Philip N. Ward

2.8k total citations
42 papers, 1.3k citations indexed

About

Philip N. Ward is a scholar working on Molecular Biology, Public Health, Environmental and Occupational Health and Microbiology. According to data from OpenAlex, Philip N. Ward has authored 42 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 17 papers in Public Health, Environmental and Occupational Health and 16 papers in Microbiology. Recurrent topics in Philip N. Ward's work include Streptococcal Infections and Treatments (17 papers), Milk Quality and Mastitis in Dairy Cows (12 papers) and Microbial infections and disease research (12 papers). Philip N. Ward is often cited by papers focused on Streptococcal Infections and Treatments (17 papers), Milk Quality and Mastitis in Dairy Cows (12 papers) and Microbial infections and disease research (12 papers). Philip N. Ward collaborates with scholars based in United Kingdom, United States and Canada. Philip N. Ward's co-authors include James A. Leigh, Terence R. Field, Tracey J. Coffey, Sharon A. Egan, Martin Maiden, Emmanuelle Maguin, William Ditcham, P Narcisi, Robert W Bentley and Allan J. Richards and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Journal of Molecular Biology.

In The Last Decade

Philip N. Ward

42 papers receiving 1.3k citations

Peers

Philip N. Ward

MICRO

PHEOH

ACS

Claudia F. Deobald United States

Cherilyn A. Elwell United States

Jodi K. Craigo United States

Adeline Mallet France

Reggie Y.C. Lo Canada

Orla Hartford Ireland

Mary Jo Hamilton United States

Virgil E.J.C. Schijns Netherlands

Marci A. Scidmore United States

Jacob Pitcovski Israel

Claudia F. Deobald United States

Philip N. Ward

134 ×0.3

MICRO

104 ×0.3

PHEOH

417 ×1.1

136 ×0.4

ACS

125 ×0.5

Citations per year, relative to Philip N. Ward Philip N. Ward (= 1×) peers Claudia F. Deobald

Countries citing papers authored by Philip N. Ward

Since Specialization

Citations

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

Fields of papers citing papers by Philip N. Ward

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Philip N. Ward. 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 Philip N. Ward. The network helps show where Philip N. Ward may publish in the future.

Co-authorship network of co-authors of Philip N. Ward

This figure shows the co-authorship network connecting the top 25 collaborators of Philip N. Ward. A scholar is included among the top collaborators of Philip N. Ward 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 Philip N. Ward. Philip N. Ward 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

Ward, Philip N., et al.. (2024). Priming from within: TLR2 dependent but receptor independent activation of the mammary macrophage inflammasome by Streptococcus uberis. Frontiers in Cellular and Infection Microbiology. 14. 1444178–1444178. 1 indexed citations

Weckener, Miriam, Bradley R. Clarke, Huanting Liu, et al.. (2023). The lipid linked oligosaccharide polymerase Wzy and its regulating co-polymerase, Wzz, from enterobacterial common antigen biosynthesis form a complex. Open Biology. 13(3). 220373–220373. 11 indexed citations

Uchański, Tomasz, Simonas Masiulis, Baptiste Fischer, et al.. (2021). Megabodies expand the nanobody toolkit for protein structure determination by single-particle cryo-EM. Nature Methods. 18(1). 60–68. 86 indexed citations

Yang, Yun, Jiwei Liu, Bradley R. Clarke, et al.. (2021). The molecular basis of regulation of bacterial capsule assembly by Wzc. Nature Communications. 12(1). 4349–4349. 40 indexed citations

Cehovin, Ana, Odile B. Harrison, Philip N. Ward, et al.. (2018). Identification of Novel Neisseria gonorrhoeae Lineages Harboring Resistance Plasmids in Coastal Kenya. The Journal of Infectious Diseases. 218(5). 801–808. 36 indexed citations

Berry, Jamie-Lee, Yingqi Xu, Philip N. Ward, et al.. (2016). A Comparative Structure/Function Analysis of Two Type IV Pilin DNA Receptors Defines a Novel Mode of DNA Binding. Structure. 24(6). 926–934. 30 indexed citations

Johnson, Steven, Lionel Tan, Stijn van der Veen, et al.. (2012). Design and Evaluation of Meningococcal Vaccines through Structure-Based Modification of Host and Pathogen Molecules. PLoS Pathogens. 8(10). e1002981–e1002981. 49 indexed citations

Leigh, James A., Sharon A. Egan, Philip N. Ward, Terence R. Field, & Tracey J. Coffey. (2010). Sortase anchored proteins ofStreptococcus uberisplay major roles in the pathogenesis of bovine mastitis in dairy cattle. Veterinary Research. 41(5). 63–63. 38 indexed citations

Leigh, James A., et al.. (2010). Differential Protein Expression in Streptococcus uberis under Planktonic and Biofilm Growth Conditions. Applied and Environmental Microbiology. 77(1). 382–384. 23 indexed citations

10.

Ward, Philip N., Matthew T. G. Holden, James A. Leigh, et al.. (2009). Evidence for niche adaptation in the genome of the bovine pathogen Streptococcus uberis. BMC Genomics. 10(1). 54–54. 86 indexed citations

11.

Ward, Philip N., et al.. (2008). Structural Consideration of the Formation of the Activation Complex between the Staphylokinase-Like Streptococcal Plasminogen Activator PadA and Bovine Plasminogen. Journal of Molecular Biology. 381(3). 734–747. 9 indexed citations

12.

Monaghan, Padraic, et al.. (2004). Localization of MtuA, an LraI homologue in Streptococcus uberis. Journal of Applied Microbiology. 97(1). 149–157. 3 indexed citations

13.

Ward, Philip N., et al.. (2004). Complex Interactions Between Bovine Plasminogen and Streptococcal Plasminogen Activator PauA. Journal of Molecular Biology. 342(4). 1101–1114. 13 indexed citations

14.

Leigh, James A., et al.. (2004). The exploitation of the genome in the search for determinants of virulence in Streptococcus uberis. Veterinary Immunology and Immunopathology. 100(3-4). 145–149. 9 indexed citations

15.

McVey, D. Scott, Jishu Shi, James A. Leigh, et al.. (2004). Identification of multiple linear epitopes of the plasminogen activator A (PauA) of Streptococcus uberis with murine monoclonal antibodies. Veterinary Immunology and Immunopathology. 104(3-4). 155–162. 4 indexed citations

16.

Rosey, Everett L., et al.. (1999). PauA: a novel plasminogen activator fromStreptococcus uberis. FEMS Microbiology Letters. 178(1). 27–33. 39 indexed citations

17.

Ward, Philip N., et al.. (1999). Epithelial invasion and cell lysis by virulent strains ofStreptococcus suisis enhanced by the presence of suilysin. FEMS Immunology & Medical Microbiology. 26(1). 25–35. 63 indexed citations

18.

Ward, Philip N., et al.. (1994). Mutation of a putative ADP‐ribosylation motif in the Pasteurella multocida toxin does not affect mitogenic activity. FEBS Letters. 342(1). 81–84. 10 indexed citations

19.

Richards, Allan J., J. C. Lloyd, P Narcisi, et al.. (1992). A 27-bp deletion from one allele of the type III collagen gene (COL3A1) in a large family with Ehlers-Danlos syndrome type IV. Human Genetics. 88(3). 325–330. 23 indexed citations

20.

Wilson, R.T., et al.. (1987). Milk Production Characteristics of the Kenana Breed of Bos indicus Cattle in Sudan. Journal of Dairy Science. 70(12). 2673–2679. 9 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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