Tran-Viet KN - Search Results

1

Common MFRP sequence variants are not associated with moderate to high hyperopia, isolated microphthalmia, and high myopia.

Metlapally R, Li YJ, Tran-Viet KN, Bulusu A, White TR, Ellis J, Kao D, Young TL. Metlapally R, et al. Mol Vis. 2008 Mar 4;14:387-93. Mol Vis. 2008. PMID: 18334955 Free PMC article.

2

Pediatric cataract, myopic astigmatism, familial exudative vitreoretinopathy and primary open-angle glaucoma co-segregating in a family.

Mackey DA, Hewitt AW, Ruddle JB, Vote B, Buttery RG, Toomes C, Metlapally R, Li YJ, Tran-Viet KN, Malecaze F, Calvas P, Rosenberg T, Guggenheim JA, Young TL. Mackey DA, et al. Among authors: tran viet kn. Mol Vis. 2011;17:2118-28. Epub 2011 Aug 10. Mol Vis. 2011. PMID: 21850187 Free PMC article.

3

Mutations in SCO2 are associated with autosomal-dominant high-grade myopia.

Tran-Viet KN, Powell C, Barathi VA, Klemm T, Maurer-Stroh S, Limviphuvadh V, Soler V, Ho C, Yanovitch T, Schneider G, Li YJ, Nading E, Metlapally R, Saw SM, Goh L, Rozen S, Young TL. Tran-Viet KN, et al. Am J Hum Genet. 2013 May 2;92(5):820-6. doi: 10.1016/j.ajhg.2013.04.005. Am J Hum Genet. 2013. PMID: 23643385 Free PMC article.

4

Identification of STRA6 and SKI sequence variants in patients with anophthalmia/microphthalmia.

White T, Lu T, Metlapally R, Katowitz J, Kherani F, Wang TY, Tran-Viet KN, Young TL. White T, et al. Mol Vis. 2008;14:2458-65. Epub 2008 Dec 26. Mol Vis. 2008. PMID: 19112531 Free PMC article.

5

Genetic association of insulin-like growth factor-1 polymorphisms with high-grade myopia in an international family cohort.

Metlapally R, Ki CS, Li YJ, Tran-Viet KN, Abbott D, Malecaze F, Calvas P, Mackey DA, Rosenberg T, Paget S, Guggenheim JA, Young TL. Metlapally R, et al. Invest Ophthalmol Vis Sci. 2010 Sep;51(9):4476-9. doi: 10.1167/iovs.09-4912. Epub 2010 Apr 30. Invest Ophthalmol Vis Sci. 2010. PMID: 20435602 Free PMC article.

6

Study of a US cohort supports the role of ZNF644 and high-grade myopia susceptibility.

Tran-Viet KN, St Germain E, Soler V, Powell C, Lim SH, Klemm T, Saw SM, Young TL. Tran-Viet KN, et al. Mol Vis. 2012;18:937-44. Epub 2012 Apr 12. Mol Vis. 2012. PMID: 22539872 Free PMC article.

7

Association mapping of the high-grade myopia MYP3 locus reveals novel candidates UHRF1BP1L, PTPRR, and PPFIA2.

Hawthorne F, Feng S, Metlapally R, Li YJ, Tran-Viet KN, Guggenheim JA, Malecaze F, Calvas P, Rosenberg T, Mackey DA, Venturini C, Hysi PG, Hammond CJ, Young TL. Hawthorne F, et al. Among authors: tran viet kn. Invest Ophthalmol Vis Sci. 2013 Mar 21;54(3):2076-86. doi: 10.1167/iovs.12-11102. Invest Ophthalmol Vis Sci. 2013. PMID: 23422819 Free PMC article.

8

Mutation in collagen II alpha 1 isoforms delineates Stickler and Wagner syndrome phenotypes.

Tran-Viet KN, Soler V, Quiette V, Powell C, Yanovitch T, Metlapally R, Luo X, Katsanis N, Nading E, Young TL. Tran-Viet KN, et al. Mol Vis. 2013 Apr 5;19:759-66. Print 2013. Mol Vis. 2013. PMID: 23592912 Free PMC article.

9

COL1A1 and COL2A1 genes and myopia susceptibility: evidence of association and suggestive linkage to the COL2A1 locus.

Metlapally R, Li YJ, Tran-Viet KN, Abbott D, Czaja GR, Malecaze F, Calvas P, Mackey D, Rosenberg T, Paget S, Zayats T, Owen MJ, Guggenheim JA, Young TL. Metlapally R, et al. Invest Ophthalmol Vis Sci. 2009 Sep;50(9):4080-6. doi: 10.1167/iovs.08-3346. Epub 2009 Apr 22. Invest Ophthalmol Vis Sci. 2009. PMID: 19387081 Free PMC article.

10

Mutational hot spot potential of a novel base pair mutation of the CSPG2 gene in a family with Wagner syndrome.

Ronan SM, Tran-Viet KN, Burner EL, Metlapally R, Toth CA, Young TL. Ronan SM, et al. Arch Ophthalmol. 2009 Nov;127(11):1511-9. doi: 10.1001/archophthalmol.2009.273. Arch Ophthalmol. 2009. PMID: 19901218 Free PMC article.

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