Chen LJ - Search Results

1

Genetic Association of the PARL-ABCC5-HTR3D-HTR3C Locus With Primary Angle-Closure Glaucoma in Chinese.

Tang FY, Ma L, Tam POS, Pang CP, Tham CC, Chen LJ. Tang FY, et al. Among authors: chen lj. Invest Ophthalmol Vis Sci. 2017 Aug 1;58(10):4384–4389. doi: 10.1167/iovs.17-22304. Invest Ophthalmol Vis Sci. 2017. PMID: 28813580

2

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.

3

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.

4

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

5

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.

6

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.

7

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. Among authors: chen lj. 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

8

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

9

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. Among authors: chen lj. Mol Vis. 2010 Feb 6;16:167-77. Mol Vis. 2010. PMID: 20142848 Free PMC article.

10

Differential pattern of RP1 mutations in retinitis pigmentosa.

Zhang X, Chen LJ, Law JP, Lai TY, Chiang SW, Tam PO, Chu KY, Wang N, Zhang M, Pang CP. Zhang X, et al. Among authors: chen lj. Mol Vis. 2010 Jul 15;16:1353-60. Mol Vis. 2010. PMID: 20664799 Free PMC article.

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