PubMed for id: 481692

Year	Number of Results
1979	1
1989	1
1993	1
1997	1
1998	2
2000	1
2001	1
2002	1
2004	4
2005	3
2006	3
2007	4
2008	3
2009	3
2010	5
2011	4
2012	4
2013	8
2014	4
2015	5
2016	6
2017	6
2018	5
2019	10
2020	6
2021	10
2022	7
2023	12
2024	1

1

Protrusion of KCNJ13 Gene Knockout Retinal Pigment Epithelium Due to Oxidative Stress-Induced Cell Death.

Kanzaki Y, Fujita H, Sato K, Hosokawa M, Matsumae H, Morizane Y, Ohuchi H. Kanzaki Y, et al. Invest Ophthalmol Vis Sci. 2022 Nov 1;63(12):29. doi: 10.1167/iovs.63.12.29. Invest Ophthalmol Vis Sci. 2022. PMID: 36413373 Free PMC article.

2

Sensing through Non-Sensing Ocular Ion Channels.

Kabra M, Pattnaik BR. Kabra M, et al. Int J Mol Sci. 2020 Sep 21;21(18):6925. doi: 10.3390/ijms21186925. Int J Mol Sci. 2020. PMID: 32967234 Free PMC article. Review.

3

KCNJ13 Gene Deletion Impairs Cell Alignment and Phagocytosis in Retinal Pigment Epithelium Derived from Human-Induced Pluripotent Stem Cells.

Kanzaki Y, Fujita H, Sato K, Hosokawa M, Matsumae H, Shiraga F, Morizane Y, Ohuchi H. Kanzaki Y, et al. Invest Ophthalmol Vis Sci. 2020 May 11;61(5):38. doi: 10.1167/iovs.61.5.38. Invest Ophthalmol Vis Sci. 2020. PMID: 32437550 Free PMC article.

4

Gene Augmentation and Readthrough Rescue Channelopathy in an iPSC-RPE Model of Congenital Blindness.

Shahi PK, Hermans D, Sinha D, Brar S, Moulton H, Stulo S, Borys KD, Capowski E, Pillers DM, Gamm DM, Pattnaik BR. Shahi PK, et al. Am J Hum Genet. 2019 Feb 7;104(2):310-318. doi: 10.1016/j.ajhg.2018.12.019. Epub 2019 Jan 24. Am J Hum Genet. 2019. PMID: 30686507 Free PMC article.

5

A Novel KCNJ13 Nonsense Mutation and Loss of Kir7.1 Channel Function Causes Leber Congenital Amaurosis (LCA16).

Pattnaik BR, Shahi PK, Marino MJ, Liu X, York N, Brar S, Chiang J, Pillers DA, Traboulsi EI. Pattnaik BR, et al. Hum Mutat. 2015 Jul;36(7):720-7. doi: 10.1002/humu.22807. Epub 2015 May 20. Hum Mutat. 2015. PMID: 25921210

6

Focus on Kir7.1: physiology and channelopathy.

Kumar M, Pattnaik BR. Kumar M, et al. Channels (Austin). 2014;8(6):488-95. doi: 10.4161/19336950.2014.959809. Channels (Austin). 2014. PMID: 25558901 Free PMC article. Review.

7

Leber Congenital Amaurosis – RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY.

Weleber RG, Francis PJ, Trzupek KM, Beattie C. Weleber RG, et al. 2004 Jul 7 [updated 2013 May 2]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2004 Jul 7 [updated 2013 May 2]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301475 Free Books & Documents. Review.

8

Foveal Hypoplasia in CRB1-Related Retinopathies.

Rodriguez-Martinez AC, Higgins BE, Tailor-Hamblin V, Malka S, Cheloni R, Collins AM, Bladen J, Henderson R, Moosajee M. Rodriguez-Martinez AC, et al. Int J Mol Sci. 2023 Sep 11;24(18):13932. doi: 10.3390/ijms241813932. Int J Mol Sci. 2023. PMID: 37762234 Free PMC article.

9

Classification and Growth Rate of Chorioretinal Atrophy after Voretigene Neparvovec-Rzyl for RPE65-Mediated Retinal Degeneration.

Bommakanti N, Young BK, Sisk RA, Berrocal AM, Duncan JL, Bakall B, Mathias MT, Ahmed I, Chorfi S, Comander J, Nagiel A, Besirli CG. Bommakanti N, et al. Ophthalmol Retina. 2024 Jan;8(1):42-48. doi: 10.1016/j.oret.2023.08.017. Epub 2023 Sep 3. Ophthalmol Retina. 2024. PMID: 37660736

10

Nonviral base editing of KCNJ13 mutation preserves vision in a model of inherited retinal channelopathy.

Kabra M, Shahi PK, Wang Y, Sinha D, Spillane A, Newby GA, Saxena S, Tong Y, Chang Y, Abdeen AA, Edwards KL, Theisen CO, Liu DR, Gamm DM, Gong S, Saha K, Pattnaik BR. Kabra M, et al. J Clin Invest. 2023 Oct 2;133(19):e171356. doi: 10.1172/JCI171356. J Clin Invest. 2023. PMID: 37561581 Free PMC article.

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