Doug D Chung
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Explore the profile of Doug D Chung including associated specialties, affiliations and a list of published articles.
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100
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Recent Articles
1.
Peshkar-Kulkarni S, Chung D, Aldave A
Ophthalmic Genet
. 2025 Jan;
1-8.
PMID: 39834031
Purpose: To assess the impact of MitoQ, a mitochondria-targeted antioxidant, on viability of human corneal endothelial cell (hCEnC) lines expressing mutations associated with congenital hereditary endothelial dystrophy (CHED) and Fuchs...
2.
Chung D, Chen A, Choo C, Zhang W, Williams D, Griffis C, et al.
PLoS One
. 2024 Jan;
19(1):e0296928.
PMID: 38252645
Mutations in the solute linked carrier family 4 member 11 (SLC4A11) gene are associated with congenital hereditary endothelial dystrophy (CHED) and Fuchs corneal endothelial dystrophy type 4 (FECD4), both characterized...
3.
Patterson K, Chong J, Chung D, Lisch W, Karp C, Dreisler E, et al.
Am J Ophthalmol
. 2023 Nov;
258:183-195.
PMID: 37972748
Purpose: To report the genetic etiology of Lisch epithelial corneal dystrophy (LECD). Design: Multicenter cohort study. Methods: A discovery cohort of 27 individuals with LECD from 17 families, including 7...
4.
Jatavallabhula K, Onyia O, Chung D, Williams D, Wang K, Aldave A
Cornea
. 2023 Oct;
43(2):253-256.
PMID: 37823852
Purpose: The aim of this study was to report a novel heterozygous variant c.1712G>T (p.Gly571Val) in the nucleotide-binding domain, leucine-rich repeat family, pyrin domain-containing 3 gene ( NLRP3 ) in...
5.
Williams D, Onyia O, Chung D, Kirakosyan A, Hovakimyan A, Payne C, et al.
Mol Vis
. 2023 Jun;
29:25-30.
PMID: 37287641
Purpose: Pre-Descemet corneal dystrophy (PDCD) with X-linked ichthyosis (XLI) is associated with mutations in or deletions of the steroid sulfatase gene (). As only three cases of genetically confirmed PDCD...
6.
Williams D, Chung D, Hovakimyan A, Davtyan A, Glasgow B, Aldave A
Cornea
. 2022 Dec;
42(4):464-469.
PMID: 36534610
Purpose: Congenital stromal corneal dystrophy (CSCD) is a rare congenital, dominantly inherited disorder characterized by diffuse stromal opacification associated with mutations in the decorin gene ( DCN ). As only...
7.
Choo C, Chung D, Ledwitch K, Kassels A, Meiler J, Aldave A
Ophthalmic Genet
. 2022 Mar;
43(4):530-533.
PMID: 35315300
Purpose: To provide the initial confirmation of the c.1772C>T (p.Ser591Phe) mutation in the transforming growth factor--induced ( gene as being associated with variant lattice corneal dystrophy (LCD). Methods: Ophthalmologic examination...
8.
Choo C, de Los Bueis A, Chung D, Aldave A
Cornea
. 2021 Aug;
41(6):779-781.
PMID: 34369396
Purpose: The aim of this study was to report the results of screening peroxiredoxin 3 (PRDX3) and PDZ domain-containing protein 8 (PDZD8) in a previously unreported pedigree with punctiform and...
9.
Yung M, Chen A, Chung D, Barrington A, Zhang J, Frausto R, et al.
Ophthalmic Genet
. 2021 May;
42(4):486-492.
PMID: 34003075
Background: Concomitant corneal ectasia and posterior lamellar corneal opacification is rare, and the genetic relationship between these two conditions is unclear. We report the genetic and clinical characterization of this...
10.
Chen A, Niruthisard D, Chung D, Chuephanich P, Aldave A
Ophthalmic Genet
. 2020 Sep;
41(6):639-644.
PMID: 32880217
Background: Most transforming growth factor beta-induced () corneal dystrophies are associated with a characteristic phenotype, clinical course, and a conserved mutation in the gene. However, we report a novel missense...