R01 EY020540/EY/NEI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2010	1
2011	2
2013	1
2014	2
2015	4
2016	2
2017	4
2018	4
2019	1
2022	1
2023	3
2024	0

1

Comprehensive Molecular Diagnosis of a Large Chinese Leber Congenital Amaurosis Cohort.

Wang H, Wang X, Zou X, Xu S, Li H, Soens ZT, Wang K, Li Y, Dong F, Chen R, Sui R. Wang H, et al. Invest Ophthalmol Vis Sci. 2015 Jun;56(6):3642-55. doi: 10.1167/iovs.14-15972. Invest Ophthalmol Vis Sci. 2015. PMID: 26047050 Free PMC article.

2

Single-cell multiomics of the human retina reveals hierarchical transcription factor collaboration in mediating cell type-specific effects of genetic variants on gene regulation.

Wang J, Cheng X, Liang Q, Owen LA, Lu J, Zheng Y, Wang M, Chen S, DeAngelis MM, Li Y, Chen R. Wang J, et al. Genome Biol. 2023 Nov 27;24(1):269. doi: 10.1186/s13059-023-03111-8. Genome Biol. 2023. PMID: 38012720 Free PMC article.

3

AAV8-Mediated Gene Therapy Rescues Retinal Degeneration Phenotype in a Tlcd3b Knockout Mouse Model.

Qian X, Liu H, Fu S, Lu J, Hung YT, Turner C, Gu H, Chen R. Qian X, et al. Invest Ophthalmol Vis Sci. 2022 Mar 2;63(3):11. doi: 10.1167/iovs.63.3.11. Invest Ophthalmol Vis Sci. 2022. PMID: 35275174 Free PMC article.

4

Conditional loss of Spata7 in photoreceptors causes progressive retinal degeneration in mice.

Eblimit A, Agrawal SA, Thomas K, Anastassov IA, Abulikemu T, Moayedi Y, Mardon G, Chen R. Eblimit A, et al. Exp Eye Res. 2018 Jan;166:120-130. doi: 10.1016/j.exer.2017.10.015. Epub 2017 Oct 31. Exp Eye Res. 2018. PMID: 29100828 Free PMC article.

5

Ceramide compensation by ceramide synthases preserves retinal function and structure in a retinal dystrophy mouse model.

Qian X, Srinivasan T, He J, Lu J, Jin Y, Gu H, Chen R. Qian X, et al. Dis Model Mech. 2023 Jul 1;16(7):dmm050168. doi: 10.1242/dmm.050168. Epub 2023 Jul 19. Dis Model Mech. 2023. PMID: 37466006 Free PMC article.

6

Gene augmentation therapy to rescue degenerative photoreceptors in a Cwc27 mutant mouse model.

Lu J, Zheng KQ, Bertrand RE, Quinlan J, Ferdous S, Srinivasan T, Oh S, Wang K, Chen R. Lu J, et al. Exp Eye Res. 2023 Sep;234:109596. doi: 10.1016/j.exer.2023.109596. Epub 2023 Jul 20. Exp Eye Res. 2023. PMID: 37479075

7

Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa.

Arno G, Agrawal SA, Eblimit A, Bellingham J, Xu M, Wang F, Chakarova C, Parfitt DA, Lane A, Burgoyne T, Hull S, Carss KJ, Fiorentino A, Hayes MJ, Munro PM, Nicols R, Pontikos N, Holder GE; UKIRDC; Asomugha C, Raymond FL, Moore AT, Plagnol V, Michaelides M, Hardcastle AJ, Li Y, Cukras C, Webster AR, Cheetham ME, Chen R. Arno G, et al. Am J Hum Genet. 2016 Dec 1;99(6):1305-1315. doi: 10.1016/j.ajhg.2016.10.008. Epub 2016 Nov 23. Am J Hum Genet. 2016. PMID: 27889058 Free PMC article.

8

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. 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.

9

SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data.

Chen Y, Zhao L, Wang Y, Cao M, Gelowani V, Xu M, Agrawal SA, Li Y, Daiger SP, Gibbs R, Wang F, Chen R. Chen Y, et al. BMC Bioinformatics. 2017 Mar 3;18(1):147. doi: 10.1186/s12859-017-1566-3. BMC Bioinformatics. 2017. PMID: 28253855 Free PMC article.

10

The candidate splicing factor Sfswap regulates growth and patterning of inner ear sensory organs.

Moayedi Y, Basch ML, Pacheco NL, Gao SS, Wang R, Harrison W, Xiao N, Oghalai JS, Overbeek PA, Mardon G, Groves AK. Moayedi Y, et al. PLoS Genet. 2014 Jan;10(1):e1004055. doi: 10.1371/journal.pgen.1004055. Epub 2014 Jan 2. PLoS Genet. 2014. PMID: 24391519 Free PMC article.

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