Genevieve Wright

2.5k total citations
35 papers, 1.4k citations indexed

About

Genevieve Wright is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Genevieve Wright has authored 35 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 21 papers in Ophthalmology and 7 papers in Genetics. Recurrent topics in Genevieve Wright's work include Retinal Development and Disorders (28 papers), Retinal Diseases and Treatments (21 papers) and Cellular transport and secretion (5 papers). Genevieve Wright is often cited by papers focused on Retinal Development and Disorders (28 papers), Retinal Diseases and Treatments (21 papers) and Cellular transport and secretion (5 papers). Genevieve Wright collaborates with scholars based in United Kingdom, United States and Japan. Genevieve Wright's co-authors include Andrew R. Webster, Anthony G. Robson, Anthony T. Moore, Graham E. Holder, Michel Michaelides, Panagiotis I. Sergouniotis, Donna S. Mackay, Zheng Li, Kaoru Fujinami and Sophie Devery and has published in prestigious journals such as PLoS ONE, Ophthalmology and The American Journal of Human Genetics.

In The Last Decade

Genevieve Wright

34 papers receiving 1.4k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Genevieve Wright United Kingdom 18 1.2k 822 215 214 214 35 1.4k
Markus N. Preising Germany 25 1.5k 1.2× 1.2k 1.5× 383 1.8× 210 1.0× 237 1.1× 77 1.8k
Abigail T. Fahim United States 18 780 0.6× 504 0.6× 225 1.0× 284 1.3× 122 0.6× 43 1.1k
Dominique Ducroq France 17 1.2k 0.9× 756 0.9× 181 0.8× 182 0.9× 246 1.1× 20 1.3k
Almudena Ávila‐Fernández Spain 24 1.3k 1.1× 645 0.8× 148 0.7× 199 0.9× 309 1.4× 52 1.4k
Ajoy Vincent Canada 18 757 0.6× 462 0.6× 188 0.9× 111 0.5× 216 1.0× 68 1.0k
Ralph J. Florijn Netherlands 21 1.0k 0.8× 470 0.6× 137 0.6× 208 1.0× 309 1.4× 46 1.3k
Blanca Garcı́a-Sandoval Spain 21 1.0k 0.8× 549 0.7× 158 0.7× 169 0.8× 187 0.9× 56 1.2k
Michalis Georgiou United Kingdom 26 1.5k 1.2× 1.3k 1.5× 368 1.7× 220 1.0× 239 1.1× 75 1.9k
Sten Kjellström United States 14 909 0.7× 416 0.5× 320 1.5× 155 0.7× 248 1.2× 23 1.0k
Naheed W. Khan United States 23 1.4k 1.1× 706 0.9× 197 0.9× 483 2.3× 183 0.9× 43 1.6k

Countries citing papers authored by Genevieve Wright

Since Specialization
Citations

This map shows the geographic impact of Genevieve Wright'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 Genevieve Wright with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Genevieve Wright more than expected).

Fields of papers citing papers by Genevieve Wright

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Genevieve Wright. 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 Genevieve Wright. The network helps show where Genevieve Wright may publish in the future.

Co-authorship network of co-authors of Genevieve Wright

This figure shows the co-authorship network connecting the top 25 collaborators of Genevieve Wright. A scholar is included among the top collaborators of Genevieve Wright based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Genevieve Wright. Genevieve Wright is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Georgiou, Michalis, Genevieve Wright, Yu Fujinami‐Yokokawa, et al.. (2024). PDE6A-Associated Retinitis Pigmentosa, Clinical Characteristics, Genetics, and Natural History. Ophthalmology Retina. 9(3). 278–287. 4 indexed citations
2.
Sen, Sagnik, Kaoru Fujinami, Yu Fujinami‐Yokokawa, et al.. (2024). IQCB1 (NPHP5)-Retinopathy: Clinical and Genetic Characterization and Natural History. American Journal of Ophthalmology. 264. 205–215. 3 indexed citations
3.
Varela, Malena Daich, Elena Schiff, Samantha Malka, et al.. (2024). PHYH c.678+5G>T Leads to In-Frame Exon Skipping and Is Associated With Attenuated Refsum Disease. Investigative Ophthalmology & Visual Science. 65(2). 38–38.
4.
Guimarães, Thales A. C. de, Anthony G. Robson, Genevieve Wright, et al.. (2024). CDH23-Associated Usher Syndrome: Clinical Features, Retinal Imaging, and Natural History. Investigative Ophthalmology & Visual Science. 65(8). 27–27. 5 indexed citations
5.
Schiff, Elena, Genevieve Wright, Naushin Waseem, et al.. (2022). Dominant Cone Rod Dystrophy, Previously Assigned to a Missense Variant in RIMS1, Is Fully Explained by Co-Inheritance of a Dominant Allele of PROM1. Investigative Ophthalmology & Visual Science. 63(9). 14–14. 6 indexed citations
6.
Muthiah, Manickam Nick, Angelos Kalitzeos, Navjit Singh, et al.. (2021). Novel disease-causing variant in RDH12 presenting with autosomal dominant retinitis pigmentosa. British Journal of Ophthalmology. 106(9). 1274–1281. 11 indexed citations
7.
Pontikos, Nikolas, Gavin Arno, Neringa Jurkutė, et al.. (2020). Genetic Basis of Inherited Retinal Disease in a Molecularly Characterized Cohort of More Than 3000 Families from the United Kingdom. Ophthalmology. 127(10). 1384–1394. 152 indexed citations
8.
Ba‐Abbad, Rola, Anthony G. Robson, Omar A. Mahroo, et al.. (2020). A clinical study of patients with novel CDHR1 genotypes associated with late-onset macular dystrophy. Eye. 35(5). 1482–1489. 6 indexed citations
9.
Casalino, Giuseppe, Kamron N. Khan, Monica Armengol, et al.. (2020). Autosomal Recessive Bestrophinopathy. Ophthalmology. 128(5). 706–718. 29 indexed citations
10.
Mahroo, Omar A., Kamron N. Khan, Genevieve Wright, et al.. (2018). Retinopathy Associated with Biallelic Mutations in PYGM (McArdle Disease). Ophthalmology. 126(2). 320–322. 12 indexed citations
11.
Fujinami, Kaoru, Jana Zernant, Genevieve Wright, et al.. (2014). Clinical and Molecular Characteristics of Childhood-Onset Stargardt Disease. Ophthalmology. 122(2). 326–334. 128 indexed citations
12.
Vincent, Ajoy, Anthony G. Robson, M. Neveu, et al.. (2013). A Phenotype–Genotype Correlation Study of X-Linked Retinoschisis. Ophthalmology. 120(7). 1454–1464. 60 indexed citations
13.
Fujinami, Kaoru, Panagiotis I. Sergouniotis, Alice E. Davidson, et al.. (2013). Clinical and Molecular Analysis of Stargardt Disease With Preserved Foveal Structure and Function. American Journal of Ophthalmology. 156(3). 487–501.e1. 90 indexed citations
14.
Davidson, Alice E., Panagiotis I. Sergouniotis, Donna S. Mackay, et al.. (2012). RP1L1Variants are Associated with a Spectrum of Inherited Retinal Diseases Including Retinitis Pigmentosa and Occult Macular Dystrophy. Human Mutation. 34(3). 506–514. 74 indexed citations
15.
Poulter, James A., Alice E. Davidson, Manir Ali, et al.. (2012). Recessive Mutations inTSPAN12Cause Retinal Dysplasia and Severe Familial Exudative Vitreoretinopathy (FEVR). Investigative Ophthalmology & Visual Science. 53(6). 2873–2873. 61 indexed citations
16.
Mackay, Donna S., Arundhati Dev Borman, Phillip Moradi, et al.. (2011). RDH12 retinopathy: novel mutations and phenotypic description.. PubMed. 17. 2706–16. 49 indexed citations
17.
Sergouniotis, Panagiotis I., Elliott H. Sohn, Zheng Li, et al.. (2011). Phenotypic Variability in RDH5 Retinopathy (Fundus Albipunctatus). Ophthalmology. 118(8). 1661–1670. 66 indexed citations
18.
Sergouniotis, Panagiotis I., Donna S. Mackay, Alexander Day, et al.. (2010). A detailed phenotypic assessment of individuals affected by MFRP-related oculopathy.. PubMed. 16. 540–8. 33 indexed citations
19.
Sergouniotis, Panagiotis I., Zheng Li, Donna S. Mackay, et al.. (2010). A Survey of DNA Variation ofC2ORF71in Probands with Progressive Autosomal Recessive Retinal Degeneration and Controls. Investigative Ophthalmology & Visual Science. 52(3). 1880–1880. 11 indexed citations
20.
Li, Zheng, Panagiotis I. Sergouniotis, Michel Michaelides, et al.. (2009). Recessive Mutations of the Gene TRPM1 Abrogate ON Bipolar Cell Function and Cause Complete Congenital Stationary Night Blindness in Humans. The American Journal of Human Genetics. 85(5). 711–719. 139 indexed citations

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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