Webster AR - Search Results

1

Evidence of association of APOE with age-related macular degeneration: a pooled analysis of 15 studies.

McKay GJ, Patterson CC, Chakravarthy U, Dasari S, Klaver CC, Vingerling JR, Ho L, de Jong PT, Fletcher AE, Young IS, Seland JH, Rahu M, Soubrane G, Tomazzoli L, Topouzis F, Vioque J, Hingorani AD, Sofat R, Dean M, Sawitzke J, Seddon JM, Peter I, Webster AR, Moore AT, Yates JR, Cipriani V, Fritsche LG, Weber BH, Keilhauer CN, Lotery AJ, Ennis S, Klein ML, Francis PJ, Stambolian D, Orlin A, Gorin MB, Weeks DE, Kuo CL, Swaroop A, Othman M, Kanda A, Chen W, Abecasis GR, Wright AF, Hayward C, Baird PN, Guymer RH, Attia J, Thakkinstian A, Silvestri G. McKay GJ, et al. Among authors: webster ar. Hum Mutat. 2011 Dec;32(12):1407-16. doi: 10.1002/humu.21577. Epub 2011 Sep 12. Hum Mutat. 2011. PMID: 21882290 Free PMC article.

2

Ocular malformations and the fruits of developmental genetics.

Webster AR, Moore AT. Webster AR, et al. Eye (Lond). 1994;8 ( Pt 5):v. doi: 10.1038/eye.1994.123. Eye (Lond). 1994. PMID: 7835439 No abstract available.

3

Clinical features and molecular genetics of Von Hippel-Lindau disease.

Maher ER, Webster AR, Moore AT. Maher ER, et al. Among authors: webster ar. Ophthalmic Genet. 1995 Sep;16(3):79-84. doi: 10.3109/13816819509059966. Ophthalmic Genet. 1995. PMID: 8556282 Review.

4

Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations.

Maher ER, Webster AR, Richards FM, Green JS, Crossey PA, Payne SJ, Moore AT. Maher ER, et al. Among authors: webster ar. J Med Genet. 1996 Apr;33(4):328-32. doi: 10.1136/jmg.33.4.328. J Med Genet. 1996. PMID: 8730290 Free PMC article.

5

An analysis of phenotypic variation in the familial cancer syndrome von Hippel-Lindau disease: evidence for modifier effects.

Webster AR, Richards FM, MacRonald FE, Moore AT, Maher ER. Webster AR, et al. Am J Hum Genet. 1998 Oct;63(4):1025-35. doi: 10.1086/302037. Am J Hum Genet. 1998. PMID: 9758595 Free PMC article.

6

Allelic variation in ABCR associated with Stargardt disease but not age-related macular degeneration.

Stone EM, Webster AR, Vandenburgh K, Streb LM, Hockey RR, Lotery AJ, Sheffield VC. Stone EM, et al. Among authors: webster ar. Nat Genet. 1998 Dec;20(4):328-9. doi: 10.1038/3798. Nat Genet. 1998. PMID: 9843201 No abstract available.

7

A clinical and molecular genetic analysis of solitary ocular angioma.

Webster AR, Maher ER, Bird AC, Gregor ZJ, Moore AT. Webster AR, et al. Ophthalmology. 1999 Mar;106(3):623-9. doi: 10.1016/S0161-6420(99)90127-6. Ophthalmology. 1999. PMID: 10080225

8

Clinical characteristics of ocular angiomatosis in von Hippel-Lindau disease and correlation with germline mutation.

Webster AR, Maher ER, Moore AT. Webster AR, et al. Arch Ophthalmol. 1999 Mar;117(3):371-8. doi: 10.1001/archopht.117.3.371. Arch Ophthalmol. 1999. PMID: 10088816

9

Mutations in the CACNA1F and NYX genes in British CSNBX families.

Zito I, Allen LE, Patel RJ, Meindl A, Bradshaw K, Yates JR, Bird AC, Erskine L, Cheetham ME, Webster AR, Poopalasundaram S, Moore AT, Trump D, Hardcastle AJ. Zito I, et al. Among authors: webster ar. Hum Mutat. 2003 Feb;21(2):169. doi: 10.1002/humu.9106. Hum Mutat. 2003. PMID: 12552565

10

Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) families.

Ebenezer ND, Michaelides M, Jenkins SA, Audo I, Webster AR, Cheetham ME, Stockman A, Maher ER, Ainsworth JR, Yates JR, Bradshaw K, Holder GE, Moore AT, Hardcastle AJ. Ebenezer ND, et al. Among authors: webster ar. Invest Ophthalmol Vis Sci. 2005 Jun;46(6):1891-8. doi: 10.1167/iovs.04-1482. Invest Ophthalmol Vis Sci. 2005. PMID: 15914600

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