R01 EY022356/EY/NEI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2013	4
2014	6
2015	11
2016	10
2017	13
2018	7
2019	5
2020	3
2021	6
2022	5
2023	6
2024	5

1

Spatial organization of the mouse retina at single cell resolution by MERFISH.

Choi J, Li J, Ferdous S, Liang Q, Moffitt JR, Chen R. Choi J, et al. Nat Commun. 2023 Aug 15;14(1):4929. doi: 10.1038/s41467-023-40674-3. Nat Commun. 2023. PMID: 37582959 Free PMC article.

2

Single-nuclei RNA-seq on human retinal tissue provides improved transcriptome profiling.

Liang Q, Dharmat R, Owen L, Shakoor A, Li Y, Kim S, Vitale A, Kim I, Morgan D, Liang S, Wu N, Chen K, DeAngelis MM, Chen R. Liang Q, et al. Nat Commun. 2019 Dec 17;10(1):5743. doi: 10.1038/s41467-019-12917-9. Nat Commun. 2019. PMID: 31848347 Free PMC article.

3

A novel statistical method for interpreting the pathogenicity of rare variants.

Wang J, Liu H, Bertrand RE, Sarrion-Perdigones A, Gonzalez Y, Venken KJT, Chen R. Wang J, et al. Genet Med. 2021 Jan;23(1):59-68. doi: 10.1038/s41436-020-00948-3. Epub 2020 Sep 4. Genet Med. 2021. PMID: 32884132 Free PMC article.

4

Comprehensive molecular diagnosis of 67 Chinese Usher syndrome probands: high rate of ethnicity specific mutations in Chinese USH patients.

Jiang L, Liang X, Li Y, Wang J, Zaneveld JE, Wang H, Xu S, Wang K, Wang B, Chen R, Sui R. Jiang L, et al. Orphanet J Rare Dis. 2015 Sep 4;10:110. doi: 10.1186/s13023-015-0329-3. Orphanet J Rare Dis. 2015. PMID: 26338283 Free PMC article.

5

Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration.

Han JH, Rodenburg K, Hayman T, Calzetti G, Kaminska K, Quinodoz M, Marra M, Wallerich S, Allon G, Nagy ZZ, Knézy K, Li Y, Chen R, Barboni MTS, Yang P, Pennesi ME, van den Born LI, Varsányi B, Szabó V, Sharon D, Banin E, Ben-Yosef T, Roosing S, Koenekoop RK, Rivolta C. Han JH, et al. Genet Med. 2024 Jun;26(6):101106. doi: 10.1016/j.gim.2024.101106. Epub 2024 Feb 28. Genet Med. 2024. PMID: 38420906 Free article.

6

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.

7

Single-cell transcriptomics identifies limbal stem cell population and cell types mapping its differentiation trajectory in limbal basal epithelium of human cornea.

Li DQ, Kim S, Li JM, Gao Q, Choi J, Bian F, Hu J, Zhang Y, Li J, Lu R, Li Y, Pflugfelder SC, Miao H, Chen R. Li DQ, et al. Ocul Surf. 2021 Apr;20:20-32. doi: 10.1016/j.jtos.2020.12.004. Epub 2021 Jan 1. Ocul Surf. 2021. PMID: 33388438 Free PMC article.

8

The many faces of the trabecular meshwork cell.

Stamer WD, Clark AF. Stamer WD, et al. Exp Eye Res. 2017 May;158:112-123. doi: 10.1016/j.exer.2016.07.009. Epub 2016 Jul 19. Exp Eye Res. 2017. PMID: 27443500 Free PMC article. Review.

9

Comprehensive single-cell atlas of the mouse retina.

Li J, Choi J, Cheng X, Ma J, Pema S, Sanes JR, Mardon G, Frankfort BJ, Tran NM, Li Y, Chen R. Li J, et al. iScience. 2024 May 8;27(6):109916. doi: 10.1016/j.isci.2024.109916. eCollection 2024 Jun 21. iScience. 2024. PMID: 38812536 Free PMC article.

10

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.

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