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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.

Mol Vis. 2012;18:937-44. Epub 2012 Apr 12.


New ZNF644 mutations identified in patients with high myopia.

Xiang X, Wang T, Tong P, Li Y, Guo H, Wan A, Xia L, Liu Y, Li Y, Tian Q, Shen L, Cai X, Tian L, Jin X, Xia K, Hu Z.

Mol Vis. 2014 Jun 30;20:939-46. eCollection 2014.


Detection of mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 families with early-onset high myopia by exome sequencing.

Jiang D, Li J, Xiao X, Li S, Jia X, Sun W, Guo X, Zhang Q.

Invest Ophthalmol Vis Sci. 2014 Dec 18;56(1):339-45. doi: 10.1167/iovs.14-14850.


Exome sequencing identifies ZNF644 mutations in high myopia.

Shi Y, Li Y, Zhang D, Zhang H, Li Y, Lu F, Liu X, He F, Gong B, Cai L, Li R, Liao S, Ma S, Lin H, Cheng J, Zheng H, Shan Y, Chen B, Hu J, Jin X, Zhao P, Chen Y, Zhang Y, Lin Y, Li X, Fan Y, Yang H, Wang J, Yang Z.

PLoS Genet. 2011 Jun;7(6):e1002084. doi: 10.1371/journal.pgen.1002084. Epub 2011 Jun 9.


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.

Mol Vis. 2008 Mar 4;14:387-93.


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.

Am J Hum Genet. 2013 May 2;92(5):820-6. doi: 10.1016/j.ajhg.2013.04.005.


[Association of ZNF644, GRM6 and CTNND2 genes polymorphisms with high myopia].

Wang H, Yang M, Su S, Kang L, Zhu R, Shi J, Guan H.

Zhonghua Yi Xue Za Zhi. 2014 May 6;94(17):1289-93. Chinese.


Assessment of exonic single nucleotide polymorphisms in the adenosine A2A receptor gene to high myopia susceptibility in Chinese subjects.

Chen X, Xue A, Chen W, Ding Y, Yan D, Peng J, Zeng C, Qu J, Zhou X.

Mol Vis. 2011;17:486-91. Epub 2011 Feb 16.


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.

Invest Ophthalmol Vis Sci. 2010 Sep;51(9):4476-9. doi: 10.1167/iovs.09-4912. Epub 2010 Apr 30.


Myocilin polymorphisms and high myopia in subjects of European origin.

Zayats T, Yanovitch T, Creer RC, McMahon G, Li YJ, Young TL, Guggenheim JA.

Mol Vis. 2009;15:213-22. Epub 2009 Jan 26.


IGF-1 gene polymorphisms in Polish families with high-grade myopia.

Rydzanicz M, Nowak DM, Karolak JA, Frajdenberg A, Podfigurna-Musielak M, Mrugacz M, Gajecka M.

Mol Vis. 2011;17:2428-39. Epub 2011 Sep 21.


Linkage and association of myocilin (MYOC) polymorphisms with high myopia in a Chinese population.

Tang WC, Yip SP, Lo KK, Ng PW, Choi PS, Lee SY, Yap MK.

Mol Vis. 2007 Apr 4;13:534-44.


Association analysis of retinoic acid receptor beta (RARbeta) gene with high myopia in Chinese subjects.

Ding Y, Chen X, Yan D, Xue A, Lu F, Qu J, Zhou X.

Mol Vis. 2010 May 13;16:855-61.


Sequence variants in the transforming growth beta-induced factor (TGIF) gene are not associated with high myopia.

Scavello GS, Paluru PC, Ganter WR, Young TL.

Invest Ophthalmol Vis Sci. 2004 Jul;45(7):2091-7.


Hepatocyte growth factor and myopia: genetic association analyses in a Caucasian population.

Yanovitch T, Li YJ, Metlapally R, Abbott D, Viet KN, Young TL.

Mol Vis. 2009 May 20;15:1028-35.


Norrie disease gene sequence variants in an ethnically diverse population with retinopathy of prematurity.

Hutcheson KA, Paluru PC, Bernstein SL, Koh J, Rappaport EF, Leach RA, Young TL.

Mol Vis. 2005 Jul 14;11:501-8.


TGFbeta-induced factor: a candidate gene for high myopia.

Lam DS, Lee WS, Leung YF, Tam PO, Fan DS, Fan BJ, Pang CP.

Invest Ophthalmol Vis Sci. 2003 Mar;44(3):1012-5.


Variation in optineurin (OPTN) allele frequencies between and within populations.

Ayala-Lugo RM, Pawar H, Reed DM, Lichter PR, Moroi SE, Page M, Eadie J, Azocar V, Maul E, Ntim-Amponsah C, Bromley W, Obeng-Nyarkoh E, Johnson AT, Kijek TG, Downs CA, Johnson JM, Perez-Grossmann RA, Guevara-Fujita ML, Fujita R, Wallace MR, Richards JE.

Mol Vis. 2007 Feb 2;13:151-63.

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