Thomas Ledger

1.2k total citations
22 papers, 898 citations indexed

About

Thomas Ledger is a scholar working on Plant Science, Molecular Biology and Pollution. According to data from OpenAlex, Thomas Ledger has authored 22 papers receiving a total of 898 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Plant Science, 7 papers in Molecular Biology and 7 papers in Pollution. Recurrent topics in Thomas Ledger's work include Plant-Microbe Interactions and Immunity (10 papers), Microbial bioremediation and biosurfactants (5 papers) and Legume Nitrogen Fixing Symbiosis (5 papers). Thomas Ledger is often cited by papers focused on Plant-Microbe Interactions and Immunity (10 papers), Microbial bioremediation and biosurfactants (5 papers) and Legume Nitrogen Fixing Symbiosis (5 papers). Thomas Ledger collaborates with scholars based in Chile, United States and Spain. Thomas Ledger's co-authors include Bernardo González, María Josefina Poupin, Danilo Pérez‐Pantoja, Raúl A. Donoso, Dietmar H. Pieper, Ana Zúñiga, Nicolás Guiliani, Rodrigo A. Gutiérrez, Marlene Manzano and Kornelia Smalla and has published in prestigious journals such as PLoS ONE, Applied and Environmental Microbiology and Scientific Reports.

In The Last Decade

Thomas Ledger

22 papers receiving 895 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas Ledger Chile 13 446 269 262 147 90 22 898
Adam E. Croxford United Kingdom 9 126 0.3× 396 1.5× 135 0.5× 112 0.8× 46 0.5× 15 693
Betsy M. Martínez-Vaz United States 8 140 0.3× 387 1.4× 187 0.7× 71 0.5× 26 0.3× 22 647
Manuella Nóbrega Dourado Brazil 19 572 1.3× 201 0.7× 331 1.3× 147 1.0× 8 0.1× 27 1.0k
María Ángeles Castillo Spain 19 269 0.6× 185 0.7× 110 0.4× 25 0.2× 27 0.3× 27 739
Sukanya Lal India 12 66 0.1× 300 1.1× 206 0.8× 108 0.7× 20 0.2× 17 536
Rekha Kumari India 11 57 0.1× 206 0.8× 209 0.8× 102 0.7× 14 0.2× 29 476
Jiajin Song China 11 146 0.3× 305 1.1× 87 0.3× 68 0.5× 80 0.9× 18 499
Sergio A. Cuozzo Argentina 14 99 0.2× 306 1.1× 157 0.6× 68 0.5× 12 0.1× 25 606
Jingyuan Chen China 16 410 0.9× 79 0.3× 255 1.0× 95 0.6× 5 0.1× 38 843

Countries citing papers authored by Thomas Ledger

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Ledger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Ledger

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Ledger. A scholar is included among the top collaborators of Thomas Ledger 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 Thomas Ledger. Thomas Ledger 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.
Vega, Andrea, et al.. (2024). Nitrogen-modulated effects of the diazotrophic bacterium Cupriavidus taiwanensis on the non-nodulating plant Arabidopsis thaliana. Plant and Soil. 506(1-2). 819–837. 2 indexed citations
3.
Poupin, María Josefina, et al.. (2023). The Arabidopsis holobiont: a (re)source of insights to understand the amazing world of plant–microbe interactions. Environmental Microbiome. 18(1). 9–9. 19 indexed citations
5.
Gazitúa, María Consuelo, Verónica Morgante, María Josefina Poupin, et al.. (2021). The microbial community from the early-plant colonizer (Baccharis linearis) is required for plant establishment on copper mine tailings. Scientific Reports. 11(1). 10448–10448. 18 indexed citations
6.
Ledger, Thomas, et al.. (2018). Non-halophilic endophytes associated with the euhalophyte Arthrocnemum macrostachyum and their plant growth promoting activity potential. FEMS Microbiology Letters. 365(19). 12 indexed citations
7.
Ruz, Gonzalo A., Daniel Ashlock, Thomas Ledger, & Eric Goles. (2017). Inferring bistable lac operen Boolean regulatory networks using evolutionary computation. 1–8. 1 indexed citations
8.
Ledger, Thomas, et al.. (2016). Volatile-Mediated Effects Predominate in Paraburkholderia phytofirmans Growth Promotion and Salt Stress Tolerance of Arabidopsis thaliana. Frontiers in Microbiology. 7. 1838–1838. 88 indexed citations
10.
Ledger, Thomas, et al.. (2015). Burkholderia phytofirmans PsJN induces long-term metabolic and transcriptional changes involved in Arabidopsis thaliana salt tolerance. Frontiers in Plant Science. 6. 466–466. 118 indexed citations
11.
Zúñiga, Ana, María Josefina Poupin, Raúl A. Donoso, et al.. (2013). Quorum Sensing and Indole-3-Acetic Acid Degradation Play a Role in Colonization and Plant Growth Promotion of Arabidopsis thaliana by Burkholderia phytofirmans PsJN. Molecular Plant-Microbe Interactions. 26(5). 546–553. 137 indexed citations
12.
Heuer, Holger, Chu Thi Thanh Binh, Sven Jechalke, et al.. (2012). IncP-1ε Plasmids are Important Vectors of Antibiotic Resistance Genes in Agricultural Systems: Diversification Driven by Class 1 Integron Gene Cassettes. Frontiers in Microbiology. 3. 2–2. 117 indexed citations
14.
Ledger, Thomas, Ana Zúñiga, Tatiana Kraiser, et al.. (2011). Aromatic compounds degradation plays a role in colonization of Arabidopsis thaliana and Acacia caven by Cupriavidus pinatubonensis JMP134. Antonie van Leeuwenhoek. 101(4). 713–723. 15 indexed citations
15.
Lykidis, Athanasios, Danilo Pérez‐Pantoja, Thomas Ledger, et al.. (2010). The Complete Multipartite Genome Sequence of Cupriavidus necator JMP134, a Versatile Pollutant Degrader. PLoS ONE. 5(3). e9729–e9729. 91 indexed citations
16.
Ledger, Thomas, Felipe F. Aceituno, & Bernardo González. (2009). 3-Chlorobenzoate is taken up by a chromosomally encoded transport system in Cupriavidus necator JMP134. Microbiology. 155(8). 2757–2765. 10 indexed citations
17.
Ledger, Thomas, Dietmar H. Pieper, & Bernardo González. (2006). Chlorophenol Hydroxylases Encoded by Plasmid pJP4 Differentially Contribute to Chlorophenoxyacetic Acid Degradation. Applied and Environmental Microbiology. 72(4). 2783–2792. 41 indexed citations
18.
19.
Pérez‐Pantoja, Danilo, Thomas Ledger, Dietmar H. Pieper, & Bernardo González. (2003). Efficient Turnover of Chlorocatechols Is Essential for Growth of Ralstonia eutropha JMP134(pJP4) in 3-Chlorobenzoic Acid. Journal of Bacteriology. 185(5). 1534–1542. 45 indexed citations
20.
Ledger, Thomas, Dietmar H. Pieper, Danilo Pérez‐Pantoja, & Bernardo González. (2002). Novel insights into the interplay between peripheral reactions encoded by xyl genes and the chlorocatechol pathway encoded by tfd genes for the degradation of chlorobenzoates by Ralstonia eutropha JMP134. Microbiology. 148(11). 3431–3440. 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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