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Thales Antonio Cabral de Guimaraes
Thales Antonio Cabral de Guimaraes
Other namesThales A. C. de Guimaraes
Clinical Research Fellow, Moorfields Eye Hospital; PhD student, UCL Institute of Ophthalmology
Verified email at ucl.ac.uk
Title
Cited by
Cited by
Year
Treatments for dry age-related macular degeneration: therapeutic avenues, clinical trials and future directions
TAC de Guimaraes, MD Varela, M Georgiou, M Michaelides
British Journal of Ophthalmology 106 (3), 297-304, 2022
1372022
Gene therapy for neovascular age-related macular degeneration: rationale, clinical trials and future directions
TAC de Guimaraes, M Georgiou, JWB Bainbridge, M Michaelides
British Journal of Ophthalmology 105 (2), 151-157, 2021
842021
Leber congenital amaurosis/early-onset severe retinal dystrophy: current management and clinical trials
MD Varela, TAC de Guimaraes, M Georgiou, M Michaelides
British Journal of Ophthalmology 106 (4), 445-451, 2022
462022
KCNV2 retinopathy: clinical features, molecular genetics and directions for future therapy
TACD Guimaraes, M Georgiou, AG Robson, M Michaelides
Ophthalmic Genetics 41 (3), 208-215, 2020
282020
Artificial intelligence in retinal disease: clinical application, challenges, and future directions
M Daich Varela, S Sen, TAC De Guimaraes, N Kabiri, N Pontikos, ...
Graefe's Archive for Clinical and Experimental Ophthalmology 261 (11), 3283-3297, 2023
212023
Structural evaluation in inherited retinal diseases
MD Varela, B Esener, SA Hashem, TAC de Guimaraes, M Georgiou, ...
British Journal of Ophthalmology 105 (12), 1623-1631, 2021
212021
KCNV2-associated retinopathy: genetics, electrophysiology, and clinical course—KCNV2 Study Group Report 1
M Georgiou, AG Robson, K Fujinami, SM Leo, A Vincent, F Nasser, ...
American journal of ophthalmology 225, 95-107, 2021
202021
KCNV2-associated retinopathy: Detailed retinal phenotype and structural endpoints—KCNV2 Study group report 2
M Georgiou, K Fujinami, A Vincent, F Nasser, S Khateb, ME Vargas, ...
American journal of ophthalmology 230, 1-11, 2021
152021
SynthEye: investigating the impact of synthetic data on artificial intelligence-assisted gene diagnosis of inherited retinal disease
YA Veturi, W Woof, T Lazebnik, I Moghul, P Woodward-Court, SK Wagner, ...
Ophthalmology Science 3 (2), 100258, 2023
112023
Inherited causes of combined vision and hearing loss: clinical features and molecular genetics
TAC de Guimaraes, E Arram, AF Shakarchi, M Georgiou, M Michaelides
British Journal of Ophthalmology 107 (10), 1403-1414, 2023
92023
Can artificial intelligence accelerate the diagnosis of inherited retinal diseases? Protocol for a data-only retrospective cohort study (Eye2Gene)
Q Nguyen, W Woof, N Kabiri, S Sen, MD Varela, TAC De Guimaraes, ...
BMJ open 13 (3), e071043, 2023
62023
RP2-associated X-linked retinopathy: clinical findings, molecular genetics, and natural history
M Georgiou, AG Robson, K Jovanovic, TAC de Guimarães, N Ali, ...
Ophthalmology 130 (4), 413-422, 2023
52023
Stargardt misdiagnosis: How ocular genetics helps
MB Ibanez IV, TAC de Guimaraes, J Capasso, N Bello, AV Levin
American Journal of Medical Genetics Part A 185 (3), 814-819, 2021
52021
AAV5-RPGR (botaretigene sparoparvovec) gene therapy for X-linked retinitis pigmentosa (XLRP) demonstrates localized improvements in static perimetry
M Michaelides, J Xu, D Wang, P Wong, A Fung, A Forbes, S Naylor, ...
Investigative Ophthalmology & Visual Science 63 (7), 3846-3846, 2022
42022
Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies …
M Georgiou, AG Robson, K Fujinami, TAC de Guimarães, ...
Progress in Retinal and Eye Research, 101244, 2024
32024
Eye2Gene: prediction of causal inherited retinal disease gene from multimodal imaging using deep-learning
N Pontikos, W Woof, A Veturi, B Javanmardi, M Ibarra-Arellano, A Hustinx, ...
32022
Best Vitelliform Macular Dystrophy Natural History Study Report 1: Clinical Features and Genetic Findings.
Y Laich, M Georgiou, K Fujinami, MD Varela, Y Fujinami-Yokokawa, ...
Ophthalmology, 2024
12024
KCNV2-associated retinopathy: genotype–phenotype correlations–KCNV2 study group report 3
TAC de Guimaraes, M Georgiou, AG Robson, K Fujinami, A Vincent, ...
British Journal of Ophthalmology, 2023
12023
Paradoxical response to carbonic anhydrase inhibitors in patients with intraretinal cystoid spaces
TAC Guimaraes, JE Capasso, AV Levin
Ophthalmic Genetics 40 (3), 213-218, 2019
12019
Sex Distributions in Non-ABCA4 Autosomal Macular Dystrophies
AV Mishra, S Vermeirsch, S Lin, MP Martin-Gutierrez, M Simcoe, ...
Investigative Ophthalmology & Visual Science 65 (5), 9-9, 2024
2024
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