Lu F - Search Results

1

Whole-exome sequencing revealed HKDC1 as a candidate gene associated with autosomal-recessive retinitis pigmentosa.

Zhang L, Sun Z, Zhao P, Huang L, Xu M, Yang Y, Chen X, Lu F, Zhang X, Wang H, Zhang S, Liu W, Jiang Z, Ma S, Chen R, Zhao C, Yang Z, Sui R, Zhu X. Zhang L, et al. Among authors: lu f. Hum Mol Genet. 2018 Dec 1;27(23):4157-4168. doi: 10.1093/hmg/ddy281. Hum Mol Genet. 2018. PMID: 30085091 Free PMC article.

2

HTRA1 variant increases risk to neovascular age-related macular degeneration in Chinese population.

Lu F, Hu J, Zhao P, Lin Y, Yang Y, Liu X, Fan Y, Chen B, Liao S, Du Q, Lei C, Cameron DJ, Zhang K, Yang Z. Lu F, et al. Vision Res. 2007 Nov;47(24):3120-3. doi: 10.1016/j.visres.2007.08.010. Epub 2007 Sep 27. Vision Res. 2007. PMID: 17904186 Free article.

3

A genome-wide scan maps a novel autosomal dominant juvenile-onset open-angle glaucoma locus to 2p15-16.

Lin Y, Liu T, Li J, Yang J, Du Q, Wang J, Yang Y, Liu X, Fan Y, Lu F, Chen Y, Pu Y, Zhang K, He X, Yang Z. Lin Y, et al. Among authors: lu f. Mol Vis. 2008 Apr 18;14:739-44. Mol Vis. 2008. PMID: 18432317 Free PMC article.

4

A novel mutation in LMX1B gene causes nail-patella syndrome in a large Chinese family.

Lin Y, Zhao J, Chen S, Zeng X, Du Q, Yang Y, Lu F, Pu Y, Yang Z. Lin Y, et al. Among authors: lu f. Bone. 2008 Sep;43(3):591-5. doi: 10.1016/j.bone.2008.04.025. Epub 2008 May 16. Bone. 2008. PMID: 18595794

5

[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.

6

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.

7

[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.

8

[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.

9

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. Mol Vis. 2010 Jan 10;16:1-6. Mol Vis. 2010. PMID: 20062564 Free PMC article.

10

Genetic and functional dissection of HTRA1 and LOC387715 in age-related macular degeneration.

Yang Z, Tong Z, Chen Y, Zeng J, Lu F, Sun X, Zhao C, Wang K, Davey L, Chen H, London N, Muramatsu D, Salasar F, Carmona R, Kasuga D, Wang X, Bedell M, Dixie M, Zhao P, Yang R, Gibbs D, Liu X, Li Y, Li C, Li Y, Campochiaro B, Constantine R, Zack DJ, Campochiaro P, Fu Y, Li DY, Katsanis N, Zhang K. Yang Z, et al. Among authors: lu f. PLoS Genet. 2010 Feb 5;6(2):e1000836. doi: 10.1371/journal.pgen.1000836. PLoS Genet. 2010. PMID: 20140183 Free PMC article.

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