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Andrew Webster
Andrew Webster
UCL Institute of Ophthalmology
Verified email at ucl.ac.uk
Title
Cited by
Cited by
Year
Retinal gene therapy in patients with choroideremia: initial findings from a phase 1/2 clinical trial
RE MacLaren, M Groppe, AR Barnard, CL Cottriall, T Tolmachova, ...
The Lancet 383 (9923), 1129-1137, 2014
8712014
Seven new loci associated with age-related macular degeneration
Nature genetics 45 (4), 433-439, 2013
8532013
Germline mutations in the Von Hippel‐Lindau disease (VHL) gene in families from North America, Europe, and Japan
B Zbar, T Kishida, F Chen, L Schmidt, ER Maher, FM Richards, ...
Human mutation 8 (4), 348-357, 1996
6151996
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
4052017
Whole-genome sequencing of patients with rare diseases in a national health system
E Turro, WJ Astle, K Megy, S Gräf, D Greene, O Shamardina, HL Allen, ...
Nature 583 (7814), 96-102, 2020
3862020
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
3592021
Genetic influence on early age-related maculopathy: a twin study
CJ Hammond, AR Webster, H Snieder, AC Bird, CE Gilbert, TD Spector
Ophthalmology 109 (4), 730-736, 2002
3372002
Biallelic mutation of BEST1 causes a distinct retinopathy in humans
R Burgess, ID Millar, BP Leroy, JE Urquhart, IM Fearon, E De Baere, ...
The American Journal of Human Genetics 82 (1), 19-31, 2008
3172008
Mutations in HPRP3, a third member ofpre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa
CF Chakarova, MM Hims, H Bolz, L Abu-Safieh, RJ Patel, ...
Human molecular genetics 11 (1), 87-92, 2002
3052002
Somatic inactivation of the VHL gene in Von Hippel-Lindau disease tumors.
AH Prowse, AR Webster, FM Richards, S Richard, S Olschwang, ...
American journal of human genetics 60 (4), 765, 1997
2881997
Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations.
ER Maher, AR Webster, FM Richards, JS Green, PA Crossey, SJ Payne, ...
Journal of Medical Genetics 33 (4), 328-332, 1996
2761996
Clinical characteristics of ocular angiomatosis in von Hippel-Lindau disease and correlation with germline mutation
AR Webster, ER Maher, AT Moore
Archives of Ophthalmology 117 (3), 371-378, 1999
2731999
An analysis of allelic variation in the ABCA4 gene
AR Webster, E Héon, AJ Lotery, K Vandenburgh, TL Casavant, KT Oh, ...
Investigative ophthalmology & visual science 42 (6), 1179-1189, 2001
2582001
An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes
G Wheway, M Schmidts, DA Mans, K Szymanska, TMT Nguyen, H Racher, ...
Nature cell biology 17 (8), 1074-1087, 2015
2442015
Allelic variation in ABCR associated with Stargardt disease but not age-related macular degeneration
AR Webster, K Vandenburgh, LM Streb, RR Hockey, AJ Lotery, ...
Nature genetics 20 (4), 328-329, 1998
2431998
Visual acuity after retinal gene therapy for choroideremia
TL Edwards, JK Jolly, M Groppe, AR Barnard, CL Cottriall, T Tolmachova, ...
New England Journal of Medicine 374 (20), 1996-1998, 2016
2232016
NMNAT1 mutations cause Leber congenital amaurosis
MJ Falk, Q Zhang, E Nakamaru-Ogiso, C Kannabiran, Z Fonseca-Kelly, ...
Nature genetics 44 (9), 1040-1045, 2012
2142012
Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia
S Kohl, D Zobor, WC Chiang, N Weisschuh, J Staller, IG Menendez, ...
Nature genetics 47 (7), 757-765, 2015
2132015
Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans
Z Li, PI Sergouniotis, M Michaelides, DS Mackay, GA Wright, S Devery, ...
The American Journal of Human Genetics 85 (5), 711-719, 2009
2112009
Comprehensive sequence analysis of nine Usher syndrome genes in the UK National Collaborative Usher Study
PLQ Stabej, Z Saihan, N Rangesh, HB Steele-Stallard, J Ambrose, ...
Journal of medical genetics 49 (1), 27-36, 2012
1902012
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