Pierre Chambrier

2.2k total citations
28 papers, 1.5k citations indexed

About

Pierre Chambrier is a scholar working on Molecular Biology, Plant Science and Cellular and Molecular Neuroscience. According to data from OpenAlex, Pierre Chambrier has authored 28 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 24 papers in Plant Science and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Pierre Chambrier's work include Plant Molecular Biology Research (18 papers), Plant Reproductive Biology (13 papers) and Photosynthetic Processes and Mechanisms (9 papers). Pierre Chambrier is often cited by papers focused on Plant Molecular Biology Research (18 papers), Plant Reproductive Biology (13 papers) and Photosynthetic Processes and Mechanisms (9 papers). Pierre Chambrier collaborates with scholars based in France, Morocco and Netherlands. Pierre Chambrier's co-authors include Frédéric Berger, Annick Berne-Dedieu, Ulríke Mayer, Gerd Jürgens, Damien Garcia, P. Morel, Michiel Vandenbussche, Claire Lionnet, Mohammed Bendahmane and Peter Rogowsky and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and The Plant Cell.

In The Last Decade

Pierre Chambrier

27 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pierre Chambrier France 21 1.1k 1.1k 185 178 60 28 1.5k
Cynthia Lincoln United States 11 2.4k 2.2× 2.2k 2.0× 53 0.3× 134 0.8× 57 0.9× 12 2.6k
Jinling Liu China 17 1.2k 1.1× 625 0.6× 158 0.9× 26 0.1× 215 3.6× 42 1.5k
Maryse Nicolaı̈ France 15 987 0.9× 698 0.6× 101 0.5× 45 0.3× 40 0.7× 16 1.2k
Lexiang Ji United States 23 1.8k 1.6× 1.3k 1.2× 302 1.6× 100 0.6× 35 0.6× 36 2.3k
Michał Jaśkiewicz Germany 8 1.4k 1.3× 570 0.5× 35 0.2× 84 0.5× 121 2.0× 10 1.7k
Michiyuki Ono Japan 17 682 0.6× 745 0.7× 41 0.2× 61 0.3× 50 0.8× 42 947
Miho Ikeda Japan 18 1.8k 1.6× 1.6k 1.5× 131 0.7× 54 0.3× 32 0.5× 36 2.1k
H. Fujisawa Japan 16 1.4k 1.3× 1.5k 1.3× 92 0.5× 60 0.3× 78 1.3× 20 1.8k
Patrick Sieber Switzerland 13 2.2k 2.0× 1.9k 1.7× 45 0.2× 118 0.7× 39 0.7× 16 2.4k
Stefanie Sprunck Germany 22 1.7k 1.5× 1.7k 1.5× 86 0.5× 348 2.0× 55 0.9× 40 2.0k

Countries citing papers authored by Pierre Chambrier

Since Specialization
Citations

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

Fields of papers citing papers by Pierre Chambrier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pierre Chambrier

This figure shows the co-authorship network connecting the top 25 collaborators of Pierre Chambrier. A scholar is included among the top collaborators of Pierre Chambrier 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 Pierre Chambrier. Pierre Chambrier 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.
Chambrier, Pierre, et al.. (2024). Evolution of the basic helix–loop–helix transcription factor SPATULA and its role in gynoecium development. Annals of Botany. 134(6). 1037–1054. 2 indexed citations
2.
Roldán, Maria Victoria Gómez, Marion Verdenaud, John Saviour Yaw Eleblu, et al.. (2020). Integrative genome-wide analysis reveals the role of WIP proteins in inhibition of growth and development. Communications Biology. 3(1). 239–239. 17 indexed citations
3.
Boltz, Véronique, Florian Brioudes, Pierre Chambrier, et al.. (2019). TCTP and CSN4 control cell cycle progression and development by regulating CULLIN1 neddylation in plants and animals. PLoS Genetics. 15(1). e1007899–e1007899. 25 indexed citations
4.
Morel, P., Pierre Chambrier, Véronique Boltz, et al.. (2019). Divergent Functional Diversification Patterns in the SEP/AGL6/AP1 MADS-Box Transcription Factor Superclade. The Plant Cell. 31(12). 3033–3056. 43 indexed citations
5.
Morel, P., Klaas Heijmans, Frédérique Rozier, et al.. (2017). Divergence of the Floral A-Function between an Asterid and a Rosid Species. The Plant Cell. 29(7). 1605–1621. 33 indexed citations
6.
Vandenbussche, Michiel, et al.. (2016). Petunia, Your Next Supermodel?. Frontiers in Plant Science. 7. 72–72. 69 indexed citations
7.
Vialette‐Guiraud, Aurélie, et al.. (2016). The analysis of Gene Regulatory Networks in plant evo-devo. Journal of Experimental Botany. 67(9). 2549–2563. 4 indexed citations
8.
9.
Chambrier, Pierre, et al.. (2015). Regulation of a maize HD – ZIP   IV transcription factor by a non‐conventional RDR 2‐dependent small RNA. The Plant Journal. 81(5). 747–758. 9 indexed citations
10.
Denay, Grégoire, Audrey Creff, Steven Moussu, et al.. (2014). Endosperm breakdown in Arabidopsis requires heterodimers of the basic helix-loop-helix proteins ZHOUPI and INDUCER OF CBP EXPRESSION 1. Development. 141(6). 1222–1227. 77 indexed citations
11.
Zelazny, Enric, Martina Santambrogio, Pierre Chambrier, et al.. (2013). Mechanisms Governing the Endosomal Membrane Recruitment of the Core Retromer in Arabidopsis. Journal of Biological Chemistry. 288(13). 8815–8825. 59 indexed citations
12.
Sosso, Davide, Ghislaine Gendrot, Annick Berne-Dedieu, et al.. (2012). PPR8522 encodes a chloroplast-targeted pentatricopeptide repeat protein necessary for maize embryogenesis and vegetative development. Journal of Experimental Botany. 63(16). 5843–5857. 51 indexed citations
13.
Depège‐Fargeix, Nathalie, Marie Javelle, Pierre Chambrier, et al.. (2010). Functional characterization of the HD-ZIP IV transcription factor OCL1 from maize. Journal of Experimental Botany. 62(1). 293–305. 47 indexed citations
14.
Finet, Cédric, Chloé Fourquin, Annick Berne-Dedieu, et al.. (2010). Parallel structural evolution of auxin response factors in the angiosperms. The Plant Journal. 63(6). 952–959. 63 indexed citations
15.
Marais, Gabriel, Roberta Bergero, Pierre Chambrier, et al.. (2008). Evidence for Degeneration of the Y Chromosome in the Dioecious Plant Silene latifolia. Current Biology. 18(7). 545–549. 95 indexed citations
16.
Fobis‐Loisy, Isabelle, Pierre Chambrier, & Thierry Gaude. (2007). Genetic transformation of Arabidopsis lyrata: specific expression of the green fluorescent protein (GFP) in pistil tissues. Plant Cell Reports. 26(6). 745–753. 16 indexed citations
17.
Fourquin, Chloé, et al.. (2007). Functional Conservation between CRABS CLAW Orthologues from Widely Diverged Angiosperms. Annals of Botany. 100(3). 651–657. 36 indexed citations
18.
Scalliet, Gabriel, Claire Lionnet, Mickael Le Béchec, et al.. (2006). Role of Petal-specific Orcinol O-methyltransferases in the Evolution of Rose Scent.. HAL (Le Centre pour la Communication Scientifique Directe).
19.
Garcia, Damien, et al.. (2003). Arabidopsis haiku Mutants Reveal New Controls of Seed Size by Endosperm. PLANT PHYSIOLOGY. 131(4). 1661–1670. 229 indexed citations
20.
Kerbœuf, Dominique, et al.. (1999). Flow cytometry analysis of drug transport mechanisms in Haemonchus contortus susceptible or resistant to anthelmintics. Parasitology Research. 85(2). 118–123. 27 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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