Works by Holder, Graham E.

Results: 41

Clinical and Molecular Characterization of Enhanced S-Cone Syndrome in Children.

Published in:

JAMA Ophthalmology, 2014, v. 132, n. 11, p. 1341, doi. 10.1001/jamaophthalmol.2014.2343

By:

Hull, Sarah;
Arno, Gavin;
Sergouniotis, Panagiotis I.;
Tiffin, Peter;
Borman, Arundhati Dev;
Chandra, Aman;
Robson, Anthony G.;
Holder, Graham E.;
Webster, Andrew R.;
Moore, Anthony T.

Publication type:

Article

Expansion of Ocular Phenotypic Features Associated With Mutations in ADAMTS18.

Published in:

JAMA Ophthalmology, 2014, v. 132, n. 8, p. 996, doi. 10.1001/jamaophthalmol.2014.940

By:

Chandra, Aman;
Arno, Gavin;
Williamson, Kathleen;
Sergouniotis, Panagiotis I.;
Preising, Markus N.;
Charteris, David G.;
Thompson, Dorothy A.;
Holder, Graham E.;
Borman, Arundhati Dev;
Davagnanam, Indran;
Webster, Andrew R.;
Lorenz, Birgit;
FitzPatrick, David R.;
Moore, Anthony T.

Publication type:

Article

Inner Retinal Dysfunction in the Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.

Published in:

2017

By:

Borruat, François-Xavier;
Holder, Graham E.;
Bremner, Fion

Publication type:

Case Study

Submacular integration of hESC-RPE monolayer xenografts in a surgical non-human primate model.

Published in:

Stem Cell Research & Therapy, 2021, v. 12, n. 1, p. 1, doi. 10.1186/s13287-021-02395-6

By:

Zengping Liu;
Ilmarinen, Tanja;
Tan, Gavin S. W.;
Hongisto, Heidi;
Wong, Edmund Y. M.;
Tsai, Andrew S. H.;
Al-Nawaiseh, Sami;
Holder, Graham E.;
Xinyi Su;
Barathi, Veluchamy Amutha;
Skottman, Heli;
Stanzel, Boris V.

Publication type:

Article

Use of genome-wide SNP homozygosity mapping in small pedigrees to identify new mutations in VSX2 causing recessive microphthalmia and a semidominant inner retinal dystrophy.

Published in:

Human Genetics, 2010, v. 128, n. 1, p. 51, doi. 10.1007/s00439-010-0823-6

By:

Iseri, Sibel Ugur;
Wyatt, Alexander W.;
Nürnberg, Gudrun;
Kluck, Christian;
Nürnberg, Peter;
Holder, Graham E.;
Blair, Ed;
Salt, Alison;
Ragge, Nicola K.

Publication type:

Article

Early midline interactions are important in mouse optic chiasm formation but are not critical in man: a significant distinction between man and mouse.

Published in:

European Journal of Neuroscience, 2006, v. 23, n. 11, p. 3034, doi. 10.1111/j.1460-9568.2006.04827.x

By:

Neveu, Magella M.;
Holder, Graham E.;
Ragge, Nicola K.;
Sloper, John J.;
Collin, J. Richard O.;
Jeffery, Glen

Publication type:

Article

Optic chiasm formation in humans is independent of foveal development.

Published in:

European Journal of Neuroscience, 2005, v. 22, n. 7, p. 1825, doi. 10.1111/j.1460-9568.2005.04364.x

By:

Neveu, Magella M.;
Holder, Graham E.;
Sloper, John J.;
Jeffery, Glen

Publication type:

Article

Age-related changes in the dynamics of human albino visual pathways.

Published in:

European Journal of Neuroscience, 2003, v. 18, n. 7, p. 1939, doi. 10.1046/j.1460-9568.2003.02929.x

By:

Neveu, Magella M.;
Jeffery, Glen;
Burton, Linda C.;
Sloper, John J.;
Holder, Graham E.

Publication type:

Article

The clinical features of retinal disease due to a dominant mutation in RPE65.

Published in:

Molecular Vision, 2016, v. 22, p. 1

By:

Hull, Sarah;
Mukherjee, Rajarshi;
Holder, Graham E.;
Moore, Anthony T.;
Webster, Andrew R.

Publication type:

Article

Three Different Cone Opsin Gene Array Mutational Mechanisms with Genotype-Phenotype Correlation and Functional Investigation of Cone Opsin Variants.

Published in:

Human Mutation, 2014, v. 35, n. 11, p. 1354, doi. 10.1002/humu.22679

By:

Gardner, Jessica C.;
Liew, Gerald;
Quan, Ying‐Hua;
Ermetal, Burcu;
Ueyama, Hisao;
Davidson, Alice E.;
Schwarz, Nele;
Kanuga, Naheed;
Chana, Ravinder;
Maher, Eamonn R.;
Webster, Andrew R.;
Holder, Graham E.;
Robson, Anthony G.;
Cheetham, Michael E.;
Liebelt, Jan;
Ruddle, Jonathan B.;
Moore, Anthony T.;
Michaelides, Michel;
Hardcastle, Alison J.

Publication type:

Article

RP1L1 Variants are Associated with a Spectrum of Inherited Retinal Diseases Including Retinitis Pigmentosa and Occult Macular Dystrophy.

Published in:

Human Mutation, 2013, v. 34, n. 3, p. 506, doi. 10.1002/humu.22264

By:

Davidson, Alice E.;
Sergouniotis, Panagiotis I.;
Mackay, Donna S.;
Wright, Genevieve A.;
Waseem, Naushin H.;
Michaelides, Michel;
Holder, Graham E.;
Robson, Anthony G.;
Moore, Anthony T.;
Plagnol, Vincent;
Webster, Andrew R.

Publication type:

Article

A randomised controlled trial investigating the effect of n-3 long-chain polyunsaturated fatty acid supplementation on cognitive and retinal function in cognitively healthy older people: the Older People And n-3 Long-chain polyunsaturated fatty acids (OPAL) study protocol [ISRCTN72331636].

Published in:

Nutrition Journal, 2006, v. 5, p. 20, doi. 10.1186/1475-2891-5-20

By:

Dangour, Alan D.;
Clemens, Felicity;
Elbourne, Diana;
Fasey, Nicky;
Fletcher, Astrid E.;
Hardy, Pollyanna;
Holder, Graham E.;
Huppert, Felicia A.;
Knight, Rosemary;
Letley, Louise;
Richards, Marcus;
Truesdale, Ann;
Vickers, Madge;
Uauy, Ricardo

Publication type:

Article

Diffuse retinal dysfunction following immune reconstitution uveitis in patients with prior cytomegalovirus retinitis: a novel observation.

Published in:

Documenta Ophthalmologica, 2023, v. 147, n. 2, p. 139, doi. 10.1007/s10633-023-09947-6

By:

Yuen, Yew Sen;
Holder, Graham E.;
Lingam, Gopal;
Shen, Tina Yu Ting

Publication type:

Article

Electronegative ERG or pseudo-negative ERG?

Published in:

Documenta Ophthalmologica, 2022, v. 145, n. 3, p. 283, doi. 10.1007/s10633-022-09881-z

By:

Holder, Graham E.;
Mahroo, Omar

Publication type:

Article

ISCEV extended protocol for the S-cone ERG.

Published in:

Documenta Ophthalmologica, 2020, v. 140, n. 2, p. 95, doi. 10.1007/s10633-019-09730-6

By:

Perlman, Ido;
Kondo, Mineo;
Chelva, Enid;
Robson, Anthony G.;
Holder, Graham E.

Publication type:

Article

ISCEV extended protocol for the photopic On-Off ERG.

Published in:

Documenta Ophthalmologica, 2018, v. 136, n. 3, p. 199, doi. 10.1007/s10633-018-9645-y

By:

Sustar, Maja;
Holder, Graham E.;
Kremers, Jan;
Barnes, Claire S.;
Lei, Bo;
Khan, Naheed W.;
Robson, Anthony G.

Publication type:

Article

ISCEV guide to visual electrodiagnostic procedures.

Published in:

Documenta Ophthalmologica, 2018, v. 136, n. 1, p. 1, doi. 10.1007/s10633-017-9621-y

By:

Robson, Anthony G.;
Nilsson, Josefin;
Li, Shiying;
Jalali, Subhadra;
Fulton, Anne B.;
Tormene, Alma Patrizia;
Holder, Graham E.;
Brodie, Scott E.

Publication type:

Article

Electrodiagnostic and two-wavelength fundus autofluorescence imaging investigations in acute idiopathic maculopathy.

Published in:

Documenta Ophthalmologica, 2010, v. 121, n. 2, p. 155, doi. 10.1007/s10633-010-9235-0

By:

Day, Alexander C.;
Rotsos, Tryfon;
Holder, Graham E.;
Tufail, Adnan;
Robson, Anthony G.

Publication type:

Article

Severe retinal vasculitis in systemic lupus erythematosus leading to vision threatening paracentral acute middle maculopathy.

Published in:

2021

By:

Chin, Daniel;
Gan, Nicola Y.;
Holder, Graham E.;
Tien, Melissa;
Agrawal, Rupesh;
Manghani, Mona

Publication type:

Case Study

Hematopoietic stem cell transplantation as rescue therapy for refractory autoimmune retinopathy: a case report.

Published in:

2025

By:

Wong, Wendy Meihua;
Loh, Yvonne;
Chan, Hwei Wuen;
Fong, Warren;
Chee, Soon-Phaik;
Koh, Adrian;
Holder, Graham E.

Publication type:

Case Study

Short Communication: Contribution of Voltage-Gated Sodium Channels to the Rabbit Cone Electroretinograms.

Published in:

Current Eye Research, 2016, v. 41, n. 4, p. 569, doi. 10.3109/02713683.2015.1029134

By:

Becker, Silke;
Jayaram, Hari;
Holder, Graham E.;
Limb, G. Astrid

Publication type:

Article

Unilateral Pigmented Paravenous Retinochoroidal Atrophy Associated With Presumed Ocular Tuberculosis.

Published in:

2017

By:

Fernandez-Sanz, Guillermo;
Carreño, Ester;
Mall, Sonia;
Neveu, Magella M.;
Holder, Graham E.;
Thomas, Dhanes

Publication type:

journal article

Acute Monocular Visual Loss Due To Carcinomatous Meningitis.

Published in:

Neuro-Ophthalmology, 2010, v. 34, n. 5/6, p. 347, doi. 10.3109/01658107.2010.500011

By:

Mathew, Rashmi;
Levin, Samantha;
Luthert, Philip J.;
Maher, Jane;
Holder, Graham E.

Publication type:

Article

Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration.

Published in:

2017

By:

Ku, Cristy A.;
Hull, Sarah;
Arno, Gavin;
Vincent, Ajoy;
Carss, Keren;
Kayton, Robert;
Weeks, Douglas;
Anderson, Glenn W.;
Geraets, Ryan;
Parker, Camille;
Pearce, David A.;
Michaelides, Michel;
MacLaren, Robert E.;
Robson, Anthony G.;
Holder, Graham E.;
Heon, Elise;
Raymond, F. Lucy;
Moore, Anthony T.;
Webster, Andrew R.;
Pennesi, Mark E.

Publication type:

journal article

Clinical Characterization of CNGB1-Related Autosomal Recessive Retinitis Pigmentosa.

Published in:

2017

By:

Hull, Sarah;
Attanasio, Marcella;
Arno, Gavin;
Carss, Keren;
Robson, Anthony G.;
Thompson, Dorothy A.;
Plagnol, Vincent;
Michaelides, Michel;
Holder, Graham E.;
Henderson, Robert H.;
Raymond, F. Lucy;
Moore, Anthony T.;
Webster, Andrew R.

Publication type:

journal article

Expanding the Phenotype of TRNT1-Related Immunodeficiency to Include Childhood Cataract and Inner Retinal Dysfunction.

Published in:

2016

By:

Hull, Sarah;
Malik, Aeesha N. J.;
Arno, Gavin;
Mackay, S.;
Plagnol, Vincent;
Michaelides, Michel;
Mansour, Sahar;
Albanese, Assunta;
Brown, Katrina Tatton;
Holder, Graham E.;
Webster, Andrew R.;
Heath, Paul T.;
Moore, Anthony T.;
Mackay, Donna S

Publication type:

journal article

Characterization of CDH3-Related Congenital Hypotrichosis With Juvenile Macular Dystrophy.

Published in:

2016

By:

Hull, Sarah;
Arno, Gavin;
Robson, Anthony G.;
Broadgate, Suzanne;
Plagnol, Vincent;
McKibbin, Martin;
Halford, Stephanie;
Michaelides, Michel;
Holder, Graham E.;
Moore, Anthony T.;
Khan, Kamron N.;
Webster, Andrew R.

Publication type:

journal article

Recessive Retinopathy Consequent on Mutant G-Protein β Subunit 3 (GNB3).

Published in:

2016

By:

Arno, Gavin;
Holder, Graham E.;
Chakarova, Christina;
Kohl, Susanne;
Pontikos, Nikolas;
Fiorentino, Alessia;
Plagnol, Vincent;
Cheetham, Michael E.;
Hardcastle, Alison J.;
Webster, Andrew R.;
Michaelides, Michel;
UK Inherited Retinal Disease Consortium

Publication type:

journal article

Molecular and Clinical Findings in Patients With Knobloch Syndrome.

Published in:

2016

By:

Hull, Sarah;
Arno, Gavin;
Ku, Cristy A.;
Zhongqi Ge;
Waseem, Naushin;
Chandra, Aman;
Webster, Andrew R.;
Robson, Anthony G.;
Michaelides, Michel;
Weleber, Richard G.;
Davagnanam, Indran;
Rui Chen;
Holder, Graham E.;
Pennesi, Mark E.;
Moore, Anthony T.;
Ge, Zhongqi;
Chen, Rui

Publication type:

journal article

Molecular modeling indicates distinct classes of missense variants with mild and severe XLRS phenotypes.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 23, p. 4756, doi. 10.1093/hmg/ddt329

By:

Sergeev, Yuri V.;
Vitale, Susan;
Sieving, Paul A.;
Vincent, Ajoy;
Robson, Anthony G.;
Moore, Anthony T.;
Webster, Andrew R.;
Holder, Graham E.

Publication type:

Article

Comparison of Fundus Autofluorescence and Minimum-Motion Measurements of Macular Pigment Distribution Profiles Derived from Identical Retinal Areas.

Published in:

Perception, 2005, v. 34, n. 8, p. 1029, doi. 10.1068/p5196

By:

Robson, Anthony G;
Harding, Glen;
van Kuijk, Frederik J G M;
Pauleikhoff, Daniel;
Holder, Graham E;
Bird, Alan C;
Fitzke, Frederick W;
Moreland, Jack D

Publication type:

Article

Macular maldevelopment in ATF6-mediated retinal dysfunction.

Published in:

Ophthalmic Genetics, 2019, v. 40, n. 6, p. 564, doi. 10.1080/13816810.2019.1706749

By:

Ritter, Markus;
Arno, Gavin;
Ba-Abbad, Rola;
Holder, Graham E.;
Webster, Andrew R.

Publication type:

Article

A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 2, p. 273, doi. 10.1093/hmg/7.2.273

By:

Payne, Annette M.;
Downes, Susan M.;
Bessant, David A.R.;
Taylor, Rachel;
Holder, Graham E.;
Warren, Martin J.;
Bird, Alan C.;
Bhattacharya, Shomi S.

Publication type:

Article

cGMP-grade human iPSC-derived retinal photoreceptor precursor cells rescue cone photoreceptor damage in non-human primates.

Published in:

Stem Cell Research & Therapy, 2021, v. 12, n. 1, p. 1, doi. 10.1186/s13287-021-02539-8

By:

Lingam, Swathi;
Liu, Zengping;
Yang, Binxia;
Wong, Wendy;
Parikh, Bhav Harshad;
Ong, Jun Yi;
Goh, Debbie;
Wong, Daniel Soo Lin;
Tan, Queenie Shu Woon;
Tan, Gavin S. W.;
Holder, Graham E.;
Regha, Kakkad;
Barathi, Veluchamy Amutha;
Hunziker, Walter;
Lingam, Gopal;
Zeng, Xianmin;
Su, Xinyi

Publication type:

Article

Macular Telangiectasia type 2: multimodal assessment of retinal function and microstructure.

Published in:

Acta Ophthalmologica (1755375X), 2022, v. 100, n. 6, p. e1240, doi. 10.1111/aos.15072

By:

Ledolter, Anna A.;
Ristl, Robin;
Palmowski‐Wolfe, Anja M.;
Montuoro, Alessio;
Deak, Gabor G.;
Sacu, Stefan;
Holder, Graham E.;
Schmidt‐Erfurth, Ursula;
Ritter, Markus

Publication type:

Article

Unilateral pigmentary retinopathy: a retrospective case series.

Published in:

Acta Ophthalmologica (1755375X), 2019, v. 97, n. 4, p. e601, doi. 10.1111/aos.13981

By:

Wong, Tracey;
Errera, Marie‐Hélène;
Robson, Anthony G.;
Hykin, Philip G.;
Pal, Bishwanath;
Sagoo, Mandeep S.;
Pavesio, Carlos E.;
Moore, Anthony T.;
Webster, Andrew R.;
Holder, Graham E.;
MacLaren, Robert E.

Publication type:

Article

Choroidal structural analysis and vascularity index in retinal dystrophies.

Published in:

Acta Ophthalmologica (1755375X), 2019, v. 97, n. 1, p. e116, doi. 10.1111/aos.13836

By:

Wei, Xin;
Mishra, Chitaranjan;
Kannan, Naresh Babu;
Holder, Graham E.;
Khandelwal, Neha;
Kim, Ramasamy;
Agrawal, Rupesh

Publication type:

Article

Ocular manifestations of microcephaly with or without chorioretinopathy, lymphedema or intellectual disability ( MCLID) syndrome associated with mutations in KIF11.

Published in:

Acta Ophthalmologica (1755375X), 2016, v. 94, n. 1, p. 92, doi. 10.1111/aos.12759

By:

Balikova, Irina;
Robson, Anthony G.;
Holder, Graham E.;
Ostergaard, Pia;
Mansour, Sahar;
Moore, Anthony T.

Publication type:

Article

Phenotypic findings in C1QTNF5 retinopathy (late-onset retinal degeneration).

Published in:

Acta Ophthalmologica (1755375X), 2013, v. 91, n. 3, p. e191, doi. 10.1111/aos.12010

By:

Soumplis, Vasileios;
Sergouniotis, Panagiotis I.;
Robson, Anthony G.;
Michaelides, Michel;
Moore, Anthony T.;
Holder, Graham E.;
Webster, Andrew R.

Publication type:

Article

A phenotypic study of congenital stationary night blindness (CSNB) associated with mutations in the GRM6 gene.

Published in:

Acta Ophthalmologica (1755375X), 2012, v. 90, n. 3, p. e192, doi. 10.1111/j.1755-3768.2011.02267.x

By:

Sergouniotis, Panagiotis I.;
Robson, Anthony G.;
Li, Zheng;
Devery, Sophie;
Holder, Graham E.;
Moore, Anthony T.;
Webster, Andrew R.

Publication type:

Article

Tobacco optic neuropathy (TON) - the historical and present concept of the disease.

Published in:

Acta Ophthalmologica (1755375X), 2011, v. 89, n. 5, p. 495, doi. 10.1111/j.1755-3768.2009.01853.x

By:

Grzybowski, Andrzej;
Holder, Graham E.

Publication type:

Article