Catherine Rameau

8.2k total citations · 2 hit papers
64 papers, 6.0k citations indexed

About

Catherine Rameau is a scholar working on Plant Science, Ecology, Evolution, Behavior and Systematics and Molecular Biology. According to data from OpenAlex, Catherine Rameau has authored 64 papers receiving a total of 6.0k indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Plant Science, 30 papers in Ecology, Evolution, Behavior and Systematics and 20 papers in Molecular Biology. Recurrent topics in Catherine Rameau's work include Plant Molecular Biology Research (40 papers), Plant Parasitism and Resistance (38 papers) and Plant and animal studies (30 papers). Catherine Rameau is often cited by papers focused on Plant Molecular Biology Research (40 papers), Plant Parasitism and Resistance (38 papers) and Plant and animal studies (30 papers). Catherine Rameau collaborates with scholars based in France, Australia and United Kingdom. Catherine Rameau's co-authors include Christine A. Beveridge, Elizabeth A. Dun, Alexandre de Saint Germain, Jean‐Paul Pillot, Philip B. Brewer, Maria Victoria Gómez Roldán, Saı̈da Danoun, Soizic Rochange, Virginie Puech‐Pagès and Guillaume Bécard and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and PLoS ONE.

In The Last Decade

Catherine Rameau

62 papers receiving 5.9k citations

Hit Papers

Strigolactone inhibition of shoot branching 2008 2026 2014 2020 2008 2011 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
Catherine Rameau France 35 5.7k 2.6k 2.0k 235 183 64 6.0k
Philip B. Brewer Australia 29 6.1k 1.1× 2.3k 0.9× 2.8k 1.4× 173 0.7× 90 0.5× 38 6.4k
Elizabeth A. Dun Australia 21 4.5k 0.8× 2.3k 0.9× 1.4k 0.7× 169 0.7× 89 0.5× 23 4.7k
Satoko Yoshida Japan 34 5.5k 1.0× 1.8k 0.7× 1.6k 0.8× 690 2.9× 104 0.6× 62 5.8k
Soizic Rochange France 14 2.9k 0.5× 1.1k 0.4× 1.0k 0.5× 134 0.6× 50 0.3× 19 3.2k
Radoslava Matúšová Slovakia 16 3.5k 0.6× 2.1k 0.8× 910 0.5× 189 0.8× 49 0.3× 27 3.8k
Virginie Puech‐Pagès France 13 4.0k 0.7× 1.6k 0.6× 709 0.4× 229 1.0× 40 0.2× 18 4.2k
Wouter Kohlen Netherlands 27 4.0k 0.7× 1.6k 0.6× 952 0.5× 431 1.8× 41 0.2× 58 4.2k
Mark T. Waters Australia 29 3.9k 0.7× 2.3k 0.9× 1.4k 0.7× 66 0.3× 48 0.3× 45 4.2k
Makoto Kusaba Japan 36 3.7k 0.7× 871 0.3× 3.2k 1.6× 87 0.4× 307 1.7× 77 4.4k
Kaori Yoneyama Japan 35 4.7k 0.8× 3.3k 1.3× 577 0.3× 240 1.0× 27 0.1× 69 4.8k

Countries citing papers authored by Catherine Rameau

Since Specialization
Citations

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

Fields of papers citing papers by Catherine Rameau

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine Rameau

This figure shows the co-authorship network connecting the top 25 collaborators of Catherine Rameau. A scholar is included among the top collaborators of Catherine Rameau 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 Catherine Rameau. Catherine Rameau 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.
Delvento, Chiara, Pasquale Luca Curci, Catherine Rameau, et al.. (2025). Field resistance to Orobanche crenata in pea (Pisum sativum L.): beyond strigolactones. BMC Plant Biology. 25(1). 1340–1340.
2.
Pillot, Jean‐Paul, Carine Géry, Laura Chauvin, et al.. (2025). Efficient and heritable gene editing through CRISPR‐Cas9 in Pisum sativum. Plant Biotechnology Journal. 23(8). 3398–3400.
3.
Cornu, David, Marion Dalmais, Abdelhafid Bendahmane, et al.. (2022). Structural and functional analyses explain Pea KAI2 receptor diversity and reveal stereoselective catalysis during signal perception. Communications Biology. 5(1). 126–126. 20 indexed citations
4.
Lopez‐Obando, Mauricio, François‐Didier Boyer, David Cornu, et al.. (2021). The Physcomitrium ( Physcomitrella ) patens PpKAI2L receptors for strigolactones and related compounds function via MAX2-dependent and -independent pathways. The Plant Cell. 33(11). 3487–3512. 26 indexed citations
5.
Lopez‐Obando, Mauricio, Beate Hoffmann, Alexandre de Saint Germain, et al.. (2018). Physcomitrella patens MAX2 characterization suggests an ancient role for this F‐box protein in photomorphogenesis rather than strigolactone signalling. New Phytologist. 219(2). 743–756. 28 indexed citations
6.
Boutet‐Mercey, Stéphanie, François Perreau, Guillaume Clavé, et al.. (2017). Validated Method for Strigolactone Quantification by Ultra High‐Performance Liquid Chromatography – Electrospray Ionisation Tandem Mass Spectrometry Using Novel Deuterium Labelled Standards. Phytochemical Analysis. 29(1). 59–68. 22 indexed citations
7.
Lopez‐Obando, Mauricio, Beate Hoffmann, Rohan Bythell‐Douglas, et al.. (2016). Structural modelling and transcriptional responses highlight a clade of PpKAI2-LIKE genes as candidate receptors for strigolactones in Physcomitrella patens. Planta. 243(6). 1441–1453. 28 indexed citations
8.
Germain, Alexandre de Saint, Guillaume Clavé, Marie‐Ange Badet‐Denisot, et al.. (2016). An histidine covalent receptor and butenolide complex mediates strigolactone perception. Nature Chemical Biology. 12(10). 787–794. 213 indexed citations
9.
Hoffmann, Beate, Hélène Proust, Katia Belcram, et al.. (2014). Strigolactones Inhibit Caulonema Elongation and Cell Division in the Moss Physcomitrella patens. PLoS ONE. 9(6). e99206–e99206. 36 indexed citations
10.
Boyer, François‐Didier, Alexandre de Saint Germain, Jean‐Bernard Pouvreau, et al.. (2013). New Strigolactone Analogs as Plant Hormones with Low Activities in the Rhizosphere. Molecular Plant. 7(4). 675–690. 81 indexed citations
11.
Weller, James L., Lim Chee Liew, Valérie Hecht, et al.. (2012). A conserved molecular basis for photoperiod adaptation in two temperate legumes. Proceedings of the National Academy of Sciences. 109(51). 21158–21163. 134 indexed citations
12.
Proust, Hélène, Beate Hoffmann, Xiaonan Xie, et al.. (2011). Strigolactones regulate protonema branching and act as a quorum sensing-like signal in the moss Physcomitrella patens. Development. 138(8). 1531–1539. 182 indexed citations
13.
Boyer, François‐Didier, et al.. (2010). Stereochemistry, Total Synthesis, and Biological Evaluation of the New Plant Hormone Solanacol. Chemistry - A European Journal. 16(47). 13941–13945. 47 indexed citations
14.
Rameau, Catherine. (2010). Strigolactones, a novel class of plant hormone controlling shoot branching. Comptes Rendus Biologies. 333(4). 344–349. 36 indexed citations
15.
Elliott, Robert C., Diane R. Lester, Catherine Rameau, et al.. (2008). The Pea DELLA Proteins LA and CRY Are Important Regulators of Gibberellin Synthesis and Root Growth . PLANT PHYSIOLOGY. 147(1). 199–205. 70 indexed citations
16.
Lejeune-Hénaut, Isabelle, Éric Hanocq, Véronique Fontaine, et al.. (2008). The flowering locus Hr colocalizes with a major QTL affecting winter frost tolerance in Pisum sativum L.. Theoretical and Applied Genetics. 116(8). 1105–1116. 85 indexed citations
17.
Roldán, Maria Victoria Gómez, Soraya Fermas, Philip B. Brewer, et al.. (2008). Strigolactone inhibition of shoot branching. Nature. 455(7210). 189–194. 1643 indexed citations breakdown →
18.
Triques, Karine, Bénédicte Sturbois, Marion Dalmais, et al.. (2007). Characterization of Arabidopsis thaliana mismatch specific endonucleases: application to mutation discovery by TILLING in pea. The Plant Journal. 51(6). 1116–1125. 102 indexed citations
19.
Deniot, Gwenaëlle, et al.. (2007). Candidate genes for quantitative resistance to Mycosphaerella pinodes in pea (Pisum sativum L.). Theoretical and Applied Genetics. 114(6). 971–984. 61 indexed citations
20.
Rameau, Catherine, et al.. (2003). The basal-branching pea mutant rms7-1. Queensland's institutional digital repository (The University of Queensland). 3 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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