Andrew R. Webster

Moorfields Eye Hospital NHS Foundation Trust

Also affiliated with Institute of Ophthalmology, Moorfields Eye Hospital, University College London

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 4%percentile

0.818Author DataRank

Indexed papers

4in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 4 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3500 Inherited Retinal Disease Patients from the United Kingdom

medRxiv(2024)10.1101/2024.03.24.24304809

Top 45%

0.405DataRank

Top 45%9 citations

Thales A. C. de Guimarães, Saoud Al‐Khuzaei, Malena Daich Varela, Sagnik Sen, Pallavi Bagga +32 more

Papers

Driven by 24 papers — median percentile 40. Top paper: “Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan”.

Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan

Human Mutation(1996)10.1002/(sici)1098-1004(1996)8:4<348::aid-humu8>3.0.co;2-3

N/A

14.7DataRank · unranked

504 citations

Takeshi Kishida, Fan Chen, Laura Schmidt, Eamonn R. Maher, Frances M. Richards +21 more

Seven new loci associated with age-related macular degeneration

Nature Genetics(2013)10.1038/ng.2578

N/A

1.0DataRank · unranked

798 citations

Lars G. Fritsche, Wei Chen, Brian L. Yaspan, Yi Yu, Guðmar Þorleifsson +141 more

An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes

Nature Cell Biology(2015)10.1038/ncb3201

N/A

0.831DataRank · unranked

253 citations

Gabrielle Wheway, Miriam Schmidts, Dorus A. Mans, Katarzyna Szymanska, Thanh-Minh T. Nguyen +71 more

Rare disease gene association discovery in the 100,000 GenomesProject

Nature(2025)10.1038/s41586-025-08623-w

N/A

0.515DataRank · unranked

18 citations

Letizia Vestito, Emma Magavern, Julius O.B. Jacobsen, Gavin Arno, Elijah R. Behr +56 more

Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3500 Inherited Retinal Disease Patients from the United Kingdom

medRxiv(2024)10.1101/2024.03.24.24304809

Top 45%

0.405DataRank

Top 45%9 citations

Thales A. C. de Guimarães, Saoud Al‐Khuzaei, Malena Daich Varela, Sagnik Sen, Pallavi Bagga +32 more

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa

Nature Genetics(2026)10.1038/s41588-025-02451-4

N/A

0.370DataRank · unranked

8 citations

Kim Rodenburg, Zuzana Cvackova, Karolina Kaminska, Suzanne E. de Bruijn, Ana Belén Iglesias-Romero +212 more

Quantification of Optical Coherence Tomography Features in >3500 Patients with Inherited Retinal Disease Reveals Novel Genotype-Phenotype Associations

medRxiv(2025)10.1101/2025.07.03.25330767

Top 60%

0.248DataRank

Top 60%4 citations

Thales A. C. de Guimarães, Saoud Al‐Khuzaei, Malena Daich Varela, Mital Shah, Gunjan Naik +32 more

SNRNP200- Associated Retinopathy: In-Depth Clinical Phenotyping and Genetic Characterization

American Journal of Ophthalmology(2025)10.1016/j.ajo.2025.08.015

Top 70%

0.165DataRank

Top 70%2 citations

Yannik Laich, Angelos Kalitzeos, Thales A. C. de Guimarães, Anthony G. Robson, Kaoru Fujinami +7 more

A large animal model of RDH5-associated retinopathy recapitulates important features of the human phenotype

Human Molecular Genetics(2021)10.1093/hmg/ddab316

N/A

0DataRank · unranked

18 citations

Anahita Daruwalla, Samantha R. De Silva, Paige A. Winkler, Kelian Sun, Nate Pasmanter +13 more

Risk factors for non-invasive (skin and soft tissue) and invasive Staphylococcus aureus infections among children and adults living in southeastern USA: a retrospective cohort study

BMJ Open(2022)10.1136/bmjopen-2021-059327

N/A

0DataRank · unranked

8 citations

Traci Leong, Andrew R. Webster, Anthony Giarrusso, Scott K. Fridkin, Susan M. Ray +3 more

KCNV2-associated retinopathy: genotype–phenotype correlations –KCNV2study group report 3

British Journal of Ophthalmology(2023)10.1136/bjo-2023-323640

N/A

0DataRank · unranked

5 citations

Michalis Georgiou, Anthony G. Robson, Kaoru Fujinami, Ajoy Vincent, Fadi Nasser +31 more

Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project data

medRxiv(2023)10.1101/2023.12.20.23300294

N/A

0DataRank · unranked

3 citations

Letizia Vestito, Emma Magavern, Julius O.B. Jacobsen, Gavin Arno, Elijah R. Behr +56 more

Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study

British Journal of Ophthalmology(2024)10.1136/bjo-2023-323747

N/A

0DataRank · unranked

7 citations

Elizabeth White, Alaa Tayyib, Lesley Everett, Ajoy Vincent, Elise Héon +52 more

Ceramide synthase TLCD3B is a novel gene associated with human recessive retinal dystrophy

Genetics in Medicine(2020)10.1038/s41436-020-01003-x

N/A

0DataRank · unranked

15 citations

Jun Wang, Kaitlyn Xiong, Chinthana Thangavel, Xinye Qian, Rola Ba‐Abbad +11 more

Next-generation phenotyping of inherited retinal diseases from multimodal imaging with Eye2Gene

Nature Machine Intelligence(2025)10.1038/s42256-025-01040-8

N/A

0DataRank · unranked

23 citations

William Woof, Siying Lin, Biraja Ghoshal, Bernardo Mendes, Yoga Advaith Veturi +42 more

Genome-Wide Insights Into the Genes and Pathways Shaping Human Foveal Development: Redefining the Genetic Landscape of Foveal Hypoplasia

Investigative Ophthalmology & Visual Science(2025)10.1167/iovs.66.12.22

N/A

0DataRank · unranked

5 citations

Ha-Jun Yoon, Alvin Lirio, Kayesha Coley, Jun Wang, Nick Shrine +16 more

Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophy

Genetics in Medicine(2025)10.1016/j.gim.2025.101401

N/A

0DataRank · unranked

4 citations

Maayan Avraham, Sandeep Sarma Asodu, Abigail R. Moye, Riccardo Sangermano, Leah Rizel +19 more

Clinical and Biochemical Characterization of Specific GUCY2D Alleles Associated With a Rare Form of Night Blindness

Investigative Ophthalmology & Visual Science(2025)10.1167/iovs.66.6.22

N/A

0DataRank · unranked

1 citations

Igor V. Peshenko, Malena Daich Varela, Siying Lin, Gavin Arno, Omar A. Mahroo +6 more

Variants in CFAP410 cause a range of retinal and skeletal phenotypes

npj Genomic Medicine(2025)10.1038/s41525-025-00489-1

N/A

0DataRank · unranked

0 citations

Amy E. Pohodich, David G. Birch, Kaylie Webb-Jones, Byron L. Lam, Emily H. Jung +44 more

Substitution of a single non-coding nucleotide upstream of TMEM216 causes non-syndromic retinitis pigmentosa and is associated with reduced TMEM216 expression

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.07.020

N/A

0DataRank · unranked

7 citations

Pooja Biswas, Anne-Marie Berry, Riccardo Sangermano, Mukhtar Ullah, Siying Lin +40 more

A genetic and clinical study of individuals with nonsyndromic retinopathy consequent upon sequence variants in HGSNAT, the gene associated with Sanfilippo C mucopolysaccharidosis

American Journal of Medical Genetics Part C Seminars in Medical Genetics(2020)10.1002/ajmg.c.31822

N/A

0DataRank · unranked

28 citations

Malena Daich Varela, Anthony G. Robson, Karen Pierpoint, Rola Ba‐Abbad, Savita Nutan +12 more

Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome

Ophthalmic Genetics(2021)10.1080/13816810.2021.1946704

N/A

0DataRank · unranked

34 citations

Cristy A. Ku, Mariana Matioli da Palma, Michalis Georgiou, Elena Schiff, Byron L. Lam +16 more

KCNV2-Associated Retinopathy: Detailed Retinal Phenotype and Structural Endpoints—KCNV2 Study Group Report 2

American Journal of Ophthalmology(2021)10.1016/j.ajo.2021.03.004

N/A

0DataRank · unranked

28 citations

Kaoru Fujinami, Ajoy Vincent, Fadi Nasser, Samer Khateb, Mauricio E. Vargas +32 more

CNGB1 ‐related rod‐cone dystrophy: A mutation review and update

Human Mutation(2021)10.1002/humu.24205

N/A

0DataRank · unranked

24 citations

Vasily Smirnov, Cyntia Solis Hernandez, Saddek Mohand‐Saïd, Christel Condroyer, Aline Antonio +28 more

Andrew R. Webster

Indexed papers

Top data-sharing exemplar

Papers