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Year | Number of Results |
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Page 1
TCF4-mediated Fuchs endothelial corneal dystrophy: Insights into a common trinucleotide repeat-associated disease.
Prog Retin Eye Res. 2021 Mar;81:100883. doi: 10.1016/j.preteyeres.2020.100883. Epub 2020 Jul 28.
Prog Retin Eye Res. 2021.
PMID: 32735996
Free PMC article.
Review.
Endothelial corneal dystrophy with annular stromal clefts.
Koay SY, Sadan AN, Gore DM, Goyal S, Tuft S.
Koay SY, et al. Among authors: sadan an.
Can J Ophthalmol. 2021 Oct;56(5):e150-e152. doi: 10.1016/j.jcjo.2021.02.029. Epub 2021 Mar 23.
Can J Ophthalmol. 2021.
PMID: 33775594
No abstract available.
Item in Clipboard
CUGC for posterior polymorphous corneal dystrophy (PPCD).
Davidson AE, Hafford-Tear NJ, Dudakova L, Sadan AN, Pontikos N, Hardcastle AJ, Tuft SJ, Liskova P.
Davidson AE, et al. Among authors: sadan an.
Eur J Hum Genet. 2020 Jan;28(1):126-131. doi: 10.1038/s41431-019-0448-8. Epub 2019 Jun 14.
Eur J Hum Genet. 2020.
PMID: 31201376
Free PMC article.
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Phenotype and genotype of concurrent keratoconus and Fuchs endothelial corneal dystrophy.
Liu S, Sadan AN, Muthusamy K, Zarouchlioti C, Jedlickova J, Pontikos N, Thaung C, Hardcastle AJ, Netukova M, Skalicka P, Dudakova L, Bunce C, Tuft SJ, Davidson AE, Liskova P.
Liu S, et al. Among authors: sadan an.
Acta Ophthalmol. 2023 Sep;101(6):679-686. doi: 10.1111/aos.15654. Epub 2023 Mar 7.
Acta Ophthalmol. 2023.
PMID: 36883248
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CRISPR/Cas9-targeted enrichment and long-read sequencing of the Fuchs endothelial corneal dystrophy-associated TCF4 triplet repeat.
Hafford-Tear NJ, Tsai YC, Sadan AN, Sanchez-Pintado B, Zarouchlioti C, Maher GJ, Liskova P, Tuft SJ, Hardcastle AJ, Clark TA, Davidson AE.
Hafford-Tear NJ, et al. Among authors: sadan an.
Genet Med. 2019 Sep;21(9):2092-2102. doi: 10.1038/s41436-019-0453-x. Epub 2019 Feb 8.
Genet Med. 2019.
PMID: 30733599
Free PMC article.
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Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease.
Bhattacharyya N, Chai N, Hafford-Tear NJ, Sadan AN, Szabo A, Zarouchlioti C, Jedlickova J, Leung SK, Liao T, Dudakova L, Skalicka P, Parekh M, Moghul I, Jeffries AR, Cheetham ME, Muthusamy K, Hardcastle AJ, Pontikos N, Liskova P, Tuft SJ, Davidson AE.
Bhattacharyya N, et al. Among authors: sadan an.
PLoS Genet. 2024 May 7;20(5):e1011230. doi: 10.1371/journal.pgen.1011230. Online ahead of print.
PLoS Genet. 2024.
PMID: 38713708
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Should Patients with Kearns-Sayre Syndrome and Corneal Endothelial Failure Be Genotyped for a TCF4 Trinucleotide Repeat, Commonly Associated with Fuchs Endothelial Corneal Dystrophy?
Dudakova L, Skalicka P, Davidson AE, Sadan AN, Chylova M, Jahnova H, Anteneova N, Tesarova M, Honzik T, Liskova P.
Dudakova L, et al. Among authors: sadan an.
Genes (Basel). 2021 Nov 29;12(12):1918. doi: 10.3390/genes12121918.
Genes (Basel). 2021.
PMID: 34946867
Free PMC article.
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