Neil D. Ebenezer

2.9k total citations
42 papers, 2.1k citations indexed

About

Neil D. Ebenezer is a scholar working on Radiology, Nuclear Medicine and Imaging, Molecular Biology and Ophthalmology. According to data from OpenAlex, Neil D. Ebenezer has authored 42 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Radiology, Nuclear Medicine and Imaging, 20 papers in Molecular Biology and 15 papers in Ophthalmology. Recurrent topics in Neil D. Ebenezer's work include Corneal surgery and disorders (19 papers), Corneal Surgery and Treatments (12 papers) and Glaucoma and retinal disorders (9 papers). Neil D. Ebenezer is often cited by papers focused on Corneal surgery and disorders (19 papers), Corneal Surgery and Treatments (12 papers) and Glaucoma and retinal disorders (9 papers). Neil D. Ebenezer collaborates with scholars based in United Kingdom, Mexico and United States. Neil D. Ebenezer's co-authors include Shomi S. Bhattacharya, Alison J. Hardcastle, Louise Ocaka, Ordan J. Lehmann, Tim Jordan, Eranga N. Vithana, Roger A. Hitchings, Petra Lišková, David M. Hunt and Chris F. Inglehearn and has published in prestigious journals such as Nature Genetics, Molecular Cell and PLoS ONE.

In The Last Decade

Neil D. Ebenezer

41 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Neil D. Ebenezer United Kingdom	27	1.2k	785	726	407	213	42	2.1k
Keiko Fujiki Japan	25	757 0.6×	628 0.8×	486 0.7×	254 0.6×	88 0.4×	86	1.6k
Gulab Zode United States	25	1.1k 0.9×	460 0.6×	1.3k 1.8×	117 0.3×	467 2.2×	45	2.2k
Cecilie Bredrup Norway	14	434 0.4×	674 0.9×	370 0.5×	163 0.4×	195 0.9×	34	1.4k
Mohammed A. Aldahmesh Saudi Arabia	32	1.2k 1.0×	303 0.4×	591 0.8×	815 2.0×	213 1.0×	61	2.0k
Kazuhide Kawase Japan	22	699 0.6×	580 0.7×	1.2k 1.6×	107 0.3×	173 0.8×	45	1.7k
Jeffrey W. Kalenak United States	13	765 0.6×	1.0k 1.3×	1.9k 2.6×	149 0.4×	269 1.3×	24	2.2k
Frédéric Mascarelli France	27	1.4k 1.2×	380 0.5×	765 1.1×	113 0.3×	336 1.6×	64	2.0k
Allan R. Shepard United States	18	775 0.7×	291 0.4×	752 1.0×	168 0.4×	189 0.9×	38	1.4k
Jacoline B. ten Brink Netherlands	22	1.3k 1.1×	282 0.4×	682 0.9×	608 1.5×	480 2.3×	49	2.0k
Yoshitsugu Saishin Japan	22	749 0.6×	727 0.9×	1.1k 1.5×	115 0.3×	66 0.3×	56	1.8k

Countries citing papers authored by Neil D. Ebenezer

Since Specialization

Citations

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

Fields of papers citing papers by Neil D. Ebenezer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Neil D. Ebenezer. 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 Neil D. Ebenezer. The network helps show where Neil D. Ebenezer may publish in the future.

Co-authorship network of co-authors of Neil D. Ebenezer

This figure shows the co-authorship network connecting the top 25 collaborators of Neil D. Ebenezer. A scholar is included among the top collaborators of Neil D. Ebenezer 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 Neil D. Ebenezer. Neil D. Ebenezer 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

Hassan, Hala, Caroline Thaung, Neil D. Ebenezer, et al.. (2012). Severe Meesmann’s epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12. Eye. 27(3). 367–373. 14 indexed citations

Lišková, Petra, Rhian Gwilliam, Martin Filipec, et al.. (2012). High Prevalence of Posterior Polymorphous Corneal Dystrophy in the Czech Republic; Linkage Disequilibrium Mapping and Dating an Ancestral Mutation. PLoS ONE. 7(9). e45495–e45495. 23 indexed citations

Gardner, Jessica C., Tom R. Webb, Naheed Kanuga, et al.. (2011). A Novel Missense Mutation in Both OPN1LW and OPN1MW Cone Opsin Genes Causes X-Linked Cone Dystrophy (XLCOD5). Advances in experimental medicine and biology. 723. 595–601. 2 indexed citations

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

Lišková, Petra, Gordon K. Klintworth, Martin Filipec, et al.. (2008). Phenotype Associated with the H626P Mutation and Other Changes in the <i>TGFBI</i> Gene in Czech Families. Ophthalmic Research. 40(2). 105–108. 7 indexed citations

Lišková, Petra, Stephen J. Tuft, Rhian Gwilliam, et al.. (2007). Novel mutations in theZEB1 gene identified in Czech and British patients with posterior polymorphous corneal dystrophy. Human Mutation. 28(6). 638–638. 64 indexed citations

Ramprasad, Vedam L., Neil D. Ebenezer, Tin Aung, et al.. (2007). NovelSLC4A11mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Human Mutation. 28(5). 522–523. 61 indexed citations

Ocaka, Louise, Neil D. Ebenezer, Glen Brice, et al.. (2007). Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel. Journal of Medical Genetics. 45(2). 87–92. 58 indexed citations

Jirsová, Kateřina, et al.. (2006). Immunohistochemical characterization of cytokeratins in the abnormal corneal endothelium of posterior polymorphous corneal dystrophy patients. Experimental Eye Research. 84(4). 680–686. 48 indexed citations

10.

Vithana, Eranga N., Patricio E. Morgan, Periasamy Sundaresan, et al.. (2006). Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2). Nature Genetics. 38(7). 755–757. 207 indexed citations

11.

Young, Robert D., Tomoya O. Akama, Petra Lišková, et al.. (2006). Differential immunogold localisation of sulphated and unsulphated keratan sulphate proteoglycans in normal and macular dystrophy cornea using sulphation motif-specific antibodies. Histochemistry and Cell Biology. 127(1). 115–120. 26 indexed citations

12.

El-Ashry, Mohamed F., Mai M. Abd El-Aziz, Simon Wilkins, et al.. (2005). Novel CHST6 nonsense and missense mutations responsible for macular corneal dystrophy. American Journal of Ophthalmology. 139(1). 192–193. 38 indexed citations

13.

Ebenezer, Neil D.. (2005). Clinical and Molecular Characterization of a Family With Autosomal Recessive Cornea Plana. Archives of Ophthalmology. 123(9). 1248–1248. 16 indexed citations

14.

El-Ashry, Mohamed F., Mai M. Abd El-Aziz, Alison J. Hardcastle, Shomi S. Bhattacharya, & Neil D. Ebenezer. (2005). A Clinical and Molecular Genetic Study of Autosomal-Dominant Stromal Corneal Dystrophy in British Population. Ophthalmic Research. 37(6). 310–317. 11 indexed citations

15.

Ebenezer, Neil D., Andrew R. Webster, Andrés Ruiz‐Linares, et al.. (2004). Recombination hotspots and block structure of linkage disequilibrium in the human genome exemplified by detailed analysis of PGM1 on 1p31. Human Molecular Genetics. 13(24). 3089–3102. 11 indexed citations

16.

Aung, Tin, Louise Ocaka, Neil D. Ebenezer, et al.. (2002). Investigating the association between OPA1 polymorphisms and glaucoma: comparison between normal tension and high tension primary open angle glaucoma. Human Genetics. 110(5). 513–514. 47 indexed citations

17.

Ebenezer, Neil D., et al.. (2001). Linkage analysis of a large Amish pedigree with glaucoma.. UCL Discovery (University College London). 1 indexed citations

18.

Aung, Tin, Louise Ocaka, Neil D. Ebenezer, et al.. (2001). A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene. Human Genetics. 110(1). 52–56. 106 indexed citations

19.

Hameed, Abdul, Shagufta Khaliq, M. Ismail, et al.. (2000). A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13.. PubMed. 41(3). 629–33. 51 indexed citations

20.

Gregory-Evans, Kevin, Alan Fryer, C.F. Inglehearn, et al.. (1994). Genetic linkage of cone–rod retinal dystrophy to chromosome 19q and evidence for segregation distortion. Nature Genetics. 6(2). 210–213. 93 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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