Mohammad I Othman
Overview
Explore the profile of Mohammad I Othman including associated specialties, affiliations and a list of published articles.
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14
Citations
1666
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Recent Articles
1.
Fahim A, Sullivan L, Bowne S, Jones K, Wheaton D, Khan N, et al.
Ophthalmol Retina
. 2020 Jan;
4(5):510-520.
PMID: 31953110
Purpose: X-linked retinitis pigmentosa can manifest in female carriers with widely variable severity, whereas others remain unaffected. The contribution of X-chromosome inactivation (XCI) to phenotypic variation has been postulated but...
2.
Garnai S, Brinkmeier M, Emery B, Aleman T, Pyle L, Veleva-Rotse B, et al.
PLoS Genet
. 2019 May;
15(5):e1008130.
PMID: 31048900
Nanophthalmos is a rare, potentially devastating eye condition characterized by small eyes with relatively normal anatomy, a high hyperopic refractive error, and frequent association with angle closure glaucoma and vision...
3.
Lundy S, Nikoopour E, Karoukis A, Ohara R, Othman M, Tagett R, et al.
Front Med (Lausanne)
. 2018 Oct;
5:249.
PMID: 30271775
Autoimmune retinopathy (AIR) causes rapidly progressive vision loss that is treatable but often is confused with other forms of retinal degeneration including retinitis pigmentosa (RP). Measurement of anti-retinal antibodies (ARA)...
4.
Fritsche L, Igl W, Cooke Bailey J, Grassmann F, Sengupta S, Bragg-Gresham J, et al.
Nat Genet
. 2015 Dec;
48(2):134-43.
PMID: 26691988
Advanced age-related macular degeneration (AMD) is the leading cause of blindness in the elderly, with limited therapeutic options. Here we report on a study of >12 million variants, including 163,714...
5.
Lo Y, Kang H, Nelson M, Othman M, Chissoe S, Ehm M, et al.
BMC Bioinformatics
. 2015 Apr;
16:75.
PMID: 25884587
Background: Sequencing studies of exonic regions aim to identify rare variants contributing to complex traits. With high coverage and large sample size, these studies tend to apply simple variant calling...
6.
Fritsche L, Chen W, Schu M, Yaspan B, Yu Y, Thorleifsson G, et al.
Nat Genet
. 2013 Mar;
45(4):433-9, 439e1-2.
PMID: 23455636
Age-related macular degeneration (AMD) is a common cause of blindness in older individuals. To accelerate the understanding of AMD biology and help design new therapies, we executed a collaborative genome-wide...
7.
Thompson D, Khan N, Othman M, Chang B, Jia L, Grahek G, et al.
PLoS One
. 2012 May;
7(5):e35865.
PMID: 22563472
Animal models of human disease are an invaluable component of studies aimed at understanding disease pathogenesis and therapeutic possibilities. Mutations in the gene encoding retinitis pigmentosa GTPase regulator (RPGR) are...
8.
Khanna H, Davis E, Murga-Zamalloa C, Estrada-Cuzcano A, Lopez I, den Hollander A, et al.
Nat Genet
. 2009 May;
41(6):739-45.
PMID: 19430481
Despite rapid advances in the identification of genes involved in disease, the predictive power of the genotype remains limited, in part owing to poorly understood effects of second-site modifiers. Here...
9.
Iannaccone A, Othman M, Cantrell A, Jennings B, Branham K, Swaroop A
Adv Exp Med Biol
. 2008 Jan;
613:221-7.
PMID: 18188948
No abstract available.
10.
Rozsa F, Reed D, Scott K, Pawar H, Moroi S, Kijek T, et al.
Mol Vis
. 2006 Mar;
12:125-41.
PMID: 16541013
Purpose: Topical use of dexamethasone has long been associated with steroid induced-glaucoma, although the mechanism is unknown. We applied a strict filtering of comparative microarray data to more than 18,000...