Lam DSC - Search Results

1

Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population.

Shi Y, Qu J, Zhang D, Zhao P, Zhang Q, Tam POS, Sun L, Zuo X, Zhou X, Xiao X, Hu J, Li Y, Cai L, Liu X, Lu F, Liao S, Chen B, He F, Gong B, Lin H, Ma S, Cheng J, Zhang J, Chen Y, Zhao F, Yang X, Chen Y, Yang C, Lam DSC, Li X, Shi F, Wu Z, Lin Y, Yang J, Li S, Ren Y, Xue A, Fan Y, Li D, Pang CP, Zhang X, Yang Z. Shi Y, et al. Among authors: lam dsc. Am J Hum Genet. 2011 Jun 10;88(6):805-813. doi: 10.1016/j.ajhg.2011.04.022. Epub 2011 Jun 6. Am J Hum Genet. 2011. PMID: 21640322 Free PMC article.

2

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

Lam DS, Lee WS, Leung YF, Tam PO, Fan DS, Fan BJ, Pang CP. Lam DS, et al. Invest Ophthalmol Vis Sci. 2003 Mar;44(3):1012-5. doi: 10.1167/iovs.02-0058. Invest Ophthalmol Vis Sci. 2003. PMID: 12601022

3

Differential occurrence of mutations causative of eye diseases in the Chinese population.

Pang CP, Lam DS. Pang CP, et al. Hum Mutat. 2002 Mar;19(3):189-208. doi: 10.1002/humu.10053. Hum Mutat. 2002. PMID: 11857735 Review.

4

AC and AG dinucleotide repeats in the PAX6 P1 promoter are associated with high myopia.

Ng TK, Lam CY, Lam DS, Chiang SW, Tam PO, Wang DY, Fan BJ, Yam GH, Fan DS, Pang CP. Ng TK, et al. Mol Vis. 2009 Nov 5;15:2239-48. Mol Vis. 2009. PMID: 19907666 Free PMC article.

5

TIGR/MYOC proximal promoter GT-repeat polymorphism is not associated with myopia.

Leung YF, Tam PO, Baum L, Lam DS, Pang CC. Leung YF, et al. Hum Mutat. 2000 Dec;16(6):533. doi: 10.1002/1098-1004(200012)16:6<533::AID-HUMU21>3.0.CO;2-8. Hum Mutat. 2000. PMID: 11102993 No abstract available.

6

Gene mapping for primary open angle glaucoma.

Fan BJ, Wang DY, Lam DS, Pang CP. Fan BJ, et al. Clin Biochem. 2006 Mar;39(3):249-58. doi: 10.1016/j.clinbiochem.2005.11.001. Epub 2005 Dec 5. Clin Biochem. 2006. PMID: 16332362 Review.

7

Molecular diagnostics of genetic eye diseases.

Fan BJ, Tam PO, Choy KW, Wang DY, Lam DS, Pang CP. Fan BJ, et al. Clin Biochem. 2006 Mar;39(3):231-9. doi: 10.1016/j.clinbiochem.2005.11.010. Epub 2006 Jan 10. Clin Biochem. 2006. PMID: 16412407 Review.

8

A novel deletion variant of gammaD-crystallin responsible for congenital nuclear cataract.

Zhang LY, Yam GH, Fan DS, Tam PO, Lam DS, Pang CP. Zhang LY, et al. Mol Vis. 2007 Nov 7;13:2096-104. Mol Vis. 2007. PMID: 18079686

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

10

Absence of trabecular meshwork-inducible stretch response (TISR)/oculomedin gene and proximal promoter mutation in primary open angle glaucoma patients.

Leung YF, Baum L, Lam DS, Fan DS, Chua JK, Pang CP. Leung YF, et al. Hum Genet. 2000 Oct;107(4):404-5. doi: 10.1007/s004390000385. Hum Genet. 2000. PMID: 11129344

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