
Experimental Eye Research|March 10, 2019
The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosisLubica Dudakova, Cerys J Evans, Nikolas Pontikos, et al.
Investigative Ophthalmology & Visual Science|August 29, 2025
Sex Distributions in the Most Frequent Autosomal Genetic Causes of Retinitis PigmentosaMark J Hughes, Tina Lamey, Elena R Schiff, et al.
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