Giles Oldroyd

28.6k total citations · 9 hit papers
124 papers, 16.5k citations indexed

About

Giles Oldroyd is a scholar working on Plant Science, Agronomy and Crop Science and Molecular Biology. According to data from OpenAlex, Giles Oldroyd has authored 124 papers receiving a total of 16.5k indexed citations (citations by other indexed papers that have themselves been cited), including 123 papers in Plant Science, 36 papers in Agronomy and Crop Science and 9 papers in Molecular Biology. Recurrent topics in Giles Oldroyd's work include Legume Nitrogen Fixing Symbiosis (109 papers), Plant nutrient uptake and metabolism (66 papers) and Agronomic Practices and Intercropping Systems (36 papers). Giles Oldroyd is often cited by papers focused on Legume Nitrogen Fixing Symbiosis (109 papers), Plant nutrient uptake and metabolism (66 papers) and Agronomic Practices and Intercropping Systems (36 papers). Giles Oldroyd collaborates with scholars based in United Kingdom, United States and France. Giles Oldroyd's co-authors include J. Allan Downie, Sharon R. Long, Jongho Sun, Jeremy D. Murray, Cyril Zipfel, Philip S. Poole, Brian J. Staskawicz, Sibylle Hirsch, Julian I. Schroeder and Jane E. Parker and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Giles Oldroyd

120 papers receiving 16.3k citations

Hit Papers

Speak, friend, and enter: signalling systems that promote... 2008 2026 2014 2020 2013 2019 2011 2008 2017 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Giles Oldroyd United Kingdom 67 15.4k 3.9k 2.2k 730 692 124 16.5k
Martin Parniske Germany 60 11.8k 0.8× 1.9k 0.5× 2.6k 1.2× 655 0.9× 378 0.5× 115 12.7k
Philip S. Poole United Kingdom 52 8.1k 0.5× 1.7k 0.4× 1.9k 0.9× 278 0.4× 1.5k 2.2× 149 10.2k
Luigi Cattivelli Italy 54 8.2k 0.5× 1.4k 0.4× 2.8k 1.3× 299 0.4× 266 0.4× 219 9.8k
Majid R. Foolad United States 41 9.8k 0.6× 636 0.2× 2.7k 1.2× 685 0.9× 297 0.4× 99 11.0k
Jean‐Michel Ané United States 41 4.9k 0.3× 937 0.2× 1.2k 0.5× 382 0.5× 309 0.4× 106 5.8k
Ε. H. Roberts United Kingdom 53 9.1k 0.6× 1.2k 0.3× 2.1k 1.0× 1.3k 1.8× 405 0.6× 191 10.1k
Ertao Wang China 41 6.3k 0.4× 573 0.1× 1.2k 0.6× 365 0.5× 283 0.4× 81 7.0k
Maria Harrison United States 65 13.4k 0.9× 564 0.1× 4.0k 1.8× 878 1.2× 220 0.3× 124 14.7k
Meixue Zhou Australia 59 9.7k 0.6× 740 0.2× 1.5k 0.7× 385 0.5× 432 0.6× 276 11.0k
Howard Thomas United Kingdom 49 6.4k 0.4× 938 0.2× 3.9k 1.8× 970 1.3× 232 0.3× 147 8.4k

Countries citing papers authored by Giles Oldroyd

Since Specialization
Citations

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

Fields of papers citing papers by Giles Oldroyd

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giles Oldroyd

This figure shows the co-authorship network connecting the top 25 collaborators of Giles Oldroyd. A scholar is included among the top collaborators of Giles Oldroyd 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 Giles Oldroyd. Giles Oldroyd 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.
Gysel, Kira, Mette Laursen, Feng Feng, et al.. (2025). The Medicago truncatulaLYR4 intracellular domain serves as a scaffold in immunity signaling independent of its phosphorylation activity. New Phytologist. 246(4). 1423–1431. 1 indexed citations
2.
Roy, Sonali, Ivone Torres‐Jerez, Shulan Zhang, et al.. (2024). The peptide GOLVEN10 alters root development and noduletaxis in Medicago truncatula. The Plant Journal. 118(3). 607–625. 12 indexed citations
3.
Zhang, Jingyi, Jongho Sun, Kangping Li, et al.. (2024). A receptor required for chitin perception facilitates arbuscular mycorrhizal associations and distinguishes root symbiosis from immunity. Current Biology. 34(8). 1705–1717.e6. 21 indexed citations
4.
Lin, Jie-shun, Jongho Sun, Xiaowei Huang, et al.. (2022). Constitutive activation of a nuclear-localized calcium channel complex in Medicago truncatula. Proceedings of the National Academy of Sciences. 119(34). e2205920119–e2205920119. 14 indexed citations
5.
Lee, Tak, Boas Pucker, Giles Oldroyd, et al.. (2021). A mycorrhiza-associated receptor-like kinase with an ancient origin in the green lineage. Proceedings of the National Academy of Sciences. 118(25). 19 indexed citations
6.
Radhakrishnan, Guru, Jean Keller, Mélanie K. Rich, et al.. (2020). An ancestral signalling pathway is conserved in intracellular symbioses-forming plant lineages. Nature Plants. 6(3). 280–289. 131 indexed citations
7.
Lee, Tak, Jungnam Cho, Boas Pucker, et al.. (2020). The negative regulator SMAX1 controls mycorrhizal symbiosis and strigolactone biosynthesis in rice. Nature Communications. 11(1). 2114–2114. 90 indexed citations
8.
Feike, Doreen, Andrey Korolev, Eleni Soumpourou, et al.. (2019). Characterizing standard genetic parts and establishing common principles for engineering legume and cereal roots. Plant Biotechnology Journal. 17(12). 2234–2245. 21 indexed citations
9.
Feng, Feng, Jongho Sun, Guru Radhakrishnan, et al.. (2019). A combination of chitooligosaccharide and lipochitooligosaccharide recognition promotes arbuscular mycorrhizal associations in Medicago truncatula. Nature Communications. 10(1). 5047–5047. 148 indexed citations
10.
Couzigou, Jean‐Malo, Katharina Schiessl, Shengbin Liu, et al.. (2018). MtNODULE ROOT1 and MtNODULE ROOT2 Are Essential for Indeterminate Nodule Identity. PLANT PHYSIOLOGY. 178(1). 295–316. 33 indexed citations
11.
Roy, Sonali, Fran Robson, Chengwu Liu, et al.. (2017). MtLAX2, a Functional Homologue of the Arabidopsis Auxin Influx Transporter AUX1, Is Required for Nodule Organogenesis. PLANT PHYSIOLOGY. 174(1). 326–338. 50 indexed citations
12.
Charpentier, Myriam, Jongho Sun, Guru Radhakrishnan, et al.. (2016). Nuclear-localized cyclic nucleotide–gated channels mediate symbiotic calcium oscillations. Science. 352(6289). 1102–1105. 201 indexed citations
13.
Miller, J. Benjamin, et al.. (2013). Phosphorylation of S344 in the calmodulin‐binding domain negatively affects CCaMK function during bacterial and fungal symbioses. The Plant Journal. 76(2). 287–296. 23 indexed citations
14.
Granqvist, Emma, Derin B. Wysham, Wojciech Kozłowski, et al.. (2012). Buffering Capacity Explains Signal Variation in Symbiotic Calcium Oscillations   . PLANT PHYSIOLOGY. 160(4). 2300–2310. 31 indexed citations
15.
Xie, Fang, Jeremy D. Murray, Jiyoung Kim, et al.. (2011). Legume pectate lyase required for root infection by rhizobia. Proceedings of the National Academy of Sciences. 109(2). 633–638. 177 indexed citations
16.
Rogers, Christian, Jiangqi Wen, Rujin Chen, & Giles Oldroyd. (2009). Deletion-Based Reverse Genetics in Medicago truncatula    . PLANT PHYSIOLOGY. 151(3). 1077–1086. 62 indexed citations
17.
Jakab, Júlia, R. Varma Penmetsa, Colby G. Starker, et al.. (2007). An ERF Transcription Factor in Medicago truncatula That Is Essential for Nod Factor Signal Transduction. The Plant Cell. 19(4). 1221–1234. 235 indexed citations
18.
Kaló, Péter, Cynthia Gleason, Anne Edwards, et al.. (2005). Nodulation Signaling in Legumes Requires NSP2, a Member of the GRAS Family of Transcriptional Regulators. Science. 308(5729). 1786–1789. 402 indexed citations
19.
Ané, Jean‐Michel, G. B. Kiss, Brendan K. Riely, et al.. (2004). Medicago truncatula DMI1 Required for Bacterial and Fungal Symbioses in Legumes. Science. 303(5662). 1364–1367. 358 indexed citations
20.
Mitra, Raka M., Cynthia Gleason, Anne Edwards, et al.. (2004). A Ca 2+ /calmodulin-dependent protein kinase required for symbiotic nodule development: Gene identification by transcript-based cloning. Proceedings of the National Academy of Sciences. 101(13). 4701–4705. 323 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026