Khanh-Nhat Tran-Viet
Overview
Explore the profile of Khanh-Nhat Tran-Viet including associated specialties, affiliations and a list of published articles.
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17
Citations
649
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Recent Articles
1.
Souma T, Tompson S, Thomson B, Siggs O, Kizhatil K, Yamaguchi S, et al.
J Clin Invest
. 2016 Jun;
126(7):2575-87.
PMID: 27270174
Primary congenital glaucoma (PCG) is a devastating eye disease and an important cause of childhood blindness worldwide. In PCG, defects in the anterior chamber aqueous humor outflow structures of the...
2.
Metlapally R, Gonzalez P, Hawthorne F, Tran-Viet K, Wildsoet C, Young T
PLoS One
. 2013 Nov;
8(10):e78984.
PMID: 24205357
Introduction: In human eyes, ocular enlargement/growth reflects active extracellular matrix remodeling of the outer scleral shell. Micro-RNAs are small non-coding RNAs that regulate gene expression by base pairing with target...
3.
Lim S, St Germain E, Tran-Viet K, Staffieri S, Marino M, Dollfus P, et al.
Ophthalmic Genet
. 2013 Jun;
35(1):1-6.
PMID: 23802135
Background: The Atonal Homolog 7 (ATOH7) gene has been implicated in association studies with optic nerve head diameter size. Hence, we screened optic nerve hypoplasia (ONH) patient DNA samples from...
4.
Tran-Viet K, Powell C, Barathi V, Klemm T, Maurer-Stroh S, Limviphuvadh V, et al.
Am J Hum Genet
. 2013 May;
92(5):820-6.
PMID: 23643385
Myopia, or near-sightedness, is an ocular refractive error of unfocused image quality in front of the retinal plane. Individuals with high-grade myopia (dioptric power greater than -6.00) are predisposed to...
5.
Tran-Viet K, Soler V, Quiette V, Powell C, Yanovitch T, Metlapally R, et al.
Mol Vis
. 2013 Apr;
19:759-66.
PMID: 23592912
Purpose: Stickler syndrome is an arthro-ophthalmopathy with phenotypic overlap with Wagner syndrome. The common Stickler syndrome type I is inherited as an autosomal dominant trait, with causal mutations in collagen...
6.
Hawthorne F, Feng S, Metlapally R, Li Y, Tran-Viet K, Guggenheim J, et al.
Invest Ophthalmol Vis Sci
. 2013 Feb;
54(3):2076-86.
PMID: 23422819
Purpose: Myopia, or nearsightedness, is a common ocular genetic disease for which over 20 candidate genomic loci have been identified. The high-grade myopia locus, MYP3, has been reported on chromosome...
7.
Soler V, Tran-Viet K, Galiacy S, Limviphuvadh V, Klemm T, St Germain E, et al.
J Med Genet
. 2013 Jan;
50(4):246-54.
PMID: 23349227
Background: Corneal intraepithelial dyskeratosis is an extremely rare condition. The classical form, affecting Native American Haliwa-Saponi tribe members, is called hereditary benign intraepithelial dyskeratosis (HBID). Herein, we present a new...
8.
Lim S, Tran-Viet K, Yanovitch T, Freedman S, Klemm T, Call W, et al.
Am J Ophthalmol
. 2012 Dec;
155(3):508-517.e5.
PMID: 23218701
Purpose: To screen primary congenital glaucoma patients in the United States for sequence variants within the CYP1B1, LTBP2, and MYOC genes using Sanger and whole exome sequencing. Design: Retrospective case-control...
9.
Tran-Viet K, St Germain E, Soler V, Powell C, Lim S, Klemm T, et al.
Mol Vis
. 2012 Apr;
18:937-44.
PMID: 22539872
Purpose: Myopia, or nearsightedness, is highly prevalent in Asian countries and is considered a serious public health issue globally. High-grade myopia can predispose individuals to myopic maculopathy, premature cataracts, retinal...
10.
Metlapally R, Ki C, Li Y, Tran-Viet K, Abbott D, Malecaze F, et al.
Invest Ophthalmol Vis Sci
. 2010 May;
51(9):4476-9.
PMID: 20435602
Purpose: Evidence from human myopia genetic mapping studies (MYP3 locus), modulated animal models, and observations of glycemic control in humans suggests that insulin-like growth factor (IGF)-1 plays a role in...