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Anthony Robson

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Kaoru Fujinami; Chris R Hogg; Graham E Holder; Noemi Lois; Mackay Donna; Anthony T Moore; Anthony G Robson; Edwin M Stone; Kazuo Tsubota; Kazushige Tsunoda; Andrew R Webster; Catey Bunce; Alice E Davidson; Michel Michaelides
A longitudinal study of stargardt disease: clinical and electrophysiologic assessment, progression, and genotype correlations.
Vasileios Soumplis; Graham E Holder; Michel Michaelides; Anthony T Moore; Anthony G Robson; Panagiotis I Sergouniotis; Andrew R Webster
Phenotypic findings in C1QTNF5 retinopathy (late-onset retinal degeneration).
Alice Davidson; Graham E Holder; Mackay Donna; Michel Michaelides; Anthony T Moore; Vincent Plagnol; Anthony G Robson; Panagiotis I Sergouniotis; Naushin Waseem; Genevieve A Wright; Andrew R Webster
RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa and occult macular dystrophy.

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2013: Kaoru Fujinami; Chris R Hogg; Graham E Holder; Noemi Lois; Mackay Donna; Anthony T Moore; Anthony G Robson; Edwin M Stone; Kazuo Tsubota; Kazushige Tsunoda; Andrew R Webster; Catey Bunce; Alice E Davidson; Michel Michaelides
A longitudinal study of stargardt disease: clinical and electrophysiologic assessment, progression, and genotype correlations.
American journal of ophthalmology 2013;155(6):1075-1088.e13.
2013: Vasileios Soumplis; Graham E Holder; Michel Michaelides; Anthony T Moore; Anthony G Robson; Panagiotis I Sergouniotis; Andrew R Webster
Phenotypic findings in C1QTNF5 retinopathy (late-onset retinal degeneration).
Acta ophthalmologica 2013;91(3):e191-5.
2013: Alice Davidson; Graham E Holder; Mackay Donna; Michel Michaelides; Anthony T Moore; Vincent Plagnol; Anthony G Robson; Panagiotis I Sergouniotis; Naushin Waseem; Genevieve A Wright; Andrew R Webster
RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa and occult macular dystrophy.
Human mutation 2013;34(3):506-14.
2012: Anthony G Robson; Janus J Kulikowski
Objective assessment of chromatic and achromatic pattern adaptation reveals the temporal response properties of different visual pathways.
Visual neuroscience 2012;29(6):301-13.
2012: Bita Manzouri; Anthony G Robson; Panagiotis I Sergouniotis; Andrew R Webster; Anthony Moore
Bietti crystalline retinopathy: report of retinal crystal deposition in male adolescent siblings.
Archives of ophthalmology 2012;130(11):1470-3.
2012: Simona Degli Esposti; Alan C Bird; Catey Bunce; Catherine Egan; Jack D Moreland; Anthony G Robson
Macular pigment parameters in patients with macular telangiectasia (MacTel) and normal subjects: implications of a novel analysis.
Investigative ophthalmology & visual science 2012;53(10):6568-75.
2012: Arundhati Dev Borman; Fred Fitzke; Georgina Hall; Robert H Henderson; Graham E Holder; Mackay Donna; Phillip Moradi; Louise A Ocaka; Caterina Ripamonti; Anthony G Robson; Andrew Stockman; Andrew R Webster; Graeme C Black; Anthony T Moore
Early onset retinal dystrophy due to mutations in LRAT: molecular analysis and detailed phenotypic study.
Investigative ophthalmology & visual science 2012;53(7):3927-38.
2012: M H Tan; H V Tran; Olivier M Vanakker; Anthony G Robson; R Groves; Graham Holder; J E Lai-Cheong; A T Moore
Angioid streaks with severe macular dysfunction and generalised retinal involvement due to a homozygous duplication in the ABCC6 gene.
Eye (London, England) 2012;26(5):753-5.
2012: Mala Subash; Adnan Tufail; Andrew R Webster; Genevieve A Wright; Anthony T Moore; Bishwanath Pal; Anthony G Robson; Tryfonas Rotsos; Sophie Devery; Graham E Holder; Michel Michaelides
Unilateral vitelliform maculopathy: a comprehensive phenotype study with molecular screening of BEST1 and PRPH2.
The British journal of ophthalmology 2012;96(5):719-22.
2012: Panagiotis I Sergouniotis; Sophie Devery; Graham E Holder; Zheng Li; Anthony T Moore; Anthony G Robson; Andrew R Webster
A phenotypic study of congenital stationary night blindness (CSNB) associated with mutations in the GRM6 gene.
Acta ophthalmologica 2012;90(3):e192-7.
2012: Eva Lenassi; Anthony G Robson; Marko Hawlina; Graham E Holder
The value of two-field pattern electroretinogram in routine clinical electrophysiologic practice.
Retina (Philadelphia, Pa.) 2012;32(3):588-99.
2012: Tom R Webb; Seyhan Yazar; Mahinda Yogarajah; Wei Ang; Tin Aung; Michael E Cheetham; Jessica C Gardner; Hala Hassan; Graham E Holder; Daniel Kelberman; Chiea C Khor; David A Mackey; Mar Matarin; Michel Michaelides; Anthony T Moore; Craig E Pennell; Anthony G Robson; Jonathan B Ruddle; Sanjay M Sisodiya; Jane C Sowden; Elias I Traboulsi; Stephen J Tuft; Alison J Hardcastle
X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment development.
American journal of human genetics 2012;90(2):247-59.
2012: Panagiotis I Sergouniotis; Andrew R Webster; Graham E Holder; Michel Michaelides; Anthony G Robson; Anthony T Moore
High-resolution optical coherence tomography imaging in KCNV2 retinopathy.
The British journal of ophthalmology 2012;96(2):213-7.
2012: Anthony G Robson; Zubin Saihan; Frederick W Fitzke; Graham Holder; Eva Lenassi; Vy Luong; Andrew R Webster
Comparison of fundus autofluorescence with photopic and scotopic fine matrix mapping in patients with retinitis pigmentosa: 4- to 8-year follow-up.
Investigative ophthalmology & visual science 2012;53(10):6187-95.
2012: Mei Hong Tan; Dorothy A Thompson; Hoai Viet Tran; Andrew R Webster; Genevieve A Wright; Phillip Moradi; Anthony G Robson; Isabelle Russell-Eggitt; Alexander J Smith; Robin R Ali; Michael Cheetham; Jill Cowing; Arundhati Dev-Borman; Robert H Henderson; Mackay Donna; Robert E MacLaren; Michel Michaelides; Anthony T Moore
Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapy.
PloS one 2012;7(3):e32330.
2011: Magella M Neveu; Anthony G Robson; Ricardo Uauy; Elizabeth Allen; Alan C Bird; Alan Dangour; Graham E Holder
Electroretinogram measures in a septuagenarian population.
Documenta ophthalmologica. Advances in ophthalmology 2011;123(2):75-81.
2011: Zubin Saihan; Polona Le Quesne Stabej; Karen P Steel; Maria Bitner-Glindzicz; Graham E Holder; Linda M Luxon; Nell Rangesh; Anthony G Robson; Anthony T Moore; Andrew R Webster
Mutations in the USH1C gene associated with sector retinitis pigmentosa and hearing loss.
Retina (Philadelphia, Pa.) 2011;31(8):1708-16.
2011: Anthony G Robson; Adnan Tufail; Alan C Bird; Fred Fitzke; Graham E Holder; Anthony T Moore; Andrew R Webster
Serial imaging and structure-function correlates of high-density rings of fundus autofluorescence in retinitis pigmentosa.
Retina (Philadelphia, Pa.) 2011;31(8):1670-9.
2011: Arundhati Dev Borman; Alice E Davidson; Elfride De Baere; Graham Holder; Bart P Leroy; Forbes D C Manson; James O'Sullivan; Anthony G Robson; Dorothy A Thompson; Andrew R Webster; Graeme C M Black; Anthony T Moore
Childhood-onset autosomal recessive bestrophinopathy.
Archives of ophthalmology 2011;129(8):1088-93.
2011: Panagiotis I Sergouniotis; Elliott H Sohn; Genevieve A Wright; Graham Holder; Zheng Li; Vikki A McBain; Anthony T Moore; Anthony G Robson; Andrew R Webster
Phenotypic variability in RDH5 retinopathy (Fundus Albipunctatus).
Ophthalmology 2011;118(8):1661-70.
2011: P I Sergouniotis; Andrew R Webster; Alice Davidson; Anthony G Robson; K Sehmi; Anthony T Moore
Mizuo-Nakamura phenomenon in Oguchi disease due to a homozygous nonsense mutation in the SAG gene.
Eye (London, England) 2011;25(8):1098-101.
2011: Robert H Henderson; Mackay Donna; Zheng Li; Phillip Moradi; Panagiotis Sergouniotis; Isabelle Russell-Eggitt; Dorothy A Thompson; Anthony G Robson; Graham E Holder; Andrew R Webster; Anthony T Moore
Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.
The British journal of ophthalmology 2011;95(6):811-7.
2011: Mackay Donna; Louise A Ocaka; Arundhati Dev Borman; Panagiotis I Sergouniotis; Robert H Henderson; Phillip Moradi; Anthony G Robson; Dorothy A Thompson; Andrew R Webster; Anthony T Moore
Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutations.
Investigative ophthalmology & visual science 2011;52(6):3032-8.
2010: Alexander C Day; Tryfon Rotsos; Graham E Holder; Adnan Tufail; Anthony G Robson
Electrodiagnostic and two-wavelength fundus autofluorescence imaging investigations in acute idiopathic maculopathy.
Documenta ophthalmologica. Advances in ophthalmology 2010;121(2):155-60.
2010: John L Barbur; E Konstantakopoulou; Marisa Rodriguez-Carmona; J Alister Harlow; Anthony G Robson; Jack D Moreland
The Macular Assessment Profile test - a new VDU-based technique for measuring the spatial distribution of the macular pigment, lens density and rapid flicker sensitivity.
Ophthalmic & physiological optics : the journal of the British College of Ophthalmic Opticians (Optometrists) 2010;30(5):470-83.
2010: Jessica C Gardner; Tom R Webb; Naheed Kanuga; Anthony G Robson; Graham Holder; Andrew Stockman; Caterina Ripamonti; Neil D Ebenezer; Olufunmilola Ogun; Sophie Devery; Genevieve A Wright; Eamonn R Maher; Michael Cheetham; Anthony T Moore; Michel Michaelides; Alison J Hardcastle
X-linked cone dystrophy caused by mutation of the red and green cone opsins.
American journal of human genetics 2010;87(1):26-39.
2010: Rajarshi Mukhopadhyay; Panagiotis I Sergouniotis; Mackay Donna; Alexander C Day; Genevieve Wright; Sophie Devery; Bart P Leroy; Anthony G Robson; Graham E Holder; Zheng Li; Andrew R Webster
A detailed phenotypic assessment of individuals affected by MFRP-related oculopathy.
Molecular vision 2010;16():540-8.
2010: Anthony G Robson; Andrew R Webster; Michel Michaelides; Susan M Downes; Jill A Cowing; David Hunt; Anthony T Moore; Graham E Holder
"Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiology.
Retina (Philadelphia, Pa.) 2010;30(1):51-62.
2009: Zheng Li; Panagiotis I Sergouniotis; Michel Michaelides; Mackay Donna; Genevieve A Wright; Sophie Devery; Anthony T Moore; Graham E Holder; Anthony G Robson; Andrew R Webster
Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.
American journal of human genetics 2009;85(5):711-9.
2009: Louisa Wickham; Fred K Chen; Geoffrey P Lewis; Germit S Uppal; Magella Neveu; Genevieve A Wright; Anthony G Robson; Andrew R Webster; Iain Grierson; Paul Hiscott; Peter Coffey; Graham Holder; Steven K Fisher; Lyndon da Cruz
Clinicopathological case series of four patients with inherited macular disease.
Investigative ophthalmology & visual science 2009;50(8):3553-61.
2009: Graham Holder; Richard P Gale; James F Acheson; Anthony G Robson
Electrodiagnostic assessment in optic nerve disease.
Current opinion in neurology 2009;22(1):3-10.
2008: Phillip Moradi; Anthony G Robson; Geoffrey E Rose; Graham Holder
Electrophysiological monitoring in a patient with an optic nerve glioma.
Documenta ophthalmologica. Advances in ophthalmology 2008;117(2):171-4.
2008: Anthony G Robson; Neil R A Parry
Measurement of macular pigment optical density and distribution using the steady-state visual evoked potential.
Visual neuroscience 2008;25(4):575-83.
2008: Isabelle Audo; Michel Michaelides; Anthony G Robson; Marko Hawlina; Veronika Vaclavik; Jennifer M Sandbach; Magella Neveu; Chris R Hogg; David Hunt; Anthony T Moore; Alan C Bird; Andrew R Webster; Graham Holder
Phenotypic variation in enhanced S-cone syndrome.
Investigative ophthalmology & visual science 2008;49(5):2082-93.
2008: Anthony G Robson; Michel Michaelides; Zubin Saihan; Alan C Bird; Andrew R Webster; Anthony T Moore; Frederick W Fitzke; Graham Holder
Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update.
Documenta ophthalmologica. Advances in ophthalmology 2008;116(2):79-89.
2008: Veronika Vaclavik; Christina F Chakarova; Shomi S Bhattacharya; Anthony G Robson; Graham Holder; Alan C Bird; Andrew R Webster
Bilateral giant macular schisis in a patient with enhanced S-cone syndrome from a family showing pseudo-dominant inheritance.
The British journal of ophthalmology 2008;92(2):299-300.
2008: Sobha Sivaprasad; Boom Ting Kung; Anthony G Robson; Graeme Black; Andrew R Webster; Alan Bird; Catherine Egan
A new phenotype of macular dystrophy associated with a mitochondrial A3243G mutation.
Clinical & experimental ophthalmology 2008;36(1):92-3.
2008: Isabelle Audo; Anthony G Robson; Graham Holder; Anthony T Moore
The negative ERG: clinical phenotypes and disease mechanisms of inner retinal dysfunction.
Survey of ophthalmology 2008;53(1):16-40.
2008: Rosemary Burgess; Ian D Millar; Bart P Leroy; Jill E Urquhart; Ian M Fearon; Elfride De Baere; Peter D Brown; Anthony G Robson; Genevieve A Wright; Philippe Kestelyn; Graham Holder; Andrew R Webster; Forbes D C Manson; Graeme C M Black
Biallelic mutation of BEST1 causes a distinct retinopathy in humans.
American journal of human genetics 2008;82(1):19-31.
2008: Anthony G Robson; Michel Michaelides; Vy Luong; Graham Holder; Alan C Bird; Andrew R Webster; Anthony T Moore; Frederick W Fitzke
Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone rod dystrophy.
The British journal of ophthalmology 2008;92(1):95-102.
2007: Isabelle Audo; Olivier M Vanakker; Alaric Smith; Bart P Leroy; Anthony G Robson; Sharon A Jenkins; Paul J Coucke; Alan C Bird; Anne De Paepe; Graham Holder; Andrew R Webster
Pseudoxanthoma elasticum with generalized retinal dysfunction, a common finding?
Investigative ophthalmology & visual science 2007;48(9):4250-6.
2007: Vikki A McBain; Anthony G Robson; Chris R Hogg; Graham Holder
Assessment of patients with suspected non-organic visual loss using pattern appearance visual evoked potentials.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 2007;245(4):502-10.
2007: Wolfgang Schalch; William Cohn; Felix M Barker; Wolfgang Köpcke; John Mellerio; Alan C Bird; Anthony G Robson; Fred F Fitzke; Frederik J G M van Kuijk
Xanthophyll accumulation in the human retina during supplementation with lutein or zeaxanthin - the LUXEA (LUtein Xanthophyll Eye Accumulation) study.
Archives of biochemistry and biophysics 2007;458(2):128-35.
2007: Veronika Vaclavik; Kenneth G-J Ooi; Alan C Bird; Anthony G Robson; Graham Holder; Andrew R Webster
Autofluorescence findings in acute exudative polymorphous vitelliform maculopathy.
Archives of ophthalmology 2007;125(2):274-7.
2007: Stephen H Tsang; Veronika Vaclavik; Alan C Bird; Anthony G Robson; Graham Holder
Novel phenotypic and genotypic findings in X-linked retinoschisis.
Archives of ophthalmology 2007;125(2):259-67.
2007: Andrew Scott; Nicholas G Strouthidis; Anthony G Robson; Joan Forsyth; Eamonn R Maher; Patricio Schlottmann; Michel Michaelides
Bilateral epiretinal membranes in Gorlin syndrome associated with a novel PTCH mutation.
American journal of ophthalmology 2007;143(2):346-8.
2006: Huimin Wu; Jill A Cowing; Michel Michaelides; Susan E Wilkie; Glen Jeffery; Sharon A Jenkins; Viktoria Mester; Alan C Bird; Anthony G Robson; Graham Holder; Anthony T Moore; David Hunt; Andrew R Webster
Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans.
American journal of human genetics 2006;79(3):574-9.
2006: Anthony G Robson; Zubin Saihan; Sharon A Jenkins; Frederick W Fitzke; Alan C Bird; Andrew R Webster; Graham Holder
Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity.
The British journal of ophthalmology 2006;90(4):472-9.
2006: Anthony G Robson; Graham Holder; Jack D Moreland; Janus J Kulikowski
Chromatic VEP assessment of human macular pigment: comparison with minimum motion and minimum flicker profiles.
Visual neuroscience 2006;23(2):275-83.
2005: Anthony G Robson; E C Richardson; A H C Koh; Carlos Pavesio; Phillip G Hykin; A Calcagni; E M Graham; Graham Holder
Unilateral electronegative ERG of non-vascular aetiology.
The British journal of ophthalmology 2005;89(12):1620-6.
2005: Graham Holder; Anthony G Robson; Carlos Pavesio; E M Graham
Electrophysiological characterisation and monitoring in the management of birdshot chorioretinopathy.
The British journal of ophthalmology 2005;89(6):709-18.
2005: Anthony G Robson; Glen Harding; Frederik J G M van Kuijk; Daniel Pauleikhoff; Graham Holder; Alan C Bird; Frederick W Fitzke; Jack D Moreland
Comparison of fundus autofluorescence and minimum-motion measurements of macular pigment distribution profiles derived from identical retinal areas.
Perception 2005;34(8):1029-34.
2004: Anthony G Robson; Catherine A Egan; Vy Luong; Alan C Bird; Graham Holder; Frederick W Fitzke
Comparison of fundus autofluorescence with photopic and scotopic fine-matrix mapping in patients with retinitis pigmentosa and normal visual acuity.
Investigative ophthalmology & visual science 2004;45(11):4119-25.
2004: Hendrik P N Scholl; N H Victor Chong; Anthony G Robson; Graham Holder; Anthony T Moore; Alan C Bird
Fundus autofluorescence in patients with leber congenital amaurosis.
Investigative ophthalmology & visual science 2004;45(8):2747-52.
2003: Anthony G Robson; Ahmed El-Amir; Claire Bailey; Catherine A Egan; Frederick W Fitzke; Andrew R Webster; Alan C Bird; Graham Holder
Pattern ERG correlates of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity.
Investigative ophthalmology & visual science 2003;44(8):3544-50.
2003: Anthony G Robson; Jack D Moreland; Daniel Pauleikhoff; Tony Morrissey; Graham Holder; Frederick W Fitzke; Alan C Bird; Frederik J G M van Kuijk
Macular pigment density and distribution: comparison of fundus autofluorescence with minimum motion photometry.
Vision research 2003;43(16):1765-75.
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.
2003: Anthony G Robson; Catherine Egan; Graham Holder; Alan C Bird; Frederick W Fitzke
Comparing rod and cone function with fundus autofluorescence images in retinitis pigmentosa.
Advances in experimental medicine and biology 2003;533():41-7.
2003: Graham Holder; Anthony G Robson; Chris R Hogg; Malaika M Kurz-Levin; Noemi Lois; Alan C Bird
Pattern ERG: clinical overview, and some observations on associated fundus autofluorescence imaging in inherited maculopathy.
Documenta ophthalmologica. Advances in ophthalmology 2003;106(1):17-23.
2002: Janus J Kulikowski; Anthony G Robson; Ian J Murray
Scalp VEPs and intra-cortical responses to chromatic and achromatic stimuli in primates.
Documenta ophthalmologica. Advances in ophthalmology 2002;105(2):243-79.
1998: Anthony G Robson; Janus J Kulikowski
Objective specification of tritanopic confusion lines using visual evoked potentials.
Vision research 1998;38(21):3499-503.
1998: Jack D Moreland; Anthony G Robson; N Soto-Leon; Janus J Kulikowski
Macular pigment and the colour-specificity of visual evoked potentials.
Vision research 1998;38(21):3241-5.
1997: Janus J Kulikowski; Declan J McKeefry; Anthony G Robson
Selective stimulation of colour mechanisms: an empirical perspective.
Spatial vision 1997;10(4):379-402.
1996: Janus J Kulikowski; Anthony G Robson; Declan J McKeefry
Specificity and selectivity of chromatic visual evoked potentials.
Vision research 1996;36(21):3397-401.