Benoît Driesschaert

929 total citations
52 papers, 693 citations indexed

About

Benoît Driesschaert is a scholar working on Biophysics, Materials Chemistry and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Benoît Driesschaert has authored 52 papers receiving a total of 693 indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Biophysics, 37 papers in Materials Chemistry and 14 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Benoît Driesschaert's work include Electron Spin Resonance Studies (45 papers), Lanthanide and Transition Metal Complexes (35 papers) and Advanced MRI Techniques and Applications (14 papers). Benoît Driesschaert is often cited by papers focused on Electron Spin Resonance Studies (45 papers), Lanthanide and Transition Metal Complexes (35 papers) and Advanced MRI Techniques and Applications (14 papers). Benoît Driesschaert collaborates with scholars based in United States, Belgium and France. Benoît Driesschaert's co-authors include Valery V. Khramtsov, Bernard Gallez, Andrey A. Bobko, Jacqueline Marchand‐Brynaert, Timothy D. Eubank, Mark Tseytlin, Ilirian Dhimitruka, Raphaël Robiette, Jason V. Evans and Elena E. Tchekneva and has published in prestigious journals such as Angewandte Chemie International Edition, SHILAP Revista de lepidopterología and The Journal of Immunology.

In The Last Decade

Benoît Driesschaert

51 papers receiving 690 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Benoît Driesschaert United States 16 464 386 140 139 116 52 693
Ilirian Dhimitruka United States 16 528 1.1× 480 1.2× 176 1.3× 145 1.0× 156 1.3× 24 884
Yuliya F. Polienko Russia 13 263 0.6× 210 0.5× 123 0.9× 23 0.2× 50 0.4× 44 501
Alexey S. Chubarov Russia 17 165 0.4× 231 0.6× 73 0.5× 64 0.5× 45 0.4× 39 643
Elias Pershagen Sweden 8 87 0.2× 303 0.8× 58 0.4× 51 0.4× 150 1.3× 9 585
Pavel B. Tsitovich United States 15 185 0.4× 580 1.5× 362 2.6× 292 2.1× 90 0.8× 15 713
Jacek L. Kolanowski Australia 16 67 0.1× 363 0.9× 78 0.6× 38 0.3× 393 3.4× 29 905
André F. Martins United States 21 76 0.2× 652 1.7× 200 1.4× 385 2.8× 203 1.8× 49 1.1k
Angelo Josue M. Lubag United States 14 186 0.4× 807 2.1× 214 1.5× 567 4.1× 207 1.8× 16 1.1k
Amandine Roux France 15 49 0.1× 340 0.9× 129 0.9× 133 1.0× 82 0.7× 29 556
Liu Qi Chen United States 8 157 0.3× 392 1.0× 80 0.6× 365 2.6× 40 0.3× 10 587

Countries citing papers authored by Benoît Driesschaert

Since Specialization
Citations

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

Fields of papers citing papers by Benoît Driesschaert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Benoît Driesschaert

This figure shows the co-authorship network connecting the top 25 collaborators of Benoît Driesschaert. A scholar is included among the top collaborators of Benoît Driesschaert 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 Benoît Driesschaert. Benoît Driesschaert 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.
Murugesan, V., et al.. (2024). Line-Shifting Triarylmethyl Radicals for Imaging of Enzyme Activity Using Overhauser-Enhanced Magnetic Resonance Imaging: Application to Alkaline Phosphatase. SHILAP Revista de lepidopterología. 3(1). 35–44. 1 indexed citations
2.
Eubank, Timothy D., et al.. (2023). In Vivo Electron Paramagnetic Resonance Molecular Profiling of Tumor Microenvironment upon Tumor Progression to Malignancy in an Animal Model of Breast Cancer. Molecular Imaging and Biology. 26(3). 424–434. 6 indexed citations
3.
Viswakarma, Navin, Werner J. Geldenhuys, Timothy D. Eubank, et al.. (2023). SOX71, A Biocompatible Succinyl Derivative of the Triarylmethyl Radical OX071 for In Vivo Quantitative Oxygen Mapping Using Electron Paramagnetic Resonance. Molecular Imaging and Biology. 26(3). 542–552. 2 indexed citations
4.
Bobko, Andrey A., Lei Wang, Gangqing Hu, et al.. (2023). Dose-Specific Intratumoral GM-CSF Modulates Breast Tumor Oxygenation and Antitumor Immunity. The Journal of Immunology. 211(10). 1589–1604. 7 indexed citations
5.
Driesschaert, Benoît, Eugene D. Barth, Mrignayani Kotecha, et al.. (2023). Toward a Nanoencapsulated EPR Imaging Agent for Clinical Use. Molecular Imaging and Biology. 26(3). 525–541. 3 indexed citations
6.
Tan, Kong Ooi, et al.. (2022). Observing Nearby Nuclei on Paramagnetic Trityls and MOFs via DNP and Electron Decoupling. Chemistry - A European Journal. 28(68). e202202556–e202202556. 7 indexed citations
7.
Eubank, Timothy D., et al.. (2022). Synthesis and characterization of a biocompatible 13C1 isotopologue of trityl radical OX071 for in vivo EPR viscometry. The Analyst. 147(24). 5643–5648. 9 indexed citations
8.
Singewald, Kevin, et al.. (2021). Cleavage-Resistant Protein Labeling With Hydrophilic Trityl Enables Distance MeasurementsIn-Cell. The Journal of Physical Chemistry B. 125(20). 5265–5274. 23 indexed citations
9.
Moore, W. Michael, et al.. (2021). Perchlorinated Triarylmethyl Radical 99% Enriched 13 C at the Central Carbon as EPR Spin Probe Highly Sensitive to Molecular Tumbling. The Journal of Physical Chemistry B. 125(27). 7380–7387. 6 indexed citations
10.
Moore, W. Michael, et al.. (2021). Impact of Chlorine Substitution on Electron Spin Relaxation of a Trityl Radical. Applied Magnetic Resonance. 53(3-5). 797–808. 2 indexed citations
11.
12.
Driesschaert, Benoît, et al.. (2020). A 13C‐Labeled Triarylmethyl Radical as an EPR Spin Probe Highly Sensitive to Molecular Tumbling. Angewandte Chemie. 132(38). 16593–16596. 4 indexed citations
13.
Driesschaert, Benoît, et al.. (2020). A 13C‐Labeled Triarylmethyl Radical as an EPR Spin Probe Highly Sensitive to Molecular Tumbling. Angewandte Chemie International Edition. 59(38). 16451–16454. 38 indexed citations
14.
Khramtsov, Valery V., et al.. (2019). Synthesis of hydroxyethyl tetrathiatriarylmethyl radicals OX063 and OX071. RSC Advances. 9(60). 35073–35076. 34 indexed citations
15.
Xu, Xuan, et al.. (2018). Imaging of Enzyme Activity by Electron Paramagnetic Resonance: Concept and Experiment Using a Paramagnetic Substrate of Alkaline Phosphatase. Angewandte Chemie International Edition. 57(36). 11701–11705. 14 indexed citations
16.
17.
Driesschaert, Benoît, et al.. (2017). Triarylmethyl-based biradical as a superoxide probe. Free Radical Research. 52(3). 373–379. 14 indexed citations
18.
Driesschaert, Benoît, Andrey A. Bobko, Valery V. Khramtsov, & Jay L. Zweíer. (2016). Nitro-Triarylmethyl Radical as Dual Oxygen and Superoxide Probe. Cell Biochemistry and Biophysics. 75(2). 241–246. 11 indexed citations
19.
Driesschaert, Benoît, et al.. (2012). A phosphonated triarylmethyl radical as a probe for measurement of pH by EPR. Chemical Communications. 48(34). 4049–4049. 35 indexed citations
20.
Driesschaert, Benoît, et al.. (2011). Chiral properties of tetrathiatriarylmethyl spin probes. Chemical Communications. 47(16). 4793–4793. 28 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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