Stephen J Tuft
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Explore the profile of Stephen J Tuft including associated specialties, affiliations and a list of published articles.
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90
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1846
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Recent Articles
1.
Liu S, Sadan A, Bhattacharyya N, Zarouchlioti C, Szabo A, Abreu Costa M, et al.
JAMA Ophthalmol
. 2025 Mar;
PMID: 40079965
Importance: Understanding the pathogenic mechanisms of Fuchs endothelial corneal dystrophy (FECD) could contribute to developing gene-targeted therapies. Objective: To investigate associations between demographic data and age at first keratoplasty in...
2.
Zarouchlioti C, Efthymiou S, Facchini S, Dominik N, Bhattacharyya N, Liu S, et al.
EBioMedicine
. 2024 Sep;
108:105328.
PMID: 39278108
Background: Fuchs endothelial corneal dystrophy (FECD) is the most common repeat-mediated disease in humans. It exclusively affects corneal endothelial cells (CECs), with ≤81% of cases associated with an intronic TCF4...
3.
Braddock F, Gardner J, Bhattacharyya N, Sanchez-Pintado B, Costa M, Zarouchlioti C, et al.
Eur J Hum Genet
. 2024 Aug;
32(12):1583-1589.
PMID: 39169229
Corneal dystrophies are phenotypically and genetically heterogeneous, often resulting in visual impairment caused by corneal opacification. We investigated the genetic cause of an autosomal dominant corneal stromal dystrophy in a...
4.
Bhattacharyya N, Chai N, Hafford-Tear N, Sadan A, Szabo A, Zarouchlioti C, et al.
PLoS Genet
. 2024 May;
20(5):e1011230.
PMID: 38713708
Fuchs endothelial corneal dystrophy (FECD) is an age-related cause of vision loss, and the most common repeat expansion-mediated disease in humans characterised to date. Up to 80% of European FECD...
5.
Li J, Maile H, Bunce C, Kandakji L, Leucci M, Allan B, et al.
Eye (Lond)
. 2024 Feb;
38(9):1681-1686.
PMID: 38409307
Objective: To define how estimates of keratoconus progression following collagen cross-linking (CXL) vary according to the parameter selected to measure corneal shape. Materials And Methods: We estimated progression following CXL...
6.
Patterson K, Chong J, Chung D, Lisch W, Karp C, Dreisler E, et al.
Am J Ophthalmol
. 2023 Nov;
258:183-195.
PMID: 37972748
Purpose: To report the genetic etiology of Lisch epithelial corneal dystrophy (LECD). Design: Multicenter cohort study. Methods: A discovery cohort of 27 individuals with LECD from 17 families, including 7...
7.
Liu S, Sadan A, Muthusamy K, Zarouchlioti C, Jedlickova J, Pontikos N, et al.
Acta Ophthalmol
. 2023 Mar;
101(6):679-686.
PMID: 36883248
Purpose: To characterise the phenotype and genotype of concurrent keratoconus and Fuchs endothelial corneal dystrophy (KC + FECD). Methods: We recruited 20 patients with concurrent KC + FECD for a...
8.
Maile H, Li J, Pontikos N, Gore D, Tuft S
Am J Ophthalmol
. 2022 Nov;
249:193.
PMID: 36379322
No abstract available.
9.
Skalicka P, Jedlickova J, Horinek A, Trkova M, Davidson A, Tuft S, et al.
J Clin Med
. 2022 Sep;
11(17).
PMID: 36079096
We report the phenotype of a 15-year-old female patient with anterior segment dysgenesis (ASD) caused by a novel heterozygous loss-of-function variant. The proband underwent an ophthalmic examination as well as...
10.
Maile H, Li J, Fortune M, Royston P, Leucci M, Moghul I, et al.
Am J Ophthalmol
. 2022 Apr;
240:321-329.
PMID: 35469790
Purpose: To generate a prognostic model to predict keratoconus progression to corneal crosslinking (CXL). Design: Retrospective cohort study. Methods: We recruited 5025 patients (9341 eyes) with early keratoconus between January...