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Stephen Tuft
Stephen Tuft
Institute of Ophthalmology
在 ucl.ac.uk 的电子邮件经过验证
标题
引用次数
年份
Spatial transcriptomics reveal isoform-specific patterns of TCF4 dysregulation in CTG18. 1 expansion positive FECD case-derived corneal endothelial cells
N Bhattacharyya, C Zarouchlioti, J Jedlickova, L Dudakova, P Skalicka, ...
Investigative Ophthalmology & Visual Science 65 (7), 644-644, 2024
2024
Novel insights into Fuchs endothelial corneal dystrophy through genetic, demographic, and phenotypic correlations
S Liu, A Sadan, A Szabo, N Bhattacharyya, C Zarouchlioti, MA Costa, ...
Investigative Ophthalmology & Visual Science 65 (7), 4229-4229, 2024
2024
A novel autosomal dominant Corneal Stromal Dystrophy associated with a SPARCL1 missense variant
FL Braddock, BS Pintado, A Szabo, N Bhattacharyya, S Mitchell, ...
Investigative Ophthalmology & Visual Science 65 (7), 2167-2167, 2024
2024
Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease
N Bhattacharyya, N Chai, NJ Hafford-Tear, AN Sadan, A Szabo, ...
PLoS Genetics 20 (5), e1011230, 2024
12024
OP-7 A comparison of keratoconus progression following collagen cross-linkage using standard or personalised keratometry thresholds
JPO Li, H Maile, C Bunce, M Leucci, B Allan, S Tuft, N Pontikos, D Gore
BMJ Open Ophthalmology 9 (Suppl 2), 2024
2024
A comparison of keratoconus progression following collagen cross-linkage using standard or personalised keratometry thresholds
JPO Li, HP Maile, C Bunce, L Kandakji, MT Leucci, BD Allan, SJ Tuft, ...
Eye, 1-6, 2024
2024
Lisch epithelial corneal dystrophy is caused by heterozygous loss-of-function variants in MCOLN1
K Patterson, JX Chong, DD Chung, W Lisch, CL Karp, E Dreisler, ...
American journal of ophthalmology 258, 183-195, 2024
12024
Antifungal susceptibility profiles for fungal isolates from corneas and contact lenses in the United Kingdom
S Tuft, NRH Stone, MJ Burton, EM Johnson, AM Borman
Eye 38 (3), 529-536, 2024
22024
Tissue-Specific Dynamics of TCF4 Triplet Repeat Instability Revealed by Optical Genome Mapping
C Zarouchlioti, S Efthymiou, S Fracchini, N Dominik, N Bhattacharyya, ...
bioRxiv, 2024.03. 27.587034, 2024
2024
Genetically refined and unsolved inherited corneal disease cohort offers opportunities for novel genomic discovery
MA Costa, A Szabo, N Bhattacharyya, C Zarouchlioti, N Hafford-Tear, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 373-374, 2024
2024
Deciphering novel TCF4-driven molecular origins and mechanisms underlying a common triplet repeat expansion-mediated disease
N Bhattacharyya, N Hafford-Tear, A Sadan, A Szabo, N Chai, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 375-375, 2024
2024
Utilising a CTG18. 1 expansion-negative Fuchs endothelial corneal dystrophy cohort to identify novel genetic risk loci
A Szabo, C Zarouchlioti, N Bhattacharyya, A Sadan, N Hafford-Tear, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 791-791, 2024
2024
Phenotype and genotype of concurrent keratoconus and Fuchs endothelial corneal dystrophy
S Liu, AN Sadan, K Muthusamy, C Zarouchlioti, J Jedlickova, N Pontikos, ...
Acta Ophthalmologica 101 (6), 679-686, 2023
2023
Reply to Comment on: Personalized model to predict keratoconus progression from demographic, topographic and genetic data
HP Maile, JPO Li, N Pontikos, DM Gore, SJ Tuft
American journal of ophthalmology 249, 193, 2023
42023
Graphical comparison of surgeon outcomes for the audit of a national corneal transplant registry (OTAG study 32)
C Hopkinson, E Curnow, DFP Larkin, J Prydal, S Tuft
Eye 37 (6), 1236-1241, 2023
22023
Antimicrobial resistance in topical treatments for microbial keratitis: protocol for a systematic review and meta-analysis
S Tuft, J Evans, I Gordon, A Leck, N Stone, T Neal, D Macleod, S Kaye, ...
BMJ open 13 (3), e069338, 2023
22023
False positive fungus results from investigation of microbial keratitis
SY Koay, S Tuft
Eye 37 (3), 574-575, 2023
12023
Utility of investigation for suspected microbial keratitis: a diagnostic accuracy study
S Tuft, C Bunce, S De, J Thomas
Eye 37 (3), 415-420, 2023
92023
Posterior corneal vesicles are not associated with the genetic variants that cause posterior polymorphous corneal dystrophy
P Liskova, NJ Hafford‐Tear, P Skalicka, F Malinka, J Jedlickova, ...
Acta Ophthalmologica 100 (7), e1426-e1430, 2022
32022
Snail Track Lesion with Flat Keratometry in Anterior Segment Dysgenesis Caused by a Novel FOXC1 Variant
P Skalicka, J Jedlickova, A Horinek, M Trkova, AE Davidson, SJ Tuft, ...
Journal of Clinical Medicine 11 (17), 5166, 2022
2022
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