Yao W - Search Results

1

Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2.

Li A, Jiao X, Munier FL, Schorderet DF, Yao W, Iwata F, Hayakawa M, Kanai A, Shy Chen M, Alan Lewis R, Heckenlively J, Weleber RG, Traboulsi EI, Zhang Q, Xiao X, Kaiser-Kupfer M, Sergeev YV, Hejtmancik JF. Li A, et al. Among authors: yao w. Am J Hum Genet. 2004 May;74(5):817-26. doi: 10.1086/383228. Epub 2004 Mar 23. Am J Hum Genet. 2004. PMID: 15042513 Free PMC article.

2

A new locus for autosomal recessive nuclear cataract mapped to chromosome 19q13 in a Pakistani family.

Riazuddin SA, Yasmeen A, Zhang Q, Yao W, Sabar MF, Ahmed Z, Riazuddin S, Hejtmancik JF. Riazuddin SA, et al. Among authors: yao w. Invest Ophthalmol Vis Sci. 2005 Feb;46(2):623-6. doi: 10.1167/iovs.04-0955. Invest Ophthalmol Vis Sci. 2005. PMID: 15671291

3

Mutations in betaB3-crystallin associated with autosomal recessive cataract in two Pakistani families.

Riazuddin SA, Yasmeen A, Yao W, Sergeev YV, Zhang Q, Zulfiqar F, Riaz A, Riazuddin S, Hejtmancik JF. Riazuddin SA, et al. Among authors: yao w. Invest Ophthalmol Vis Sci. 2005 Jun;46(6):2100-6. doi: 10.1167/iovs.04-1481. Invest Ophthalmol Vis Sci. 2005. PMID: 15914629

4

Mutations in the gene encoding the alpha-subunit of rod phosphodiesterase in consanguineous Pakistani families.

Riazuddin SA, Zulfiqar F, Zhang Q, Yao W, Li S, Jiao X, Shahzadi A, Amer M, Iqbal M, Hussnain T, Sieving PA, Riazuddin S, Hejtmancik JF. Riazuddin SA, et al. Among authors: yao w. Mol Vis. 2006 Oct 26;12:1283-91. Mol Vis. 2006. PMID: 17110911 Free article.

5

Crystallin gene mutations in Indian families with inherited pediatric cataract.

Devi RR, Yao W, Vijayalakshmi P, Sergeev YV, Sundaresan P, Hejtmancik JF. Devi RR, et al. Among authors: yao w. Mol Vis. 2008 Jun 16;14:1157-70. Mol Vis. 2008. PMID: 18587492 Free PMC article.

6

Evaluation of the association between OPA1 polymorphisms and primary open-angle glaucoma in Barbados families.

Yao W, Jiao X, Hejtmancik JF, Leske MC, Hennis A, Nemesure B; Barbados Family Study Group. Yao W, et al. Mol Vis. 2006 Jun 12;12:649-54. Mol Vis. 2006. PMID: 16785854 Free article.

7

Overexpression of human γC-crystallin 5 bp duplication disrupts lens morphology in transgenic mice.

Ma Z, Yao W, Theendakara V, Chan CC, Wawrousek E, Hejtmancik JF. Ma Z, et al. Among authors: yao w. Invest Ophthalmol Vis Sci. 2011 Jul 23;52(8):5369-75. doi: 10.1167/iovs.11-7168. Invest Ophthalmol Vis Sci. 2011. PMID: 21436266 Free PMC article.

8

Human βA3/A1-crystallin splicing mutation causes cataracts by activating the unfolded protein response and inducing apoptosis in differentiating lens fiber cells.

Ma Z, Yao W, Chan CC, Kannabiran C, Wawrousek E, Hejtmancik JF. Ma Z, et al. Among authors: yao w. Biochim Biophys Acta. 2016 Jun;1862(6):1214-27. doi: 10.1016/j.bbadis.2016.02.003. Epub 2016 Feb 4. Biochim Biophys Acta. 2016. PMID: 26851658 Free PMC article.

9

Genetic heterogeneity in microcornea-cataract: five novel mutations in CRYAA, CRYGD, and GJA8.

Hansen L, Yao W, Eiberg H, Kjaer KW, Baggesen K, Hejtmancik JF, Rosenberg T. Hansen L, et al. Among authors: yao w. Invest Ophthalmol Vis Sci. 2007 Sep;48(9):3937-44. doi: 10.1167/iovs.07-0013. Invest Ophthalmol Vis Sci. 2007. PMID: 17724170

10

The congenital "ant-egg" cataract phenotype is caused by a missense mutation in connexin46.

Hansen L, Yao W, Eiberg H, Funding M, Riise R, Kjaer KW, Hejtmancik JF, Rosenberg T. Hansen L, et al. Among authors: yao w. Mol Vis. 2006 Sep 1;12:1033-9. Mol Vis. 2006. PMID: 16971895 Free article.

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