Marianne G. Rots

5.9k total citations
111 papers, 4.0k citations indexed

About

Marianne G. Rots is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Marianne G. Rots has authored 111 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 80 papers in Molecular Biology, 29 papers in Genetics and 17 papers in Oncology. Recurrent topics in Marianne G. Rots's work include Epigenetics and DNA Methylation (39 papers), CRISPR and Genetic Engineering (28 papers) and Virus-based gene therapy research (16 papers). Marianne G. Rots is often cited by papers focused on Epigenetics and DNA Methylation (39 papers), CRISPR and Genetic Engineering (28 papers) and Virus-based gene therapy research (16 papers). Marianne G. Rots collaborates with scholars based in Netherlands, United States and Germany. Marianne G. Rots's co-authors include Marcel H.J. Ruiters, Monique G.P. van der Wijst, Rutger A. F. Gjaltema, Hidde J. Haisma, Bernardina T.F. van der Gun, David Cano-Rodríguez, Pernette J. Verschure, Godefridus J. Peters, Gerrit Jansen and A. Veerman and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Marianne G. Rots

107 papers receiving 4.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marianne G. Rots Netherlands 36 2.8k 602 587 371 352 111 4.0k
Masatoshi Takagi Japan 34 2.6k 0.9× 357 0.6× 943 1.6× 490 1.3× 656 1.9× 181 4.2k
Hong Yin China 32 1.8k 0.6× 391 0.6× 531 0.9× 880 2.4× 360 1.0× 90 3.6k
Fernando López‐Casillas Mexico 35 3.3k 1.2× 367 0.6× 839 1.4× 483 1.3× 267 0.8× 82 4.8k
Ofer Reizes United States 30 3.1k 1.1× 452 0.8× 894 1.5× 725 2.0× 424 1.2× 86 5.4k
Lucio Pastore Italy 34 2.5k 0.9× 945 1.6× 730 1.2× 591 1.6× 346 1.0× 122 4.3k
Young Il Yeom South Korea 36 3.0k 1.1× 662 1.1× 585 1.0× 848 2.3× 526 1.5× 99 4.2k
Kwang‐Hyun Baek South Korea 36 2.7k 1.0× 410 0.7× 762 1.3× 390 1.1× 675 1.9× 195 4.3k
Steen Kølvraa Denmark 39 2.6k 0.9× 752 1.2× 344 0.6× 329 0.9× 299 0.8× 154 4.8k
Lucia Manzoli Italy 38 3.6k 1.3× 286 0.5× 471 0.8× 399 1.1× 408 1.2× 174 5.0k
Hua Pan United States 37 2.7k 1.0× 459 0.8× 314 0.5× 670 1.8× 546 1.6× 160 4.7k

Countries citing papers authored by Marianne G. Rots

Since Specialization
Citations

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

Fields of papers citing papers by Marianne G. Rots

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marianne G. Rots. 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 Marianne G. Rots. The network helps show where Marianne G. Rots may publish in the future.

Co-authorship network of co-authors of Marianne G. Rots

This figure shows the co-authorship network connecting the top 25 collaborators of Marianne G. Rots. A scholar is included among the top collaborators of Marianne G. Rots 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 Marianne G. Rots. Marianne G. Rots 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.
Bintu, Lacramioara, et al.. (2025). Epigenetic editing: from concept to clinic. Nature Reviews Drug Discovery. 25(3). 227–248.
2.
Guryev, Victor, Maaike Goris, Hjalmar R. Bouma, et al.. (2023). Liver transcriptomic and methylomic analyses identify transcriptional mitogen-activated protein kinase regulation in facultative hibernation of Syrian hamster. Proceedings of the Royal Society B Biological Sciences. 290(1999). 20230368–20230368. 7 indexed citations
3.
Dalpé, Gratien, Charles Dupras, Katherine Cheung, et al.. (2023). Defusing the legal and ethical minefield of epigenetic applications in the military, defense, and security context. Journal of Law and the Biosciences. 10(2). lsad034–lsad034. 3 indexed citations
4.
Ibrahim, Joe, Ligia Mateiu, Tim De Pooter, et al.. (2023). Mitochondrial GpC and CpG DNA Hypermethylation Cause Metabolic Stress-Induced Mitophagy and Cholestophagy. International Journal of Molecular Sciences. 24(22). 16412–16412. 10 indexed citations
5.
Cortés-Mancera, Fabián, Janette Heegsma, Bart van de Sluis, et al.. (2023). Mitochondrial DNA methylation in metabolic associated fatty liver disease. Frontiers in Nutrition. 10. 964337–964337. 14 indexed citations
6.
Hof, Ingrid H., Pytrick Jellema, Tom J. de Koning, et al.. (2022). The Mitochondrial Epigenome: An Unexplored Avenue to Explain Unexplained Myopathies?. International Journal of Molecular Sciences. 23(4). 2197–2197. 12 indexed citations
7.
Sarno, Federica, Emilie Logie, Christophe Deben, et al.. (2022). Functional Validation of the Putative Oncogenic Activity of PLAU. Biomedicines. 11(1). 102–102. 7 indexed citations
8.
Rots, Marianne G., et al.. (2021). The Endothelium as a Target for Anti-Atherogenic Therapy: A Focus on the Epigenetic Enzymes EZH2 and SIRT1. Journal of Personalized Medicine. 11(2). 103–103. 21 indexed citations
9.
Vlahov, Nikola, Sander Christiaan Steenbeek, Anna M. Grawenda, et al.. (2021). RASSF1C oncogene elicits amoeboid invasion, cancer stemness, and extracellular vesicle release via a SRC/Rho axis. The EMBO Journal. 40(20). e107680–e107680. 13 indexed citations
10.
Wu, Dandan, Yan‐Ming Xu, Machteld N. Hylkema, et al.. (2020). Ubiquitin carboxyl-terminal hydrolase isozyme L1/UCHL1 suppresses epithelial–mesenchymal transition and is under-expressed in cadmium-transformed human bronchial epithelial cells. Cell Biology and Toxicology. 37(4). 497–513. 8 indexed citations
11.
Wijst, Monique G.P. van der, et al.. (2018). Importance of Metal-Ion Exchange for the Biological Activity of Coordination Complexes of the Biomimetic Ligand N4Py. Inorganic Chemistry. 57(13). 7748–7756. 24 indexed citations
12.
Wu, Dandan, Juan Song, Sabine Bartel, et al.. (2017). The potential for targeted rewriting of epigenetic marks in COPD as a new therapeutic approach. Pharmacology & Therapeutics. 182. 1–14. 38 indexed citations
13.
Wijst, Monique G.P. van der, et al.. (2015). Targeting Nrf2 in healthy and malignant ovarian epithelial cells: Protection versus promotion. Molecular Oncology. 9(7). 1259–1273. 20 indexed citations
14.
Rots, Marianne G., et al.. (2015). The role of neutrophil gelatinase associated lipocalin (NGAL) as biological constituent linking depression and cardiovascular disease. Brain Behavior and Immunity. 46. 23–32. 40 indexed citations
15.
Huisman, Christian, G. Bea A. Wisman, Hinke G. Kazemier, et al.. (2013). Functional validation of putative tumor suppressor gene C13ORF18 in cervical cancer by Artificial Transcription Factors. Molecular Oncology. 7(3). 669–679. 37 indexed citations
16.
Falahi, Fahimeh, Christian Huisman, Hinke G. Kazemier, et al.. (2013). Towards Sustained Silencing of HER2/neu in Cancer By Epigenetic Editing. Molecular Cancer Research. 11(9). 1029–1039. 60 indexed citations
17.
Stolzenburg, Sabine, et al.. (2008). Modulation of epigenetic marks controlling the expression of the pancarcinoma antigen epithelial cell adhesion molecule. Data Archiving and Networked Services (DANS).
18.
Oosterhuis, Dorenda, Igor P. Dmitriev, Jerome Schaack, et al.. (2006). Towards a double controlled conditionally replicative adenovirus for potent and specific melanoma cell kill. Journal of Controlled Release. 116(2). e64–e66.
19.
Harmsen, Martin C., et al.. (2005). The carcinoma-specific epithelial glycoprotein-2 promoter controls efficient and selective gene expression in an adenoviral context. Cancer Gene Therapy. 13(2). 150–158. 8 indexed citations
20.
Westra, Johanna, Sigrídur A. Ásgeirsdóttir, Robbert J. Kok, et al.. (2005). Differential effects of NF-κB and p38 MAPK inhibitors and combinations thereof on TNF-α- and IL-1β-induced proinflammatory status of endothelial cells in vitro. American Journal of Physiology-Cell Physiology. 289(5). C1229–C1239. 127 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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