Charng J - Search Results

1

Imaging Lenticular Autofluorescence in Older Subjects.

Charng J, Tan R, Luu CD, Sadigh S, Stambolian D, Guymer RH, Jacobson SG, Cideciyan AV. Charng J, et al. Invest Ophthalmol Vis Sci. 2017 Oct 1;58(12):4940-4947. doi: 10.1167/iovs.17-22540. Invest Ophthalmol Vis Sci. 2017. PMID: 28973367 Free PMC article.

2

Age-related retinal function changes in albino and pigmented rats.

Charng J, Nguyen CT, Bui BV, Vingrys AJ. Charng J, et al. Invest Ophthalmol Vis Sci. 2011 Nov 17;52(12):8891-9. doi: 10.1167/iovs.11-7602. Invest Ophthalmol Vis Sci. 2011. PMID: 22003116

3

Developing an Outcome Measure With High Luminance for Optogenetics Treatment of Severe Retinal Degenerations and for Gene Therapy of Cone Diseases.

Cideciyan AV, Roman AJ, Jacobson SG, Yan B, Pascolini M, Charng J, Pajaro S, Nirenberg S. Cideciyan AV, et al. Among authors: charng j. Invest Ophthalmol Vis Sci. 2016 Jun 1;57(7):3211-21. doi: 10.1167/iovs.16-19586. Invest Ophthalmol Vis Sci. 2016. PMID: 27309625 Free PMC article.

4

Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration.

Charng J, Cideciyan AV, Jacobson SG, Sumaroka A, Schwartz SB, Swider M, Roman AJ, Sheplock R, Anand M, Peden MC, Khanna H, Heon E, Wright AF, Swaroop A. Charng J, et al. Hum Mol Genet. 2016 Dec 15;25(24):5444-5459. doi: 10.1093/hmg/ddw361. Hum Mol Genet. 2016. PMID: 27798110 Free PMC article.

5

Defining Outcomes for Clinical Trials of Leber Congenital Amaurosis Caused by GUCY2D Mutations.

Jacobson SG, Cideciyan AV, Sumaroka A, Roman AJ, Charng J, Lu M, Choudhury S, Schwartz SB, Heon E, Fishman GA, Boye SE. Jacobson SG, et al. Among authors: charng j. Am J Ophthalmol. 2017 May;177:44-57. doi: 10.1016/j.ajo.2017.02.003. Epub 2017 Feb 16. Am J Ophthalmol. 2017. PMID: 28212877

6

Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 Gene.

Jacobson SG, Cideciyan AV, Sumaroka A, Roman AJ, Charng J, Lu M, Choi W, Sheplock R, Swider M, Kosyk MS, Schwartz SB, Stone EM, Fishman GA. Jacobson SG, et al. Among authors: charng j. Invest Ophthalmol Vis Sci. 2017 May 1;58(5):2609-2622. doi: 10.1167/iovs.17-21560. Invest Ophthalmol Vis Sci. 2017. PMID: 28510626 Free article.

7

Pupillary Light Reflexes in Severe Photoreceptor Blindness Isolate the Melanopic Component of Intrinsically Photosensitive Retinal Ganglion Cells.

Charng J, Jacobson SG, Heon E, Roman AJ, McGuigan DB 3rd, Sheplock R, Kosyk MS, Swider M, Cideciyan AV. Charng J, et al. Invest Ophthalmol Vis Sci. 2017 Jun 1;58(7):3215-3224. doi: 10.1167/iovs.17-21909. Invest Ophthalmol Vis Sci. 2017. PMID: 28660274 Free PMC article.

8

Efficacy Outcome Measures for Clinical Trials of USH2A Caused by the Common c.2299delG Mutation.

Calzetti G, Levy RA, Cideciyan AV, Garafalo AV, Roman AJ, Sumaroka A, Charng J, Heon E, Jacobson SG. Calzetti G, et al. Among authors: charng j. Am J Ophthalmol. 2018 Sep;193:114-129. doi: 10.1016/j.ajo.2018.06.017. Epub 2018 Jun 25. Am J Ophthalmol. 2018. PMID: 29953849

9

Progression in X-linked Retinitis Pigmentosa Due to ORF15-RPGR Mutations: Assessment of Localized Vision Changes Over 2 Years.

Cideciyan AV, Charng J, Roman AJ, Sheplock R, Garafalo AV, Heon E, Jacobson SG. Cideciyan AV, et al. Among authors: charng j. Invest Ophthalmol Vis Sci. 2018 Sep 4;59(11):4558-4566. doi: 10.1167/iovs.18-24931. Invest Ophthalmol Vis Sci. 2018. PMID: 30208424

10

Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration.

Charng J, Cideciyan AV, Jacobson SG, Sumaroka A, Schwartz SB, Swider M, Roman AJ, Sheplock R, Anand M, Peden MC, Khanna H, Heon E, Wright AF, Swaroop A. Charng J, et al. Hum Mol Genet. 2019 Jan 1;28(1):175. doi: 10.1093/hmg/ddy342. Hum Mol Genet. 2019. PMID: 30285110 Free PMC article. No abstract available.

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