Chen L - Search Results

1

A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population.

Shi Y, Gong B, Chen L, Zuo X, Liu X, Tam PO, Zhou X, Zhao P, Lu F, Qu J, Sun L, Zhao F, Chen H, Zhang Y, Zhang D, Lin Y, Lin H, Ma S, Cheng J, Yang J, Huang L, Zhang M, Zhang X, Pang CP, Yang Z. Shi Y, et al. Among authors: chen l, chen h. Hum Mol Genet. 2013 Jun 1;22(11):2325-33. doi: 10.1093/hmg/ddt066. Epub 2013 Feb 12. Hum Mol Genet. 2013. PMID: 23406873

2

[Blockade of (+/-) 12-chloroscoulerine on feed-back regulation of dopamine D2 autoreceptors].

Chen LJ, Zhang XX, Guo X. Chen LJ, et al. Zhongguo Yao Li Xue Bao. 1996 Sep;17(5):477-80. Zhongguo Yao Li Xue Bao. 1996. PMID: 9863180 Free article. Chinese.

3

Association of complement factor H polymorphisms with exudative age-related macular degeneration.

Chen LJ, Liu DT, Tam PO, Chan WM, Liu K, Chong KK, Lam DS, Pang CP. Chen LJ, et al. Mol Vis. 2006 Dec 5;12:1536-42. Mol Vis. 2006. PMID: 17167412 Free article.

4

HTRA1 variants in exudative age-related macular degeneration and interactions with smoking and CFH.

Tam PO, Ng TK, Liu DT, Chan WM, Chiang SW, Chen LJ, DeWan A, Hoh J, Lam DS, Pang CP. Tam PO, et al. Among authors: chen lj. Invest Ophthalmol Vis Sci. 2008 Jun;49(6):2357-65. doi: 10.1167/iovs.07-1520. Epub 2008 Mar 3. Invest Ophthalmol Vis Sci. 2008. PMID: 18316707 Free PMC article.

5

Multiple gene polymorphisms in the complement factor h gene are associated with exudative age-related macular degeneration in chinese.

Ng TK, Chen LJ, Liu DT, Tam PO, Chan WM, Liu K, Hu YJ, Chong KK, Lau CS, Chiang SW, Lam DS, Pang CP. Ng TK, et al. Among authors: chen lj. Invest Ophthalmol Vis Sci. 2008 Aug;49(8):3312-7. doi: 10.1167/iovs.07-1517. Epub 2008 Apr 17. Invest Ophthalmol Vis Sci. 2008. PMID: 18421087

6

Evaluation of LOXL1 polymorphisms in primary open-angle glaucoma in southern and northern Chinese.

Gong WF, Chiang SW, Chen LJ, Tam PO, Jia LY, Leung DY, Geng YQ, Tham CC, Lam DS, Ritch R, Wang N, Pang CP. Gong WF, et al. Among authors: chen lj. Mol Vis. 2008;14:2381-9. Epub 2008 Dec 19. Mol Vis. 2008. PMID: 19098994 Free PMC article.

7

Autosomal-dominant retinitis pigmentosa caused by a mutation in SNRNP200, a gene required for unwinding of U4/U6 snRNAs.

Zhao C, Bellur DL, Lu S, Zhao F, Grassi MA, Bowne SJ, Sullivan LS, Daiger SP, Chen LJ, Pang CP, Zhao K, Staley JP, Larsson C. Zhao C, et al. Among authors: chen lj. Am J Hum Genet. 2009 Nov;85(5):617-27. doi: 10.1016/j.ajhg.2009.09.020. Epub 2009 Oct 29. Am J Hum Genet. 2009. PMID: 19878916 Free PMC article.

8

Association of NR2E3 but not NRL mutations with retinitis pigmentosa in the Chinese population.

Yang Y, Zhang X, Chen LJ, Chiang SW, Tam PO, Lai TY, Chan CK, Wang N, Lam DS, Pang CP. Yang Y, et al. Invest Ophthalmol Vis Sci. 2010 Apr;51(4):2229-35. doi: 10.1167/iovs.09-4299. Epub 2009 Nov 20. Invest Ophthalmol Vis Sci. 2010. PMID: 19933183

9

Compound heterozygosity of two novel truncation mutations in RP1 causing autosomal recessive retinitis pigmentosa.

Chen LJ, Lai TY, Tam PO, Chiang SW, Zhang X, Lam S, Lai RY, Lam DS, Pang CP. Chen LJ, et al. Invest Ophthalmol Vis Sci. 2010 Apr;51(4):2236-42. doi: 10.1167/iovs.09-4437. Epub 2009 Nov 20. Invest Ophthalmol Vis Sci. 2010. PMID: 19933189

10

Ethnicity-based subgroup meta-analysis of the association of LOXL1 polymorphisms with glaucoma.

Chen H, Chen LJ, Zhang M, Gong W, Tam PO, Lam DS, Pang CP. Chen H, et al. Mol Vis. 2010 Feb 6;16:167-77. Mol Vis. 2010. PMID: 20142848 Free PMC article.

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