Othman M - Search Results

1

A variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration.

Kanda A, Chen W, Othman M, Branham KE, Brooks M, Khanna R, He S, Lyons R, Abecasis GR, Swaroop A. Kanda A, et al. Among authors: othman m. Proc Natl Acad Sci U S A. 2007 Oct 9;104(41):16227-32. doi: 10.1073/pnas.0703933104. Epub 2007 Sep 20. Proc Natl Acad Sci U S A. 2007. PMID: 17884985 Free PMC article.

2

Mouse eye gene microarrays for investigating ocular development and disease.

Farjo R, Yu J, Othman MI, Yoshida S, Sheth S, Glaser T, Baehr W, Swaroop A. Farjo R, et al. Vision Res. 2002 Feb;42(4):463-70. doi: 10.1016/s0042-6989(01)00219-x. Vision Res. 2002. PMID: 11853762 Free article.

3

Evaluation and optimization of procedures for target labeling and hybridization of cDNA microarrays.

Yu J, Othman MI, Farjo R, Zareparsi S, MacNee SP, Yoshida S, Swaroop A. Yu J, et al. Mol Vis. 2002 Apr 26;8:130-7. Mol Vis. 2002. PMID: 12011805 Free article.

4

Gene expression signatures and biomarkers of noninvasive and invasive breast cancer cells: comprehensive profiles by representational difference analysis, microarrays and proteomics.

Nagaraja GM, Othman M, Fox BP, Alsaber R, Pellegrino CM, Zeng Y, Khanna R, Tamburini P, Swaroop A, Kandpal RP. Nagaraja GM, et al. Among authors: othman m. Oncogene. 2006 Apr 13;25(16):2328-38. doi: 10.1038/sj.onc.1209265. Oncogene. 2006. PMID: 16314837

5

CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration.

Li M, Atmaca-Sonmez P, Othman M, Branham KE, Khanna R, Wade MS, Li Y, Liang L, Zareparsi S, Swaroop A, Abecasis GR. Li M, et al. Among authors: othman m. Nat Genet. 2006 Sep;38(9):1049-54. doi: 10.1038/ng1871. Epub 2006 Aug 27. Nat Genet. 2006. PMID: 16936733 Free PMC article.

6

Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration.

Friedman JS, Chang B, Kannabiran C, Chakarova C, Singh HP, Jalali S, Hawes NL, Branham K, Othman M, Filippova E, Thompson DA, Webster AR, Andréasson S, Jacobson SG, Bhattacharya SS, Heckenlively JR, Swaroop A. Friedman JS, et al. Among authors: othman m. Am J Hum Genet. 2006 Dec;79(6):1059-70. doi: 10.1086/510021. Epub 2006 Oct 23. Am J Hum Genet. 2006. PMID: 17186464 Free PMC article.

7

High-resolution imaging with adaptive optics in patients with inherited retinal degeneration.

Duncan JL, Zhang Y, Gandhi J, Nakanishi C, Othman M, Branham KE, Swaroop A, Roorda A. Duncan JL, et al. Among authors: othman m. Invest Ophthalmol Vis Sci. 2007 Jul;48(7):3283-91. doi: 10.1167/iovs.06-1422. Invest Ophthalmol Vis Sci. 2007. PMID: 17591900

8

Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations.

Aleman TS, Cideciyan AV, Sumaroka A, Schwartz SB, Roman AJ, Windsor EA, Steinberg JD, Branham K, Othman M, Swaroop A, Jacobson SG. Aleman TS, et al. Among authors: othman m. Invest Ophthalmol Vis Sci. 2007 Oct;48(10):4759-65. doi: 10.1167/iovs.07-0453. Invest Ophthalmol Vis Sci. 2007. PMID: 17898302 Free PMC article.

9

Retinal phenotype of an X-linked pseudo-Usher syndrome in association with the G173R mutation in the RPGR gene.

Iannaccone A, Othman MI, Cantrell AD, Jennings BJ, Branham K, Swaroop A. Iannaccone A, et al. Adv Exp Med Biol. 2008;613:221-7. doi: 10.1007/978-0-387-74904-4_25. Adv Exp Med Biol. 2008. PMID: 18188948 No abstract available.

10

Discordant phenotypes in fraternal twins having an identical mutation in exon ORF15 of the RPGR gene.

Walia S, Fishman GA, Swaroop A, Branham KE, Lindeman M, Othman M, Weleber RG. Walia S, et al. Among authors: othman m. Arch Ophthalmol. 2008 Mar;126(3):379-84. doi: 10.1001/archophthalmol.2007.72. Arch Ophthalmol. 2008. PMID: 18332319

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