Leila Touat‐Todeschini

489 total citations
11 papers, 358 citations indexed

About

Leila Touat‐Todeschini is a scholar working on Molecular Biology, Plant Science and Cancer Research. According to data from OpenAlex, Leila Touat‐Todeschini has authored 11 papers receiving a total of 358 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 2 papers in Plant Science and 2 papers in Cancer Research. Recurrent topics in Leila Touat‐Todeschini's work include RNA Research and Splicing (6 papers), Genomics and Chromatin Dynamics (6 papers) and RNA modifications and cancer (5 papers). Leila Touat‐Todeschini is often cited by papers focused on RNA Research and Splicing (6 papers), Genomics and Chromatin Dynamics (6 papers) and RNA modifications and cancer (5 papers). Leila Touat‐Todeschini collaborates with scholars based in France, United States and Japan. Leila Touat‐Todeschini's co-authors include André Verdel, Yuichi Shichino, Edwige Hiriart, Masayuki Yamamoto, Akira Yamashita, Da‐Qiao Ding, Hirotsugu Tanaka, Yasushi Hiraoka, Dimitrios A. Skoufias and Emeline Lambert and has published in prestigious journals such as Nature Communications, The EMBO Journal and Molecular Cell.

In The Last Decade

Leila Touat‐Todeschini

11 papers receiving 354 citations

Peers

Leila Touat‐Todeschini
Jothy Dhakshnamoorthy United States
Cristina Cotobal United Kingdom
Erwan Lejeune United Kingdom
Guifen Wu China
Leila Touat‐Todeschini
Citations per year, relative to Leila Touat‐Todeschini Leila Touat‐Todeschini (= 1×) peers Vanivilasini Balachandran

Countries citing papers authored by Leila Touat‐Todeschini

Since Specialization
Citations

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

Fields of papers citing papers by Leila Touat‐Todeschini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Leila Touat‐Todeschini. 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 Leila Touat‐Todeschini. The network helps show where Leila Touat‐Todeschini may publish in the future.

Co-authorship network of co-authors of Leila Touat‐Todeschini

This figure shows the co-authorship network connecting the top 25 collaborators of Leila Touat‐Todeschini. A scholar is included among the top collaborators of Leila Touat‐Todeschini 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 Leila Touat‐Todeschini. Leila Touat‐Todeschini is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

11 of 11 papers shown
1.
Roche, Benjamin, Leila Touat‐Todeschini, Karine Fréon, et al.. (2025). Transcription-replication conflict resolution by nuclear RNA interference. Molecular Cell. 85(21). 3930–3946.e5. 1 indexed citations
2.
Kim, Hyun Soo, Benjamin Roche, Sonali Bhattacharjee, et al.. (2024). Clr4SUV39H1 ubiquitination and non-coding RNA mediate transcriptional silencing of heterochromatin via Swi6 phase separation. Nature Communications. 15(1). 9384–9384. 4 indexed citations
3.
Seigneurin‐Berny, Daphné, et al.. (2023). Protocol to study the role of a human nuclear m6A RNA reader on chromatin-associated RNA targets. STAR Protocols. 4(3). 102528–102528. 1 indexed citations
4.
Touat‐Todeschini, Leila, Marie‐Christine Carpentier, Florent Chuffart, et al.. (2022). Chromatin-associated YTHDC1 coordinates heat-induced reprogramming of gene expression. Cell Reports. 41(11). 111784–111784. 11 indexed citations
5.
Touat‐Todeschini, Leila, Samira Acajjaoui, Montserrat Soler‐López, et al.. (2022). Structural analysis of Red1 as a conserved scaffold of the RNA-targeting MTREC/PAXT complex. Nature Communications. 13(1). 4969–4969. 16 indexed citations
6.
Touat‐Todeschini, Leila, Yuichi Shichino, Nicolas Thierry‐Mieg, et al.. (2017). Selective termination of lnc RNA transcription promotes heterochromatin silencing and cell differentiation. The EMBO Journal. 36(17). 2626–2641. 42 indexed citations
7.
Hiriart, Edwige, Leila Touat‐Todeschini, Akira Yamashita, et al.. (2012). Mmi1 RNA surveillance machinery directs RNAi complex RITS to specific meiotic genes in fission yeast. The EMBO Journal. 31(10). 2296–2308. 71 indexed citations
8.
Yamashita, Akira, Yuichi Shichino, Hirotsugu Tanaka, et al.. (2012). Hexanucleotide motifs mediate recruitment of the RNA elimination machinery to silent meiotic genes. Open Biology. 2(3). 120014–120014. 90 indexed citations
9.
Touat‐Todeschini, Leila, et al.. (2009). SMC5 and MMS21 are required for chromosome cohesion and mitotic progression. Cell Cycle. 8(14). 2211–2218. 32 indexed citations
10.
Verdel, André, et al.. (2009). Common themes in siRNA-mediated epigenetic silencing pathways. The International Journal of Developmental Biology. 53(2-3). 245–257. 88 indexed citations
11.
Martin, P. J., Peggy Parroche, Laurence Chatel, et al.. (2006). Optimized vaccination regimen linked to exhaustive screening approaches identifies 2 novel HLA-B7 restricted epitopes within hepatitis C virus NS3 protein. Microbes and Infection. 8(9-10). 2432–2441. 2 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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