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Robert H Henderson
Robert H Henderson
Consultant Ophthalmologist, Moorfields Eye Hospital, Great Ormond Street Hospital
Verified email at gosh.nhs.uk - Homepage
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
23812008
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
Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1
RH Henderson, DS Mackay, Z Li, P Moradi, P Sergouniotis, ...
British journal of ophthalmology 95 (6), 811-817, 2011
1282011
Novel mutations in MERTK associated with childhood onset rod-cone dystrophy
DS Mackay, RH Henderson, PI Sergouniotis, Z Li, P Moradi, GE Holder, ...
Molecular vision 16, 369, 2010
1032010
A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunction
RH Henderson, KA Williamson, JS Kennedy, AR Webster, GE Holder, ...
Molecular vision 15, 2442, 2009
962009
The oculome panel test: next-generation sequencing to diagnose a diverse range of genetic developmental eye disorders
A Patel, JD Hayward, V Tailor, R Nyanhete, H Ahlfors, C Gabriel, ...
Ophthalmology 126 (6), 888-907, 2019
822019
A Homozygous Mutation in the TUB Gene Associated with Retinal Dystrophy and Obesity
AD Borman, LR Pearce, DS Mackay, K Nagel‐Wolfrum, AE Davidson, ...
Human mutation 35 (3), 289-293, 2014
812014
RDH12 retinopathy: novel mutations and phenotypic description
DS Mackay, AD Borman, P Moradi, RH Henderson, Z Li, GA Wright, ...
Molecular vision 17, 2706, 2011
802011
An assessment of the apex microarray technology in genotyping patients with Leber congenital amaurosis and early-onset severe retinal dystrophy
RH Henderson, N Waseem, R Searle, J van der Spuy, I Russell-Eggitt, ...
Investigative ophthalmology & visual science 48 (12), 5684-5689, 2007
802007
Wound‐related complications and clinical outcomes following open globe injury repair
GYX Kong, RH Henderson, SS Sandhu, RW Essex, PJ Allen, ...
Clinical & experimental ophthalmology 43 (6), 508-513, 2015
662015
Biallelic mutation of protocadherin-21 (PCDH21) causes retinal degeneration in humans
RH Henderson, Z Li, MM Abd El Aziz, DS Mackay, MA Eljinini, M Zeidan, ...
Molecular vision 16, 46, 2010
642010
Comprehensive cancer-predisposition gene testing in an adult multiple primary tumor series shows a broad range of deleterious variants and atypical tumor phenotypes
J Whitworth, PS Smith, JE Martin, H West, A Luchetti, F Rodger, G Clark, ...
The American Journal of Human Genetics 103 (1), 3-18, 2018
602018
Bi-allelic loss-of-function CACNA1B mutations in progressive epilepsy-dyskinesia
KM Gorman, E Meyer, D Grozeva, E Spinelli, A McTague, A Sanchis-Juan, ...
The American Journal of Human Genetics 104 (5), 948-956, 2019
582019
Early onset retinal dystrophy due to mutations in LRAT: molecular analysis and detailed phenotypic study
AD Borman, LA Ocaka, DS Mackay, C Ripamonti, RH Henderson, ...
Investigative ophthalmology & visual science 53 (7), 3927-3938, 2012
512012
Visual impairment, severe visual impairment, and blindness in children in Britain (BCVIS2): a national observational study
LJ Teoh, AL Solebo, JS Rahi, J Abbott, W Abdullah, G Adams, L Allen, ...
The Lancet Child & Adolescent Health 5 (3), 190-200, 2021
482021
Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutations
DS Mackay, LA Ocaka, AD Borman, PI Sergouniotis, RH Henderson, ...
Investigative ophthalmology & visual science 52 (6), 3032-3038, 2011
442011
Immediate sequential bilateral pediatric vitreoretinal surgery: an international multicenter study
Y Yonekawa, WC Wu, S Kusaka, J Robinson, D Tsujioka, KB Kang, ...
Ophthalmology 123 (8), 1802-1808, 2016
422016
De novo truncating mutations in WASF1 cause intellectual disability with seizures
Y Ito, KJ Carss, ST Duarte, T Hartley, B Keren, MA Kurian, I Marey, ...
The American Journal of Human Genetics 103 (1), 144-153, 2018
362018
Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapy
MH Tan, DS Mackay, J Cowing, HV Tran, AJ Smith, GA Wright, ...
PloS one 7 (3), e32330, 2012
362012
Biallelic mutation of ARHGEF18, involved in the determination of epithelial apicobasal polarity, causes adult-onset retinal degeneration
G Arno, KJ Carss, S Hull, C Zihni, AG Robson, A Fiorentino, G Black, ...
The American Journal of Human Genetics 100 (2), 334-342, 2017
302017
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