Andrew R Webster

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 16

Top Topics

Artificial Intelligence

Diabetic Retinopathy

Cross Sectional

Top Venues

Ophthalmic genetics

American journal of medical genetics. Part A

Science (New York, N.Y.)

This page only lists publications with an associated author ORCID identifier.

Publications

William Woof, Thales Antonio Cabral de Guimaraes, Saoud Al-Khuzaei, Malena Daich Varela, Sagnik Sen, Pallavi Bagga, Bernardo Mendes, Mital Shah, Paula Burke, David Parry, Siying Lin, Gunjan Naik, Biraja Ghoshal, Bart Liefers, Dun Jack Fu, Michalis Georgiou, Quang Nguyen, Alan Sousa da Silva, Yichen Liu, Yu Fujinami-Yokokawa, Nathaniel Kabiri, Dayyanah Sumodhee, Praveen J Patel, Jennifer Furman, Ismail Moghul, Juliana Maria Ferraz Sallum, Samantha Roshani De Silva, Birgit Lorenz, Frank G Holz, Kaoru Fujinami, Andrew R Webster, Omar A Mahroo, Susan M Downes, Savita Madhusudhan, Konstantinos Balaskas, Michel Michaelides, Nikolas Pontikos
Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3000 Inherited Retinal Disease Patients from the United Kingdom. medRxiv : the preprint server for health sciences (2024)
Quang Nguyen, William Woof, Nathaniel Kabiri, Sagnik Sen, Malena Daich Varela, Thales Antonio Cabral de Guimaraes, Mital Shah, Dayyanah Sumodhee, Ismail Moghul, Saoud Al-Khuzaei, Yichen Liu, Catherine Hollyhead, Bhavna Tailor, Loy Lobo, Carl Veal, Stephen Archer, Jennifer Furman, Gavin Arno, Manuel Gomes, Kaoru Fujinami, Savita Madhusudhan, Omar A Mahroo, Andrew R Webster, Konstantinos Balaskas, Susan M Downes, Michel Michaelides, Nikolas Pontikos, null null
Can artificial intelligence accelerate the diagnosis of inherited retinal diseases? Protocol for a data-only retrospective cohort study (Eye2Gene). BMJ open 13 (3) (2023)
Quang Nguyen, William Woof, Nathaniel Kabiri, Sagnik Sen, Malena Daich Varela, Thales Antonio Cabral de Guimaraes, Mital Shah, Dayyanah Sumodhee, Ismail Moghul, Saoud Al-Khuzaei, Yichen Liu, Catherine Hollyhead, Bhavna Tailor, Loy Lobo, Carl Veal, Stephen Archer, Jennifer Furman, Gavin Arno, Manuel Gomes, Kaoru Fujinami, Savita Madhusudhan, Omar A Mahroo, Andrew R Webster, Konstantinos Balaskas, Susan M Downes, Michel Michaelides, Nikolas Pontikos, null null
Can artificial intelligence accelerate the diagnosis of inherited retinal diseases? Protocol for a data-only retrospective cohort study (Eye2Gene). BMJ open 13 (3) (2023)
Quang Nguyen, William Woof, Nathaniel Kabiri, Sagnik Sen, Malena Daich Varela, Thales Antonio Cabral de Guimaraes, Mital Shah, Dayyanah Sumodhee, Ismail Moghul, Saoud Al-Khuzaei, Yichen Liu, Catherine Hollyhead, Bhavna Tailor, Loy Lobo, Carl Veal, Stephen Archer, Jennifer Furman, Gavin Arno, Manuel Gomes, Kaoru Fujinami, Savita Madhusudhan, Omar A Mahroo, Andrew R Webster, Konstantinos Balaskas, Susan M Downes, Michel Michaelides, Nikolas Pontikos, null null
Can artificial intelligence accelerate the diagnosis of inherited retinal diseases? Protocol for a data-only retrospective cohort study (Eye2Gene). BMJ open 13 (3) (2023)
Quang Nguyen, William Woof, Nathaniel Kabiri, Sagnik Sen, Malena Daich Varela, Thales Antonio Cabral de Guimaraes, Mital Shah, Dayyanah Sumodhee, Ismail Moghul, Saoud Al-Khuzaei, Yichen Liu, Catherine Hollyhead, Bhavna Tailor, Loy Lobo, Carl Veal, Stephen Archer, Jennifer Furman, Gavin Arno, Manuel Gomes, Kaoru Fujinami, Savita Madhusudhan, Omar A Mahroo, Andrew R Webster, Konstantinos Balaskas, Susan M Downes, Michel Michaelides, Nikolas Pontikos, null null
Can artificial intelligence accelerate the diagnosis of inherited retinal diseases? Protocol for a data-only retrospective cohort study (Eye2Gene). BMJ open 13 (3) (2023)
Elena R Schiff, Nancy Aychoua, Savita Nutan, Indran Davagnanam, Anthony T Moore, Anthony G Robson, C K Patel, Andrew R Webster, Gavin Arno
Variability of retinopathy consequent upon novel mutations in LAMA1. Ophthalmic genetics 43 (5) (2022)
Rose M Gilbert, Dayyanah Sumodhee, Nikolas Pontikos, Catherine Hollyhead, Angus Patrick, Samuel Scarles, Sabrina Van Der Smissen, Rodrigo M Young, Nick Nettleton, Andrew R Webster, Jocelyn Cammack
Collaborative Research and Development of a Novel, Patient-Centered Digital Platform (MyEyeSite) for Rare Inherited Retinal Disease Data: Acceptability and Feasibility Study. JMIR formative research 6 (1) (2022)
Austin D Igelman, Cristy Ku, Mariana Matioli da Palma, Michalis Georgiou, Elena R Schiff, Byron L Lam, Eeva-Marja Sankila, Jeeyun Ahn, Lindsey Pyers, Ajoy Vincent, Juliana Maria Ferraz Sallum, Wadih M Zein, Jin Kyun Oh, Maldonado Ramiro S, Joseph Ryu, Stephen H Tsang, Michael B Gorin, Andrew R Webster, Michel Michaelides, Paul Yang, Mark E Pennesi
Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome. Ophthalmic genetics 42 (6) (2021)
Rola Ba-Abbad, Anthony G Robson, Becky MacPhee, Andrew R Webster, Michel Michaelides
Rod-cone dystrophy associated with the Gly167Asp variant in PRPH2. Ophthalmic genetics 40 (2) (2020)
Markus Ritter, Gavin Arno, Rola Ba-Abbad, Graham E Holder, Andrew R Webster
Macular maldevelopment in ATF6-mediated retinal dysfunction. Ophthalmic genetics 40 (6) (2020)
Rola Ba-Abbad, Gavin Arno, Anthony G Robson, Konstantinos Bouras, Michalis Georgiou, Genevieve Wright, Andrew R Webster, Michel Michaelides
Macula-predominant retinopathy associated with biallelic variants in RDH12. Ophthalmic genetics 41 (6) (2020)
Wei Wei, Salih Tuna, Michael J Keogh, Katherine R Smith, Timothy J Aitman, Philip L Beales, David L H Bennett, Daniel P Gale, Maria A K Bitner-Glindzicz, Graeme C Black, Paul Brennan, Perry Mark Elliott, Frances A Flinter, R Andres Floto, Henry Houlden, Melita Irving, Ania Koziell, Eamonn R Maher, Hugh Stephen Markus, Nicholas W Morrell, William G Newman, Irene Roberts, John Andrew Sayer, Kenneth G C Smith, Jenny C Taylor, Hugh C Watkins, Andrew R Webster, Andrew O M Wilkie, Catherine Williamson, null null, null null, Sofie Ashford, Christopher J Penkett, Kathleen E Stirrups, Augusto Rendon, Willem H Ouwehand, John R Bradley, F Lucy Raymond, Mark Caulfield, Ernest Turro, Patrick F Chinnery
Germline selection shapes human mitochondrial DNA diversity. Science (New York, N.Y.) 364 (6442) (2019)
James Fasham, Gavin Arno, Siying Lin, Mingchu Xu, Keren J Carss, Sarah Hull, Amelia Lane, Anthony G Robson, Olivia Wenger, Jay E Self, Gaurav V Harlalka, Claire G Salter, Lynn Schema, Timothy J Moss, Michael E Cheetham, Anthony T Moore, F Lucy Raymond, Rui Chen, Andrew H Crosby, Andrew R Webster, Andrew H Crosby, null null
Delineating the expanding phenotype associated with SCAPER gene mutation. American journal of medical genetics. Part A 179 (8) (2019)
Sancy Low, Ryian Mohamed, Alice Davidson, Maria Papadopoulos, Piergiacomo Grassi, Andrew R Webster, Graeme C M Black, Paul J Foster, David F Garway-Heath, Philip A Bloom
A new paradigm for delivering personalised care: integrating genetics with surgical interventions in BEST1 mutations. Eye (London, England) 34 (3) (2019)
Shyamanga Borooah, Chloe M Stanton, Joseph Marsh, Keren J Carss, Naushin Waseem, Pooja Biswas, Georgios Agorogiannis, Lucy Raymond, Gavin Arno, Andrew R Webster
Whole genome sequencing reveals novel mutations causing autosomal dominant inherited macular degeneration. Ophthalmic genetics 39 (6) (2018)
Sancy Low, Ryian Mohamed, Michelle Ting, Andrew R Webster, David F Garway-Heath
The treatment of refractory angle-closure glaucoma in a patient with X-linked juvenile retinoschisis. Ophthalmic genetics 39 (5) (2018)