Wang F - Search Results

1

Integrative genomic analysis reveals novel regulatory mechanisms of eyeless during Drosophila eye development.

Yeung K, Wang F, Li Y, Wang K, Mardon G, Chen R. Yeung K, et al. Among authors: wang f, wang k. Nucleic Acids Res. 2018 Dec 14;46(22):11743-11758. doi: 10.1093/nar/gky892. Nucleic Acids Res. 2018. PMID: 30295802 Free PMC article.

2

Regulation of Drosophila eye development by the transcription factor Sine oculis.

Jusiak B, Karandikar UC, Kwak SJ, Wang F, Wang H, Chen R, Mardon G. Jusiak B, et al. Among authors: wang h, wang f. PLoS One. 2014 Feb 25;9(2):e89695. doi: 10.1371/journal.pone.0089695. eCollection 2014. PLoS One. 2014. PMID: 24586968 Free PMC article.

3

Integrative subcellular proteomic analysis allows accurate prediction of human disease-causing genes.

Zhao L, Chen Y, Bajaj AO, Eblimit A, Xu M, Soens ZT, Wang F, Ge Z, Jung SY, He F, Li Y, Wensel TG, Qin J, Chen R. Zhao L, et al. Among authors: wang f. Genome Res. 2016 May;26(5):660-9. doi: 10.1101/gr.198911.115. Epub 2016 Feb 24. Genome Res. 2016. PMID: 26912414 Free PMC article.

4

Genome-wide DNA binding pattern of the homeodomain transcription factor Sine oculis (So) in the developing eye of Drosophila melanogaster.

Jusiak B, Wang F, Karandikar UC, Kwak SJ, Wang H, Chen R, Mardon G. Jusiak B, et al. Among authors: wang h, wang f. Genom Data. 2014 Dec 1;2:153-155. doi: 10.1016/j.gdata.2014.06.016. Genom Data. 2014. PMID: 25126519 Free PMC article.

5

ATF6 Is Mutated in Early Onset Photoreceptor Degeneration With Macular Involvement.

Xu M, Gelowani V, Eblimit A, Wang F, Young MP, Sawyer BL, Zhao L, Jenkins G, Creel DJ, Wang K, Ge Z, Wang H, Li Y, Hartnett ME, Chen R. Xu M, et al. Among authors: wang h, wang f, wang k. Invest Ophthalmol Vis Sci. 2015 Jun;56(6):3889-95. doi: 10.1167/iovs.15-16778. Invest Ophthalmol Vis Sci. 2015. PMID: 26070061 Free PMC article.

6

NGS-based Molecular diagnosis of 105 eyeGENE(®) probands with Retinitis Pigmentosa.

Ge Z, Bowles K, Goetz K, Scholl HP, Wang F, Wang X, Xu S, Wang K, Wang H, Chen R. Ge Z, et al. Among authors: wang x, wang h, wang f, wang k. Sci Rep. 2015 Dec 15;5:18287. doi: 10.1038/srep18287. Sci Rep. 2015. PMID: 26667666 Free PMC article.

7

Next-generation sequencing-based molecular diagnosis of 82 retinitis pigmentosa probands from Northern Ireland.

Zhao L, Wang F, Wang H, Li Y, Alexander S, Wang K, Willoughby CE, Zaneveld JE, Jiang L, Soens ZT, Earle P, Simpson D, Silvestri G, Chen R. Zhao L, et al. Among authors: wang h, wang f, wang k. Hum Genet. 2015 Feb;134(2):217-30. doi: 10.1007/s00439-014-1512-7. Epub 2014 Dec 4. Hum Genet. 2015. PMID: 25472526 Free PMC article. Clinical Trial.

8

Comprehensive analysis of patients with Stargardt macular dystrophy reveals new genotype-phenotype correlations and unexpected diagnostic revisions.

Zaneveld J, Siddiqui S, Li H, Wang X, Wang H, Wang K, Li H, Ren H, Lopez I, Dorfman A, Khan A, Wang F, Salvo J, Gelowani V, Li Y, Sui R, Koenekoop R, Chen R. Zaneveld J, et al. Among authors: wang x, wang h, wang f, wang k. Genet Med. 2015 Apr;17(4):262-70. doi: 10.1038/gim.2014.174. Epub 2014 Dec 4. Genet Med. 2015. PMID: 25474345 Free PMC article.

9

Mutations in human IFT140 cause non-syndromic retinal degeneration.

Xu M, Yang L, Wang F, Li H, Wang X, Wang W, Ge Z, Wang K, Zhao L, Li H, Li Y, Sui R, Chen R. Xu M, et al. Among authors: wang x, wang w, wang f, wang k. Hum Genet. 2015 Oct;134(10):1069-78. doi: 10.1007/s00439-015-1586-x. Epub 2015 Jul 28. Hum Genet. 2015. PMID: 26216056 Free PMC article.

10

Next-generation sequencing and novel variant determination in a cohort of 92 familial exudative vitreoretinopathy patients.

Salvo J, Lyubasyuk V, Xu M, Wang H, Wang F, Nguyen D, Wang K, Luo H, Wen C, Shi C, Lin D, Zhang K, Chen R. Salvo J, et al. Among authors: wang h, wang f, wang k. Invest Ophthalmol Vis Sci. 2015 Feb 24;56(3):1937-46. doi: 10.1167/iovs.14-16065. Invest Ophthalmol Vis Sci. 2015. PMID: 25711638 Free PMC article.

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