Andrew Webster
University College London
H-index: 79
Europe-United Kingdom
Top articles of Andrew Webster
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
RP2-Associated X-linked Retinopathy: Clinical Findings, Molecular Genetics, and Natural History in a Large Cohort of Female Carriers | American Journal of Ophthalmology | Michalis Georgiou Anthony G Robson Sami H Uwaydat Marco H Ji Ahmed F Shakarchi | 2024/5/1 |
Typical best vitelliform dystrophy secondary to biallelic variants in BEST1 | Ophthalmic Genetics | Pankaja Dhoble Anthony G Robson Andrew R Webster Michel Michaelides | 2024/1/2 |
IMPG2-related maculopathy | American Journal of Ophthalmology | Johannes Birtel Richard Caswell Samantha R De Silva Philipp Herrmann Salwah Rehman | 2024/2/1 |
PHYH c. 678+ 5G> T Leads to In-Frame Exon Skipping and Is Associated With Attenuated Refsum Disease | Investigative Ophthalmology & Visual Science | Malena Daich Varela Elena Schiff Samantha Malka Genevieve Wright Omar A Mahroo | 2024/2/1 |
Representation of Women Among Individuals With Mild Variants in ABCA4-Associated Retinopathy: A Meta-Analysis | JAMA ophthalmology | Stéphanie S Cornelis Joanna IntHout Esmee H Runhart Olivier Grunewald Siying Lin | 2024/4/11 |
Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3000 Inherited Retinal Disease Patients from the United Kingdom | medRxiv | William Woof Thales AC de Guimaraes Saoud Al-Khuzaei Malena Daich Varela Sagnik Sen | 2024 |
Best Vitelliform Macular Dystrophy Natural History Study Report 1: Clinical Features and Genetic Findings. | Ophthalmology | Yannik Laich Michalis Georgiou Kaoru Fujinami Malena Daich Varela Yu Fujinami-Yokokawa | 2024/1/24 |
Mutations in SAMD7 cause autosomal-recessive macular dystrophy with or without cone dysfunction | The American Journal of Human Genetics | Miriam Bauwens Elifnaz Celik Dinah Zur Siying Lin Mathieu Quinodoz | 2024/2/1 |
Congenital Stationary Night Blindness: Structure, Function and Genotype–Phenotype Correlations in a cohort of 122 patients. | Ophthalmology Retina | Mohamed Katta Thales AC de Guimaraes Yu Fujinami-Yokokawa Kaoru Fujinami Michalis Georgiou | 2024/3/24 |
Discrepancies in central foveal intensity with different autofluorescence modalities in CNGB3‐associated achromatopsia and correlation with integrity of ellipsoid zone on … | Acta Ophthalmologica | Haseeb Akhtar Jeffrey Lam Gavin Arno Andrew R Webster Michel Michaelides | 2024/1 |
Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies … | Michalis Georgiou Anthony G Robson Kaoru Fujinami Thales AC de Guimarães Yu Fujinami-Yokokawa | 2024/1/24 | |
Cone-driven strong flash electroretinograms in healthy adults: Prevalence of negative waveforms | Documenta Ophthalmologica | Xiaofan Jiang Taha Bhatti Ambreen Tariq Shaun M Leo Nancy Aychoua | 2024/2 |
IQCB1 (NPHP5)-retinopathy: Clinical and Genetic Characterization and Natural History | American Journal of Ophthalmology | Sagnik Sen Lorenzo Fabozzi Kaoru Fujinami Yu Fujinami-Yokokawa Genevieve A Wright | 2024/3/23 |
Localised loss of sheen in Optos pseudocolour images in Oguchi disease following prior short wavelength autofluorescence imaging | Acta Ophthalmologica | Haseeb Akhtar Luke Nicholson Zoe Ockrim Magella Neveu Andrew R Webster | 2024/1 |
Spectrum of Genetic Variants in the Most Common Genes Causing Inherited Retinal Disease in a Large Molecularly Characterized United Kingdom Cohort | Ophthalmology Retina | Siying Lin Sandra Vermeirsch Nikolas Pontikos Maria Pilar Martin-Gutierrez Malena Daich Varela | 2024/1/12 |
Visual Acuity by Decade in 139 Males with RPGR-Associated Retinitis Pigmentosa | Ophthalmology Science | Samantha R De Silva Hwei Wuen Chan Aditi Agarwal Andrew R Webster Michel Michaelides | 2024/3/1 |
Hyperreflectivity of the outer portion of the outer nuclear layer seen on optical coherence tomography in some cases of NR2E3‐associated retinopathy | Acta Ophthalmologica | Sammi Wing Fai Fong Gavin Arno Andrew R Webster Michel Michaelides Omar Mahroo | 2024/1 |
Combining a prioritization strategy and functional studies nominates 5’UTR variants underlying inherited retinal disease | Genome Medicine | Alfredo Dueñas Rey Marta del Pozo Valero Manon Bouckaert Katherine A Wood Filip Van den Broeck | 2024/1/6 |
RBP3-Retinopathy—Inherited High Myopia and Retinal Dystrophy: Genetic Characterization, Natural History, and Deep Phenotyping | American Journal of Ophthalmology | Michalis Georgiou Kaoru Fujinami Anthony G Robson Yu Fujinami-Yokokawa Ahmed F Shakarchi | 2024/2/1 |
Genetics, Clinical Characteristics, and Natural History of PDE6B-Associated Retinal Dystrophy | American Journal of Ophthalmology | Shaima Awadh Hashem Michalis Georgiou Yu Fujinami-Yokokawa Yannik Laich Malena Daich Varela | 2024/2/15 |
