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Andrew R. Webster

Moorfields Eye Hospital NHS Foundation Trust

76H-index
658Paper Count
2.2WCitation Count
Published Papers 242
Publication Date
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Non-truncating FRMD7 variants are more penetrant than truncating variants in heterozygous female carriers of infantile nystagmus
errOphthalmology Science
IF4.6
err2026-08-14
err0
errOAAI
errCallum Hunt; Lilian Zevlaris; Benjamin Wong; Gail D.E. Maconachie; Zhanhan Tu; Omar A. Mahroo; Mariya Moosajee; Michel Michaelides; Andrew R. Webster; Jinu Han; Pradeep Vasudevan; Irene Gottlob; Yolanda Markaki; Mervyn G. Thomas
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Retinopathy caused by a primary immune regulatory disorder - the spectrum of AIRE-associated retinopathy: case series and literature review
errEye
IF3.2
err2026-04-09
err0
errOAAI
errMohammad Anas; Andrew C. Browning; Siying Lin; Omar A. Mahroo; Andrew R. Webster; Margaret Reynolds; Tatyana Milman; Ralph C. Eagle; Richard Vile; Marc Toso; Gregory S. Hageman; Hossein Nazari; Erik J. Van Kuijk; Jose S. Pulido
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De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa
errNature Genetics
IF29
err2026-01-09
err0
errOAAI
errMathieu Quinodoz; Kim Rodenburg; Zuzana Cvackova; Karolina Kaminska; Suzanne E. de Bruijn; Ana Belén Iglesias-Romero; Erica G. M. Boonen; Mukhtar Ullah; Nick Zomer; Marc Folcher; Jacques Bijon; Lara K. Holtes; Stephen H. Tsang; Zelia Corradi; K. Bailey Freund; Stefanida Shliaga; Daan M. Panneman; Rebekkah J. Hitti-Malin; Manir Ali; Ala’a AlTalbishi; Sten Andréasson; Georg Ansari; Gavin Arno; Galuh D. N. Astuti; Carmen Ayuso; Radha Ayyagari; Sandro Banfi; Eyal Banin; Tahsin Stefan Barakat; Mirella T. S. Barboni; Miriam Bauwens; Tamar Ben-Yosef; Virginie Bernard; David G. Birch; Pooja Biswas; Fiona Blanco-Kelly; Beatrice Bocquet; Camiel J. F. Boon; Kari Branham; Dominique Bremond-Gignac; Alexis Ceecee Britten-Jones; Kinga M. Bujakowska; Cyril Burin des Roziers; Elizabeth L. Cadena; Giacomo Calzetti; Francesca Cancellieri; Luca Cattaneo; Naomi Chadderton; Peter Charbel Issa; Luísa Coutinho-Santos; Stephen P. Daiger; Elfride De Baere; Marieke De Bruyne; Berta de la Cerda; John N. De Roach; Julie De Zaeytijd; Ronny Derks; Claire-Marie Dhaenens; Lubica Dudakova; Jacque L. Duncan; G. Jane Farrar; Nicolas Feltgen; Beau J. Fenner; Lidia Fernández-Caballero; Juliana M. Ferraz Sallum; Simone Gana; Alejandro Garanto; Jessica C. Gardner; Christian Gilissen; Roser Gonzàlez-Duarte; Kensuke Goto; Sam Griffiths-Jones; Tobias B. Haack; Lonneke Haer-Wigman; Alison J. Hardcastle; Takaaki Hayashi; Elise Héon; Lies H. Hoefsloot; Alexander Hoischen; Josephine P. Holtan; Carel B. Hoyng; Manuel Benjamin B. Ibanez; Chris F. Inglehearn; Takeshi Iwata; Brynjar O. Jensson; Kaylie Jones; Vasiliki Kalatzis; Smaragda Kamakari; Marianthi Karali; Ulrich Kellner; Caroline C. W. Klaver; Krisztina Knézy; Robert K. Koenekoop; Susanne Kohl; Taro Kominami; Laura Kühlewein; Tina M. Lamey; Rina Leibu; Bart P. Leroy; Petra Liskova; Irma Lopez; Victor R. de J. López-Rodríguez; Quinten Mahieu; Omar A. Mahroo; Gaël Manes; Luke Mansard; M. Pilar Martín-Gutiérrez; Nelson Martins; Laura Mauring; Martin McKibbin; Terri L. McLaren; Isabelle Meunier; Michel Michaelides; José M. Millán; Kei Mizobuchi; Rajarshi Mukherjee; Zoltán Zsolt Nagy; Kornelia Neveling; Monika Ołdak; Michiel Oorsprong; Yang Pan; Anastasia Papachristou; Antonio Percesepe; Maximilian Pfau; Eric A. Pierce; Emily Place; Raj Ramesar; Francis Ramond; Florence Andrée Rasquin; Gillian I. Rice; Lisa Roberts; María Rodríguez-Hidalgo; Javier Ruiz-Ederra; Ataf H. Sabir; Ai Fujita Sajiki; Ana Isabel Sánchez-Barbero; Asodu Sandeep Sarma; Riccardo Sangermano; Cristina M. Santos; Margherita Scarpato; Hendrik P. N. Scholl; Dror Sharon; Sabrina G. Signorini; Francesca Simonelli; Ana Berta Sousa; Maria Stefaniotou; Kari Stefansson; Katarina Stingl; Akiko Suga; Patrick Sulem; Lori S. Sullivan; Viktória Szabó; Jacek P. Szaflik; Gita Taurina; Alberta A. H. J. Thiadens; Carmel Toomes; Viet H. Tran; Miltiadis K. Tsilimbaris; Pavlina Tsoka; Veronika Vaclavik; Marie Vajter; Sandra Valeina; Enza Maria Valente; Casey Valentine; Rebeca Valero; Sophie Valleix; Joseph van Aerschot; L. Ingeborgh van den Born; Mattias Van Heetvelde; Virginie J. M. Verhoeven; Andrea L. Vincent; Andrew R. Webster; Laura Whelan; Bernd Wissinger; Georgia G. Yioti; Kazutoshi Yoshitake; Juan C. Zenteno; Roberta Zeuli; Theresia Zuleger; Chaim Landau; Allan I. Jacob; Siying Lin; Frans P. M. Cremers; Winston Lee; Jamie M. Ellingford; David Stanek; Susanne Roosing; Carlo Rivolta
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RP9 revisited; RP9 p.(H137L) remains a likely cause of dominant splicing factor-Retinitis Pigmentosa
errEuropean Journal of Human Genetics
IF4.6
err2025-10-23
err0
errOAAI
errLeon Chang; James A. Poulter; Andrew R. Webster; Gavin Arno; Rajarshi Mukherjee; Andrew Lotery; Alison J. Hardcastle; Christopher M. Watson; Chris F. Inglehearn
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errSave
SNRNP200- associated Retinopathy: In-depth Clinical Phenotyping and Genetic Characterization.
errAmerican Journal of Ophthalmology
IF4.2
err2025-08-16
err0
errOAAI
errJuan C. Romo-Aguas; Yannik Laich; Angelos Kalitzeos; Thales A.C. de Guimarāes; Anthony G. Robson; Kaoru Fujinami; Yu Fujinami-Yokokawa; Michalis Georgiou; Eduardo Di Piero; Omar A. Mahroo; Andrew R. Webster; Michel Michaelides
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errSave
Next-generation phenotyping of inherited retinal diseases from multimodal imaging with Eye2Gene
errNature Machine Intelligence
IF23.9
err2025-06-18
err0
errOAAI
errNikolas Pontikos; William A. Woof; Siying Lin; Biraja Ghoshal; Bernardo S. Mendes; Advaith Veturi; Quang Nguyen; Behnam Javanmardi; Michalis Georgiou; Alexander Hustinx; Miguel A. Ibarra-Arellano; Ismail Moghul; Yichen Liu; Kristina Pfau; Maximilian Pfau; Mital Shah; Jing Yu; Saoud Al-Khuzaei; Siegfried K. Wagner; Malena Daich Varela; Thales Antonio Cabral de Guimarães; Sagnik Sen; Gunjan Naik; Dayyanah Sumodhee; Dun Jack Fu; Nathaniel Kabiri; Jennifer Furman; Bart Liefers; Aaron Y. Lee; Samantha R. De Silva; Caio Marques; Fabiana Motta; Yu Fujinami-Yokokawa; Alison J. Hardcastle; Gavin Arno; Birgit Lorenz; Philipp Herrmann; Kaoru Fujinami; Juliana Sallum; Savita Madhusudhan; Susan M. Downes; Frank G. Holz; Konstantinos Balaskas; Andrew R. Webster; Omar A. Mahroo; Peter M. Krawitz; Michel Michaelides
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errSave
Retinograd-AI: An Open-Source Automated Fundus Autofluorescence Retinal Image Gradability Assessment for Inherited Retinal Diseases
errOphthalmology Science
IF4.6
err2025-06-04
err0
errOAAI
errGunjan Naik; Saoud Al-Khuzaei; Ismail Moghul; Thales A.C. de Guimaraes; Sagnik Sen; Malena Daich Varela; Yichen Liu; Pallavi Bagga; Vincent Rocco; Dun Jack Fu; Mariya Moosajee; Savita Madhusudhan; Andrew R. Webster; Samantha De Silva; Praveen J. Patel; Omar A. Mahroo; Susan M. Downes; Michel Michaelides; Konstantinos Balaskas; Nikolas Pontikos; William Woof A.
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Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophy
errGENETICS IN MEDICINE
IF6.2
err2025-06-01
err0
errOAAI
errEhrenberg, Miriam; Avraham, Maayan; Asodu, Sandeep Sarma; Moye, Abigail R.; Sangermano, Riccardo; Rizel, Leah; Ali-Nasser, Tahleel; Sher, Ifat; Gurwitz, David; Chao, Katherine R.; Rivera, Antonio; Webster, Andrew R.; Rivolta, Carlo; Newman, Hadas; Pras, Eran; Rotenstreich, Ygal; Banin, Eyal; Pierce, Eric A.; Zur, Dinah; Arno, Gavin; Bujakowska, Kinga M.; Lin, Siying; Sharon, Dror; Ben-Yosef, Tamar
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Variants in CFAP410 cause a range of retinal and skeletal phenotypes
errNPJ GENOMIC MEDICINE
IF4.8
err2025-04-17
err0
errOAAI
errSchmidt, Ryan E.; Pohodich, Amy E.; Birch, David; Jones, Kaylie; Lam, Byron L.; Jung, Emily H.; Jain, Nieraj; Georgiou, Michalis; Mahroo, Omar A.; Webster, Andrew R.; Michaelides, Michel; Bakall, Benjamin; Iannaccone, Alessandro; Vincent, Ajoy; Parameswarappa, Deepika C.; Heon, Elise; Scholl, Hendrik P. N.; Janeschitz-Kriegl, Lucas; Traboulsi, Elias I.; Zein, Wadih; Brooks, Brian P.; Cukras, Catherine; Hufnagel, Robert; Aleman, Tomas S.; Sylla, Mohamed M.; Tsang, Stephen H.; Alabek, Michelle; Sahel, Jose; Gorin, Michael B.; van Genderen, Maria M.; Stingl, Katarina; Reith, Milda; Kohl, Susanne; Amaral, Rebeca Azevedo Souza; Sallum, Juliana Maria Ferraz; Vincent, Andrea L.; Hull, Sarah; Duncan, Jacque L.; Hanson, James V. M.; Tedeus, Matthias; Maggi, Jordi; Graf, Urs; Koller, Samuel; Berger, Wolfgang; Gerth-Kahlert, Christina; Marra, Molly; Everett, Lesley A.; Yang, Paul; Pennesi, Mark E.
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Bi-allelic variants in three genes encoding distinct subunits of the vesicular AP-5 complex cause hereditary macular dystrophy
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2025-04-01
err0
errOAAI
errKaminska, Karolina; Cancellieri, Francesca; Quinodoz, Mathieu; Moye, Abigail R.; Bauwens, Miriam; Lin, Siying; Janeschitz-Kriegl, Lucas; Hayman, Tamar; Barberan-Martinez, Pilar; Schlaeger, Regina; van den Broeck, Filip; Fernandez, Almudena Avila; Fernandez-Caballero, Lidia; Perea-Romero, Irene; Garcia-Garcia, Gema; Salom, David; Mazzola, Pascale; Zuleger, Theresia; Poths, Karin; Haack, Tobias B.; Jacob, Julie; Vermeer, Sascha; Terbeek, Frederique; Feltgen, Nicolas; Moulin, Alexandre P.; Koutroumanou, Louisa; Papadakis, George; Browning, Andrew C.; Madhusudhan, Savita; Granse, Lotta; Banin, Eyal; Sousa, Ana Berta; Santos, Luisa Coutinho; Kuehlewein, Laura; De Angeli, Pietro; Leroy, Bart P.; Mahroo, Omar A.; Sedgwick, Fay; Eden, James; Pfau, Maximilian; Andreasson, Sten; Scholl, Hendrik P. N.; Ayuso, Carmen; Millan, Jose M.; Sharon, Dror; Tsilimbaris, Miltiadis K.; Vaclavik, Veronika; Tran, Hoai, V; Ben-Yosef, Tamar; De Baere, Elfride; Webster, Andrew R.; Arno, Gavin; Sergouniotis, Panagiotis I.; Kohl, Susanne; Santos, Cristina; Rivolta, Carlo
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Detailed Clinical, Ophthalmic, and Genetic Characterization of MYO7A-Associated Usher Syndrome
errINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
IF4.7
err2025-04-01
err0
errOAAI
errRomo-Aguas, Juan C.; de Guimaraes, Thales A. C.; Kalitzeos, Angelos; Aychoua, Nancy; Tsika, Chrysanthi; Robson, Anthony G.; Fujinami-Yokokawa, Yu; Fujinami, Kaoru; Mahroo, Omar A.; Webster, Andrew R.; Michaelides, Michel
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errSave
Best Vitelliform Macular Dystrophy Natural History Study Report 2
errOphthalmology Retina
IF5.7
err2025-03-12
err0
errOAAI
errYannik Laich; Michalis Georgiou; Kaoru Fujinami; Malena Daich Varela; Yu Fujinami-Yokokawa; Shaima Awadh Hashem; Thales A.C. de Guimaraes; Omar A. Mahroo; Andrew R. Webster; Michel Michaelides
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Clinical, Genetic, Imaging and Electrophysiological Findings in a Cohort of Patients With GUCA1A-Associated Retinopathy
errINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
IF4.7
err2025-02-19
err0
errOAAI
errAllon, Gilad; Lin, Siying; Robson, Anthony G.; Arno, Gavin; Neveu, Magella M.; Hysi, Pirro G.; Michaelides, Michel; Webster, Andrew R.; Mahroo, Omar A.
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Symptom management in melanoma associated retinopathy following intravitreal dexamethasone
errACTA OPHTHALMOLOGICA
IF2.8
err2025-01-19
err0
PREAI
errIlyas, A; Mahroo, O; Tan, JK; Trepatchayakorn, S; Bloch, E; Robson, AG; Plant, G; Virgo, J; Webster, AR; Pavesio, C; Mohamed, M
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errSave
The Electroretinogram I-Wave, a Component Originating in the Retinal OFF-Pathway, Associates With a Myopia Genetic Risk Polymorphism
errINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
IF4.7
err2024-11-12
err0
errOAAI
errXu, Zihe; Tan, Jit Kai; Vetrivel, Krishnika; Jiang, Xiaofan; Leo, Shaun M.; Bhatti, Taha; Tariq, Ambreen; Webster, Andrew R.; Robson, Anthony G.; Hammond, Christopher J.; Hysi, Pirro G.; Mahroo, Omar A.
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Bi-allelic variants in COQ8B, a gene involved in the biosynthesis of coenzyme Q10, lead to non-syndromic retinitis pigmentosa
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2024-10-01
err1
errOAAI
errIglesias-Romero, Ana Belen; Kaminska, Karolina; Quinodoz, Mathieu; Folcher, Marc; Lin, Siying; Arno, Gavin; Calado, Joaquim; Webster, Andrew R.; Moulin, Alexandre; Sousa, Ana Berta; Coutinho-Santos, Luisa; Santos, Cristina; Rivolta, Carlo
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errSave
Clinical, Ophthalmic, and Genetic Characterization of RPGRIP1-Associated Leber Congenital Amaurosis/Early-Onset Severe Retinal Dystrophy
errAMERICAN JOURNAL OF OPHTHALMOLOGY
IF4.2
err2024-10-01
err0
errOAAI
errVarela, Malena Daich; Jeste, Mrunmayi; De Guimaraes, Thales A. C.; Mahroo, Omar A.; Arno, Gavin; Webster, Andrew R.; Michaelides, Michel
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errSave
Substitution of a single non-coding nucleotide upstream of TMEM216 causes non-syndromic retinitis pigmentosa and is associated with reduced TMEM216 expression
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2024-09-01
err1
errOAAI
errMalka, Samantha; Biswas, Pooja; Berry, Anne-Marie; Sangermano, Riccardo; Ullah, Mukhtar; Lin, Siying; D'Antonio, Matteo; Jestin, Aleksandr; Jiao, Xiaodong; Quinodoz, Mathieu; Sullivan, Lori; Gardner, Jessica C.; Place, Emily M.; Michaelides, Michel; Kaminska, Karolina; Mahroo, Omar A.; Schiff, Elena; Wright, Genevieve; Cancellieri, Francesca; Vaclavik, Veronika; Santos, Cristina; Rehman, Atta Ur; Mehrotra, Sudeep; Baig, Hafiz Muhammad Azhar; Iqbal, Muhammad; Nsar, Muhammad A.; Santos, Luisa Coutinho; Sousa, Ana Berta; Tran, Viet H.; Matsui, Hiroko; Bhatia, Anjana; Naeem, Muhammad Asif; Akram, Shehla J.; Akram, Javed; Riazuddin, Sheikh; Ayuso, Carmen; Pierce, Eric A.; Hardcastle, Alison J.; Riazuddin, S. Amer; Frazer, Kelly A.; Hejtmancik, J. Fielding; Rivolta, Carlo; Bujakowska, Kinga M.; Arno, Gavin; Webster, Andrew R.; Ayyagari, Radha
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errSave
IQCB1 (NPHP5)-Retinopathy: Clinical and Genetic Characterization and Natural History
errAMERICAN JOURNAL OF OPHTHALMOLOGY
IF4.2
err2024-08-01
err1
errOAAI
errSen, Sagnik; Fabozzi, Lorenzo; Fujinami, Kaoru; Fujinami-Yokokawa, Yu; Wright, Genevieve A.; Webster, Andrew; Mahroo, Omar; Robson, Anthony G.; Georgiou, Michalis; Michaelides, Michel
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Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study
errBRITISH JOURNAL OF OPHTHALMOLOGY
IF3.5
err2024-07-30
err2
PREAI
errIgelman, Austin D.; White, Elizabeth; Tayyib, Alaa; Everett, Lesley; Vincent, Ajoy; Heon, Elise; Zeitz, Christina; Michaelides, Michel; Mahroo, Omar A.; Katta, Mohamed; Webster, Andrew; Preising, Markus; Lorenz, Birgit; Khateb, Samer; Banin, Eyal; Sharon, Dror; Luski, Shahar; Van Den Broeck, Filip; Leroy, Bart Peter; De Baere, Elfride; Walraedt, Sophie; Stingl, Katarina; Kuehlewein, Laura; Kohl, Susanne; Reith, Milda; Fulton, Anne; Raghuram, Aparna; Meunier, Isabelle; Dollfus, Helene; Aleman, Tomas S.; Bedoukian, Emma C.; O'Neil, Erin C.; Krauss, Emily; Vincent, Andrea; Jordan, Charlotte; Iannaccone, Alessandro; Sen, Parveen; Sundaramurthy, Srilekha; Nagasamy, Soumittra; Balikova, Irina; Casteels, Ingele; Borooah, Shyamanga; Yassin, Shaden; Nagiel, Aaron; Schwartz, Hillary; Zanlonghi, Xavier; Gottlob, Irene; Mclean, Rebecca J.; Munier, Francis L.; Stephenson, Andrew; Sisk, Robert; Koenekoop, Robert; Wilson, Lorri B.; Fredrick, Douglas; Choi, Dongseok; Yang, Paul; Pennesi, Mark Edward
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Research Directions

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