| 中国学者近期发表的论文 |
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| 1. | Novel susceptibility genes associated with diabetic cataract in a Taiwanese population.
Author: Lin HJ, Huang YC, Lin JM, Liao WL, Wu JY, Chen CH, Chou YC, Chen LA, Lin CJ, Tsai FJ.
Journal: Ophthalmic Genet. 2013 Mar-Jun;34(1-2):35-42. doi: 10.3109/13816810.2012.736590. Epub 2012 Nov 9. | | 2. | Ophthalmic findings in a family with early-onset isolated ectopia lentis and the p.Arg62Cys mutation of the fibrillin-1 gene (FBN1).
Author: Zhao JH, Jin TB, Liu QB, Chen C, Hu HT.
Journal: Ophthalmic Genet. 2013 Mar-Jun;34(1-2):21-6. doi: 10.3109/13816810.2012.718029. Epub 2012 Sep 6. | | 3. | Ten SNPs of PAX6, Lumican, and MYOC genes are not associated with high myopia in Han Chinese.
Author: Dai L, Li Y, Du CY, Gong LM, Han CC, Li XG, Fan P, Fu SB.
Journal: Ophthalmic Genet. 2012 Sep;33(3):171-8. doi: 10.3109/13816810.2012.675397. Epub 2012 Jul 18. | | 4. | Nitric oxide synthase 3 (NOS3) 4b/a, T-786C and G894T polymorphisms in association with diabetic retinopathy susceptibility: a meta-analysis.
Author: Zhao S, Li T, Zheng B, Zheng Z.
Journal: Ophthalmic Genet. 2012 Dec;33(4):200-7. doi: 10.3109/13816810.2012.675398. Epub 2012 Apr 17. | | 5. | Identification of the p. R116H mutation in a Chinese family with novel variable cataract phenotype: evidence for a mutational hot spot in αA-crystallin gene.
Author: Wang B, Wang KJ, Zhu SQ, Wang J, Ma X.
Journal: Ophthalmic Genet. 2012 Sep;33(3):134-8. doi: 10.3109/13816810.2011.642451. Epub 2012 Jan 4. | | 6. | An rs9621532 variant near the TIMP3 gene is not associated with neovascular age-related macular degeneration and polypoidal choroidal vasculopathy in a Chinese Han population.
Author: Zeng R, Wen F, Zhang X, Zuo C, Li M, Chen H, Wu K.
Journal: Ophthalmic Genet. 2012 Sep;33(3):139-43. doi: 10.3109/13816810.2011.643440. Epub 2011 Dec 15. | | 7. | Thirty-two years follow-up of X-linked juvenile retinoschisis in a Chinese patient with RS1 mutation.
Author: Xu F, Sui R, Dong F.
Journal: Ophthalmic Genet. 2012 Jun;33(2):77-82. doi: 10.3109/13816810.2011.628359. Epub 2011 Dec 15. | | 8. | Vitreous amyloidosis in two large mainland Chinese kindreds resulting from transthyretin variant Lys35Thr and Leu55Arg.
Author: Long D, Zeng J, Wu LQ, Tang LS, Wang HL, Wang H.
Journal: Ophthalmic Genet. 2012 Mar;33(1):28-33. doi: 10.3109/13816810.2011.599356. Epub 2011 Aug 15. | | 9. | Matrix metalloproteinase-1 rs1799750 polymorphism and glaucoma: A meta-analysis.
Author: He M, Wang W, Han X, Huang W.
Journal: Ophthalmic Genet. 2016 Jul 18:1-6. [Epub ahead of print] | | 10. | Mutation screening of the LRIT3, CABP4, and GPR179 genes in Chinese patients with Schubert-Bornschein congenital stationary night blindness.
Author: Dan H, Song X, Li J, Xing Y, Li T.
Journal: Ophthalmic Genet. 2016 Jul 18:1-5. [Epub ahead of print] |
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