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Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese.
Li YJ, Goh L, Khor CC, Fan Q, Yu M, Han S, Sim X, Ong RT, Wong TY, Vithana EN, Yap E, Nakanishi H, Matsuda F, Ohno-Matsui K, Yoshimura N, Seielstad M, Tai ES, Young TL, Saw SM. Li YJ, et al. Among authors: yap e. Ophthalmology. 2011 Feb;118(2):368-75. doi: 10.1016/j.ophtha.2010.06.016. Epub 2010 Nov 20. Ophthalmology. 2011. PMID: 21095009 Free PMC article.
Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia.
Khor CC, Miyake M, Chen LJ, Shi Y, Barathi VA, Qiao F, Nakata I, Yamashiro K, Zhou X, Tam PO, Cheng CY, Tai ES, Vithana EN, Aung T, Teo YY, Wong TY, Moriyama M, Ohno-Matsui K, Mochizuki M, Matsuda F; Nagahama Study Group; Yong RY, Yap EP, Yang Z, Pang CP, Saw SM, Yoshimura N. Khor CC, et al. Among authors: yap ep. Hum Mol Genet. 2013 Dec 20;22(25):5288-94. doi: 10.1093/hmg/ddt385. Epub 2013 Aug 9. Hum Mol Genet. 2013. PMID: 23933737
Myopia: gene-environment interaction.
Saw SM, Chua WH, Wu HM, Yap E, Chia KS, Stone RA. Saw SM, et al. Among authors: yap e. Ann Acad Med Singap. 2000 May;29(3):290-7. Ann Acad Med Singap. 2000. PMID: 10976381 Review.
465 results