Marc Kschonsak

1.5k total citations
26 papers, 891 citations indexed

About

Marc Kschonsak is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Oncology. According to data from OpenAlex, Marc Kschonsak has authored 26 papers receiving a total of 891 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 4 papers in Cardiology and Cardiovascular Medicine and 3 papers in Oncology. Recurrent topics in Marc Kschonsak's work include Genomics and Chromatin Dynamics (10 papers), RNA and protein synthesis mechanisms (8 papers) and RNA Research and Splicing (7 papers). Marc Kschonsak is often cited by papers focused on Genomics and Chromatin Dynamics (10 papers), RNA and protein synthesis mechanisms (8 papers) and RNA Research and Splicing (7 papers). Marc Kschonsak collaborates with scholars based in Germany, United States and France. Marc Kschonsak's co-authors include Christian H. Haering, Markus Hassler, Jutta Metz, S. Bisht, Jorine M. Eeftens, Cees Dekker, Vladimir Rybin, Christopher P. Arthur, Claudio Ciferri and Ilia Kats and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Marc Kschonsak

24 papers receiving 876 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marc Kschonsak Germany 17 757 117 95 90 76 26 891
Stefanie Böhm Sweden 18 892 1.2× 90 0.8× 151 1.6× 131 1.5× 72 0.9× 31 1.0k
Yehuda Brody Israel 13 1.4k 1.8× 53 0.5× 92 1.0× 65 0.7× 43 0.6× 23 1.5k
Yunhe Bao United States 13 1.6k 2.1× 190 1.6× 88 0.9× 94 1.0× 34 0.4× 14 1.7k
Tracy K. Hale New Zealand 12 661 0.9× 100 0.9× 57 0.6× 94 1.0× 27 0.4× 24 848
Carrie Bernecky Germany 10 1.1k 1.4× 99 0.8× 54 0.6× 112 1.2× 28 0.4× 12 1.2k
Alec Heckert United States 7 1.3k 1.7× 119 1.0× 50 0.5× 44 0.5× 45 0.6× 10 1.4k
Fabien Bonneau Germany 24 1.9k 2.6× 80 0.7× 136 1.4× 53 0.6× 56 0.7× 37 2.2k
Laura Baranello United States 19 1.4k 1.8× 140 1.2× 58 0.6× 238 2.6× 26 0.3× 30 1.5k
Olexandr Dybkov Germany 22 2.0k 2.6× 46 0.4× 58 0.6× 45 0.5× 42 0.6× 36 2.1k
Paolo Swuec Italy 15 759 1.0× 48 0.4× 56 0.6× 74 0.8× 31 0.4× 24 857

Countries citing papers authored by Marc Kschonsak

Since Specialization
Citations

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

Fields of papers citing papers by Marc Kschonsak

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marc Kschonsak

This figure shows the co-authorship network connecting the top 25 collaborators of Marc Kschonsak. A scholar is included among the top collaborators of Marc Kschonsak 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 Marc Kschonsak. Marc Kschonsak 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.
Ro, Soo Y., Christine C. Jao, Angela J. Oh, et al.. (2025). Fab-Induced Stabilization of an Ion Channel Receptor Enables Mechanistic Characterization of Small-Molecule Therapeutics. Analytical Chemistry. 97(9). 5102–5108.
2.
Usher, Samuel, Estelle Toulmé, Stanislau Yatskevich, et al.. (2025). The sodium leak channel NALCN is regulated by neuronal SNARE complex proteins. Science Advances. 11(11). eads6004–eads6004.
3.
Karayel, Özge, Allison Soung, Alexander F. Schubert, et al.. (2025). Impairment of DET1 causes neurological defects and lethality in mice and humans. Proceedings of the National Academy of Sciences. 122(7). e2422631122–e2422631122. 2 indexed citations
4.
Rosenberg, Scott, Fergus Shanahan, Sayumi Yamazoe, et al.. (2023). Ternary complex dissociation kinetics contribute to mutant-selective EGFR degradation. Cell chemical biology. 30(2). 175–187.e15. 10 indexed citations
5.
Kschonsak, Marc, Christine C. Jao, Christopher P. Arthur, et al.. (2023). Cryo-EM reveals an unprecedented binding site for NaV1.7 inhibitors enabling rational design of potent hybrid inhibitors. eLife. 12. 17 indexed citations
6.
Noland, Cameron L., Han Chow Chua, Marc Kschonsak, et al.. (2022). Structure-guided unlocking of NaX reveals a non-selective tetrodotoxin-sensitive cation channel. Nature Communications. 13(1). 1416–1416. 19 indexed citations
7.
Kschonsak, Marc, Han Chow Chua, Cameron L. Noland, et al.. (2021). Structural architecture of the human NALCN channelosome. Nature. 603(7899). 180–186. 20 indexed citations
8.
Kschonsak, Marc, Lionel Rougé, Christopher P. Arthur, et al.. (2021). Structures of HCMV Trimer reveal the basis for receptor recognition and cell entry. Cell. 184(5). 1232–1244.e16. 34 indexed citations
9.
Kats, Ilia, et al.. (2021). Up-regulation of ubiquitin–proteasome activity upon loss of NatA-dependent N-terminal acetylation. Life Science Alliance. 5(2). e202000730–e202000730. 11 indexed citations
10.
Kschonsak, Marc, Han Chow Chua, Cameron L. Noland, et al.. (2020). Structure of the human sodium leak channel NALCN. Nature. 587(7833). 313–318. 38 indexed citations
11.
Kschonsak, Marc, et al.. (2020). Cryoelectron Microscopy Structure of a Yeast Centromeric Nucleosome at 2.7 Å Resolution. Structure. 28(3). 363–370.e3. 16 indexed citations
12.
Lee, Byung‐Gil, Matteo Allegretti, Markus Hassler, et al.. (2020). Cryo-EM structures of holo condensin reveal a subunit flip-flop mechanism. Nature Structural & Molecular Biology. 27(8). 743–751. 73 indexed citations
13.
Hassler, Markus, Indra A. Shaltiël, Marc Kschonsak, et al.. (2019). Structural Basis of an Asymmetric Condensin ATPase Cycle. Molecular Cell. 74(6). 1175–1188.e9. 58 indexed citations
14.
Estevez, Alberto, et al.. (2019). Building Cryo-EM at Genentech to Enable Research and Drug Discovery. Microscopy and Microanalysis. 25(S2). 1314–1315. 2 indexed citations
15.
Kats, Ilia, Anton Khmelinskii, Marc Kschonsak, et al.. (2018). Mapping Degradation Signals and Pathways in a Eukaryotic N-terminome. Molecular Cell. 70(3). 488–501.e5. 72 indexed citations
16.
Eeftens, Jorine M., S. Bisht, Jacob Kerssemakers, et al.. (2017). Real‐time detection of condensin‐driven DNA compaction reveals a multistep binding mechanism. The EMBO Journal. 36(23). 3448–3457. 60 indexed citations
17.
Kschonsak, Marc, S. Bisht, Jutta Metz, et al.. (2017). Structural Basis for a Safety-Belt Mechanism That Anchors Condensin to Chromosomes. Cell. 171(3). 588–600.e24. 106 indexed citations
18.
Muir, Kyle, Marc Kschonsak, Yan Li, et al.. (2016). Structure of the Pds5-Scc1 Complex and Implications for Cohesin Function. Cell Reports. 14(9). 2116–2126. 35 indexed citations
19.
Eeftens, Jorine M., Allard J. Katan, Marc Kschonsak, et al.. (2016). Single-Molecule Experiments to Resolve Structural and Mechanical Properties of Condensin. Biophysical Journal. 110(3). 528a–528a. 1 indexed citations
20.
Eeftens, Jorine M., Allard J. Katan, Marc Kschonsak, et al.. (2016). Condensin Smc2-Smc4 Dimers Are Flexible and Dynamic. Cell Reports. 14(8). 1813–1818. 67 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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