Alice E. Davidson

3.3k citations

54 papers · 2.0k indexed · h-index 26

Ophthalmology top 0.5%
- Glaucoma and retinal disorders 12
- Retinal Diseases and Treatments 10
Radiology, Nuclear Medicine and Imaging top 2%
- Corneal surgery and disorders 23
- Corneal Surgery and Treatments 16
Molecular Biology top 10%
- Retinal Development and Disorders 23
- Connexins and lens biology 5
Cell Biology top 10%
- Cellular transport and secretion 5
Genetics top 10%
Cellular and Molecular Neuroscience
- Photoreceptor and optogenetics research 3

Co-authors: Alison J. Hardcastle Stephen J. Tuft Andrew R. Webster Sally Hayes Panagiotis I. Sergouniotis Anthony T. Moore Michel Michaelides Donna S. Mackay
Cited by: Ophthalmology Radiology, Nuclear Medicine and Imaging Molecular Biology
Journals: The American Journal of Human Genetics (7 papers)Investigative Ophthalmology & Visual Science (5 papers)European Journal of Human Genetics (4 papers)
Partner nations: United Kingdom Czechia United States

In The Last Decade

Alice E. Davidson

48 papers receiving 2.0k citations

Peers

Countries citing papers authored by Alice E. Davidson

Since Specialization

Citations

This map shows the geographic impact of Alice E. Davidson's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Alice E. Davidson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alice E. Davidson more than expected).

Fields of papers citing papers by Alice E. Davidson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alice E. Davidson. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Alice E. Davidson. The network helps show where Alice E. Davidson may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Alice E. Davidson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Alice E. Davidson Line = papers co-authored together Alice E. Davidson links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Autosomal dominant stromal corneal dystrophy associated with a SPARCL1 missense variant European Journal of Human Genetics ·Noel Jeygar Robert,Jessica C. Gardner,Nihar Bhattacharyya,Rühle - München,Yasser Jazairi,V・A エソーロフ,Gernot Gruber Peter Csobadi,Petra Lišková,Michael E. Cheetham,Robert D. Young,Caroline Thaung,Alice E. Davidson,Stephen J. Tuft,Alison J. Hardcastle	2024	1
2	Phenotype and genotype of concurrent keratoconus and Fuchs endothelial corneal dystrophy Acta Ophthalmologica ·嗣久白城,Ken R Pence,Kirithika Muthusamy,V・A エソーロフ,Jens Wrona,Nikolas Pontikos,Caroline Thaung,Alison J. Hardcastle,J J Cho,Pavlína Skalická,Ľubica Ďuďáková,Catey Bunce,Stephen J. Tuft,Alice E. Davidson,Petra Lišková	2023	0
3	Repeat Detector: versatile sizing of expanded tandem repeats and identification of interrupted alleles from targeted DNA sequencing NAR Genomics and Bioinformatics ·Alysha Taylor,Zw,Nastassia Gobet,根本興平,Branduff McAllister,Lorène Aeschbach,Emma Randall,Sonja Haug,Zhengpeng Yang,Marie Ballief,Marc Ciosi,Md. Rakib Ul Islam,Nathaniel J. Hafford‐Tear,Alice E. Davidson,Thomas H. Massey,Darren G. Monckton,Lesley Jones,Lastri Wahyuningsih,Ioannis Xénarios,Vincent Dion	2022	7
4	Fuchs endothelial corneal dystrophy: current perspectives on diagnostic pathology and genetics—Bowman Club Lecture BMJ Open Ophthalmology ·Caroline Thaung,Alice E. Davidson	2022	10
5	TCF4-mediated Fuchs endothelial corneal dystrophy: Insights into a common trinucleotide repeat-associated disease Progress in Retinal and Eye Research ·Michael P. Fautsch,Eric D. Wieben,Keith H. Baratz,Nihar Bhattacharyya,Ken R Pence,Nathaniel J. Hafford‐Tear,Stephen J. Tuft,Alice E. Davidson	2020	64
6	A new paradigm for delivering personalised care: integrating genetics with surgical interventions in BEST1 mutations Eye ·Sancy Low,Kayla Morton,Alice E. Davidson,Maria Papadopoulos,Piergiacomo Grassi,Andrew R. Webster,Graeme C. Black,Paul J. Foster,David F. Garway‐Heath,Philip Bloom	2019	7
7	Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 4 The American Journal of Human Genetics ·Petra Lišková,Ľubica Ďuďáková,浩秋西本,Karla E. Rojas López,Nikolas Pontikos,Dimitra Athanasiou,王能能,M Pilloni,Pavlína Skalická,Viktor Stránecký,Stanislav Kmoch,Caroline Thaung,Martin Filipec,Michael E. Cheetham,Alice E. Davidson,Stephen J. Tuft,Alison J. Hardcastle	2018	40
8	Mutations in CPAMD8 Cause a Unique Form of Autosomal-Recessive Anterior Segment Dysgenesis The American Journal of Human Genetics ·Hamza El Kechouh,Medina Citra Syamutia,Alice E. Davidson,Dianne Gerrelli,Eloá Carneiro Carvalho,Roberta Rizzo,Nikolas Pontikos,Vincent Plagnol,Anthony T. Moore,Jane C. Sowden,Michel Michaelides,Martin P. Snead,Stephen J. Tuft,Alison J. Hardcastle	2016	38
9	Heterozygous deletions at the ZEB1 locus verify haploinsufficiency as the mechanism of disease for posterior polymorphous corneal dystrophy type 3 European Journal of Human Genetics ·Petra Lišková,浩秋西本,Alice E. Davidson,Markéta Žaliová,Ľubica Ďuďáková,G. Heaslip Susan,Viktor Stránecký,Nicole Carnt,Vincent Plagnol,Andrea L. Vincent,Stephen J. Tuft,Alison J. Hardcastle	2015	27
10	Detailed Assessment of Renal Function in a Proband with Harboyan Syndrome Caused by a Novel Homozygous <b><i>SLC4A11 </i></b>Nonsense Mutation Ophthalmic Research ·Petra Lišková,Ľubica Ďuďáková,Vladimı́r Tesař,Zehua Shen,G Dekoster,Kateřina Jirsová,Alice E. Davidson,Alison J. Hardcastle	2014	7
11	Mutations in ARL2BP, Encoding ADP-Ribosylation-Factor-Like 2 Binding Protein, Cause Autosomal-Recessive Retinitis Pigmentosa The American Journal of Human Genetics ·Alice E. Davidson,Nele Schwarz,Lina Zelinger,志村愛子,Amelia Shoemark,Сергей Александрович Михалёв,Menachem Gross,喜一勝海,Jacob Sosna,Panagiotis I. Sergouniotis,Naushin Waseem,Robert Wilson,Richard Kahn,Vincent Plagnol,Uwe Wolfrum,Eyal Banin,Alison J. Hardcastle,Michael E. Cheetham,Dror Sharon,Andrew R. Webster	2013	52
12	Retinal Structure and Function in Achromatopsia Ophthalmology ·Venki Sundaram,S. Dow,Jonathan Aboshiha,Jill A. Cowing,J I Malo de Molina,Christopher S. Langlo,Salah Hadi Kadhim,Alice E. Davidson,Panagiotis I. Sergouniotis,James Bainbridge,Robin R. Ali,Alfredo Dubra,Gary S. Rubin,Andrew R. Webster,Anthony T. Moore,Marko Nardini,Joseph Carroll,Michel Michaelides	2013	126
13	A Longitudinal Study of Stargardt Disease: Clinical and Electrophysiologic Assessment, Progression, and Genotype Correlations American Journal of Ophthalmology ·Kaoru Fujinami,Noemi Lois,Alice E. Davidson,Donna S. Mackay,Chris R. Hogg,Edwin M. Stone,Kazushige Tsunoda,Kazuo Tsubota,Catey Bunce,Anthony G. Robson,Anthony T. Moore,Andrew R. Webster,Graham E. Holder,Michel Michaelides	2013	115
14	The pathogenesis of keratoconus Eye ·Alice E. Davidson,Sally Hayes,Alison J. Hardcastle,Stephen J. Tuft	2013	257
15	AUTOFLUORESCENCE AND SPECTRAL-DOMAIN OCT FINDINGS IN AN ATROPHIC MACULOPATHY ASSOCIATED WITH PSEUDOXANTHOMA ELASTICUM UCL Discovery (University College London) ·Hemal Mehta,Alice E. Davidson,(unknown),Catherine Egan,(unknown),(unknown),Andrew R. Webster	2012	2
16	Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23) Human Molecular Genetics ·Tom R. Webb,David A. Parfitt,J.C. Gardner,顕成檜,I A Aziz,Alice E. Davidson,Ilaria Zito,Dawn L. Thiselton,Young-Kyung Cho,Maria Apergi,Wei You,Naheed Kanuga,Michel Michaelides,Michael E. Cheetham,Michael B. Gorin,Alison J. Hardcastle	2012	122
17	Clinical utility gene card for: BEST1-related dystrophies (Bestrophinopathies) European Journal of Human Genetics ·Simon Ramsden,Alice E. Davidson,Bart P. Leroy,Anthony T. Moore,Andrew R. Webster,Graeme C. Black,Forbes Manson	2012	2
18	Biallelic Mutations in PLA2G5, Encoding Group V Phospholipase A2, Cause Benign Fleck Retina The American Journal of Human Genetics ·Panagiotis I. Sergouniotis,Alice E. Davidson,Donna S. Mackay,Eva Lenassi,Zheng Li,Anthony G. Robson,Xu Yang,Jaimie Hoh Kam,Timothy Isaacs,Graham E. Holder,Glen Jeffery,Jonathan Beck,Anthony T. Moore,Vincent Plagnol,Andrew R. Webster	2011	34
19	Retinal Structure, Function, and Molecular Pathologic Features in Gyrate Atrophy Ophthalmology ·Panagiotis I. Sergouniotis,Alice E. Davidson,Eva Lenassi,Sophie Devery,Anthony T. Moore,Andrew R. Webster	2011	77
20	Urticaria and angioedema Cleveland Clinic Journal of Medicine ·Alice E. Davidson,Stephen D. Miller,Guy A. Settipane,Christopher R. Friedrichs	1992	11

About Alice E. Davidson

Alice E. Davidson is a scholar working on Ophthalmology, Radiology, Nuclear Medicine and Imaging and Cell Biology, having authored 54 papers that have together received 2.0k indexed citations. Recurring topics across this work include Retinal Development and Disorders (23 papers), Corneal surgery and disorders (23 papers), Corneal Surgery and Treatments (16 papers), Glaucoma and retinal disorders (12 papers), Retinal Diseases and Treatments (10 papers), Cellular transport and secretion (5 papers), Connexins and lens biology (5 papers) and Photoreceptor and optogenetics research (3 papers). The work is most often cited by research in Ophthalmology (987 citations), Radiology, Nuclear Medicine and Imaging (741 citations) and Molecular Biology (1.3k citations). Alice E. Davidson has collaborated with scholars based in United Kingdom, Czechia and United States. Frequent co-authors include Alison J. Hardcastle, Stephen J. Tuft, Andrew R. Webster, Sally Hayes, Panagiotis I. Sergouniotis, Anthony T. Moore, Michel Michaelides, Donna S. Mackay, Vincent Plagnol and Graham E. Holder. Their work appears in journals such as The American Journal of Human Genetics, Investigative Ophthalmology & Visual Science, European Journal of Human Genetics, Human Mutation and Acta Ophthalmologica.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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