PubMed for id: 6247

Year	Number of Results
1991	1
1993	1
1996	1
1997	1
1998	1
1999	5
2000	1
2002	6
2003	5
2004	3
2005	2
2006	4
2007	10
2008	6
2009	7
2010	5
2011	8
2012	5
2013	4
2014	5
2015	3
2016	3
2017	2
2018	3
2019	3
2020	4
2021	3
2022	4
2023	4
2024	0

1

Vitreous Hemorrhage in Pediatric Patients With X-Linked Retinoschisis: Characteristics and Outcomes.

da Cruz NFS, Sengillo JD, Al-Khersan H, Negron CI, Felder MB, Patel NA, Berrocal AM. da Cruz NFS, et al. Ophthalmic Surg Lasers Imaging Retina. 2023 Sep;54(9):513-518. doi: 10.3928/23258160-20230803-01. Epub 2023 Aug 1. Ophthalmic Surg Lasers Imaging Retina. 2023. PMID: 37642422 Free article.

2

Identification and molecular characterization of two recurrent missense mutations in the RS1 gene in two families with X-linked retinoschisis from North India.

Chatterjee S, Gupta S, Kirola L, Chandra A, Mukherjee A, Mutsuddi M. Chatterjee S, et al. Am J Med Genet A. 2023 Oct;191(10):2524-2535. doi: 10.1002/ajmg.a.63327. Epub 2023 Jun 15. Am J Med Genet A. 2023. PMID: 37317958

3

Advances in understanding the molecular structure of retinoschisin while questions remain of biological function.

Heymann JB, Vijayasarathy C, Fariss RN, Sieving PA. Heymann JB, et al. Prog Retin Eye Res. 2023 Jul;95:101147. doi: 10.1016/j.preteyeres.2022.101147. Epub 2022 Nov 16. Prog Retin Eye Res. 2023. PMID: 36402656 Review.

4

[Analysis of RS1 gene variant in a Chinese pedigree affected with X-linked congenital retinal splitters].

Luo P, Liu Q, Xing X, Liu Q, Luo Y. Luo P, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Apr 10;39(4):378-382. doi: 10.3760/cma.j.cn511374-20200729-00566. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35446970 Chinese.

5

Clinical and genetic features of retinoschisis in 120 families with RS1 mutations.

Xiao S, Sun W, Xiao X, Li S, Luo H, Jia X, Ouyang J, Li X, Wang Y, Jiang Y, Wang P, Zhang Q. Xiao S, et al. Br J Ophthalmol. 2023 Mar;107(3):367-372. doi: 10.1136/bjophthalmol-2021-319668. Epub 2021 Oct 13. Br J Ophthalmol. 2023. PMID: 34645606

6

X-Linked Retinoschisis: Novel Clinical Observations and Genetic Spectrum in 340 Patients.

Hahn LC, van Schooneveld MJ, Wesseling NL, Florijn RJ, Ten Brink JB, Lissenberg-Witte BI, Strubbe I, Meester-Smoor MA, Thiadens AA, Diederen RM, van Cauwenbergh C, de Zaeytijd J, Walraedt S, de Baere E, Klaver CCW, Ossewaarde-van Norel J, van den Born LI, Hoyng CB, van Genderen MM, Sieving PA, Leroy BP, Bergen AA, Boon CJF. Hahn LC, et al. Ophthalmology. 2022 Feb;129(2):191-202. doi: 10.1016/j.ophtha.2021.09.021. Epub 2021 Oct 6. Ophthalmology. 2022. PMID: 34624300 Free article.

7

Spontaneous resolution of schitic cavities in XLRS.

Campbell TG, Elder J, Ruddle J. Campbell TG, et al. Ophthalmic Genet. 2021 Dec;42(6):765-767. doi: 10.1080/13816810.2021.1946705. Epub 2021 Jul 5. Ophthalmic Genet. 2021. PMID: 34223802

8

Clinical findings and RS1 genotype in 90 Chinese families with X-linked retinoschisis.

Chen C, Xie Y, Sun T, Tian L, Xu K, Zhang X, Li Y. Chen C, et al. Mol Vis. 2020 Apr 11;26:291-298. eCollection 2020. Mol Vis. 2020. PMID: 32300273 Free PMC article.

9

X-linked peripheral retinoschisis without macular involvement: a case series with RS1 genetic confirmation.

Smith LM, Cernichiaro-Espinosa LA, McKeown CA, Tekin M, Lam BL, Chiang J, Russell JF, Berrocal AM. Smith LM, et al. Ophthalmic Genet. 2020 Feb;41(1):57-62. doi: 10.1080/13816810.2020.1723115. Epub 2020 Mar 3. Ophthalmic Genet. 2020. PMID: 32124668

10

Establishment of a human induced pluripotent stem cell line (CSUASOi005-A), from peripheral blood mononuclear cells of a patient with X-linked juvenile retinoschisis carrying a novel mutation in RS1 gene.

Mao S, Ding C, Zhou Y, Jing Y, Chen J, Guo Y, Liu J, Cui Z, Yan X, Gu J, Wang Y, Chen J, Tang S. Mao S, et al. Stem Cell Res. 2020 Mar;43:101718. doi: 10.1016/j.scr.2020.101718. Epub 2020 Feb 4. Stem Cell Res. 2020. PMID: 32050117 Free article.

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