M. W. Shaw

6.9k total citations · 1 hit paper
174 papers, 5.2k citations indexed

About

M. W. Shaw is a scholar working on Plant Science, Ecology, Evolution, Behavior and Systematics and Cell Biology. According to data from OpenAlex, M. W. Shaw has authored 174 papers receiving a total of 5.2k indexed citations (citations by other indexed papers that have themselves been cited), including 137 papers in Plant Science, 58 papers in Ecology, Evolution, Behavior and Systematics and 47 papers in Cell Biology. Recurrent topics in M. W. Shaw's work include Plant Pathogens and Fungal Diseases (47 papers), Fungal Plant Pathogen Control (44 papers) and Plant Disease Resistance and Genetics (34 papers). M. W. Shaw is often cited by papers focused on Plant Pathogens and Fungal Diseases (47 papers), Fungal Plant Pathogen Control (44 papers) and Plant Disease Resistance and Genetics (34 papers). M. W. Shaw collaborates with scholars based in United Kingdom, United States and Sri Lanka. M. W. Shaw's co-authors include D.J. Royle, B. A. Fraaije, Frank van den Bosch, Bruce D.L. Fitt, Marco Pautasso, G. M. Hewitt, N. D. Paveley, Mojgan Rabiey, Thomas M. Osborne and S. R. Parker and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and SHILAP Revista de lepidopterología.

In The Last Decade

M. W. Shaw

171 papers receiving 4.8k citations

Hit Papers

Biological control of pla... 2022 2026 2023 2024 2022 50 100 150

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
M. W. Shaw 4.0k 1.3k 1.2k 801 775 174 5.2k
Christopher C. Mundt 5.4k 1.3× 722 0.6× 1.0k 0.8× 755 0.9× 1.3k 1.7× 140 6.5k
M. J. Jeger 3.1k 0.8× 479 0.4× 941 0.8× 360 0.4× 387 0.5× 97 3.9k
Hirokazu Toju 2.5k 0.6× 1.1k 0.9× 893 0.7× 875 1.1× 363 0.5× 65 4.3k
John Rozewicki 2.3k 0.6× 1.1k 0.9× 1.2k 0.9× 2.7k 3.4× 715 0.9× 8 6.4k
Scott O. Rogers 2.5k 0.6× 604 0.5× 669 0.5× 1.7k 2.1× 527 0.7× 73 4.5k
Niklaus J. Grünwald 6.6k 1.6× 987 0.8× 3.5k 2.9× 2.8k 3.5× 1.5k 2.0× 190 9.2k
François Delmotte 2.3k 0.6× 818 0.6× 1.0k 0.8× 787 1.0× 662 0.9× 74 3.5k
Christopher M. Richards 2.0k 0.5× 1.1k 0.8× 281 0.2× 813 1.0× 1.1k 1.4× 96 3.4k
Corbin D. Jones 3.7k 0.9× 808 0.6× 534 0.4× 2.9k 3.7× 1.6k 2.1× 115 7.6k
Bruce D.L. Fitt 7.0k 1.7× 1.1k 0.8× 3.3k 2.7× 960 1.2× 279 0.4× 350 7.9k

Countries citing papers authored by M. W. Shaw

Since Specialization
Citations

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

Fields of papers citing papers by M. W. Shaw

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. W. Shaw. 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 M. W. Shaw. The network helps show where M. W. Shaw may publish in the future.

Co-authorship network of co-authors of M. W. Shaw

This figure shows the co-authorship network connecting the top 25 collaborators of M. W. Shaw. A scholar is included among the top collaborators of M. W. Shaw 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 M. W. Shaw. M. W. Shaw 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.
Mikaberidze, Alexey, et al.. (2025). Dose Splitting Increases Selection for Both Target‐Site and Non‐Target‐Site Fungicide Resistance—A Modelling Analysis. Plant Pathology. 74(4). 1152–1167. 1 indexed citations
2.
Roberts, Caleb P., Michael Ferrara, Lauren Luther, et al.. (2025). Rallus elegans (King Rail) occupancy is stable, but habitat is in short supply in the Arkansas Delta. Ornithological applications. 128(1). 1–9.
3.
Shaw, M. W., et al.. (2024). Spatial spread of Ditylenchus gigas and its interaction with Botrytis fabae on Vicia faba. Annals of Applied Biology. 186(2). 125–131.
4.
Shaw, M. W., et al.. (2022). Field application of Bacillus subtilis and Aureobasidium pullulans to reduce Monilinia laxa post-harvest rot on cherry. European Journal of Plant Pathology. 163(3). 761–766. 6 indexed citations
5.
Schoonbeek, Henk‐jan, et al.. (2022). Microscope studies of symptomless growth of Botrytis cinerea in Lactuca sativa and Arabidopsis thaliana. Plant Pathology. 72(3). 564–581. 2 indexed citations
6.
Xu, Xiangming, et al.. (2021). Biocontrol agents to manage brown rot disease on cherry. European Journal of Plant Pathology. 161(3). 493–502. 11 indexed citations
7.
Passey, Tom, et al.. (2020). Genomic sequencing indicates non‐random mating of Venturia inaequalis in a mixed cultivar orchard. Plant Pathology. 69(4). 669–676. 5 indexed citations
8.
Ritchie, Faye, et al.. (2020). Inter‐individual genetic variation in the temperature response of Leptosphaeria species pathogenic on oilseed rape. Plant Pathology. 69(8). 1469–1481. 6 indexed citations
9.
Shaw, M. W., et al.. (2020). Cross‐resistance between myclobutanil and tebuconazole and the genetic basis of tebuconazole resistance in Venturia inaequalis. Pest Management Science. 77(2). 844–850. 24 indexed citations
10.
Shaw, M. W., et al.. (2020). The effect of competition on the control of invading plant pathogens. Journal of Applied Ecology. 57(7). 1403–1412. 2 indexed citations
11.
12.
Hawkins, Nichola J., et al.. (2017). Dose‐dependent selection drives lineage replacement during the experimental evolution of SDHI fungicide resistance in Zymoseptoria tritici. Evolutionary Applications. 10(10). 1055–1066. 30 indexed citations
13.
Saslis‐Lagoudakis, C. Haris, et al.. (2015). Genetic diversity and specialisation of Eudarluca caricis on some graminaceous Puccinia species. Fungal ecology. 14. 116–124. 2 indexed citations
14.
Rabiey, Mojgan, Ihsan Ullah, & M. W. Shaw. (2013). The effect of Piriformospora indica, an endophytic fungus, on wheat resistance to Fusarium disease.. Aspects of applied biology. 91–94. 1 indexed citations
15.
Wilkinson, M. J., J. Allainguillaume, M. W. Shaw, et al.. (2003). Hybridization Between Brassica napus and B. rapa on a National Scale in the United Kingdom. Science. 302(5644). 457–459. 129 indexed citations
16.
Shaw, M. W., et al.. (2002). Effect of dose rate and mixture on selection for reduced sensitivity to triazole fungicides in Mycosphaerella graminicola.. 859–864. 3 indexed citations
17.
Otim‐Nape, G. W., J. M. Thresh, & M. W. Shaw. (1998). THE INCIDENCE AND SEVERITY OF CASSAVA MOSAIC VIRUS DISEASE IN UGANDA: 1990-92. Tropical Science. 38(1). 25–37. 23 indexed citations
18.
Shaw, M. W. & D.J. Royle. (1986). Saving septoria fungicide sprays: the use of disease forecasts.. 3. 1193–1200. 10 indexed citations
19.
Shaw, M. W., et al.. (1975). Polymporphism of human C-band heterochromatin. II. Family studies with suggestive evidence for somatic crossing over.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 27(2). 178–89. 90 indexed citations
20.
Shaw, M. W.. (1957). Aphids and seed-potato growing in Scotland.. Agricultural Reviews. 3. 28–36. 1 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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