Moore AT - Search Results

1

Clinical features, molecular genetics, and pathophysiology of dominant optic atrophy.

Votruba M, Moore AT, Bhattacharya SS. Votruba M, et al. Among authors: moore at. J Med Genet. 1998 Oct;35(10):793-800. doi: 10.1136/jmg.35.10.793. J Med Genet. 1998. PMID: 9783700 Free PMC article. Review.

2

Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19.

al-Maghtheh M, Inglehearn CF, Keen TJ, Evans K, Moore AT, Jay M, Bird AC, Bhattacharya SS. al-Maghtheh M, et al. Among authors: moore at. Hum Mol Genet. 1994 Feb;3(2):351-4. doi: 10.1093/hmg/3.2.351. Hum Mol Genet. 1994. PMID: 8004108

3

Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic study.

Moore AT, Fitzke F, Jay M, Arden GB, Inglehearn CF, Keen TJ, Bhattacharya SS, Bird AC. Moore AT, et al. Br J Ophthalmol. 1993 Aug;77(8):473-9. doi: 10.1136/bjo.77.8.473. Br J Ophthalmol. 1993. PMID: 8025041 Free PMC article.

4

Further refinement of the location for autosomal dominant retinitis pigmentosa on chromosome 7p (RP9).

Inglehearn CF, Keen TJ, al-Maghtheh M, Gregory CY, Jay MR, Moore AT, Bird AC, Bhattacharya SS. Inglehearn CF, et al. Among authors: moore at. Am J Hum Genet. 1994 Apr;54(4):675-80. Am J Hum Genet. 1994. PMID: 8128965 Free PMC article.

5

A locus for autosomal dominant anterior polar cataract on chromosome 17p.

Berry V, Ionides AC, Moore AT, Plant C, Bhattacharya SS, Shiels A. Berry V, et al. Among authors: moore at. Hum Mol Genet. 1996 Mar;5(3):415-9. doi: 10.1093/hmg/5.3.415. Hum Mol Genet. 1996. PMID: 8852669

6

A locus for autosomal dominant posterior polar cataract on chromosome 1p.

Ionides AC, Berry V, Mackay DS, Moore AT, Bhattacharya SS, Shiels A. Ionides AC, et al. Among authors: moore at. Hum Mol Genet. 1997 Jan;6(1):47-51. doi: 10.1093/hmg/6.1.47. Hum Mol Genet. 1997. PMID: 9002669

7

Genetic refinement of dominant optic atrophy (OPA1) locus to within a 2 cM interval of chromosome 3q.

Votruba M, Moore AT, Bhattacharya SS. Votruba M, et al. Among authors: moore at. J Med Genet. 1997 Feb;34(2):117-21. doi: 10.1136/jmg.34.2.117. J Med Genet. 1997. PMID: 9039986 Free PMC article.

8

Demonstration of a founder effect and fine mapping of dominant optic atrophy locus on 3q28-qter by linkage disequilibrium method: a study of 38 British Isles pedigrees.

Votruba M, Moore AT, Bhattacharya SS. Votruba M, et al. Among authors: moore at. Hum Genet. 1998 Jan;102(1):79-86. doi: 10.1007/s004390050657. Hum Genet. 1998. PMID: 9490303

9

Clinical features in affected individuals from 21 pedigrees with dominant optic atrophy.

Votruba M, Fitzke FW, Holder GE, Carter A, Bhattacharya SS, Moore AT. Votruba M, et al. Among authors: moore at. Arch Ophthalmol. 1998 Mar;116(3):351-8. doi: 10.1001/archopht.116.3.351. Arch Ophthalmol. 1998. PMID: 9514489

10

Dominant optic atrophy: exclusion and fine genetic mapping of the candidate gene, HRY.

Votruba M, Payne A, Moore AT, Bhattacharya SS. Votruba M, et al. Among authors: moore at. Mamm Genome. 1998 Oct;9(10):784-7. doi: 10.1007/s003359900867. Mamm Genome. 1998. PMID: 9745030

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