Ma S - Search Results

1

[Linkage analysis of a family with familial hypertriglyceridemia].

Tang X, Lin Y, Liu B, Ma S, Yang Y, Yang ZL. Tang X, et al. Among authors: ma s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Oct;26(5):499-503. doi: 10.3760/cma.j.issn.1003-9406.2009.05.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19806567 Chinese.

2

[Disease gene screening of known loci in a Chinese family with autosomal dominant retinitis pigmentosa].

Liu W, Lu F, Qia LF, Sha ZQ, Liu XO, Ma S, Tang X, Chang JX, Yang ZL, Ye B. Liu W, et al. Among authors: ma s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Feb;26(1):70-3. doi: 10.3760/cma.j.issn.1003-9406.2009.01.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19199256 Chinese.

3

An association study of SERPING1 gene and age-related macular degeneration in a Han Chinese population.

Lu F, Zhao P, Fan Y, Tang S, Hu J, Liu X, Yang X, Chen Y, Li T, Lei C, Yang J, Lin Y, Ma S, Li C, Shi Y, Yang Z. Lu F, et al. Among authors: ma s. Mol Vis. 2010 Jan 10;16:1-6. Mol Vis. 2010. PMID: 20062564 Free PMC article.

4

Association study of complement factor H, C2, CFB, and C3 and age-related macular degeneration in a Han Chinese population.

Liu X, Zhao P, Tang S, Lu F, Hu J, Lei C, Yang X, Lin Y, Ma S, Yang J, Zhang D, Shi Y, Li T, Chen Y, Fan Y, Yang Z. Liu X, et al. Among authors: ma s. Retina. 2010 Sep;30(8):1177-84. doi: 10.1097/IAE.0b013e3181cea676. Retina. 2010. PMID: 20523265

5

[Association study on single nucleotide polymorphisms in HTRA1 gene and rheumatoid arthritis].

Luo RJ, Zhang DD, Zhu J, Zhou B, Ma S, Lu F, Liu J, Long WB, Yang ZL, Zhang CJ. Luo RJ, et al. Among authors: ma s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Jun;27(3):305-9. doi: 10.3760/cma.j.issn.1003-9406.2010.0.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 20533271 Chinese.

6

Association study of genetic variants in eight genes/loci with type 2 diabetes in a Han Chinese population.

Lin Y, Li P, Cai L, Zhang B, Tang X, Zhang X, Li Y, Xian Y, Yang Y, Wang L, Lu F, Liu X, Rao S, Chen M, Ma S, Shi Y, Bao M, Wu J, Yang Y, Yang J, Yang Z. Lin Y, et al. Among authors: ma s. BMC Med Genet. 2010 Jun 15;11:97. doi: 10.1186/1471-2350-11-97. BMC Med Genet. 2010. PMID: 20550665 Free PMC article.

7

Mutation in connexin 32 causes Charcot-Marie-Tooth disease in a large Chinese family.

Guo F, Shi Y, Lin Y, Liu X, Liu B, Liu Y, Yang Y, Lu F, Ma S, Yang Z. Guo F, et al. Among authors: ma s. Muscle Nerve. 2010 Nov;42(5):715-21. doi: 10.1002/mus.21756. Muscle Nerve. 2010. PMID: 20730878

8

Single nucleotide polymorphisms at the TRAF1/C5 locus are associated with rheumatoid arthritis in a Han Chinese population.

Zhu J, Zhang D, Wu F, He F, Liu X, Wu L, Zhou B, Liu J, Lu F, Liu J, Luo R, Long W, Yang M, Ma S, Wu X, Shi Y, Wu T, Lin Y, Yang J, Yuan G, Yang Z. Zhu J, et al. Among authors: ma s. BMC Med Genet. 2011 Apr 14;12:53. doi: 10.1186/1471-2350-12-53. BMC Med Genet. 2011. PMID: 21492465 Free PMC article.

9

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: ma s. 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.

10

Exome sequencing identifies ZNF644 mutations in high myopia.

Shi Y, Li Y, Zhang D, Zhang H, Li Y, Lu F, Liu X, He F, Gong B, Cai L, Li R, Liao S, Ma S, Lin H, Cheng J, Zheng H, Shan Y, Chen B, Hu J, Jin X, Zhao P, Chen Y, Zhang Y, Lin Y, Li X, Fan Y, Yang H, Wang J, Yang Z. Shi Y, et al. Among authors: ma s. PLoS Genet. 2011 Jun;7(6):e1002084. doi: 10.1371/journal.pgen.1002084. Epub 2011 Jun 9. PLoS Genet. 2011. PMID: 21695231 Free PMC article.

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