Riazuddin SA - Search Results

1

Eghrari AO, Riazuddin SA, Gottsch JD. Eghrari AO, et al. Among authors: riazuddin sa. Prog Mol Biol Transl Sci. 2015;134:79-97. doi: 10.1016/bs.pmbts.2015.04.005. Epub 2015 Jul 15. Prog Mol Biol Transl Sci. 2015. PMID: 26310151 Review.

2

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. Riazuddin SA, et al. Invest Ophthalmol Vis Sci. 2009 Dec;50(12):5667-71. doi: 10.1167/iovs.09-3764. Epub 2009 Jul 15. Invest Ophthalmol Vis Sci. 2009. PMID: 19608540

3

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. Meadows DN, et al. Among authors: riazuddin sa. Invest Ophthalmol Vis Sci. 2009 Dec;50(12):5662-6. doi: 10.1167/iovs.09-3568. Epub 2009 Jul 15. Invest Ophthalmol Vis Sci. 2009. PMID: 19608546

4

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. Riazuddin SA, et al. Am J Hum Genet. 2010 Jan;86(1):45-53. doi: 10.1016/j.ajhg.2009.12.001. Epub 2009 Dec 31. Am J Hum Genet. 2010. PMID: 20036349 Free PMC article.

5

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. McGlumphy EJ, et al. Among authors: riazuddin sa. Invest Ophthalmol Vis Sci. 2010 Dec;51(12):6298-302. doi: 10.1167/iovs.10-5187. Epub 2010 Sep 1. Invest Ophthalmol Vis Sci. 2010. PMID: 20811064 Free PMC article.

6

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. Riazuddin SA, et al. Hum Mutat. 2010 Nov;31(11):1261-8. doi: 10.1002/humu.21356. Epub 2010 Oct 14. Hum Mutat. 2010. PMID: 20848555 Free PMC article.

7

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. Riazuddin SA, et al. Invest Ophthalmol Vis Sci. 2011 Apr 27;52(5):2825-9. doi: 10.1167/iovs.10-6497. Print 2011 Apr. Invest Ophthalmol Vis Sci. 2011. PMID: 21245398 Free PMC article.

8

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. Li YJ, et al. Among authors: riazuddin sa. PLoS One. 2011 Apr 20;6(4):e18044. doi: 10.1371/journal.pone.0018044. PLoS One. 2011. PMID: 21533127 Free PMC article.

9

A single-base substitution in the seed region of miR-184 causes EDICT syndrome.

Iliff BW, Riazuddin SA, Gottsch JD. Iliff BW, et al. Among authors: riazuddin sa. Invest Ophthalmol Vis Sci. 2012 Jan 25;53(1):348-53. doi: 10.1167/iovs.11-8783. Invest Ophthalmol Vis Sci. 2012. PMID: 22131394 Free PMC article.

10

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. Eghrari AO, et al. Among authors: riazuddin sa. Am J Ophthalmol. 2012 Jun;153(6):1067-72. doi: 10.1016/j.ajo.2011.11.033. Epub 2012 Feb 8. Am J Ophthalmol. 2012. PMID: 22321803 Free PMC article.

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