Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 103


Prevalence and severity of fuchs corneal dystrophy in Tangier Island.

Eghrari AO, McGlumphy EJ, Iliff BW, Wang J, Emmert D, Riazuddin SA, Katsanis N, Gottsch JD.

Am J Ophthalmol. 2012 Jun;153(6):1067-72. doi: 10.1016/j.ajo.2011.11.033. Epub 2012 Feb 8.


Replication of the TCF4 intronic variant in late-onset Fuchs corneal dystrophy and evidence of independence from the FCD2 locus.

Riazuddin SA, McGlumphy EJ, Yeo WS, Wang J, Katsanis N, Gottsch JD.

Invest Ophthalmol Vis Sci. 2011 Apr 27;52(5):2825-9. doi: 10.1167/iovs.10-6497. Print 2011 Apr.


[TGC Repeats in Intron 2 of the TCF4 Gene have a Good Predictive Power Regarding to Fuchs Endothelial Corneal Dystrophy].

Luther M, Grünauer-Kloevekorn C, Weidle E, Passarge E, Rupprecht A, Hoffmann K, Foja S.

Klin Monbl Augenheilkd. 2016 Feb;233(2):187-94. doi: 10.1055/s-0035-1546138. Epub 2015 Aug 17. German.


Age-severity relationships in families linked to FCD2 with retroillumination photography.

McGlumphy EJ, Yeo WS, Riazuddin SA, Al-Saif A, Wang J, Eghrari AO, Meadows DN, Emmert DG, Katsanis N, Gottsch JD.

Invest Ophthalmol Vis Sci. 2010 Dec;51(12):6298-302. doi: 10.1167/iovs.10-5187. Epub 2010 Sep 1.


Genetic association of TCF4 intronic polymorphisms, CTG18.1 and rs17089887, with Fuchs' endothelial corneal dystrophy in an Indian population.

Nanda GG, Padhy B, Samal S, Das S, Alone DP.

Invest Ophthalmol Vis Sci. 2014 Oct 23;55(11):7674-80. doi: 10.1167/iovs.14-15297.


Expansion of CTG18.1 Trinucleotide Repeat in TCF4 Is a Potent Driver of Fuchs' Corneal Dystrophy.

Vasanth S, Eghrari AO, Gapsis BC, Wang J, Haller NF, Stark WJ, Katsanis N, Riazuddin SA, Gottsch JD.

Invest Ophthalmol Vis Sci. 2015 Jul;56(8):4531-6. doi: 10.1167/iovs.14-16122.


Association of TCF4 gene polymorphisms with Fuchs' corneal dystrophy in the Chinese.

Thalamuthu A, Khor CC, Venkataraman D, Koh LW, Tan DT, Aung T, Mehta JS, Vithana EN.

Invest Ophthalmol Vis Sci. 2011 Jul 29;52(8):5573-8. doi: 10.1167/iovs.11-7568.


Correlation of Severity of Fuchs Endothelial Corneal Dystrophy With Triplet Repeat Expansion in TCF4.

Soliman AZ, Xing C, Radwan SH, Gong X, Mootha VV.

JAMA Ophthalmol. 2015 Dec;133(12):1386-91. doi: 10.1001/jamaophthalmol.2015.3430.


Comprehensive assessment of genetic variants within TCF4 in Fuchs' endothelial corneal dystrophy.

Wieben ED, Aleff RA, Eckloff BW, Atkinson EJ, Baheti S, Middha S, Brown WL, Patel SV, Kocher JP, Baratz KH.

Invest Ophthalmol Vis Sci. 2014 Aug 28;55(9):6101-7. doi: 10.1167/iovs.14-14958.


Linkage of a mild late-onset phenotype of Fuchs corneal dystrophy to a novel locus at 5q33.1-q35.2.

Riazuddin SA, Eghrari AO, Al-Saif A, Davey L, Meadows DN, Katsanis N, Gottsch JD.

Invest Ophthalmol Vis Sci. 2009 Dec;50(12):5667-71. doi: 10.1167/iovs.09-3764. Epub 2009 Jul 15.


Association of ZEB1 and TCF4 rs613872 changes with late onset Fuchs endothelial corneal dystrophy in patients from northern India.

Gupta R, Kumawat BL, Paliwal P, Tandon R, Sharma N, Sen S, Kashyap S, Nag TC, Vajpayee RB, Sharma A.

Mol Vis. 2015 Oct 30;21:1252-60. eCollection 2015.


Fuchs Endothelial Corneal Dystrophy: Strong Association with rs613872 Not Paralleled by Changes in Corneal Endothelial TCF4 mRNA Level.

Ołdak M, Ruszkowska E, Udziela M, Oziębło D, Bińczyk E, Ścieżyńska A, Płoski R, Szaflik JP.

Biomed Res Int. 2015;2015:640234. doi: 10.1155/2015/640234. Epub 2015 Sep 16.


Analysis of SLC4A11, ZEB1, LOXHD1, COL8A2 and TCF4 gene sequences in a multi-generational family with late-onset Fuchs corneal dystrophy.

Tang H, Zhang W, Yan XM, Wang LP, Dong H, Shou T, Lei H, Guo Q.

Int J Mol Med. 2016 Jun;37(6):1487-500. doi: 10.3892/ijmm.2016.2570. Epub 2016 Apr 20.


Role of the TCF4 gene intronic variant in normal variation of corneal endothelium.

Mackey DA, Warrington NM, Hewitt AW, Oates SK, Yazar S, Soloshenko A, Crawford GJ, Mountain JA, Pennell CE.

Cornea. 2012 Feb;31(2):162-6. doi: 10.1097/ICO.0b013e318226155f.


Confirmation of the association between the TCF4 risk allele and Fuchs endothelial corneal dystrophy in patients from the Midwestern United States.

Stamler JF, Roos BR, Wagoner MD, Goins KM, Kitzmann AS, Riley JB, Stone EM, Fingert JH.

Ophthalmic Genet. 2013 Mar-Jun;34(1-2):32-4. doi: 10.3109/13816810.2012.726396. Epub 2012 Sep 24.


CTG18.1 Expansion in TCF4 Increases Likelihood of Transplantation in Fuchs Corneal Dystrophy.

Eghrari AO, Vasanth S, Wang J, Vahedi F, Riazuddin SA, Gottsch JD.

Cornea. 2017 Jan;36(1):40-43.


Association and familial segregation of CTG18.1 trinucleotide repeat expansion of TCF4 gene in Fuchs' endothelial corneal dystrophy.

Mootha VV, Gong X, Ku HC, Xing C.

Invest Ophthalmol Vis Sci. 2014 Jan 2;55(1):33-42. doi: 10.1167/iovs.13-12611.


Mutations in AGBL1 cause dominant late-onset Fuchs corneal dystrophy and alter protein-protein interaction with TCF4.

Riazuddin SA, Vasanth S, Katsanis N, Gottsch JD.

Am J Hum Genet. 2013 Oct 3;93(4):758-64. doi: 10.1016/j.ajhg.2013.08.010.


Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy.

Li YJ, Minear MA, Qin X, Rimmler J, Hauser MA, Allingham RR, Igo RP, Lass JH, Iyengar SK, Klintworth GK, Afshari NA, Gregory SG; FECD Genetics Consortium.

Invest Ophthalmol Vis Sci. 2014 Jun 10;55(7):4577-84. doi: 10.1167/iovs.13-13517.


Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy.

Li YJ, Minear MA, Rimmler J, Zhao B, Balajonda E, Hauser MA, Allingham RR, Eghrari AO, Riazuddin SA, Katsanis N, Gottsch JD, Gregory SG, Klintworth GK, Afshari NA.

PLoS One. 2011 Apr 20;6(4):e18044. doi: 10.1371/journal.pone.0018044.

Supplemental Content

Support Center