Thorsten Trimbuch

5.8k total citations · 1 hit paper
48 papers, 3.2k citations indexed

About

Thorsten Trimbuch is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Thorsten Trimbuch has authored 48 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 33 papers in Cell Biology and 30 papers in Cellular and Molecular Neuroscience. Recurrent topics in Thorsten Trimbuch's work include Cellular transport and secretion (33 papers), Neuroscience and Neuropharmacology Research (24 papers) and Lipid Membrane Structure and Behavior (23 papers). Thorsten Trimbuch is often cited by papers focused on Cellular transport and secretion (33 papers), Neuroscience and Neuropharmacology Research (24 papers) and Lipid Membrane Structure and Behavior (23 papers). Thorsten Trimbuch collaborates with scholars based in Germany, United States and United Kingdom. Thorsten Trimbuch's co-authors include Christian Rosenmund, Marcial Camacho, Pascal Fenske, Shuwen Chang, Sebastian Memczak, Petar Glažar, Mireya Plass, Luis R. Hernández-Miranda, Susanne A. Wolf and Vera Zywitza and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Thorsten Trimbuch

46 papers receiving 3.2k citations

Hit Papers

Loss of a mammalian circular RNA locus causes miRNA dereg... 2017 2026 2020 2023 2017 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thorsten Trimbuch Germany 27 2.4k 1.2k 959 834 254 48 3.2k
JeongSeop Rhee Germany 28 2.4k 1.0× 1.4k 1.1× 1.6k 1.7× 370 0.4× 290 1.1× 50 3.6k
Uri Ashery Israel 35 2.8k 1.2× 2.0k 1.6× 1.4k 1.5× 234 0.3× 475 1.9× 80 4.3k
Nael Nadif Kasri Netherlands 37 2.3k 1.0× 516 0.4× 959 1.0× 283 0.3× 277 1.1× 103 3.5k
Hiroshi Gomi Japan 25 1.2k 0.5× 718 0.6× 571 0.6× 287 0.3× 339 1.3× 55 2.5k
Annie Andrieux France 39 2.7k 1.2× 2.2k 1.8× 1.0k 1.1× 165 0.2× 425 1.7× 108 4.9k
Michihiro Igarashi Japan 31 1.6k 0.7× 1.1k 0.9× 1.1k 1.1× 201 0.2× 221 0.9× 87 3.0k
Valeria Cavalli United States 33 2.4k 1.0× 1.1k 0.9× 2.0k 2.1× 154 0.2× 558 2.2× 66 4.5k
Kimberley F. Tolias United States 30 2.9k 1.2× 1.4k 1.2× 1.1k 1.2× 124 0.1× 367 1.4× 44 4.5k
Silvia Coco Italy 27 1.3k 0.6× 729 0.6× 1.3k 1.4× 165 0.2× 339 1.3× 41 2.6k
Jeffery L. Twiss United States 45 4.5k 1.9× 1.1k 0.9× 3.0k 3.2× 372 0.4× 601 2.4× 98 6.9k

Countries citing papers authored by Thorsten Trimbuch

Since Specialization
Citations

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

Fields of papers citing papers by Thorsten Trimbuch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thorsten Trimbuch

This figure shows the co-authorship network connecting the top 25 collaborators of Thorsten Trimbuch. A scholar is included among the top collaborators of Thorsten Trimbuch 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 Thorsten Trimbuch. Thorsten Trimbuch 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.
Cabré, Noemí, Marcos F. Fondevila, Tomoo Yamazaki, et al.. (2025). Activation of intestinal endogenous retroviruses by alcohol exacerbates liver disease. Journal of Clinical Investigation. 135(13). 3 indexed citations
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.
4.
Ledderose, Julia, Timothy A. Zolnik, Thorsten Trimbuch, et al.. (2023). Layer 1 of somatosensory cortex: an important site for input to a tiny cortical compartment. Cerebral Cortex. 33(23). 11354–11372. 11 indexed citations
5.
Knierim, Ellen, Johannes Vogt, Michael Kintscher, et al.. (2023). Mutations in plasticity-related-gene-1 (PRG-1) protein contribute to hippocampal seizure susceptibility and modify epileptic phenotype. Cerebral Cortex. 33(12). 7454–7467. 2 indexed citations
7.
Brockmann, Marisa M., et al.. (2021). Reexamination of N-terminal domains of syntaxin-1 in vesicle fusion from central murine synapses. eLife. 10. 12 indexed citations
8.
Weber‐Boyvat, Marion, et al.. (2020). ORP/Osh mediate cross-talk between ER-plasma membrane contact site components and plasma membrane SNAREs. Cellular and Molecular Life Sciences. 78(4). 1689–1708. 19 indexed citations
9.
Malsam, Jörg, Thorsten Trimbuch, Andreas F.‐P. Sonnen, et al.. (2020). Complexin Suppresses Spontaneous Exocytosis by Capturing the Membrane-Proximal Regions of VAMP2 and SNAP25. Cell Reports. 32(3). 107926–107926. 28 indexed citations
10.
Camacho, Marcial, et al.. (2020). Disentangling the Roles of RIM and Munc13 in Synaptic Vesicle Localization and Neurotransmission. Journal of Neuroscience. 40(49). 9372–9385. 23 indexed citations
11.
Fuchs, Joachim, Julia Ledderose, Michiel T. van Diepen, et al.. (2019). The Axonal Membrane Protein PRG2 Inhibits PTEN and Directs Growth to Branches. Cell Reports. 29(7). 2028–2040.e8. 26 indexed citations
12.
Orlando, Marta, et al.. (2019). Light-Activated ROS Production Induces Synaptic Autophagy. Journal of Neuroscience. 39(12). 2163–2183. 53 indexed citations
13.
Watanabe, Shigeki, Lauren Mamer, Sumana Raychaudhuri, et al.. (2018). Synaptojanin and Endophilin Mediate Neck Formation during Ultrafast Endocytosis. Neuron. 98(6). 1184–1197.e6. 71 indexed citations
14.
Piwecka, Monika, Petar Glažar, Luis R. Hernández-Miranda, et al.. (2017). Loss of a mammalian circular RNA locus causes miRNA deregulation and affects brain function. Science. 357(6357). 959 indexed citations breakdown →
15.
Watanabe, Shigeki, Thorsten Trimbuch, Marcial Camacho, et al.. (2014). Clathrin regenerates synaptic vesicles from endosomes. Nature. 515(7526). 228–233. 221 indexed citations
16.
Kononenko, Natalia L., Dmytro Puchkov, Alexander M. Walter, et al.. (2014). Clathrin/AP-2 Mediate Synaptic Vesicle Reformation from Endosome-like Vacuoles but Are Not Essential for Membrane Retrieval at Central Synapses. Neuron. 82(5). 981–988. 158 indexed citations
17.
Arancillo, Marife, Sangwon Min, Stefan Gerber, et al.. (2013). Titration of Syntaxin1 in Mammalian Synapses Reveals Multiple Roles in Vesicle Docking, Priming, and Release Probability. Journal of Neuroscience. 33(42). 16698–16714. 47 indexed citations
18.
Rupprecht, Anne, Olaf Ninnemann, Martin Jabůrek, et al.. (2010). Role of the Transmembrane Potential in the Membrane Proton Leak. Biophysical Journal. 98(8). 1503–1511. 64 indexed citations
19.
Lehnardt, Seija, et al.. (2008). A Vicious Cycle Involving Release of Heat Shock Protein 60 from Injured Cells and Activation of Toll-Like Receptor 4 Mediates Neurodegeneration in the CNS. Journal of Neuroscience. 28(10). 2320–2331. 220 indexed citations
20.
McGurk, Leeanne, et al.. (2008). The RGS gene loco is essential for male reproductive system differentiation in Drosophila melanogaster. BMC Developmental Biology. 8(1). 37–37. 2 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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