Valentin Stein

7.8k total citations · 1 hit paper
50 papers, 5.9k citations indexed

About

Valentin Stein is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Valentin Stein has authored 50 papers receiving a total of 5.9k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 32 papers in Cellular and Molecular Neuroscience and 11 papers in Cell Biology. Recurrent topics in Valentin Stein's work include Neuroscience and Neuropharmacology Research (29 papers), Ion channel regulation and function (12 papers) and Lipid Membrane Structure and Behavior (7 papers). Valentin Stein is often cited by papers focused on Neuroscience and Neuropharmacology Research (29 papers), Ion channel regulation and function (12 papers) and Lipid Membrane Structure and Behavior (7 papers). Valentin Stein collaborates with scholars based in Germany, United States and France. Valentin Stein's co-authors include Thomas J. Jentsch, Anselm A. Zdebik, Frank Weinreich, Roger A. Nicoll, David S. Bredt, Christian A. Hübner, Irm Hermans‐Borgmeyer, Christian Kubisch, Björn C. Schroeder and Klaus Ballanyi and has published in prestigious journals such as Nature, Neuron and Nature Genetics.

In The Last Decade

Valentin Stein

49 papers receiving 5.8k citations

Hit Papers

Molecular Structure and P... 2002 2026 2010 2018 2002 250 500 750 1000

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Valentin Stein 4.1k 3.4k 683 650 540 50 5.9k
Mark L. Dell’Acqua 4.1k 1.0× 3.0k 0.9× 667 1.0× 600 0.9× 476 0.9× 89 5.8k
Zhuan Zhou 3.1k 0.8× 2.6k 0.8× 701 1.0× 409 0.6× 566 1.0× 124 5.2k
Gary A. Wayman 4.5k 1.1× 3.2k 0.9× 794 1.2× 450 0.7× 599 1.1× 66 7.2k
Rüdiger W. Veh 4.7k 1.2× 4.3k 1.3× 948 1.4× 673 1.0× 939 1.7× 156 8.0k
Dušan Bartsch 3.0k 0.7× 3.3k 1.0× 689 1.0× 427 0.7× 1.2k 2.2× 97 6.4k
Edward C. Cooper 3.3k 0.8× 3.0k 0.9× 577 0.8× 989 1.5× 419 0.8× 77 5.2k
Nikolaj Klöcker 2.9k 0.7× 2.2k 0.6× 402 0.6× 429 0.7× 498 0.9× 81 5.1k
Stefan Herlitze 3.7k 0.9× 3.9k 1.2× 346 0.5× 449 0.7× 1.2k 2.2× 81 6.4k
Lu‐Yang Wang 3.4k 0.8× 3.3k 1.0× 571 0.8× 420 0.6× 1.3k 2.3× 130 5.6k
Christian A. Hübner 4.4k 1.1× 2.7k 0.8× 1.3k 1.8× 381 0.6× 554 1.0× 154 7.9k

Countries citing papers authored by Valentin Stein

Since Specialization
Citations

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

Fields of papers citing papers by Valentin Stein

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Valentin Stein

This figure shows the co-authorship network connecting the top 25 collaborators of Valentin Stein. A scholar is included among the top collaborators of Valentin Stein 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 Valentin Stein. Valentin Stein 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.
Leidmaa, Este, Andreas Zimmer, Valentin Stein, & Anne‐Kathrin Gellner. (2025). Acute high-fat high-sugar diet rapidly increases blood-brain barrier permeability in mice. The journal of nutrition health & aging. 29(7). 100574–100574. 2 indexed citations
2.
Mass, Elvira, Valentin Stein, Thorsten Lang, et al.. (2025). Glucose tasting depletes intracellular calcium stores and impairs macrophage functionality. iScience. 28(11). 113770–113770.
3.
Arévalo, Lena, et al.. (2023). Genome-scale CRISPR screen reveals neddylation to contribute to cisplatin resistance of testicular germ cell tumours. British Journal of Cancer. 128(12). 2270–2282. 11 indexed citations
4.
Komorowska‐Müller, Joanna Agnieszka, et al.. (2023). Chronic low-dose Δ9-tetrahydrocannabinol (THC) treatment stabilizes dendritic spines in 18-month-old mice. Scientific Reports. 13(1). 1390–1390. 10 indexed citations
5.
Gellner, Anne‐Kathrin, et al.. (2022). Stress vulnerability shapes disruption of motor cortical neuroplasticity. Translational Psychiatry. 12(1). 91–91. 17 indexed citations
6.
Gellner, Anne‐Kathrin, Ulrike Schmidt, Eva C. Beins, et al.. (2020). Molecular and neurocircuitry mechanisms of social avoidance. Cellular and Molecular Life Sciences. 78(4). 1163–1189. 28 indexed citations
7.
Doengi, Michael, et al.. (2019). Merlin modulates process outgrowth and synaptogenesis in the cerebellum. Brain Structure and Function. 224(6). 2121–2142. 8 indexed citations
8.
Brockmann, Marisa M., et al.. (2019). Neddylation regulates excitatory synaptic transmission and plasticity. Scientific Reports. 9(1). 17935–17935. 20 indexed citations
9.
Schrod, Nikolas, Dimitri Vanhecke, Ulrike Laugks, et al.. (2018). Pleomorphic linkers as ubiquitous structural organizers of vesicles in axons. PLoS ONE. 13(6). e0197886–e0197886. 24 indexed citations
10.
Vogl, Annette M., Marisa M. Brockmann, Sebastián A. Giusti, et al.. (2015). Neddylation inhibition impairs spine development, destabilizes synapses and deteriorates cognition. Nature Neuroscience. 18(2). 239–251. 74 indexed citations
11.
Mishra, Archana, et al.. (2014). Genetic Evidence for the Adhesion Protein IgSF9/Dasm1 to Regulate Inhibitory Synapse Development Independent of its Intracellular Domain. Journal of Neuroscience. 34(12). 4187–4199. 25 indexed citations
12.
Harmel, Nadine, Gerd Zolles, Henrike Berkefeld, et al.. (2012). AMPA Receptors Commandeer an Ancient Cargo Exporter for Use as an Auxiliary Subunit for Signaling. PLoS ONE. 7(1). e30681–e30681. 33 indexed citations
13.
Robbins, Elissa M., Karen Perez de Arce, Adam I. Fogel, et al.. (2010). SynCAM 1 Adhesion Dynamically Regulates Synapse Number and Impacts Plasticity and Learning. Neuron. 68(5). 894–906. 128 indexed citations
14.
Essmann, Clara L., et al.. (2008). Serine phosphorylation of ephrinB2 regulates trafficking of synaptic AMPA receptors. Nature Neuroscience. 11(9). 1035–1043. 64 indexed citations
15.
Elias, Guillermo M., et al.. (2007). Synapse-Specific and Developmentally Regulated Targeting of AMPA Receptors by a Family of MAGUK Scaffolding Proteins. Neuron. 53(3). 465–465. 13 indexed citations
16.
Elias, Guillermo M., et al.. (2006). Synapse-Specific and Developmentally Regulated Targeting of AMPA Receptors by a Family of MAGUK Scaffolding Proteins. Neuron. 52(2). 307–320. 316 indexed citations
17.
Tomita, Susumu, et al.. (2005). Bidirectional Synaptic Plasticity Regulated by Phosphorylation of Stargazin-like TARPs. Neuron. 45(2). 269–277. 268 indexed citations
18.
Hübner, Christian A., Valentin Stein, Irm Hermans‐Borgmeyer, et al.. (2001). Disruption of KCC2 Reveals an Essential Role of K-Cl Cotransport Already in Early Synaptic Inhibition. Neuron. 30(2). 515–524. 467 indexed citations
19.
Bösl, Michael R., Valentin Stein, Christian A. Hübner, et al.. (2001). Male germ cells and photoreceptors, both dependent on close cell–cell interactions, degenerate upon ClC-2 Cl− channel disruption. The EMBO Journal. 20(6). 1289–1299. 234 indexed citations
20.
Jentsch, Thomas J., et al.. (2000). Pathophysiology of KCNQ Channels: Neonatal Epilepsy and Progressive Deafness. Epilepsia. 41(8). 1068–1069. 29 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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