Annette Payne
Title
Cited by
Cited by
Year
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)
AI den Hollander, B Jacoline, YJM de Kok, S van Soest, LI van den Born, ...
Nature genetics 23 (2), 217-221, 1999
4781999
Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis
MM Sohocki, SJ Bowne, LS Sullivan, S Blackshaw, CL Cepko, AM Payne, ...
Nature genetics 24 (1), 79-83, 2000
3002000
A mutation in NRL is associated with autosomal dominant retinitis pigmentosa
DAR Bessant, AM Payne, KP Mitton, QL Wang, PK Swain, C Plant, ...
Nature genetics 21 (4), 355-356, 1999
2421999
Mutations in the retinal guanylate cyclase (RETGC-1) gene in dominant cone-rod dystrophy
RE Kelsell, K Gregory-Evans, AM Payne, I Perrault, J Kaplan, RB Yang, ...
Human molecular genetics 7 (7), 1179-1184, 1998
2371998
A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21. 1
AM Payne, SM Downes, DAR Bessant, R Taylor, GE Holder, MJ Warren, ...
Human molecular genetics 7 (2), 273-277, 1998
2301998
Prevalence of AIPL1 mutations in inherited retinal degenerative disease
MM Sohocki, I Perrault, BP Leroy, AM Payne, S Dharmaraj, ...
Molecular genetics and metabolism 70 (2), 142-150, 2000
1842000
Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma
OJ Lehmann, ND Ebenezer, T Jordan, M Fox, L Ocaka, A Payne, ...
The American Journal of Human Genetics 67 (5), 1129-1135, 2000
1522000
GCAP1 (Y99C) mutant is constitutively active in autosomal dominant cone dystrophy
I Sokal, N Li, I Surgucheva, MJ Warren, AM Payne, SS Bhattacharya, ...
Molecular cell 2 (1), 129-133, 1998
1361998
The phenotype of Leber congenital amaurosis in patients with AIPL1 mutations
S Dharmaraj, BP Leroy, MM Sohocki, RK Koenekoop, I Perrault, K Anwar, ...
Archives of ophthalmology 122 (7), 1029-1037, 2004
1092004
Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1
SM Downes, GE Holder, FW Fitzke, AM Payne, MJ Warren, ...
Archives of ophthalmology 119 (1), 96-105, 2001
1092001
Computer simulations improve university instructional laboratories
NJ Gibbons, C Evans, A Payne, K Shah, DK Griffin
Cell Biology Education 3 (4), 263-269, 2004
812004
The Wellcome trust UK–Irish bipolar affective disorder sibling-pair genome screen: first stage report
P Bennett, R Segurado, I Jones, S Bort, F McCandless, D Lambert, ...
Molecular psychiatry 7 (2), 189-200, 2002
782002
Application of combinatorial procedures in the search for serine‐protease‐like activity with focus on the acyl transfer step
H De Muynck, A Madder, N Farcy, PJ De Clercq, MN Pérez‐Payán, ...
Angewandte Chemie International Edition 39 (1), 145-148, 2000
772000
An analysis of ABCR mutations in British patients with recessive retinal dystrophies
M Papaioannou, L Ocaka, D Bessant, N Lois, A Bird, A Payne, ...
Investigative ophthalmology & visual science 41 (1), 16-19, 2000
722000
A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13
A Hameed, S Khaliq, M Ismail, K Anwar, ND Ebenezer, T Jordan, ...
Investigative ophthalmology & visual science 41 (3), 629-633, 2000
712000
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1
SM Downes, AM Payne, RE Kelsell, FW Fitzke, GE Holder, DM Hunt, ...
Archives of ophthalmology 119 (11), 1667-1673, 2001
702001
Filial cannibalism improves survival and development of beaugregory damselfish embryos
AG Payne, C Smith, AC Campbell
Proceedings of the Royal Society of London. Series B: Biological Sciences …, 2002
692002
Clinical Features of Codon 172 RDSMacular Dystrophy: Similar Phenotype in 12 Families
SM Downes, FW Fitzke, GE Holder, AM Payne, DAR Bessant, ...
Archives of Ophthalmology 117 (10), 1373-1383, 1999
661999
Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies
AM Payne, AG Morris, SM Downes, S Johnson, AC Bird, AT Moore, ...
Journal of medical genetics 38 (9), 611-614, 2001
602001
Familial cavernous hemangioma: an expanding ocular spectrum
D Sarraf, AM Payne, ND Kitchen, KS Sehmi, SM Downes, AC Bird
Archives of ophthalmology 118 (7), 969-973, 2000
602000
The system can't perform the operation now. Try again later.
Articles 1–20