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Western Australia Atropine for the Treatment of Myopia (WA-ATOM) study: Rationale, methodology and participant baseline characteristics.
Lee SSY, Mackey DA, Lingham G, Crewe JM, Richards MD, Chen FK, Charng J, Ng F, Flitcroft I, Loughman JJ, Azuara-Blanco A, Logan NS, Hammond CJ, Chia A, Truong TT, Clark A. Lee SSY, et al. Among authors: charng j. Clin Exp Ophthalmol. 2020 Jul;48(5):569-579. doi: 10.1111/ceo.13736. Epub 2020 Apr 1. Clin Exp Ophthalmol. 2020. PMID: 32100917 Clinical Trial.
Rationale and protocol for the 7- and 8-year longitudinal assessments of eye health in a cohort of young adults in the Raine Study.
Lee SS, Lingham G, Yazar S, Sanfilippo PG, Charng J, Chen FK, Hewitt AW, Ng F, Hammond C, Straker LM, Eastwood PR, MacGregor S, Rose KA, Lucas RM, Guggenheim JA, Saw SM, Coroneo MT, He M, Mackey DA. Lee SS, et al. Among authors: charng j. BMJ Open. 2020 Mar 25;10(3):e033440. doi: 10.1136/bmjopen-2019-033440. BMJ Open. 2020. PMID: 32217560 Free PMC article.
Phenotype-genotype correlations in a pseudodominant Stargardt disease pedigree due to a novel ABCA4 deletion-insertion variant causing a splicing defect.
Huang D, Thompson JA, Charng J, Chelva E, McLenachan S, Chen SC, Zhang D, McLaren TL, Lamey TM, Constable IJ, De Roach JN, Aung-Htut MT, Adams A, Fletcher S, Wilton SD, Chen FK. Huang D, et al. Among authors: charng j. Mol Genet Genomic Med. 2020 Jul;8(7):e1259. doi: 10.1002/mgg3.1259. Epub 2020 Apr 23. Mol Genet Genomic Med. 2020. PMID: 32627976 Free PMC article.
Characterization of CRB1 splicing in retinal organoids derived from a patient with adult-onset rod-cone dystrophy caused by the c.1892A>G and c.2548G>A variants.
Zhang X, Thompson JA, Zhang D, Charng J, Arunachalam S, McLaren TL, Lamey TM, De Roach JN, Jennings L, McLenachan S, Chen FK. Zhang X, et al. Among authors: charng j. Mol Genet Genomic Med. 2020 Nov;8(11):e1489. doi: 10.1002/mgg3.1489. Epub 2020 Sep 15. Mol Genet Genomic Med. 2020. PMID: 32931148 Free PMC article.
Exploring microperimetry and autofluorescence endpoints for monitoring disease progression in PRPF31-associated retinopathy.
Roshandel D, Thompson JA, Charng J, Zhang D, Chelva E, Arunachalam S, Attia MS, Lamey TM, McLaren TL, De Roach JN, Mackey DA, Wilton SD, Fletcher S, McLenachan S, Chen FK. Roshandel D, et al. Among authors: charng j. Ophthalmic Genet. 2021 Feb;42(1):1-14. doi: 10.1080/13816810.2020.1827442. Epub 2020 Sep 27. Ophthalmic Genet. 2021. PMID: 32985313
57 results