David P. Dimasi

1.5k total citations
26 papers, 893 citations indexed

About

David P. Dimasi is a scholar working on Ophthalmology, Molecular Biology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, David P. Dimasi has authored 26 papers receiving a total of 893 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Ophthalmology, 10 papers in Molecular Biology and 8 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in David P. Dimasi's work include Glaucoma and retinal disorders (14 papers), Corneal surgery and disorders (8 papers) and Retinal Diseases and Treatments (7 papers). David P. Dimasi is often cited by papers focused on Glaucoma and retinal disorders (14 papers), Corneal surgery and disorders (8 papers) and Retinal Diseases and Treatments (7 papers). David P. Dimasi collaborates with scholars based in Australia, United States and United Kingdom. David P. Dimasi's co-authors include Jamie E. Craig, Kathryn P. Burdon, Alex W. Hewitt, David A. Mackey, Claudine S. Bonder, Shiwani Sharma, Paul Mitchell, Wai Yan Sun, J. J. Wang and Paul N. Baird and has published in prestigious journals such as The Journal of Immunology, PLoS ONE and Human Molecular Genetics.

In The Last Decade

David P. Dimasi

26 papers receiving 879 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David P. Dimasi Australia 16 524 345 319 90 79 26 893
Dhananjay Shukla India 19 831 1.6× 539 1.6× 317 1.0× 59 0.7× 37 0.5× 74 1.1k
John D. Dickinson United States 16 283 0.5× 168 0.5× 247 0.8× 110 1.2× 27 0.3× 38 951
Yangfan Yang China 15 308 0.6× 200 0.6× 173 0.5× 24 0.3× 97 1.2× 45 613
Vinodh Kakkassery Germany 13 378 0.7× 175 0.5× 158 0.5× 28 0.3× 161 2.0× 92 754
Ryoji Yamakawa Japan 14 427 0.8× 221 0.6× 148 0.5× 33 0.4× 29 0.4× 54 679
Danial Roshandel Iran 16 219 0.4× 378 1.1× 140 0.4× 57 0.6× 187 2.4× 49 740
Wakako Adachi Japan 17 324 0.6× 757 2.2× 278 0.9× 85 0.9× 478 6.1× 21 1.2k
ANNE M. V. BROOKS Australia 20 958 1.8× 556 1.6× 123 0.4× 46 0.5× 207 2.6× 84 1.2k
Anirudh Sethi United States 8 245 0.5× 132 0.4× 292 0.9× 63 0.7× 13 0.2× 10 516
Mizuki Kitamura Japan 11 318 0.6× 73 0.2× 348 1.1× 28 0.3× 31 0.4× 22 659

Countries citing papers authored by David P. Dimasi

Since Specialization
Citations

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

Fields of papers citing papers by David P. Dimasi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David P. Dimasi. 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 David P. Dimasi. The network helps show where David P. Dimasi may publish in the future.

Co-authorship network of co-authors of David P. Dimasi

This figure shows the co-authorship network connecting the top 25 collaborators of David P. Dimasi. A scholar is included among the top collaborators of David P. Dimasi 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 David P. Dimasi. David P. Dimasi 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.
Wardill, Hannah R., Chris Mavrangelos, Melissa A. Campaniello, et al.. (2018). Colonic migrating motor complexes are inhibited in acute tri-nitro benzene sulphonic acid colitis. PLoS ONE. 13(6). e0199394–e0199394. 15 indexed citations
2.
Bihari, Shailesh, Dani‐Louise Dixon, Mark Lawrence, et al.. (2017). Fluid-induced lung injury—role of TRPV4 channels. Pflügers Archiv - European Journal of Physiology. 469(9). 1121–1134. 22 indexed citations
3.
Sun, Wai Yan, David P. Dimasi, Melissa R. Pitman, et al.. (2016). Topical Application of Fingolimod Perturbs Cutaneous Inflammation. The Journal of Immunology. 196(9). 3854–3864. 12 indexed citations
4.
Helbig, Karla J., David P. Dimasi, Michael R. Beard, et al.. (2015). Dengue Virus Infection of Primary Endothelial Cells Induces Innate Immune Responses, Changes in Endothelial Cells Function and Is Restricted by Interferon-Stimulated Responses. Journal of Interferon & Cytokine Research. 35(8). 654–665. 31 indexed citations
5.
Chidlow, Glyn, John P. M. Wood, Shiwani Sharma, et al.. (2013). Ocular Expression and Distribution of Products of the POAG-Associated Chromosome 9p21 Gene Region. PLoS ONE. 8(9). e75067–e75067. 8 indexed citations
6.
Dimasi, David P., Wai Yan Sun, & Claudine S. Bonder. (2013). Neutrophil interactions with the vascular endothelium. International Immunopharmacology. 17(4). 1167–1175. 46 indexed citations
7.
Wiggs, Janey L., Alex W. Hewitt, Baojian Fan, et al.. (2012). The p53 Codon 72 PRO/PRO Genotype May Be Associated with Initial Central Visual Field Defects in Caucasians with Primary Open Angle Glaucoma. PLoS ONE. 7(9). e45613–e45613. 50 indexed citations
8.
Dimasi, David P., Kathryn P. Burdon, Alex W. Hewitt, et al.. (2012). Genetic Investigation into the Endophenotypic Status of Central Corneal Thickness and Optic Disc Parameters in Relation to Open-Angle Glaucoma. American Journal of Ophthalmology. 154(5). 833–842.e2. 21 indexed citations
9.
Dimasi, David P., Alex W. Hewitt, Bastien Llamas, et al.. (2011). Ethnic and Mouse Strain Differences in Central Corneal Thickness and Association with Pigmentation Phenotype. PLoS ONE. 6(8). e22103–e22103. 17 indexed citations
10.
Dimasi, David P., Kathryn P. Burdon, Alex W. Hewitt, et al.. (2010). Candidate gene study to investigate the genetic determinants of normal variation in central corneal thickness.. PubMed. 16. 562–9. 14 indexed citations
11.
Dimasi, David P., Alex W. Hewitt, Sonja Klebe, et al.. (2009). Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes. Human Genetics. 127(1). 33–44. 29 indexed citations
12.
Dimasi, David P., Kathryn P. Burdon, & Jamie E. Craig. (2009). The genetics of central corneal thickness. British Journal of Ophthalmology. 94(8). 971–976. 80 indexed citations
13.
Balaratnasingam, Chandrakumar, William H. Morgan, John W. Nelson, et al.. (2007). Abnormal Iris Processes May Be a Marker of Glaucoma Gene Carrier Status in Some Cases of Primary Infantile Glaucoma. Ophthalmic Genetics. 28(3). 157–162. 1 indexed citations
14.
Hewitt, Alex W., Shiwani Sharma, Kathryn P. Burdon, et al.. (2007). Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people. Human Molecular Genetics. 17(5). 710–716. 128 indexed citations
15.
Sharma, Shiwani, David P. Dimasi, Stefan Bröer, Raman Kumar, & Neil G. Della. (2007). Heme carrier protein 1 (HCP1) expression and functional analysis in the retina and retinal pigment epithelium. Experimental Cell Research. 313(6). 1251–1259. 10 indexed citations
16.
Burdon, Kathryn P., Shiwani Sharma, Celia S. Chen, et al.. (2007). A novel deletion in theFTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site. Human Mutation. 28(7). 742–742. 20 indexed citations
17.
Hewitt, Alex W., et al.. (2006). A Myocilin Gln368STOP Homozygote Does Not Exhibit a More Severe Glaucoma Phenotype Than Heterozygous Cases. American Journal of Ophthalmology. 141(2). 402–403. 12 indexed citations
18.
Hewitt, Alex W., David P. Dimasi, David A. Mackey, & Jamie E. Craig. (2006). A Glaucoma Case-control Study of the WDR36 Gene D658G Sequence Variant. American Journal of Ophthalmology. 142(2). 324–325. 54 indexed citations
19.
Craig, Jamie E., Alex W. Hewitt, David P. Dimasi, et al.. (2006). The role of the Met98Lys optineurin variant in inherited optic nerve diseases. British Journal of Ophthalmology. 90(11). 1420–1424. 13 indexed citations
20.
Sharma, Shiwani, et al.. (2004). RZF, a zinc-finger protein in the photoreceptors of human retina. Gene. 342(2). 219–229. 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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