Alison J. Hardcastle

9.1k total citations
127 papers, 4.2k citations indexed

About

Alison J. Hardcastle is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Alison J. Hardcastle has authored 127 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 85 papers in Molecular Biology, 44 papers in Ophthalmology and 40 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Alison J. Hardcastle's work include Retinal Development and Disorders (65 papers), Corneal surgery and disorders (32 papers) and Retinal Diseases and Treatments (29 papers). Alison J. Hardcastle is often cited by papers focused on Retinal Development and Disorders (65 papers), Corneal surgery and disorders (32 papers) and Retinal Diseases and Treatments (29 papers). Alison J. Hardcastle collaborates with scholars based in United Kingdom, United States and Czechia. Alison J. Hardcastle's co-authors include Michael E. Cheetham, Michel Michaelides, Stephen J. Tuft, Alice E. Davidson, Anthony T. Moore, Nele Schwarz, Sally Hayes, Neil D. Ebenezer, David M. Hunt and Petra Lišková and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Alison J. Hardcastle

123 papers receiving 4.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Alison J. Hardcastle United Kingdom	39	3.0k	1.6k	1.1k	763	703	127	4.2k
Masaru Inatani Japan	39	2.1k 0.7×	3.0k 1.9×	1.6k 1.5×	315 0.4×	787 1.1×	180	5.1k
Elise Héon Canada	44	5.1k 1.7×	3.9k 2.5×	1.5k 1.4×	1.7k 2.2×	775 1.1×	144	7.3k
Bart P. Leroy Belgium	37	3.6k 1.2×	2.0k 1.3×	579 0.5×	1.5k 1.9×	484 0.7×	157	4.8k
Paul F. Kenna Ireland	38	3.9k 1.3×	1.4k 0.9×	504 0.5×	666 0.9×	1.3k 1.8×	121	4.8k
B. Jeroen Klevering Netherlands	38	3.3k 1.1×	3.4k 2.2×	1.5k 1.3×	435 0.6×	484 0.7×	102	4.9k
Robert K. Koenekoop Canada	39	4.5k 1.5×	2.4k 1.5×	636 0.6×	1.3k 1.7×	748 1.1×	119	5.2k
Rob W.J. Collin Netherlands	38	4.5k 1.5×	1.8k 1.1×	560 0.5×	986 1.3×	758 1.1×	138	5.1k
Motokazu Tsujikawa Japan	35	1.3k 0.4×	1.8k 1.2×	1.8k 1.6×	395 0.5×	163 0.2×	102	3.6k
Marian M. Humphries Ireland	32	2.8k 0.9×	1.1k 0.7×	370 0.3×	386 0.5×	930 1.3×	68	3.5k
August F. Deutman Netherlands	36	2.7k 0.9×	2.9k 1.9×	885 0.8×	403 0.5×	301 0.4×	120	4.5k

Countries citing papers authored by Alison J. Hardcastle

Since Specialization

Citations

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

Fields of papers citing papers by Alison J. Hardcastle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alison J. Hardcastle. 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 Alison J. Hardcastle. The network helps show where Alison J. Hardcastle may publish in the future.

Co-authorship network of co-authors of Alison J. Hardcastle

This figure shows the co-authorship network connecting the top 25 collaborators of Alison J. Hardcastle. A scholar is included among the top collaborators of Alison J. Hardcastle 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 Alison J. Hardcastle. Alison J. Hardcastle 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

Gardner, Jessica C., Nihar Bhattacharyya, Petra Lišková, et al.. (2024). Autosomal dominant stromal corneal dystrophy associated with a SPARCL1 missense variant. European Journal of Human Genetics. 32(12). 1583–1589. 1 indexed citations

Georgiou, Michalis, Anthony G. Robson, Sami H. Uwaydat, et al.. (2023). RP2-Associated X-linked Retinopathy: Clinical Findings, Molecular Genetics, and Natural History in a Large Cohort of Female Carriers. American Journal of Ophthalmology. 261. 112–120. 2 indexed citations

Carnt, Nicole, Chi Nam Ignatius Pang, Kathryn P. Burdon, et al.. (2020). The association of Interleukin 8 gene SNP with severe inflammatory complications in contact lens wearers experiencing Acanthamoeba Keratitis. Investigative Ophthalmology & Visual Science. 61(7). 3998–3998. 1 indexed citations

Patterson, Emily J, Angelos Kalitzeos, Navjit Singh, et al.. (2020). Longitudinal assessment of foveal cone structure in blue cone monochromacy. Investigative Ophthalmology & Visual Science. 61(7). 5270–5270. 1 indexed citations

Lane, Amelia, Katarina Jovanović, Diego Ottaviani, et al.. (2020). Modeling and Rescue of RP2 Retinitis Pigmentosa Using iPSC-Derived Retinal Organoids. Stem Cell Reports. 15(1). 67–79. 125 indexed citations

Choquet, Hélène, Ronald B. Melles, Jie Yin, et al.. (2020). A multiethnic genome-wide analysis of 44,039 individuals identifies 41 new loci associated with central corneal thickness. Communications Biology. 3(1). 301–301. 26 indexed citations

Ottaviani, Diego, Amelia Lane, David A. Parfitt, et al.. (2019). Temporal resolution of alternative splicing in the developing human retina using 3D retinal organoids. Investigative Ophthalmology & Visual Science. 60(9). 3333–3333. 1 indexed citations

Gardner, Jessica C., Petra Lišková, Jonathan B. Ruddle, et al.. (2018). X-linked cone dystrophy and Blue Cone Monochromacy caused by novel and rare L/M opsin interchange haplotypes.. Investigative Ophthalmology & Visual Science. 59(9). 2325–2325. 1 indexed citations

Lišková, Petra, Ľubica Ďuďáková, Karla E. Rojas López, et al.. (2018). 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. 102(3). 447–459. 40 indexed citations

10.

Fiorentino, Alessia, Gavin Arno, Nikolas Pontikos, et al.. (2017). Mutations in the X-linked gene PRPS1 cause retinal degeneration in females. Investigative Ophthalmology & Visual Science. 58(8). 1243–1243. 1 indexed citations

11.

Patterson, Emily J, James Tee, Jay Neitz, et al.. (2015). Assessing cone mosaic disruption in patients with X-linked cone dysfunction. Investigative Ophthalmology & Visual Science. 56(7). 88–88. 2 indexed citations

12.

Lišková, Petra, Ľubica Ďuďáková, Vladimı́r Tesař, et al.. (2014). 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. 53(1). 30–35. 7 indexed citations

13.

Davidson, Alice E., Nele Schwarz, Lina Zelinger, et al.. (2013). Mutations in ARL2BP, Encoding ADP-Ribosylation-Factor-Like 2 Binding Protein, Cause Autosomal-Recessive Retinitis Pigmentosa. The American Journal of Human Genetics. 93(2). 321–329. 52 indexed citations

14.

Pryce, Gareth, Cristina Visintin, Sreeram V Ramagopalan, et al.. (2013). Control of spasticity in a multiple sclerosis model using central nervous system‐excluded CB ₁ cannabinoid receptor agonists. The FASEB Journal. 28(1). 117–130. 23 indexed citations

15.

Gardner, Jessica C., Michel Michaelides, Graham E. Holder, et al.. (2009). Blue cone monochromacy: causative mutations and associated phenotypes.. PubMed. 15. 876–84. 51 indexed citations

16.

Ruddle, Jonathan B., et al.. (2009). RPGR ORF15 genotype and clinical variability of retinal degeneration in an Australian population. British Journal of Ophthalmology. 93(9). 1151–1154. 26 indexed citations

17.

Bhattacharya, Siladitya, Ronak Patel, Leen Abu‐Safieh, et al.. (2003). Evaluation of the Retbindin Gene as a Candidate for Retinal Diseases. Investigative Ophthalmology & Visual Science. 44(13). 2322–2322. 1 indexed citations

18.

Zito, Ilaria, et al.. (2001). Evidence for a new X-linked syndrome involving retinitis pigmentosa. UCL Discovery (University College London). 3 indexed citations

19.

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

20.

Hardcastle, Alison J., Zoë K. David-Gray, M Jay, A.C. Bird, & Shoumo Bhattacharya. (1997). Localization of CSNBX (CSNB4) between the retinitis pigmentosa loci RP2 and RP3 on proximal Xp.. PubMed. 38(13). 2750–5. 13 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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