Follow
Anthony Moore
Anthony Moore
UCL Institute of Ophthalmology
Verified email at ucsf.edu
Title
Cited by
Cited by
Year
Effect of gene therapy on visual function in Leber's congenital amaurosis
JWB Bainbridge, AJ Smith, SS Barker, S Robbie, R Henderson, ...
New England Journal of Medicine 358 (21), 2231-2239, 2008
24022008
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
C Alexander, M Votruba, UEA Pesch, DL Thiselton, S Mayer, A Moore, ...
Nature genetics 26 (2), 211-215, 2000
15672000
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
LG Fritsche, W Igl, JNC Bailey, F Grassmann, S Sengupta, ...
Nature genetics 48 (2), 134-143, 2016
14252016
Clinical features and natural history of von Hippel-Lindau disease
ER Maher, JRW Yates, R Harries, C Benjamin, R Harris, AT Moore, ...
QJM: An International Journal of Medicine 77 (2), 1151-1163, 1990
11441990
Complement C3 variant and the risk of age-related macular degeneration
JRW Yates, T Sepp, BK Matharu, JC Khan, DA Thurlby, H Shahid, ...
New England Journal of Medicine 357 (6), 553-561, 2007
11192007
Seven new loci associated with age-related macular degeneration
Nature genetics 45 (4), 433-439, 2013
8582013
Long-term effect of gene therapy on Leber’s congenital amaurosis
JWB Bainbridge, MS Mehat, V Sundaram, SJ Robbie, SE Barker, ...
New England Journal of Medicine 372 (20), 1887-1897, 2015
7972015
Smoking and age related macular degeneration: the number of pack years of cigarette smoking is a major determinant of risk for both geographic atrophy and choroidal …
JC Khan, DA Thurlby, H Shahid, DG Clayton, JRW Yates, M Bradley, ...
British Journal of Ophthalmology 90 (1), 75-80, 2006
4712006
Comprehensive rare variant analysis via whole-genome sequencing to determine the molecular pathology of inherited retinal disease
KJ Carss, G Arno, M Erwood, J Stephens, A Sanchis-Juan, S Hull, K Megy, ...
The American Journal of Human Genetics 100 (1), 75-90, 2017
4162017
A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant “zonular pulverulent” cataract, on chromosome 1q
A Shiels, D Mackay, A Ionides, V Berry, A Moore, S Bhattacharya
The American Journal of Human Genetics 62 (3), 526-532, 1998
4141998
A human homolog of yeast pre-mRNA splicing gene, PRP31, underlies autosomal dominant retinitis pigmentosa on chromosome 19q13. 4 (RP11)
EN Vithana, L Abu-Safieh, MJ Allen, A Carey, M Papaioannou, ...
Molecular cell 8 (2), 375-381, 2001
4052001
100,000 genomes pilot on rare-disease diagnosis in health care—preliminary report
100,000 Genomes Project Pilot Investigators
New England Journal of Medicine 385 (20), 1868-1880, 2021
3782021
Missense mutations in MIP underlie autosomal dominant ‘polymorphic’and lamellar cataracts linked to 12q
V Berry, P Francis, S Kaushal, A Moore, S Bhattacharya
Nature genetics 25 (1), 15-17, 2000
3562000
Connexin46 mutations in autosomal dominant congenital cataract
D Mackay, A Ionides, Z Kibar, G Rouleau, V Berry, A Moore, A Shiels, ...
The American Journal of Human Genetics 64 (5), 1357-1364, 1999
3441999
Reviews of evidence regarding interventions to reduce tobacco use and exposure to environmental tobacco smoke
DP Hopkins, PA Briss, CJ Ricard, CG Husten, VG Carande-Kulis, ...
American journal of preventive medicine 20 (2), 16-66, 2001
3352001
Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans
V Berry, P Francis, MA Reddy, D Collyer, E Vithana, I MacKay, G Dawson, ...
The American Journal of Human Genetics 69 (5), 1141-1145, 2001
3242001
Identification and correction of mechanisms underlying inherited blindness in human iPSC-derived optic cups
DA Parfitt, A Lane, CM Ramsden, AJF Carr, PM Munro, K Jovanovic, ...
Cell stem cell 18 (6), 769-781, 2016
3182016
Two infant vision screening programmes: prediction and prevention of strabismus and amblyopia from photo-and videorefractive screening
J Atkinson, O Braddick, B Bobier, S Anker, D Ehrlich, J King, P Watson, ...
Eye 10 (2), 189-198, 1996
3161996
Molecular genetic basis of inherited cataract and associated phenotypes
MA Reddy, PJ Francis, V Berry, SS Bhattacharya, AT Moore
Survey of ophthalmology 49 (3), 300-315, 2004
3142004
Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions
N Kumaran, AT Moore, RG Weleber, M Michaelides
British journal of ophthalmology 101 (9), 1147-1154, 2017
3092017
The system can't perform the operation now. Try again later.
Articles 1–20