Ludivine Taconnat

5.8k total citations · 1 hit paper
35 papers, 4.3k citations indexed

About

Ludivine Taconnat is a scholar working on Plant Science, Molecular Biology and Pollution. According to data from OpenAlex, Ludivine Taconnat has authored 35 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Plant Science, 26 papers in Molecular Biology and 1 paper in Pollution. Recurrent topics in Ludivine Taconnat's work include Plant Stress Responses and Tolerance (12 papers), Plant Molecular Biology Research (12 papers) and Photosynthetic Processes and Mechanisms (10 papers). Ludivine Taconnat is often cited by papers focused on Plant Stress Responses and Tolerance (12 papers), Plant Molecular Biology Research (12 papers) and Photosynthetic Processes and Mechanisms (10 papers). Ludivine Taconnat collaborates with scholars based in France, Morocco and Germany. Ludivine Taconnat's co-authors include Jean‐Pierre Renou, Marie‐Laure Martin‐Magniette, Alain Lecharny, Monique Le Ret, Claire Lurin, Mohammed Bellaoui, Boris Szurek, Michel Caboche, Hakim Mireau and Nemo Peeters and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and The Plant Cell.

In The Last Decade

Ludivine Taconnat

35 papers receiving 4.2k citations

Hit Papers

Genome-Wide Analysis of Arabidopsis Pentatricopeptide Rep... 2004 2026 2011 2018 2004 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
Ludivine Taconnat France 28 3.3k 2.4k 172 140 136 35 4.3k
Chengchao Zheng China 40 4.8k 1.4× 3.1k 1.3× 68 0.4× 93 0.7× 82 0.6× 113 5.9k
Jeong Dong Bahk South Korea 30 2.3k 0.7× 1.9k 0.8× 197 1.1× 68 0.5× 77 0.6× 72 3.2k
Zhi‐Sheng Xu China 35 3.4k 1.0× 3.0k 1.3× 70 0.4× 132 0.9× 46 0.3× 135 4.8k
Suk‐Yoon Kwon South Korea 35 3.6k 1.1× 2.0k 0.9× 76 0.4× 126 0.9× 36 0.3× 161 4.3k
Zhangliang Chen China 30 3.3k 1.0× 2.9k 1.2× 52 0.3× 145 1.0× 62 0.5× 94 4.1k
Changai Wu China 37 4.5k 1.3× 2.9k 1.2× 49 0.3× 67 0.5× 71 0.5× 80 5.1k
Étienne Delannoy France 27 1.8k 0.5× 2.5k 1.1× 72 0.4× 51 0.4× 99 0.7× 62 3.3k
Francisco M. Cánovas Spain 40 3.0k 0.9× 2.3k 1.0× 50 0.3× 61 0.4× 102 0.8× 132 4.0k
Tomasz Czechowski Germany 16 4.5k 1.4× 3.0k 1.3× 37 0.2× 145 1.0× 148 1.1× 22 5.9k
Mohammad‐Reza Hajirezaei Germany 40 3.4k 1.0× 1.9k 0.8× 71 0.4× 52 0.4× 81 0.6× 83 4.2k

Countries citing papers authored by Ludivine Taconnat

Since Specialization
Citations

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

Fields of papers citing papers by Ludivine Taconnat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ludivine Taconnat

This figure shows the co-authorship network connecting the top 25 collaborators of Ludivine Taconnat. A scholar is included among the top collaborators of Ludivine Taconnat 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 Ludivine Taconnat. Ludivine Taconnat 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.
Jardinaud, Marie‐Françoise, Marie‐Christine Auriac, Sandra Moreau, et al.. (2022). MtEFD and MtEFD2: Two transcription factors with distinct neofunctionalization in symbiotic nodule development. PLANT PHYSIOLOGY. 189(3). 1587–1607. 8 indexed citations
2.
Creff, Audrey, Lysiane Brocard, Jérôme Joubès, et al.. (2019). A stress-response-related inter-compartmental signalling pathway regulates embryonic cuticle integrity in Arabidopsis. PLoS Genetics. 15(4). e1007847–e1007847. 37 indexed citations
3.
Armezzani, Alessia, Olivier Ali, Antoine Larrieu, et al.. (2018). Transcriptional induction of cell wall remodelling genes is coupled to microtubule-driven growth isotropy at the shoot apex in Arabidopsis. Development. 145(11). 40 indexed citations
4.
Sakai, Kaori, Ludivine Taconnat, Néro Borrega, et al.. (2018). Combining laser-assisted microdissection (LAM) and RNA-seq allows to perform a comprehensive transcriptomic analysis of epidermal cells of Arabidopsis embryo. Plant Methods. 14(1). 10–10. 26 indexed citations
5.
Taconnat, Ludivine, Evangelos Barbas, Guillem Rigaill, et al.. (2016). Unraveling the early molecular and physiological mechanisms involved in response to phenanthrene exposure. BMC Genomics. 17(1). 818–818. 21 indexed citations
6.
Eisenhut, Marion, Séverine Planchais, Cécile Cabassa, et al.. (2012). Arabidopsis A BOUT DE SOUFFLE is a putative mitochondrial transporter involved in photorespiratory metabolism and is required for meristem growth at ambient CO 2 levels. The Plant Journal. 73(5). 836–849. 56 indexed citations
7.
Markakis, Marios Nektarios, Tinne De Cnodder, Damien Simon, et al.. (2012). Identification of genes involved in the ACC-mediated control of root cell elongation in Arabidopsis thaliana. BMC Plant Biology. 12(1). 208–208. 51 indexed citations
8.
Moreau, Manon, Marianne Azzopardi, Gilles Clément, et al.. (2012). Mutations in the Arabidopsis Homolog of LST8/GβL, a Partner of the Target of Rapamycin Kinase, Impair Plant Growth, Flowering, and Metabolic Adaptation to Long Days. The Plant Cell. 24(2). 463–481. 195 indexed citations
9.
Lozano‐Durán, Rosa, Tábata Rosas‐Díaz, Giuliana Gusmaroli, et al.. (2011). Geminiviruses Subvert Ubiquitination by Altering CSN-Mediated Derubylation of SCF E3 Ligase Complexes and Inhibit Jasmonate Signaling in Arabidopsis thaliana    . The Plant Cell. 23(3). 1014–1032. 182 indexed citations
10.
Jay, Florence, Yu Wang, Agnès Yu, et al.. (2011). Misregulation of AUXIN RESPONSE FACTOR 8 Underlies the Developmental Abnormalities Caused by Three Distinct Viral Silencing Suppressors in Arabidopsis. PLoS Pathogens. 7(5). e1002035–e1002035. 73 indexed citations
11.
Latrasse, David, Sophie Germann, Nicole Houba‐Hérin, et al.. (2011). Control of Flowering and Cell Fate by LIF2, an RNA Binding Partner of the Polycomb Complex Component LHP1. PLoS ONE. 6(1). e16592–e16592. 54 indexed citations
13.
Klein, Elodie, Ludivine Taconnat, Els Prinsen, et al.. (2010). Expression of the Beet necrotic yellow vein virus p25 protein induces hormonal changes and a root branching phenotype in Arabidopsis thaliana. Transgenic Research. 20(3). 443–466. 25 indexed citations
14.
Benhamed, Moussa, Marie‐Laure Martin‐Magniette, Ludivine Taconnat, et al.. (2008). Genome‐scale Arabidopsis promoter array identifies targets of the histone acetyltransferase GCN5. The Plant Journal. 56(3). 493–504. 107 indexed citations
15.
Bashandy, Talaat, Ludivine Taconnat, Jean‐Pierre Renou, Yves Meyer, & Jean‐Philippe Reichheld. (2008). Accumulation of Flavonoids in an ntra ntrb Mutant Leads to Tolerance to UV-C. Molecular Plant. 2(2). 249–258. 47 indexed citations
16.
Castaings, Loren, Antonio Camargo, Yves Texier, et al.. (2008). The nodule inception‐like protein 7 modulates nitrate sensing and metabolism in Arabidopsis. The Plant Journal. 57(3). 426–435. 357 indexed citations
17.
Gagnot, Séverine, Marie‐Laure Martin‐Magniette, Frédérique Bitton, et al.. (2007). CATdb: a public access to Arabidopsis transcriptome data from the URGV-CATMA platform. Nucleic Acids Research. 36(Database). D986–D990. 143 indexed citations
18.
Ramel, Frédéric, Cécile Sulmon, Francisco Cabello‐Hurtado, et al.. (2007). Genome-wide interacting effects of sucrose and herbicide-mediated stress in Arabidopsis thaliana: novel insights into atrazine toxicity and sucrose-induced tolerance. BMC Genomics. 8(1). 450–450. 77 indexed citations
19.
Herbette, Stéphane, Ludivine Taconnat, Véronique Hugouvieux, et al.. (2006). Genome-wide transcriptome profiling of the early cadmium response of Arabidopsis roots and shoots. Biochimie. 88(11). 1751–1765. 276 indexed citations
20.
Lurin, Claire, Mohammed Bellaoui, Michel Caboche, et al.. (2004). Genome-Wide Analysis of Arabidopsis Pentatricopeptide Repeat Proteins Reveals Their Essential Role in Organelle Biogenesis[W]. The Plant Cell. 16(8). 2089–2103. 1051 indexed citations breakdown →

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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