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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1983 1
1987 2
1988 3
1989 1
1990 3
1992 1
1996 2
1997 2
2001 4
2002 1
2004 2
2005 1
2007 4
2008 4
2009 12
2010 14
2011 14
2012 6
2013 8
2014 10
2015 9
2016 7
2017 14
2018 25
2019 13
2020 13
2021 18
2022 18
2023 20
2024 6

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215 results

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Page 1
Correspondence.
Chen N, Hsiao MC, Wang NK. Chen N, et al. Among authors: wang nk. Retina. 2023 Feb 1;43(2):e9-e11. doi: 10.1097/IAE.0000000000003664. Retina. 2023. PMID: 36695807 Free PMC article. No abstract available.
Correspondence.
Huang CY, Kang EY, Wu WC, Wang NK. Huang CY, et al. Among authors: wang nk. Retina. 2018 Aug;38(8):e72-e73. doi: 10.1097/IAE.0000000000002256. Retina. 2018. PMID: 30028441 No abstract available.
Systemic Cytokines in Retinopathy of Prematurity.
Wu PY, Fu YK, Lien RI, Chiang MC, Lee CC, Chen HC, Hsueh YJ, Chen KJ, Wang NK, Liu L, Chen YP, Hwang YS, Lai CC, Wu WC. Wu PY, et al. Among authors: wang nk. J Pers Med. 2023 Feb 5;13(2):291. doi: 10.3390/jpm13020291. J Pers Med. 2023. PMID: 36836525 Free PMC article. Review.
Ocular Complications of Obstructive Sleep Apnea.
Liu PK, Chiu TY, Wang NK, Levi SR, Tsai MJ. Liu PK, et al. Among authors: wang nk. J Clin Med. 2021 Jul 31;10(15):3422. doi: 10.3390/jcm10153422. J Clin Med. 2021. PMID: 34362205 Free PMC article. Review.
Familial Exudative Vitreoretinopathy.
Chen KJ, Wang NK, Wu WC. Chen KJ, et al. Among authors: wang nk. JAMA Ophthalmol. 2017 Apr 13;135(4):e165487. doi: 10.1001/jamaophthalmol.2016.5487. Epub 2017 Apr 13. JAMA Ophthalmol. 2017. PMID: 28418565 No abstract available.
Associations of VEGF Polymorphisms With Retinopathy of Prematurity.
Ling XC, Kang EY, Chen KJ, Wang NK, Liu L, Chen YP, Hwang YS, Lai CC, Yang SF, Wu WC. Ling XC, et al. Among authors: wang nk. Invest Ophthalmol Vis Sci. 2023 Jun 1;64(7):11. doi: 10.1167/iovs.64.7.11. Invest Ophthalmol Vis Sci. 2023. PMID: 37272765 Free PMC article.
Response to Cody.
Wang NK, Chiang JPW. Wang NK, et al. Genet Med. 2020 Jan;22(1):236-237. doi: 10.1038/s41436-019-0621-z. Epub 2019 Aug 9. Genet Med. 2020. PMID: 31395943 Free PMC article. No abstract available.
CNGB1-related rod-cone dystrophy: A mutation review and update.
Nassisi M, Smirnov VM, Solis Hernandez C, Mohand-Saïd S, Condroyer C, Antonio A, Kühlewein L, Kempf M, Kohl S, Wissinger B, Nasser F, Ragi SD, Wang NK, Sparrow JR, Greenstein VC, Michalakis S, Mahroo OA, Ba-Abbad R, Michaelides M, Webster AR, Degli Esposti S, Saffren B, Capasso J, Levin A, Hauswirth WW, Dhaenens CM, Defoort-Dhellemmes S, Tsang SH, Zrenner E, Sahel JA, Petersen-Jones SM, Zeitz C, Audo I. Nassisi M, et al. Among authors: wang nk. Hum Mutat. 2021 Jun;42(6):641-666. doi: 10.1002/humu.24205. Epub 2021 May 16. Hum Mutat. 2021. PMID: 33847019 Free PMC article. Review.
Congenital Stationary Night Blindness: Clinical and Genetic Features.
Kim AH, Liu PK, Chang YH, Kang EY, Wang HH, Chen N, Tseng YJ, Seo GH, Lee H, Liu L, Chao AN, Chen KJ, Hwang YS, Wu WC, Lai CC, Tsang SH, Hsiao MC, Wang NK. Kim AH, et al. Among authors: wang nk. Int J Mol Sci. 2022 Nov 29;23(23):14965. doi: 10.3390/ijms232314965. Int J Mol Sci. 2022. PMID: 36499293 Free PMC article.
215 results