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A Moore

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Vanita Berry; Ziheng Yang; P K F Addison; Peter J Francis; A C W Ionides; G Karan; L Jiang; W Lin; J Hu; R Yang; A Moore; K Zhang; Shomi S Bhattacharya
Recurrent 17 bp duplication in PITX3 is primarily associated with posterior polar cataract (CPP4).
Peter J Francis; Anthony G Robson; Graham Holder; A Moore; P Francis; A Moore; Sundeep Kaushal
Inherited retinal dystrophy and asymmetric axial length.
Vanita Berry; Peter J Francis; M Ashwin Reddy; D Collyer; Eranga N Vithana; Ian Mackay; Gary Dawson; Alisoun Carey; A Moore; Shomi S Bhattacharya; R A Quinlan
Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans.

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All Publications

2004: Vanita Berry; Ziheng Yang; P K F Addison; Peter J Francis; A C W Ionides; G Karan; L Jiang; W Lin; J Hu; R Yang; A Moore; K Zhang; Shomi S Bhattacharya
Recurrent 17 bp duplication in PITX3 is primarily associated with posterior polar cataract (CPP4).
Journal of medical genetics 2004;41(8):e109.
2003: Peter J Francis; Anthony G Robson; Graham Holder; A Moore; P Francis; A Moore; Sundeep Kaushal
Inherited retinal dystrophy and asymmetric axial length.
The British journal of ophthalmology 2003;87(4):503-4.
2001: Vanita Berry; Peter J Francis; M Ashwin Reddy; D Collyer; Eranga N Vithana; Ian Mackay; Gary Dawson; Alisoun Carey; A Moore; Shomi S Bhattacharya; R A Quinlan
Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans.
American journal of human genetics 2001;69(5):1141-5.
2000: Peter J Francis; Vanita Berry; Shomi Bhattacharya; A Moore
Congenital progressive polymorphic cataract caused by a mutation in the major intrinsic protein of the lens, MIP (AQP0).
The British journal of ophthalmology 2000;84(12):1376-9.
2000: Christiane Alexander; Marcela Votruba; Ulrike E A Pesch; Dawn L Thiselton; S Mayer; A Moore; M Rodriguez; Ulrich Kellner; Beate Leo-Kottler; G Auburger; Shomi S Bhattacharya; Bernd Wissinger
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28.
Nature genetics 2000;26(2):211-5.
2000: Peter J Francis; J J Chung; M Yasui; Vanita Berry; A Moore; M Keith Wyatt; Graeme Wistow; Shomi S Bhattacharya; Peter Agre
Functional impairment of lens aquaporin in two families with dominantly inherited cataracts.
Human molecular genetics 2000;9(15):2329-34.
2000: Vanita Berry; Peter J Francis; Sundeep Kaushal; A Moore; Shomi Bhattacharya
Missense mutations in MIP underlie autosomal dominant 'polymorphic' and lamellar cataracts linked to 12q.
Nature genetics 2000;25(1):15-7.
1999: A C W Ionides; Peter J Francis; Vanita Berry; Mackay Donna; Shomi Bhattacharya; Alan Shiels; A Moore
Clinical and genetic heterogeneity in autosomal dominant cataract.
The British journal of ophthalmology 1999;83(7):802-8.
1999: Mackay Donna; A C W Ionides; Z Kibar; G Rouleau; Vanita Berry; A Moore; Alan Shiels; Shomi Bhattacharya
Connexin46 mutations in autosomal dominant congenital cataract.
American journal of human genetics 1999;64(5):1357-64.
1998: Alan Shiels; Mackay Donna; A C W Ionides; Vanita Berry; A Moore; Shomi Bhattacharya
A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome 1q.
American journal of human genetics 1998;62(3):526-32.
1998: A C W Ionides; Vanita Berry; Mackay Donna; Alan Shiels; Shomi Bhattacharya; A Moore
Anterior polar cataract: clinical spectrum and genetic linkage in a single family.
Eye (London, England) 1998;12 ( Pt 2)():224-6.
1997: Mackay Donna; A C W Ionides; Vanita Berry; A Moore; Shomi Bhattacharya; Alan Shiels
A new locus for dominant "zonular pulverulent" cataract, on chromosome 13.
American journal of human genetics 1997;60(6):1474-8.