Mathieu Lupien

17.5k total citations · 1 hit paper
101 papers, 6.7k citations indexed

About

Mathieu Lupien is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Mathieu Lupien has authored 101 papers receiving a total of 6.7k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Molecular Biology, 30 papers in Genetics and 25 papers in Cancer Research. Recurrent topics in Mathieu Lupien's work include Genomics and Chromatin Dynamics (45 papers), Epigenetics and DNA Methylation (24 papers) and RNA Research and Splicing (17 papers). Mathieu Lupien is often cited by papers focused on Genomics and Chromatin Dynamics (45 papers), Epigenetics and DNA Methylation (24 papers) and RNA Research and Splicing (17 papers). Mathieu Lupien collaborates with scholars based in Canada, United States and United Kingdom. Mathieu Lupien's co-authors include Myles Brown, Jérôme Eeckhoute, Clifford A. Meyer, Jason S. Carroll, Xiaoyang Zhang, Richard Cowper‐Sal·lari, Swneke D. Bailey, Luca Magnani, Yong Zhang and Qianben Wang and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Mathieu Lupien

95 papers receiving 6.7k citations

Hit Papers

FoxA1 Translates Epigenetic Signatures into Enhancer-Driv... 2008 2026 2014 2020 2008 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mathieu Lupien Canada 40 5.3k 1.6k 1.4k 1.1k 836 101 6.7k
Kurtis E. Bachman United States 30 6.5k 1.2× 1.1k 0.7× 1.2k 0.9× 1.4k 1.3× 574 0.7× 51 7.6k
Qianben Wang United States 37 4.6k 0.9× 1.7k 1.1× 1.3k 1.0× 849 0.8× 1.8k 2.1× 67 6.1k
Ceshi Chen China 49 5.2k 1.0× 915 0.6× 1.6k 1.1× 1.6k 1.5× 629 0.8× 182 6.8k
Johan Vallon‐Christersson Sweden 35 2.9k 0.5× 953 0.6× 2.0k 1.5× 1.4k 1.3× 524 0.6× 90 4.8k
Roseline Godbout Canada 44 4.9k 0.9× 1.1k 0.7× 1.5k 1.1× 1.7k 1.6× 389 0.5× 132 6.9k
Wilbert Zwart Netherlands 39 3.9k 0.7× 1.2k 0.8× 1.2k 0.9× 1.4k 1.3× 1.1k 1.3× 152 6.5k
Shuichi Tsutsumi Japan 43 4.4k 0.8× 606 0.4× 1.2k 0.9× 773 0.7× 520 0.6× 83 5.8k
Aaron L. Sarver United States 36 3.0k 0.6× 1.1k 0.7× 1.6k 1.2× 488 0.5× 707 0.8× 76 4.5k
Tim H.‐M. Huang United States 37 3.5k 0.7× 584 0.4× 1.0k 0.8× 852 0.8× 505 0.6× 118 4.7k
Edward A. Fox United States 33 4.8k 0.9× 1.8k 1.1× 1.2k 0.9× 1.7k 1.6× 709 0.8× 53 7.4k

Countries citing papers authored by Mathieu Lupien

Since Specialization
Citations

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

Fields of papers citing papers by Mathieu Lupien

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mathieu Lupien

This figure shows the co-authorship network connecting the top 25 collaborators of Mathieu Lupien. A scholar is included among the top collaborators of Mathieu Lupien 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 Lupien. Mathieu Lupien 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.
Luo, Wu, Mona Teng, Weilong Guo, et al.. (2026). METTL3-based epitranscriptomic editing screening identifies functional m6A sites in cancers. Nature Cancer.
2.
Shrestha, Raunak, Lisa N. Chesner, Meng Zhang, et al.. (2024). An Atlas of Accessible Chromatin in Advanced Prostate Cancer Reveals the Epigenetic Evolution during Tumor Progression. Cancer Research. 84(18). 3086–3100. 7 indexed citations
3.
Lupien, Mathieu, et al.. (2024). Epigenomic heterogeneity as a source of tumour evolution. Nature reviews. Cancer. 25(1). 7–26. 20 indexed citations
4.
Medina, Tiago da Silva, Alex Murison, Michelle I. Smith, et al.. (2023). The chromatin and single-cell transcriptional landscapes of CD4 T cells in inflammatory bowel disease link risk loci with a proinflammatory Th17 cell population. Frontiers in Immunology. 14. 1161901–1161901. 7 indexed citations
5.
Grillo, Giacomo, Simon Linder, Christopher Arlidge, et al.. (2023). Transposable Elements Are Co-opted as Oncogenic Regulatory Elements by Lineage-Specific Transcription Factors in Prostate Cancer. Cancer Discovery. 13(11). 2470–2487. 21 indexed citations
6.
Payer, Lindsay M., Jared P. Steranka, Giacomo Grillo, et al.. (2021). Alu insertion variants alter gene transcript levels. Genome Research. 31(12). 2236–2248. 22 indexed citations
7.
Bailey, Swneke D., et al.. (2018). C3D: a tool to predict 3D genomic interactions between cis-regulatory elements. Bioinformatics. 35(5). 877–879. 9 indexed citations
8.
Sonzogni, Olmo, Jennifer Haynes, Kai Huang, et al.. (2018). Reporters to mark and eliminate basal or luminal epithelial cells in culture and in vivo. PLoS Biology. 16(6). e2004049–e2004049. 16 indexed citations
9.
Kron, Ken J., Alexander Murison, Stanley Zhou, et al.. (2017). TMPRSS2–ERG fusion co-opts master transcription factors and activates NOTCH signaling in primary prostate cancer. Nature Genetics. 49(9). 1336–1345. 117 indexed citations
10.
Bhat‐Nakshatri, Poornima, Chirayu Goswami, Sunil Badve, et al.. (2016). Molecular Insights of Pathways Resulting from Two Common PIK3CA Mutations in Breast Cancer. Cancer Research. 76(13). 3989–4001. 18 indexed citations
11.
Malorni, Luca, Mario Giuliano, Ilenia Migliaccio, et al.. (2016). Blockade of AP-1 Potentiates Endocrine Therapy and Overcomes Resistance. Molecular Cancer Research. 14(5). 470–481. 31 indexed citations
12.
Brunelle, Mylène, et al.. (2015). The histone variant H2A.Z is an important regulator of enhancer activity. Nucleic Acids Research. 43(20). gkv825–gkv825. 62 indexed citations
13.
Corradin, Olivia, Alina Saiakhova, Batool Akhtar‐Zaidi, et al.. (2013). Combinatorial effects of multiple enhancer variants in linkage disequilibrium dictate levels of gene expression to confer susceptibility to common traits. Genome Research. 24(1). 1–13. 240 indexed citations
14.
Jalili, Ahmad, Christine Wagner, Мikhail Pashenkov, et al.. (2012). Dual Suppression of the Cyclin-Dependent Kinase Inhibitors CDKN2C and CDKN1A in Human Melanoma. JNCI Journal of the National Cancer Institute. 104(21). 1673–1679. 33 indexed citations
15.
Tang, Qianzi, Yiwen Chen, Clifford A. Meyer, et al.. (2011). A Comprehensive View of Nuclear Receptor Cancer Cistromes. Cancer Research. 71(22). 6940–6947. 109 indexed citations
16.
Sérandour, Aurélien A., Stéphane Avner, Frédéric Percevault, et al.. (2011). Epigenetic switch involved in activation of pioneer factor FOXA1-dependent enhancers. Genome Research. 21(4). 555–565. 171 indexed citations
17.
Boros, Joanna, Ian J. Donaldson, Amanda O’Donnell, et al.. (2009). Elucidation of the ELK1 target gene network reveals a role in the coordinate regulation of core components of the gene regulation machinery. Genome Research. 19(11). 1963–1973. 113 indexed citations
18.
Frietze, Seth, Mathieu Lupien, Pamela A. Silver, & Myles Brown. (2008). CARM1 Regulates Estrogen-Stimulated Breast Cancer Growth through Up-regulation of E2F1. Cancer Research. 68(1). 301–306. 164 indexed citations
19.
Eeckhoute, Jérôme, Erika Krasnickas Keeton, Mathieu Lupien, et al.. (2007). Positive Cross-Regulatory Loop Ties GATA-3 to Estrogen Receptor α Expression in Breast Cancer. Cancer Research. 67(13). 6477–6483. 274 indexed citations
20.
Hu, Chunyan, Anne Diévart, Mathieu Lupien, et al.. (2006). Overexpression of Activated Murine Notch1 and Notch3 in Transgenic Mice Blocks Mammary Gland Development and Induces Mammary Tumors. American Journal Of Pathology. 168(3). 973–990. 157 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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