Lu F - Search Results

1

[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: lu f. 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.

2

[Linkage analysis of one family with autosomal dominant high myopia].

Chang JX, Zhang DD, Lin Y, Liu B, Lu F, Tang X, Yang Y, Chen B, Zhang CJ, Yang ZL. Chang JX, et al. Among authors: lu f. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Aug;25(4):424-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 18683142 Chinese.

3

[Mutation analysis of the PAX6 gene in a family with congenital aniridia and cataract].

Lin Y, Li J, Yang Y, Yang JY, Zhang B, Tang X, Liu XQ, Lu F, Yang ZL. Lin Y, et al. Among authors: lu f. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Oct;26(5):542-5. doi: 10.3760/cma.j.issn.1003-9406.2009.05.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19806578 Chinese.

4

A novel PRPF31 mutation in a large Chinese family with autosomal dominant retinitis pigmentosa and macular degeneration.

Lu F, Huang L, Lei C, Sha G, Zheng H, Liu X, Yang J, Shi Y, Lin Y, Gong B, Zhu X, Ma S, Qiao L, Lin H, Cheng J, Yang Z. Lu F, et al. PLoS One. 2013 Nov 11;8(11):e78274. doi: 10.1371/journal.pone.0078274. eCollection 2013. PLoS One. 2013. PMID: 24244300 Free PMC article. Clinical Trial.

5

A novel mutation in BBS7 gene causes Bardet-Biedl syndrome in a Chinese family.

Yang Z, Yang Y, Zhao P, Chen K, Chen B, Lin Y, Guo F, Chen Y, Liu X, Lu F, Shi Y, Zhang D, Liao S, Xia Q. Yang Z, et al. Among authors: lu f. Mol Vis. 2008;14:2304-8. Epub 2008 Dec 12. Mol Vis. 2008. PMID: 19093007 Free PMC article.

6

[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: lu f. 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.

7

Whole-exome Sequencing Analysis Identifies Mutations in the EYS Gene in Retinitis Pigmentosa in the Indian Population.

Di Y, Huang L, Sundaresan P, Li S, Kim R, Ballav Saikia B, Qu C, Zhu X, Zhou Y, Jiang Z, Zhang L, Lin Y, Zhang D, Li Y, Zhang H, Yin Y, Lu F, Zhu X, Yang Z. Di Y, et al. Among authors: lu f. Sci Rep. 2016 Jan 20;6:19432. doi: 10.1038/srep19432. Sci Rep. 2016. PMID: 26787102 Free PMC article.

8

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: lu f. BMC Med Genet. 2010 Jun 15;11:97. doi: 10.1186/1471-2350-11-97. BMC Med Genet. 2010. PMID: 20550665 Free PMC article.

9

[Association study between age-related macular degeneration and R1210C mutation of CFH gene in Chinese population].

Shen SK, Liu XQ, Lu F, Yang ZL, Shi Y. Shen SK, et al. Among authors: lu f. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Oct;29(5):570-2. doi: 10.3760/cma.j.issn.1003-9406.2012.05.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 23042396 Chinese.

10

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: lu f. Muscle Nerve. 2010 Nov;42(5):715-21. doi: 10.1002/mus.21756. Muscle Nerve. 2010. PMID: 20730878

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