J. Basquin

4.3k total citations
63 papers, 2.5k citations indexed

About

J. Basquin is a scholar working on Molecular Biology, Materials Chemistry and Genetics. According to data from OpenAlex, J. Basquin has authored 63 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Molecular Biology, 11 papers in Materials Chemistry and 7 papers in Genetics. Recurrent topics in J. Basquin's work include RNA and protein synthesis mechanisms (25 papers), RNA Research and Splicing (21 papers) and RNA modifications and cancer (17 papers). J. Basquin is often cited by papers focused on RNA and protein synthesis mechanisms (25 papers), RNA Research and Splicing (21 papers) and RNA modifications and cancer (17 papers). J. Basquin collaborates with scholars based in Germany, United Kingdom and France. J. Basquin's co-authors include Elena Conti, Esben Lorentzen, Fabien Bonneau, Andrzej Dziembowski, J. Ebert, Sevim Ozgur, Dietrich Suck, Witold Filipowicz, Michael Sattler and Stephan Gruber and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

J. Basquin

62 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
J. Basquin Germany 29 2.2k 328 157 138 135 63 2.5k
Meindert H. Lamers Netherlands 22 1.8k 0.8× 378 1.2× 122 0.8× 98 0.7× 79 0.6× 46 2.2k
Achim Dickmanns Germany 33 2.4k 1.1× 375 1.1× 220 1.4× 205 1.5× 206 1.5× 70 3.1k
Daiqing Liao United States 27 1.7k 0.7× 388 1.2× 109 0.7× 217 1.6× 120 0.9× 54 2.3k
Gregory D. Bowman United States 34 2.6k 1.2× 369 1.1× 105 0.7× 267 1.9× 92 0.7× 59 2.9k
Chris Oubridge United Kingdom 21 3.4k 1.5× 402 1.2× 256 1.6× 144 1.0× 200 1.5× 35 3.7k
Anton Meinhart Germany 29 2.2k 1.0× 508 1.5× 142 0.9× 177 1.3× 338 2.5× 51 2.9k
Daniel R. Boutz United States 22 1.5k 0.7× 244 0.7× 164 1.0× 69 0.5× 123 0.9× 33 2.2k
Logan W. Donaldson Canada 23 1.6k 0.7× 247 0.8× 213 1.4× 104 0.8× 292 2.2× 52 2.1k
Susan E. Tsutakawa United States 34 2.6k 1.2× 327 1.0× 410 2.6× 118 0.9× 114 0.8× 66 2.8k
Brandt F. Eichman United States 31 2.8k 1.3× 471 1.4× 109 0.7× 236 1.7× 111 0.8× 76 3.0k

Countries citing papers authored by J. Basquin

Since Specialization
Citations

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

Fields of papers citing papers by J. Basquin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Basquin

This figure shows the co-authorship network connecting the top 25 collaborators of J. Basquin. A scholar is included among the top collaborators of J. Basquin 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 J. Basquin. J. Basquin 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.
Kobayashi, Wataru, Daniel Bollschweiler, J. Basquin, et al.. (2024). Nucleosome-bound NR5A2 structure reveals pioneer factor mechanism by DNA minor groove anchor competition. Nature Structural & Molecular Biology. 31(5). 757–766. 14 indexed citations
2.
Basquin, J., et al.. (2024). UPF1 helicase orchestrates mutually exclusive interactions with the SMG6 endonuclease and UPF2. Nucleic Acids Research. 52(10). 6036–6048. 7 indexed citations
3.
Becker, Sidney, et al.. (2023). Purine nucleosides replace cAMP in allosteric regulation of PKA in trypanosomatid pathogens. eLife. 12. 4 indexed citations
4.
Manjula, R., J. Basquin, Regina Feederle, et al.. (2023). Plant MDL proteins synergize with the cytokine MIF at CXCR2 and CXCR4 receptors in human cells. Science Signaling. 16(812). eadg2621–eadg2621. 2 indexed citations
5.
Bonneau, Fabien, et al.. (2023). Nuclear mRNPs are compact particles packaged with a network of proteins promoting RNA–RNA interactions. Genes & Development. 37(11-12). 505–517. 23 indexed citations
6.
Gerlach, Piotr, William A. Garland, Fabien Bonneau, et al.. (2022). Structure and regulation of the nuclear exosome targeting complex guides RNA substrates to the exosome. Molecular Cell. 82(13). 2505–2518.e7. 22 indexed citations
7.
Kubacka, Dorota, et al.. (2022). Substrate-Based Design of Cytosolic Nucleotidase IIIB Inhibitors and Structural Insights into Inhibition Mechanism. Pharmaceuticals. 15(5). 554–554. 2 indexed citations
8.
Lozada, Néstor J. Hernández, Benke Hong, Joshua C. Wood, et al.. (2022). Biocatalytic routes to stereo-divergent iridoids. Nature Communications. 13(1). 4718–4718. 15 indexed citations
9.
Prabu, J. Rajan, Kheewoong Baek, Daniel Horn‐Ghetko, et al.. (2021). CUL5-ARIH2 E3-E3 ubiquitin ligase structure reveals cullin-specific NEDD8 activation. Nature Chemical Biology. 17(10). 1075–1083. 41 indexed citations
10.
Malinverni, Roberto, Vanesa Valero, Michelle M. Leger, et al.. (2021). Evolution of a histone variant involved in compartmental regulation of NAD metabolism. Nature Structural & Molecular Biology. 28(12). 1009–1019. 9 indexed citations
11.
Lichtenberger, Raffael, Emil Karaulanov, Bernd Simon, et al.. (2021). Structural basis of PETISCO complex assembly during piRNA biogenesis in C. elegans. Genes & Development. 35(17-18). 1304–1323. 11 indexed citations
12.
Täschner, Michael, J. Basquin, Barbara Steigenberger, et al.. (2021). Nse5/6 inhibits the Smc5/6 ATPase and modulates DNA substrate binding. The EMBO Journal. 40(15). e107807–e107807. 35 indexed citations
13.
Zinzula, Luca, J. Basquin, Stefan Bohn, et al.. (2020). High-resolution structure and biophysical characterization of the nucleocapsid phosphoprotein dimerization domain from the Covid-19 severe acute respiratory syndrome coronavirus 2. Biochemical and Biophysical Research Communications. 538. 54–62. 86 indexed citations
14.
Schuller, Sandra K., Jan M. Schuller, J. Rajan Prabu, et al.. (2020). Structural insights into the nucleic acid remodeling mechanisms of the yeast THO-Sub2 complex. eLife. 9. 34 indexed citations
15.
Soh, Young‐Min, Iain F. Davidson, Stefano Zamuner, et al.. (2019). Self-organization of parS centromeres by the ParB CTP hydrolase. Science. 366(6469). 1129–1133. 94 indexed citations
16.
Han, Zhong, J. Basquin, Fabien Bonneau, et al.. (2017). Sen1 has unique structural features grafted on the architecture of the Upf1‐like helicase family. The EMBO Journal. 36(11). 1590–1604. 40 indexed citations
17.
Basquin, J., et al.. (2015). Architecture of the Ubiquitylation Module of the Yeast Ccr4-Not Complex. Structure. 23(5). 921–928. 29 indexed citations
18.
Lorentzen, Esben, J. Basquin, & Elena Conti. (2008). Structural organization of the RNA-degrading exosome. Current Opinion in Structural Biology. 18(6). 709–713. 37 indexed citations
19.
Lorentzen, Esben, J. Basquin, Rafał Tomecki, Andrzej Dziembowski, & Elena Conti. (2008). Structure of the Active Subunit of the Yeast Exosome Core, Rrp44: Diverse Modes of Substrate Recruitment in the RNase II Nuclease Family. Molecular Cell. 29(6). 717–728. 158 indexed citations
20.
Hothorn, Michael, et al.. (2006). Structural basis of yeast aminoacyl-tRNA synthetase complex formation revealed by crystal structures of two binary sub-complexes. Nucleic Acids Research. 34(14). 3968–3979. 55 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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