Olivier Mathieu

3.5k total citations
39 papers, 2.5k citations indexed

About

Olivier Mathieu is a scholar working on Plant Science, Molecular Biology and Infectious Diseases. According to data from OpenAlex, Olivier Mathieu has authored 39 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Plant Science, 22 papers in Molecular Biology and 5 papers in Infectious Diseases. Recurrent topics in Olivier Mathieu's work include Plant Molecular Biology Research (23 papers), Chromosomal and Genetic Variations (12 papers) and Plant nutrient uptake and metabolism (10 papers). Olivier Mathieu is often cited by papers focused on Plant Molecular Biology Research (23 papers), Chromosomal and Genetic Variations (12 papers) and Plant nutrient uptake and metabolism (10 papers). Olivier Mathieu collaborates with scholars based in France, Canada and Switzerland. Olivier Mathieu's co-authors include Jerzy Paszkowski, Jon Reinders, Marian Čaikovski, Aline V. Probst, Isabelle Vaillant, Sylvette Tourmente, Etienne Bucher, Thomas A. Tompkins, Akie Kobayashi and Asuka Miura and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Olivier Mathieu

38 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Olivier Mathieu France 23 1.9k 1.6k 196 178 82 39 2.5k
Joseph M. Sturino United States 15 310 0.2× 661 0.4× 99 0.5× 265 1.5× 216 2.6× 21 1.3k
Anne‐Laure Abraham France 13 443 0.2× 661 0.4× 83 0.4× 83 0.5× 202 2.5× 18 1.1k
Pradeep Reddy Marri United States 19 647 0.3× 788 0.5× 205 1.0× 306 1.7× 62 0.8× 27 1.6k
Nathan T. Porter United States 13 196 0.1× 867 0.6× 343 1.8× 139 0.8× 252 3.1× 16 1.4k
Hideki Yoshida Japan 16 568 0.3× 356 0.2× 74 0.4× 94 0.5× 36 0.4× 58 963
Rupak Mitra India 12 239 0.1× 513 0.3× 86 0.4× 144 0.8× 192 2.3× 17 1.2k
Alexandre Jamet France 12 403 0.2× 323 0.2× 63 0.3× 55 0.3× 72 0.9× 13 883
Alexandra Tauzin Canada 15 462 0.2× 679 0.4× 221 1.1× 67 0.4× 247 3.0× 44 1.4k
George Kallstrom United States 14 137 0.1× 1.3k 0.8× 452 2.3× 109 0.6× 166 2.0× 23 1.8k
Shenglong Wu China 19 134 0.1× 567 0.4× 162 0.8× 220 1.2× 121 1.5× 124 1.1k

Countries citing papers authored by Olivier Mathieu

Since Specialization
Citations

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

Fields of papers citing papers by Olivier Mathieu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Olivier Mathieu

This figure shows the co-authorship network connecting the top 25 collaborators of Olivier Mathieu. A scholar is included among the top collaborators of Olivier Mathieu 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 Olivier Mathieu. Olivier Mathieu 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.
Pélissier, Thierry, Marie-Noëlle Pouch-Pélissier, Julie Descombin, et al.. (2025). Plant mobile domain protein–DNA motif modules counteract Polycomb silencing to stabilize gene expression. Nature Plants. 11(11). 2286–2299.
2.
Wang, Gang, Renata Rehak, Annie Tremblay, et al.. (2024). Spatially and temporally precise microbiome profiling in the small intestine using the SIMBA capsule with X-ray tracking. SHILAP Revista de lepidopterología. 3. 1321624–1321624. 6 indexed citations
3.
Pouch-Pélissier, Marie-Noëlle, Thierry Pélissier, Ying Huang, et al.. (2023). RTEL1 is required for silencing and epigenome stability. Nucleic Acids Research. 51(16). 8463–8479. 1 indexed citations
4.
Schmücker, Anna, Zdravko J. Lorković, Matías Capella, et al.. (2021). Crosstalk between H2A variant-specific modifications impacts vital cell functions. PLoS Genetics. 17(6). e1009601–e1009601. 10 indexed citations
5.
Picard, Colette L., Ramesh Yelagandula, Thierry Pélissier, et al.. (2021). The histone variant H2A.W and linker histone H1 co-regulate heterochromatin accessibility and DNA methylation. Nature Communications. 12(1). 2683–2683. 62 indexed citations
6.
López‐González, Leticia, Marie-Noëlle Pouch-Pélissier, Ángeles Gómez‐Zambrano, et al.. (2018). A role for MED14 and UVH6 in heterochromatin transcription upon destabilization of silencing. Life Science Alliance. 1(6). e201800197–e201800197. 11 indexed citations
7.
Lin, Qiuye, Olivier Mathieu, Thomas A. Tompkins, Nicole Buckley, & Julia M. Green-Johnson. (2016). Modulation of the TNFα-induced gene expression profile of intestinal epithelial cells by soy fermented with lactic acid bacteria. Journal of Functional Foods. 23. 400–411. 9 indexed citations
8.
Mathieu, Olivier & Nicolas Bouché. (2014). Interplay between chromatin and RNA processing. Current Opinion in Plant Biology. 18. 60–65. 9 indexed citations
9.
Kevei, Zoltán, et al.. (2012). DNA methylation in an intron of the IBM1 histone demethylase gene stabilizes chromatin modification patterns. The EMBO Journal. 31(13). 2981–2993. 82 indexed citations
10.
11.
Mathieu, Olivier, et al.. (2011). A “mille-feuille” of silencing: Epigenetic control of transposable elements. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1809(8). 452–458. 76 indexed citations
12.
Tittel-Elmer, Mireille, Etienne Bucher, Larissa Broger, et al.. (2010). Stress-Induced Activation of Heterochromatic Transcription. PLoS Genetics. 6(10). e1001175–e1001175. 186 indexed citations
13.
Kobayashi, Akie, et al.. (2009). Bursts of retrotransposition reproduced in Arabidopsis. Nature. 461(7262). 423–426. 286 indexed citations
14.
Houde, Andrée-Anne, Bruce D. Murphy, Olivier Mathieu, Vilceu Bordignon, & Marie‐France Palin. (2008). Characterization of swine adiponectin and adiponectin receptor polymorphisms and their association with reproductive traits. Animal Genetics. 39(3). 249–257. 30 indexed citations
15.
Čaikovski, Marian, et al.. (2008). Divergent Evolution of CHD3 Proteins Resulted in MOM1 Refining Epigenetic Control in Vascular Plants. PLoS Genetics. 4(8). e1000165–e1000165. 27 indexed citations
16.
Mathieu, Olivier, et al.. (2007). Transgenerational Stability of the Arabidopsis Epigenome Is Coordinated by CG Methylation. Cell. 130(5). 851–862. 325 indexed citations
17.
Habu, Yoshiki, Olivier Mathieu, Muhammad Tariq, et al.. (2006). Epigenetic regulation of transcription in intermediate heterochromatin. EMBO Reports. 7(12). 1279–1284. 52 indexed citations
18.
Vaillant, Isabelle, Ingo Schubert, Sylvette Tourmente, & Olivier Mathieu. (2006). MOM1 mediates DNA‐methylation‐independent silencing of repetitive sequences in Arabidopsis. EMBO Reports. 7(12). 1273–1278. 85 indexed citations
19.
Mathieu, Olivier. (2003). Identification and characterization of transcription factor IIIA and ribosomal protein L5 from Arabidopsis thaliana. Nucleic Acids Research. 31(9). 2424–2433. 41 indexed citations
20.
Cloix, Catherine, et al.. (2000). Analysis of 5S rDNA Arrays in Arabidopsis thaliana: Physical Mapping and Chromosome-Specific Polymorphisms. Genome Research. 10(5). 679–690. 68 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Joseph M. Sturino Breakdown of academic impact, for papers by Anne‐Laure Abraham Breakdown of academic impact, for papers by Pradeep Reddy Marri Breakdown of academic impact, for papers by Nathan T. Porter Breakdown of academic impact, for papers by Hideki Yoshida Breakdown of academic impact, for papers by Rupak Mitra Breakdown of academic impact, for papers by Alexandre Jamet Breakdown of academic impact, for papers by Alexandra Tauzin Breakdown of academic impact, for papers by George Kallstrom Breakdown of academic impact, for papers by Shenglong Wu
Rankless by CCL
2026