Catherine Plant

952 total citations
20 papers, 472 citations indexed

About

Catherine Plant is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Catherine Plant has authored 20 papers receiving a total of 472 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 8 papers in Ophthalmology and 3 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Catherine Plant's work include Retinal Development and Disorders (11 papers), Retinal Diseases and Treatments (8 papers) and Connexins and lens biology (3 papers). Catherine Plant is often cited by papers focused on Retinal Development and Disorders (11 papers), Retinal Diseases and Treatments (8 papers) and Connexins and lens biology (3 papers). Catherine Plant collaborates with scholars based in United Kingdom, United States and Mexico. Catherine Plant's co-authors include Alan C. Bird, Shomi S. Bhattacharya, Chris F. Inglehearn, Noemi Lois, Graham E. Holder, F.W. Fitzke, Naoki Toma, Linda Ficker, Neil D. Ebenezer and Alison J. Hardcastle and has published in prestigious journals such as Human Molecular Genetics, Journal of Medical Genetics and Human Mutation.

In The Last Decade

Catherine Plant

20 papers receiving 439 citations

Peers

Catherine Plant

OPHTH

RNMI

CMN

Megan Riker United States

J. Timothy Stout United States

T. P. Dryja United States

Tomomi Metoki Japan

Birgit Lorenz Germany

Julie E. Smith United States

Silke Becker United Kingdom

Tasneem P. Sharma United States

Saloni Walia United States

Yusuf K. Durlu Türkiye

Megan Riker United States

Catherine Plant

463 ×1.3

207 ×0.9

OPHTH

129 ×1.3

RNMI

88 ×1.4

CMN

25 ×0.5

Citations per year, relative to Catherine Plant Catherine Plant (= 1×) peers Megan Riker

Countries citing papers authored by Catherine Plant

Since Specialization

Citations

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

Fields of papers citing papers by Catherine Plant

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine Plant

This figure shows the co-authorship network connecting the top 25 collaborators of Catherine Plant. A scholar is included among the top collaborators of Catherine Plant 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 Catherine Plant. Catherine Plant is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Thiselton, Dawn L., Ilaria Zito, Catherine Plant, et al.. (2000). Novel frameshift mutations in theRP2 gene and polymorphic variants. Human Mutation. 15(6). 580–580. 21 indexed citations

Bessant, David, Annette Payne, Catherine Plant, et al.. (2000). NRL S50T mutation and the importance of ‘founder effects’ in inherited retinal dystrophies. European Journal of Human Genetics. 8(10). 783–787. 20 indexed citations

Zito, Ilaria, Michael B. Gorin, Catherine Plant, et al.. (2000). Novel mutations of theRPGR gene in RP3 families. Human Mutation. 15(4). 386–386. 10 indexed citations

Hardcastle, Alison J., et al.. (1999). Mutations in the RP2 gene cause disease in 10% of familial XLRP assessed in this study. UCL Discovery (University College London). 9 indexed citations

Zito, Ilaria, Dawn L. Thiselton, Michael B. Gorin, et al.. (1999). Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locus. Human Genetics. 105(1-2). 57–62. 39 indexed citations

Gregory-Evans, Kevin, Emma E. Tarttelin, James Bellingham, et al.. (1999). Refined genetic and physical positioning of the gene for Doyne honeycomb retinal dystrophy (DHRD). Human Genetics. 104(1). 77–82. 12 indexed citations

Zito, Ilaria, Dawn L. Thiselton, J. Timothy Stout, et al.. (1999). Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locus. Human Genetics. 105(1-2). 57–62. 19 indexed citations

Payne, Annette, Susan M. Downes, David Bessant, et al.. (1999). Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies: Table 1. Journal of Medical Genetics. 36(9). 691–693. 32 indexed citations

Payne, Annette, et al.. (1999). A mutation in the bZIP transcription factor NRL is associated with autosomal dominant retinitis pigmentosa in a family linked to a novel locus on 14p. 3 indexed citations

10.

Lois, Noemi, Graham E. Holder, F.W. Fitzke, Catherine Plant, & Alan C. Bird. (1999). Intrafamilial variation of phenotype in Stargardt macular dystrophy-Fundus flavimaculatus.. PubMed. 40(11). 2668–75. 86 indexed citations

11.

Bessant, David, Annette Payne, Catherine Plant, A.C. Bird, & Shomi S. Bhattacharya. (1998). Further refinement of the Usher 2A locus at 1q41.. Journal of Medical Genetics. 35(9). 773–774. 7 indexed citations

12.

Inglehearn, Chris F., Emma E. Tarttelin, Catherine Plant, et al.. (1998). A linkage survey of 20 dominant retinitis pigmentosa families: frequencies of the nine known loci and evidence for further heterogeneity.. Journal of Medical Genetics. 35(1). 1–5. 29 indexed citations

13.

Gregory-Evans, Kevin, et al.. (1996). The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16 (vol 5, pg 1055, 1996). UCL Discovery (University College London). 22 indexed citations

14.

Payne, Annette, et al.. (1996). The prevalence and effect of peripherin/RDS mutations in autosomal dominant pattern dystrophy.. UCL Discovery (University College London). 1 indexed citations

15.

Jay, Marcelle, Catherine Plant, Kevin Gregory-Evans, & Cheryl Y. Gregory. (1996). Doyne revisited. Eye. 10(4). 469–472. 2 indexed citations

16.

Tarttelin, Emma E., Catherine Plant, J. Weissenbach, et al.. (1996). A new family linked to the RP13 locus for autosomal dominant retinitis pigmentosa on distal 17p.. Journal of Medical Genetics. 33(6). 518–520. 17 indexed citations

17.

Kelsell, Rosemary E., Bernard F. Godley, Kevin Gregory-Evans, et al.. (1995). Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6q. Human Molecular Genetics. 4(9). 1653–1656. 38 indexed citations

18.

Toma, Naoki, Neil D. Ebenezer, Chris F. Inglehearn, et al.. (1995). Linkage of congenital hereditary endothelial dystrophy to chromosome 20. Human Molecular Genetics. 4(12). 2395–2398. 85 indexed citations

19.

Plant, Catherine, et al.. (1973). A computer model for lighting prediction. Building Science. 8(4). 351–361. 10 indexed citations

20.

Plant, Catherine, et al.. (1971). Preferred luminance distribution in windowless spaces. Lighting Research & Technology. 3(3). 219–231. 10 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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