Lu F - Search Results

1

Loss of Tmem30a leads to photoreceptor degeneration.

Zhang L, Yang Y, Li S, Zhang S, Zhu X, Tai Z, Yang M, Liu Y, Guo X, Chen B, Jiang Z, Lu F, Zhu X. Zhang L, et al. Among authors: lu f. Sci Rep. 2017 Aug 24;7(1):9296. doi: 10.1038/s41598-017-09506-5. Sci Rep. 2017. PMID: 28839191 Free PMC article.

2

Evaluation of MMP2 as a candidate gene for high myopia.

Gong B, Liu X, Zhang D, Wang P, Huang L, Lin Y, Lu F, Ma S, Cheng J, Chen R, Li X, Lin H, Zeng G, Zhu X, Hu J, Yang Z, Shi Y. Gong B, et al. Among authors: lu f. Mol Vis. 2013;19:121-7. Epub 2013 Jan 28. Mol Vis. 2013. PMID: 23378725 Free PMC article.

3

A genetic variant in the SKIV2L gene is significantly associated with age-related macular degeneration in a Han Chinese population.

Lu F, Shi Y, Qu C, Zhao P, Liu X, Gong B, Ma S, Zhou Y, Zhang Q, Fei P, Xu Y, Hu J, Fan Y, Lin Y, Zhu X, Yang Z. Lu F, et al. Invest Ophthalmol Vis Sci. 2013 Apr 26;54(4):2911-7. doi: 10.1167/iovs.12-11381. Invest Ophthalmol Vis Sci. 2013. PMID: 23557739

4

[Association of single nucleotide polymorphisms of CSPG2 and HSPG2 genes with intracranial aneurysm in ethnic Han Chinese population].

Zhu X, Shi Y, Lu F, Huang GF, Hu LJ. Zhu X, et al. Among authors: lu f. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Apr;30(2):218-21. doi: 10.3760/cma.j.issn.1003-9406.2013.04.022. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23568740 Chinese.

5

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.

6

Genetic variants in PVRL2-TOMM40-APOE region are associated with human longevity in a Han Chinese population.

Lu F, Guan H, Gong B, Liu X, Zhu R, Wang Y, Qian J, Zhou T, Lan X, Wang P, Lin Y, Ma S, Lin H, Zhu X, Chen R, Zhu X, Shi Y, Yang Z. Lu F, et al. PLoS One. 2014 Jun 12;9(6):e99580. doi: 10.1371/journal.pone.0099580. eCollection 2014. PLoS One. 2014. PMID: 24924924 Free PMC article.

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

Associations of 6p21.3 Region with Age-related Macular Degeneration and Polypoidal Choroidal Vasculopathy.

Ye Z, Shuai P, Zhai Y, Li F, Jiang L, Lu F, Wen F, Huang L, Zhang D, Liu X, Lin Y, Luo H, Zhang H, Zhu X, Wu Z, Yang Z, Gong B, Shi Y. Ye Z, et al. Among authors: lu f. Sci Rep. 2016 Feb 10;6:20914. doi: 10.1038/srep20914. Sci Rep. 2016. PMID: 26861912 Free PMC article.

9

A missense variant in FGD6 confers increased risk of polypoidal choroidal vasculopathy.

Huang L, Zhang H, Cheng CY, Wen F, Tam PO, Zhao P, Chen H, Li Z, Chen L, Tai Z, Yamashiro K, Deng S, Zhu X, Chen W, Cai L, Lu F, Li Y, Cheung CM, Shi Y, Miyake M, Lin Y, Gong B, Liu X, Sim KS, Yang J, Mori K, Zhang X, Cackett PD, Tsujikawa M, Nishida K, Hao F, Ma S, Lin H, Cheng J, Fei P, Lai TY, Tang S, Laude A, Inoue S, Yeo IY, Sakurada Y, Zhou Y, Iijima H, Honda S, Lei C, Zhang L, Zheng H, Jiang D, Zhu X, Wong TY, Khor CC, Pang CP, Yoshimura N, Yang Z. Huang L, et al. Among authors: lu f. Nat Genet. 2016 Jun;48(6):640-7. doi: 10.1038/ng.3546. Epub 2016 Apr 18. Nat Genet. 2016. PMID: 27089177

10

Association study of candidate genes for susceptibility to Kashin-Beck disease in a Tibetan population.

Tai Z, Huang L, Lu F, Shi Y, Ma S, Cheng J, Lin H, Liu X, Li Y, Yang Z. Tai Z, et al. Among authors: lu f. BMC Med Genet. 2017 Jun 26;18(1):69. doi: 10.1186/s12881-017-0423-6. BMC Med Genet. 2017. PMID: 28651521 Free PMC article.

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