Carl Robinson

1.6k total citations
40 papers, 967 citations indexed

About

Carl Robinson is a scholar working on Public Health, Environmental and Occupational Health, Microbiology and Infectious Diseases. According to data from OpenAlex, Carl Robinson has authored 40 papers receiving a total of 967 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Public Health, Environmental and Occupational Health, 18 papers in Microbiology and 10 papers in Infectious Diseases. Recurrent topics in Carl Robinson's work include Streptococcal Infections and Treatments (28 papers), Microbial infections and disease research (18 papers) and Neonatal and Maternal Infections (9 papers). Carl Robinson is often cited by papers focused on Streptococcal Infections and Treatments (28 papers), Microbial infections and disease research (18 papers) and Neonatal and Maternal Infections (9 papers). Carl Robinson collaborates with scholars based in United Kingdom, Sweden and France. Carl Robinson's co-authors include Andrew S. Waller, Karen F. Steward, J. R. Newton, K. Webb, Keith A. Jolley, Bernard M. Corfe, Martin Maiden, Matthew T. G. Holden, Romain Paillot and Nicholas Davis‐Poynter and has published in prestigious journals such as International Journal of Molecular Sciences, Genome Research and Journal of Clinical Microbiology.

In The Last Decade

Carl Robinson

39 papers receiving 932 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carl Robinson United Kingdom 19 694 464 258 194 158 40 967
César B. Gutiérrez‐Martín Spain 21 239 0.3× 893 1.9× 256 1.0× 148 0.8× 196 1.2× 78 1.3k
Corinne Marois‐Créhan France 18 330 0.5× 566 1.2× 281 1.1× 241 1.2× 68 0.4× 30 1.0k
Astrid de Greeff Netherlands 19 789 1.1× 218 0.5× 387 1.5× 196 1.0× 218 1.4× 38 1.1k
Reinhard Sting Germany 18 113 0.2× 384 0.8× 310 1.2× 236 1.2× 183 1.2× 81 1.1k
U. Vecht Netherlands 19 1.1k 1.6× 266 0.6× 600 2.3× 251 1.3× 122 0.8× 32 1.3k
Marylène Kobisch France 19 448 0.6× 548 1.2× 217 0.8× 187 1.0× 155 1.0× 30 1.1k
Qinning Wang Australia 19 132 0.2× 205 0.4× 370 1.4× 282 1.5× 265 1.7× 68 1.1k
H. E. Smith Netherlands 14 846 1.2× 245 0.5× 436 1.7× 194 1.0× 129 0.8× 18 1.0k
Jiaqi Tang China 20 876 1.3× 179 0.4× 430 1.7× 171 0.9× 272 1.7× 50 1.2k
Corrie Schot Netherlands 16 164 0.2× 144 0.3× 583 2.3× 309 1.6× 145 0.9× 24 1.1k

Countries citing papers authored by Carl Robinson

Since Specialization
Citations

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

Fields of papers citing papers by Carl Robinson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carl Robinson

This figure shows the co-authorship network connecting the top 25 collaborators of Carl Robinson. A scholar is included among the top collaborators of Carl Robinson 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 Carl Robinson. Carl Robinson 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.
Robinson, Carl, Andrew S. Waller, Lars Frykberg, et al.. (2020). Intramuscular vaccination with Strangvac is safe and induces protection against equine strangles caused by Streptococcus equi. Vaccine. 38(31). 4861–4868. 26 indexed citations
2.
Taylor, Emma, Carl Robinson, Amy K. Cain, et al.. (2020). Identification of genes required for the fitness of Streptococcus equi subsp. equi in whole equine blood and hydrogen peroxide. Microbial Genomics. 6(4). 5 indexed citations
3.
Waern, Ida, Jens Eriksson, Fábio Rabelo Melo, et al.. (2019). StreptococcalsagAactivates a proinflammatory response in mast cells by a sublytic mechanism. Cellular Microbiology. 21(9). e13064–e13064. 8 indexed citations
4.
Björnsdóttir, Sigríður, Simon R. Harris, Vilhjálmur Svansson, et al.. (2017). Genomic Dissection of an Icelandic Epidemic of Respiratory Disease in Horses and Associated Zoonotic Cases. mBio. 8(4). 26 indexed citations
5.
Steward, Karen F., Carl Robinson, Matthew T. G. Holden, et al.. (2017). Diversity of Streptococcus equi subsp. zooepidemicus strains isolated from the Spanish sheep and goat population and the identification, function and prevalence of a novel arbutin utilisation system. Veterinary Microbiology. 207. 231–238. 11 indexed citations
6.
Forman, Oliver P., Amy K. Cain, Carl Robinson, et al.. (2017). Defining the ABC of gene essentiality in streptococci. BMC Genomics. 18(1). 426–426. 23 indexed citations
7.
Newton, J. R., Carl Robinson, & Andrew S. Waller. (2016). Use of vaccination in the eradication of strangles: the importance of differentiating infected from vaccinated animals (DIVA). Journal of Equine Veterinary Science. 39. S92–S92. 1 indexed citations
8.
Zhang, Meng, Dean J. Harrington, Carl Robinson, et al.. (2015). Characterisation of SEQ0694 (PrsA/PrtM) of Streptococcus equi as a functional peptidyl-prolyl isomerase affecting multiple secreted protein substrates. Molecular BioSystems. 11(12). 3279–3286. 7 indexed citations
9.
Harris, Simon R., Carl Robinson, Karen F. Steward, et al.. (2015). Genome specialization and decay of the strangles pathogen, Streptococcus equi , is driven by persistent infection. Genome Research. 25(9). 1360–1371. 56 indexed citations
10.
Robinson, Carl, Josh Slater, Karen F. Steward, et al.. (2015). Vaccination with a live multi-gene deletion strain protects horses against virulent challenge with Streptococcus equi. Vaccine. 33(9). 1160–1167. 10 indexed citations
11.
McLean, Rebecca, et al.. (2015). Localised mitogenic activity in horses following infection with Streptococcus equi. Research in Veterinary Science. 100. 100–104. 4 indexed citations
12.
Robinson, Carl, et al.. (2014). Prevalence and disease associations of superantigens szeF, szeN and szeP in the S. zooepidemicus population and possible functional redundancy of szeF. Research in Veterinary Science. 97(3). 481–487. 8 indexed citations
13.
Robinson, Carl, Karen F. Steward, Colin Barker, et al.. (2013). Combining two serological assays optimises sensitivity and specificity for the identification of Streptococcus equi subsp. equi exposure. The Veterinary Journal. 197(2). 188–191. 52 indexed citations
14.
Webb, K., Colin Barker, Karen F. Steward, et al.. (2012). Detection of Streptococcus equi subspecies equi using a triplex qPCR assay. The Veterinary Journal. 195(3). 300–304. 46 indexed citations
15.
Matthews, David A., K. Webb, J. R. Newton, et al.. (2010). Molecular characterisation of ‘strangles’ outbreaks in the UK: The use of M‐protein typing of Streptococcus equi ssp. equi. Equine Veterinary Journal. 43(3). 359–364. 35 indexed citations
16.
Webb, K., Keith A. Jolley, Carl Robinson, et al.. (2008). Development of an unambiguous and discriminatory multilocus sequence typing scheme for the Streptococcus zooepidemicus group. Microbiology. 154(10). 3016–3024. 92 indexed citations
17.
Waller, Andrew S., Margareta Flock, Ken Smith, et al.. (2007). Vaccination of horses against strangles using recombinant antigens from Streptococcus equi. Vaccine. 25(18). 3629–3635. 27 indexed citations
18.
Robinson, Carl, Iain C. Sutcliffe, Josh Slater, et al.. (2006). Mutation of the Maturase Lipoprotein Attenuates the Virulence ofStreptococcus equito a Greater Extent than Does Loss of General Lipoprotein Lipidation. Infection and Immunity. 74(12). 6907–6919. 50 indexed citations
19.
Robinson, Carl, et al.. (1996). Alanine germination receptors of Bacillus subtailis. Letters in Applied Microbiology. 23(5). 290–294. 29 indexed citations
20.
Herbert, Corentin, et al.. (1994). Human eosinophils and recombinant matrix metalloproteinase-2 increase permeability of the bovine and porcine bronchial mucosa. UWA Profiles and Research Repository (University of Western Australia). 2 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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2026