Ge Z - Search Results

1

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: ge z. 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.

2

IFT81 as a Candidate Gene for Nonsyndromic Retinal Degeneration.

Dharmat R, Liu W, Ge Z, Sun Z, Yang L, Li Y, Wang K, Thomas K, Sui R, Chen R. Dharmat R, et al. Among authors: ge z. Invest Ophthalmol Vis Sci. 2017 May 1;58(5):2483-2490. doi: 10.1167/iovs.16-19133. Invest Ophthalmol Vis Sci. 2017. PMID: 28460050 Free PMC article.

3

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: ge z. 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.

4

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. Sci Rep. 2015 Dec 15;5:18287. doi: 10.1038/srep18287. Sci Rep. 2015. PMID: 26667666 Free PMC article.

5

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: ge z. 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.

6

PHENOTYPIC VARIABILITY OF RECESSIVE RDH12-ASSOCIATED RETINAL DYSTROPHY.

Zou X, Fu Q, Fang S, Li H, Ge Z, Yang L, Xu M, Sun Z, Li H, Li Y, Dong F, Chen R, Sui R. Zou X, et al. Among authors: ge z. Retina. 2019 Oct;39(10):2040-2052. doi: 10.1097/IAE.0000000000002242. Retina. 2019. PMID: 30134391

7

GRIPT: a novel case-control analysis method for Mendelian disease gene discovery.

Wang J, Zhao L, Wang X, Chen Y, Xu M, Soens ZT, Ge Z, Wang PR, Wang F, Chen R. Wang J, et al. Among authors: ge z. Genome Biol. 2018 Nov 26;19(1):203. doi: 10.1186/s13059-018-1579-x. Genome Biol. 2018. PMID: 30477545 Free PMC article.

8

Molecular and Clinical Findings in Patients With Knobloch Syndrome.

Hull S, Arno G, Ku CA, Ge Z, Waseem N, Chandra A, Webster AR, Robson AG, Michaelides M, Weleber RG, Davagnanam I, Chen R, Holder GE, Pennesi ME, Moore AT. Hull S, et al. Among authors: ge z. JAMA Ophthalmol. 2016 Jul 1;134(7):753-62. doi: 10.1001/jamaophthalmol.2016.1073. JAMA Ophthalmol. 2016. PMID: 27259167

9

Transcriptome-Wide Analysis of Human Chondrocyte Expansion on Synoviocyte Matrix.

Kean TJ, Ge Z, Li Y, Chen R, Dennis JE. Kean TJ, et al. Among authors: ge z. Cells. 2019 Jan 24;8(2):85. doi: 10.3390/cells8020085. Cells. 2019. PMID: 30678371 Free PMC article.

10

Identification of novel direct targets of Drosophila Sine oculis and Eyes absent by integration of genome-wide data sets.

Jin M, Aibar S, Ge Z, Chen R, Aerts S, Mardon G. Jin M, et al. Among authors: ge z. Dev Biol. 2016 Jul 1;415(1):157-167. doi: 10.1016/j.ydbio.2016.05.007. Epub 2016 May 10. Dev Biol. 2016. PMID: 27178668 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

2,823 results

Search Page

Filters