Mathieu Boulard

1.6k total citations · 1 hit paper
31 papers, 1.1k citations indexed

About

Mathieu Boulard is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Mathieu Boulard has authored 31 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 8 papers in Physiology and 5 papers in Genetics. Recurrent topics in Mathieu Boulard's work include Epigenetics and DNA Methylation (9 papers), Erythrocyte Function and Pathophysiology (8 papers) and Genomics and Chromatin Dynamics (6 papers). Mathieu Boulard is often cited by papers focused on Epigenetics and DNA Methylation (9 papers), Erythrocyte Function and Pathophysiology (8 papers) and Genomics and Chromatin Dynamics (6 papers). Mathieu Boulard collaborates with scholars based in France, United States and Italy. Mathieu Boulard's co-authors include Timothy H. Bestor, John R. Edwards, Olya Yarychkivska, Philippe Bouvet, Karl G. Blume, Ernest Beutler, Stéfan Dimitrov, Y Najean, Tapas K. Kundu and Dimitar Angelov and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Mathieu Boulard

28 papers receiving 1.1k citations

Hit Papers

DNA methylation and DNA methyltransferases 2017 2026 2020 2023 2017 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mathieu Boulard France 14 860 200 119 100 87 31 1.1k
Sarah Hevi United States 10 1.6k 1.9× 368 1.8× 122 1.0× 136 1.4× 64 0.7× 12 1.8k
Kelwyn Thomas United States 17 830 1.0× 260 1.3× 95 0.8× 42 0.4× 77 0.9× 28 1.2k
Shintaro Yagi Japan 18 879 1.0× 256 1.3× 70 0.6× 125 1.3× 76 0.9× 36 1.3k
W R Baumbach United States 19 671 0.8× 292 1.5× 188 1.6× 75 0.8× 117 1.3× 31 1.5k
Iris Hart United States 15 833 1.0× 324 1.6× 103 0.9× 61 0.6× 53 0.6× 21 1.2k
John R. Morrison Australia 23 1.0k 1.2× 267 1.3× 99 0.8× 54 0.5× 38 0.4× 30 1.6k
Adam Burton United Kingdom 14 1.3k 1.5× 162 0.8× 124 1.0× 60 0.6× 88 1.0× 18 1.6k
Santiago Uribe‐Lewis United Kingdom 14 1.3k 1.6× 311 1.6× 207 1.7× 222 2.2× 127 1.5× 24 1.6k
Fumiko Saito Japan 14 593 0.7× 107 0.5× 96 0.8× 60 0.6× 50 0.6× 46 886

Countries citing papers authored by Mathieu Boulard

Since Specialization
Citations

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

Fields of papers citing papers by Mathieu Boulard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mathieu Boulard

This figure shows the co-authorship network connecting the top 25 collaborators of Mathieu Boulard. A scholar is included among the top collaborators of Mathieu Boulard 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 Mathieu Boulard. Mathieu Boulard 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.
Ganter, Kerstin, et al.. (2025). Genetic gradual reduction of OGT activity unveils the essential role of O-GlcNAc in the mouse embryo. PLoS Genetics. 21(1). e1011507–e1011507. 2 indexed citations
2.
Descostes, Nicolas, et al.. (2025). Functional genomic profiling of O-GlcNAc reveals its context-specific interplay with RNA polymerase II. Genome biology. 26(1). 69–69. 2 indexed citations
3.
Petrosino, Giuseppe, Anke Busch, Marion Scheibe, et al.. (2025). DNA methylation at retrotransposons protects the germline by preventing NRF1-mediated activation. EMBO Reports. 26(17). 4312–4339.
4.
Tabaro, Francesco, Ferdinando Scavizzi, Marcello Raspa, et al.. (2024). Trim66’s paternal deficiency causes intrauterine overgrowth. Life Science Alliance. 7(7). e202302512–e202302512.
5.
Toda, Tomohisa, Tracy A. Bedrosian, Simon T. Schafer, et al.. (2024). Long interspersed nuclear elements safeguard neural progenitors from precocious differentiation. Cell Reports. 43(2). 113774–113774. 10 indexed citations
6.
Smet, Annie De, Jianke Ren, Kathrin Muegge, et al.. (2023). Germinal center output is sustained by HELLS-dependent DNA-methylation-maintenance in B cells. Nature Communications. 14(1). 5695–5695. 8 indexed citations
7.
Yarychkivska, Olya, et al.. (2018). BAH domains and a histone-like motif in DNA methyltransferase 1 (DNMT1) regulate de novo and maintenance methylation in vivo. Journal of Biological Chemistry. 293(50). 19466–19475. 45 indexed citations
8.
Edwards, John R., Olya Yarychkivska, Mathieu Boulard, & Timothy H. Bestor. (2017). DNA methylation and DNA methyltransferases. Epigenetics & Chromatin. 10(1). 23–23. 341 indexed citations breakdown →
9.
Boulard, Mathieu, John R. Edwards, & Timothy H. Bestor. (2016). Abnormal X chromosome inactivation and sex-specific gene dysregulation after ablation of FBXL10. Epigenetics & Chromatin. 9(1). 22–22. 16 indexed citations
10.
Boulard, Mathieu, John R. Edwards, & Timothy H. Bestor. (2015). FBXL10 protects Polycomb-bound genes from hypermethylation. Nature Genetics. 47(5). 479–485. 108 indexed citations
11.
Bestor, Timothy H., John R. Edwards, & Mathieu Boulard. (2014). Notes on the role of dynamic DNA methylation in mammalian development. Proceedings of the National Academy of Sciences. 112(22). 6796–6799. 159 indexed citations
12.
Boulard, Mathieu, et al.. (2010). Histone variant macroH2A1 deletion in mice causes female-specific steatosis. Epigenetics & Chromatin. 3(1). 8–8. 52 indexed citations
13.
Syed, Sajad Hussain, Mathieu Boulard, Manu Shukla, et al.. (2009). The incorporation of the novel histone variant H2AL2 confers unusual structural and functional properties of the nucleosome. Nucleic Acids Research. 37(14). 4684–4695. 34 indexed citations
14.
Madsen, Bo Eskerod, Eliana Marisa Ramos, Mathieu Boulard, et al.. (2008). Germline Mutation in RNASEL Predicts Increased Risk of Head and Neck, Uterine Cervix and Breast Cancer. PLoS ONE. 3(6). e2492–e2492. 46 indexed citations
15.
Boulard, Mathieu, Philippe Bouvet, Tapas K. Kundu, & Stéfan Dimitrov. (2007). Histone variant nucleosomes: structure, function and implication in disease.. PubMed. 41. 71–89. 38 indexed citations
16.
Bornes, Stéphanie, Mathieu Boulard, Corinne Hiéblot, et al.. (2004). Control of the Vascular Endothelial Growth Factor Internal Ribosome Entry Site (IRES) Activity and Translation Initiation by Alternatively Spliced Coding Sequences. Journal of Biological Chemistry. 279(18). 18717–18726. 53 indexed citations
18.
Tallineau, C., et al.. (1984). Evidence for the involvement of (Cu-ATP)2− in the inhibition of human erythrocyte (Ca2+ + Mg2+-ATPase by copper. Biochimica et Biophysica Acta (BBA) - Biomembranes. 775(1). 51–56. 13 indexed citations
19.
Boulard, Mathieu, et al.. (1972). Identification and Purification of a New Non-Heme, Non-Ferritin Iron Protein. Experimental Biology and Medicine. 139(4). 1379–1384. 10 indexed citations
20.
Boulard, Mathieu, et al.. (1970). [In vitro replacement of human erythrocyte phospholipids by means of incorporation of inorganic phosphorus 32].. PubMed. 100(46). 1969–71. 1 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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