Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 86

1.

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.

2.

Progression of Fuchs corneal dystrophy in a family linked to the FCD1 locus.

Meadows DN, Eghrari AO, Riazuddin SA, Emmert DG, Katsanis N, Gottsch JD.

Invest Ophthalmol Vis Sci. 2009 Dec;50(12):5662-6. doi: 10.1167/iovs.09-3568. Epub 2009 Jul 15.

PMID:
19608546
3.

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.

PMID:
19608540
4.

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.

5.

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.

6.

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.

7.

A common locus for late-onset Fuchs corneal dystrophy maps to 18q21.2-q21.32.

Sundin OH, Broman KW, Chang HH, Vito EC, Stark WJ, Gottsch JD.

Invest Ophthalmol Vis Sci. 2006 Sep;47(9):3919-26.

PMID:
16936105
8.

Linkage of late-onset Fuchs corneal dystrophy to a novel locus at 13pTel-13q12.13.

Sundin OH, Jun AS, Broman KW, Liu SH, Sheehan SE, Vito EC, Stark WJ, Gottsch JD.

Invest Ophthalmol Vis Sci. 2006 Jan;47(1):140-5.

PMID:
16384955
9.

Analysis and documentation of progression of Fuchs corneal dystrophy with retroillumination photography.

Gottsch JD, Sundin OH, Rencs EV, Emmert DG, Stark WJ, Cheng CJ, Schmidt GW.

Cornea. 2006 May;25(4):485-9.

PMID:
16670493
10.

Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p.

Riazuddin SA, Zaghloul NA, Al-Saif A, Davey L, Diplas BH, Meadows DN, Eghrari AO, Minear MA, Li YJ, Klintworth GK, Afshari N, Gregory SG, Gottsch JD, Katsanis N.

Am J Hum Genet. 2010 Jan;86(1):45-53. doi: 10.1016/j.ajhg.2009.12.001. Epub 2009 Dec 31.

11.

Mutations in LOXHD1, a recessive-deafness locus, cause dominant late-onset Fuchs corneal dystrophy.

Riazuddin SA, Parker DS, McGlumphy EJ, Oh EC, Iliff BW, Schmedt T, Jurkunas U, Schleif R, Katsanis N, Gottsch JD.

Am J Hum Genet. 2012 Mar 9;90(3):533-9. doi: 10.1016/j.ajhg.2012.01.013. Epub 2012 Feb 16.

12.

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.

13.

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.

14.

Retroillumination Photography Analysis Enhances Clinical Definition of Severe Fuchs Corneal Dystrophy.

Eghrari AO, Garrett BS, Mumtaz AA, Edalati AE, Meadows DN, McGlumphy EJ, Iliff BW, Gottsch JD.

Cornea. 2015 Dec;34(12):1623-6. doi: 10.1097/ICO.0000000000000656.

15.

Inheritance of a novel COL8A2 mutation defines a distinct early-onset subtype of fuchs corneal dystrophy.

Gottsch JD, Sundin OH, Liu SH, Jun AS, Broman KW, Stark WJ, Vito EC, Narang AK, Thompson JM, Magovern M.

Invest Ophthalmol Vis Sci. 2005 Jun;46(6):1934-9.

PMID:
15914606
16.

Automated Retroillumination Photography Analysis for Objective Assessment of Fuchs Corneal Dystrophy.

Eghrari AO, Mumtaz AA, Garrett B, Rezaei M, Akhavan MS, Riazuddin SA, Gottsch JD.

Cornea. 2017 Jan;36(1):44-47.

PMID:
27811565
17.

A novel PITX2 mutation and a polymorphism in a 5-generation family with Axenfeld-Rieger anomaly and coexisting Fuchs' endothelial dystrophy.

Kniestedt C, Taralczak M, Thiel MA, Stuermer J, Baumer A, Gloor BP.

Ophthalmology. 2006 Oct;113(10):1791.e1-8. Epub 2006 Jul 31.

PMID:
16876867
18.

Genetic screen of African Americans with Fuchs endothelial corneal dystrophy.

Minear MA, Li YJ, Rimmler J, Balajonda E, Watson S, Allingham RR, Hauser MA, Klintworth GK, Afshari NA, Gregory SG.

Mol Vis. 2013 Dec 12;19:2508-16. eCollection 2013.

19.

Missense mutations in the sodium borate cotransporter SLC4A11 cause late-onset Fuchs corneal dystrophy.

Riazuddin SA, Vithana EN, Seet LF, Liu Y, Al-Saif A, Koh LW, Heng YM, Aung T, Meadows DN, Eghrari AO, Gottsch JD, Katsanis N.

Hum Mutat. 2010 Nov;31(11):1261-8. doi: 10.1002/humu.21356. Epub 2010 Oct 14.

20.

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.

Supplemental Content

Support Center