Robert D. Turner

4.7k total citations · 2 hit papers
64 papers, 3.5k citations indexed

About

Robert D. Turner is a scholar working on Molecular Biology, Genetics and Infectious Diseases. According to data from OpenAlex, Robert D. Turner has authored 64 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 13 papers in Genetics and 9 papers in Infectious Diseases. Recurrent topics in Robert D. Turner's work include Bacterial Genetics and Biotechnology (13 papers), Bacteriophages and microbial interactions (8 papers) and Glycosylation and Glycoproteins Research (6 papers). Robert D. Turner is often cited by papers focused on Bacterial Genetics and Biotechnology (13 papers), Bacteriophages and microbial interactions (8 papers) and Glycosylation and Glycoproteins Research (6 papers). Robert D. Turner collaborates with scholars based in United Kingdom, United States and France. Robert D. Turner's co-authors include R Holman, Simon J. Foster, Jamie K. Hobbs, Waldemar Vollmer, E.H. Cooper, Nic Mullin, Raveen K. J. Tank, Per A. Bullough, Sandip Kumar and Stéphane Mesnage and has published in prestigious journals such as Nature, The Lancet and Nature Communications.

In The Last Decade

Robert D. Turner

59 papers receiving 3.3k citations

Hit Papers

Tight blood pressure control and risk of macrovascular an... 1998 2026 2007 2016 1998 2020 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert D. Turner United Kingdom 21 921 793 792 412 297 64 3.5k
Peter Kierulf Norway 43 647 0.7× 787 1.0× 1.5k 1.8× 326 0.8× 1.8k 5.9× 234 7.9k
Wen Zhang China 31 257 0.3× 282 0.4× 2.6k 3.3× 608 1.5× 270 0.9× 107 4.0k
Kazuo Yoshida Japan 34 136 0.1× 361 0.5× 1.3k 1.6× 229 0.6× 367 1.2× 341 4.4k
Masaki Fujita Japan 37 131 0.1× 299 0.4× 1.1k 1.4× 328 0.8× 621 2.1× 240 5.0k
Takeshi Itoh Japan 27 450 0.5× 235 0.3× 749 0.9× 616 1.5× 109 0.4× 156 3.3k
John R. Barr United States 46 862 0.9× 183 0.2× 2.3k 2.9× 483 1.2× 669 2.3× 223 7.9k
Mary J. Bartholomew United States 26 302 0.3× 166 0.2× 512 0.6× 247 0.6× 183 0.6× 64 2.2k
Sang Ho Lee South Korea 41 428 0.5× 278 0.4× 2.9k 3.6× 402 1.0× 426 1.4× 297 6.7k
Yvon Berland France 43 555 0.6× 496 0.6× 1.7k 2.2× 319 0.8× 582 2.0× 213 6.2k
Mi Yeon Lee South Korea 28 260 0.3× 190 0.2× 657 0.8× 108 0.3× 311 1.0× 208 2.7k

Countries citing papers authored by Robert D. Turner

Since Specialization
Citations

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

Fields of papers citing papers by Robert D. Turner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robert D. Turner

This figure shows the co-authorship network connecting the top 25 collaborators of Robert D. Turner. A scholar is included among the top collaborators of Robert D. Turner 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 Robert D. Turner. Robert D. Turner 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.
Crook, Derrick W., Tim Peto, Philip W. Fowler, et al.. (2025). Evaluating 12 automated, whole-genome sequencing analysis pipelines for Mycobacterium tuberculosis complex: a comparative study. The Lancet Microbe. 6(12). 101210–101210. 1 indexed citations
2.
Ledermann, Raphael, Neil Shephard, Caroline A. Evans, et al.. (2025). A software tool and strategy for peptidoglycomics, the high-resolution analysis of bacterial peptidoglycans via LC-MS/MS. Communications Chemistry. 8(1). 91–91. 1 indexed citations
4.
Brown, Matilda J. M., Barnaby E. Walker, Rafaël Govaerts, et al.. (2023). rWCVP: a companion R package for the World Checklist of Vascular Plants. New Phytologist. 240(4). 1355–1365. 48 indexed citations
5.
Salamaga, Bartłomiej, et al.. (2023). A moonlighting role for LysM peptidoglycan binding domains underpins Enterococcus faecalis daughter cell separation. Communications Biology. 6(1). 428–428. 7 indexed citations
6.
Murdoch, Craig, Simon G. Danby, Hirofumi Nakanishi, et al.. (2021). Determination of Chemical Irritation Potential Using a Defined Gene Signature Set on Tissue-Engineered Human Skin Equivalents. SHILAP Revista de lepidopterología. 1(2). 100011–100011. 4 indexed citations
7.
Turner, Robert D., Aline Rifflet, Andrew Nichols, et al.. (2021). PGFinder, a novel analysis pipeline for the consistent, reproducible, and high-resolution structural analysis of bacterial peptidoglycans. eLife. 10. 17 indexed citations
8.
Pasquina-Lemonche, Laia, Robert D. Turner, Sandip Kumar, et al.. (2020). The architecture of the Gram-positive bacterial cell wall. Nature. 582(7811). 294–297. 343 indexed citations breakdown →
9.
Paterson, Thomas E., Alessandra Bari, Anthony J. Bullock, et al.. (2020). Multifunctional Copper-Containing Mesoporous Glass Nanoparticles as Antibacterial and Proangiogenic Agents for Chronic Wounds. Frontiers in Bioengineering and Biotechnology. 8. 246–246. 40 indexed citations
10.
Turner, Robert D., Stéphane Mesnage, Jamie K. Hobbs, & Simon J. Foster. (2018). Molecular imaging of glycan chains couples cell-wall polysaccharide architecture to bacterial cell morphology. Nature Communications. 9(1). 1263–1263. 72 indexed citations
11.
Manton, James D., Yao Xiao, Robert D. Turner, Graham Christie, & Eric J. Rees. (2018). ELM: super-resolution analysis of wide-field images of fluorescent shell structures. Methods and Applications in Fluorescence. 6(3). 37001–37001. 4 indexed citations
12.
Turner, Robert D., Jamie K. Hobbs, & Simon J. Foster. (2016). Atomic Force Microscopy Analysis of Bacterial Cell Wall Peptidoglycan Architecture. Methods in molecular biology. 1440. 3–9. 14 indexed citations
13.
Bailey, Richard G., et al.. (2014). The Interplay between Cell Wall Mechanical Properties and the Cell Cycle in Staphylococcus aureus. Biophysical Journal. 107(11). 2538–2545. 44 indexed citations
14.
Turner, Robert D., Emma C. Ratcliffe, Richard Wheeler, et al.. (2010). Peptidoglycan architecture can specify division planes in Staphylococcus aureus. Nature Communications. 1(1). 26–26. 107 indexed citations
15.
Turner, Robert D., Neil H. Thomson, J. Kirkham, & Deirdre DeVine. (2009). Improvement of the pore trapping method to immobilize vital coccoid bacteria for high‐resolution AFM: a study of Staphylococcus aureus. Journal of Microscopy. 238(2). 102–110. 15 indexed citations
16.
Turner, Robert D.. (2001). The treatment of rhinovirus infections: progress and potential. Antiviral Research. 49(1). 1–14. 75 indexed citations
18.
Turner, Robert D.. (1984). The Limitations of Material History: A Museological Perspective. Material Culture Review / Revue de la culture matérielle. 20. 1 indexed citations
19.
Cooper, E H, Robert D. Turner, Linda Steele, & J C Goligher. (1974). Blood Muramidase Activity in Colorectal Cancer. BMJ. 3(5932). 662–664. 11 indexed citations
20.
Turner, Robert D.. (1956). The diffraction of a cylindrical pulse by a half-plane. Quarterly of Applied Mathematics. 14(1). 63–73. 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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