Laurent Théodore

855 total citations
20 papers, 710 citations indexed

About

Laurent Théodore is a scholar working on Molecular Biology, Nutrition and Dietetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Laurent Théodore has authored 20 papers receiving a total of 710 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 4 papers in Nutrition and Dietetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Laurent Théodore's work include RNA Research and Splicing (7 papers), Developmental Biology and Gene Regulation (6 papers) and Trace Elements in Health (4 papers). Laurent Théodore is often cited by papers focused on RNA Research and Splicing (7 papers), Developmental Biology and Gene Regulation (6 papers) and Trace Elements in Health (4 papers). Laurent Théodore collaborates with scholars based in France, United States and Morocco. Laurent Théodore's co-authors include Alain Prochiantz, Maurice Wegnez, Bernard Mignotte, Sylvain Brun, Sébastien Gaumer, Isabelle Guénal, Gustavo Maroni, Christophe Antoniewski, Muriel Perron and Philippe Silar and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Neuroscience and PLoS ONE.

In The Last Decade

Laurent Théodore

20 papers receiving 697 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Laurent Théodore France 14 507 125 92 87 76 20 710
So Yeon Kwon United Kingdom 15 1.3k 2.6× 200 1.6× 141 1.5× 243 2.8× 46 0.6× 21 1.7k
Peter Rücknagel Germany 9 581 1.1× 50 0.4× 23 0.3× 95 1.1× 26 0.3× 10 677
Maria Lind Sweden 13 987 1.9× 35 0.3× 102 1.1× 198 2.3× 34 0.4× 21 1.3k
Xia Fan China 13 334 0.7× 69 0.6× 32 0.3× 117 1.3× 8 0.1× 21 604
Victoria Finnerty United States 16 720 1.4× 201 1.6× 21 0.2× 99 1.1× 20 0.3× 26 1.0k
William J. Mackay United States 12 450 0.9× 46 0.4× 13 0.1× 26 0.3× 50 0.7× 18 610
Jiawei Zhu China 11 323 0.6× 111 0.9× 17 0.2× 61 0.7× 51 0.7× 36 533
J.P. LePennec France 8 631 1.2× 72 0.6× 28 0.3× 69 0.8× 16 0.2× 8 899
Anand Sitaram United States 11 396 0.8× 49 0.4× 157 1.7× 70 0.8× 18 0.2× 12 683
Maria Vogelauer United States 14 1.3k 2.6× 167 1.3× 52 0.6× 42 0.5× 15 0.2× 16 1.5k

Countries citing papers authored by Laurent Théodore

Since Specialization
Citations

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

Fields of papers citing papers by Laurent Théodore

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laurent Théodore

This figure shows the co-authorship network connecting the top 25 collaborators of Laurent Théodore. A scholar is included among the top collaborators of Laurent Théodore 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 Laurent Théodore. Laurent Théodore 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.
2.
Marchal, Christelle, Matthieu Sanial, Anne Plessis, et al.. (2012). The HIV-1 Vpu Protein Induces Apoptosis in Drosophila via Activation of JNK Signaling. PLoS ONE. 7(3). e34310–e34310. 17 indexed citations
3.
Rubin, Thomas, et al.. (2012). Genetic Basis for Developmental Homeostasis of Germline Stem Cell Niche Number: A Network of Tramtrack-Group Nuclear BTB Factors. PLoS ONE. 7(11). e49958–e49958. 16 indexed citations
4.
Fagegaltier, Delphine, Anne-Laure Bougé, Bassam Berry, et al.. (2009). The endogenous siRNA pathway is involved in heterochromatin formation in Drosophila. Proceedings of the National Academy of Sciences. 106(50). 21258–21263. 118 indexed citations
5.
Rubin, Thomas, et al.. (2007). Drosophila retinal pigment cell death is regulated in a position-dependent manner by a cell memory gene. The International Journal of Developmental Biology. 52(1). 21–31. 12 indexed citations
6.
Roignant, Jean‐Yves, et al.. (2003). batman Interacts with Polycomb and trithorax Group Genes and Encodes a BTB/POZ Protein That Is Included in a Complex Containing GAGA Factor. Molecular and Cellular Biology. 23(4). 1181–1195. 47 indexed citations
7.
Théodore, Laurent, et al.. (2001). Developmental Dynamics of a Polyhomeotic-EGFP Fusion in Vivo. DNA and Cell Biology. 20(8). 483–492. 15 indexed citations
8.
Bloyer, Sébastien, et al.. (2001). Advantages of a P-element construct containing MtnA sequences for the identification of patterning and cell determination genes in Drosophila melanogaster. Molecular Genetics and Genomics. 265(1). 14–22. 8 indexed citations
9.
Gaumer, Sébastien, Isabelle Guénal, Sylvain Brun, Laurent Théodore, & Bernard Mignotte. (2000). Bcl-2 and Bax mammalian regulators of apoptosis are functional in Drosophila. Cell Death and Differentiation. 7(9). 804–814. 111 indexed citations
10.
Perron, Muriel, et al.. (1999). Misexpression of the RNA-binding protein ELRB in Xenopus presumptive neurectoderm induces proliferation arrest and programmed cell death. The International Journal of Developmental Biology. 43(4). 295–303. 7 indexed citations
11.
Perron, Muriel, et al.. (1999). Xenopus elav-like genes are differentially expressed during neurogenesis. Mechanisms of Development. 84(1-2). 139–142. 27 indexed citations
12.
Perron, Muriel, et al.. (1997). Subcellular Distribution of Xenopus XEL-1 Protein, a Member of the Neuron-Specific ELAV/Hu Family, Revealed by Epitope Tagging. DNA and Cell Biology. 16(5). 579–587. 11 indexed citations
13.
Bonneton, François, Laurent Théodore, Philippe Silar, Gustavo Maroni, & Maurice Wegnez. (1996). Response of Drosophila metallothionein promoters to metallic, heat shock and oxidative stresses. FEBS Letters. 380(1-2). 33–38. 40 indexed citations
14.
Prochiantz, Alain & Laurent Théodore. (1995). Nuclear/growth factors. BioEssays. 17(1). 39–44. 40 indexed citations
15.
Maroni, Gustavo, et al.. (1995). Genetic control of cadmium tolerance in Drosophila melanogaster.. Environmental Health Perspectives. 103(12). 1116–1118. 13 indexed citations
16.
Perron, Muriel, Laurent Théodore, & Maurice Wegnez. (1995). Isolation and embryonic expression of Xel-1, a nervous system-specific Xenopus gene related to the elav gene family. Mechanisms of Development. 51(2-3). 235–249. 17 indexed citations
17.
Maroni, Gustavo, et al.. (1995). Genetic Control of Cadmium Tolerance in Drosophila melanogaster. Environmental Health Perspectives. 103(12). 1116–1116. 3 indexed citations
18.
Théodore, Laurent, Daniele Derossi, Gérard Chassaing, et al.. (1995). Intraneuronal delivery of protein kinase C pseudosubstrate leads to growth cone collapse. Journal of Neuroscience. 15(11). 7158–7167. 135 indexed citations
19.
Théodore, Laurent, et al.. (1991). Recent evolutionary history of the metallothionein geneMtninDrosophila. Genetics Research. 58(3). 203–210. 24 indexed citations
20.
Silar, Philippe, et al.. (1990). Metallothionein Mto gene of Drosophila melanogaster: Structure and regulation. Journal of Molecular Biology. 215(2). 217–224. 45 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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