David Lutz

987 total citations
36 papers, 767 citations indexed

About

David Lutz is a scholar working on Cellular and Molecular Neuroscience, Developmental Neuroscience and Molecular Biology. According to data from OpenAlex, David Lutz has authored 36 papers receiving a total of 767 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Cellular and Molecular Neuroscience, 18 papers in Developmental Neuroscience and 13 papers in Molecular Biology. Recurrent topics in David Lutz's work include Neurogenesis and neuroplasticity mechanisms (18 papers), Nerve injury and regeneration (10 papers) and Neuroscience and Neuropharmacology Research (8 papers). David Lutz is often cited by papers focused on Neurogenesis and neuroplasticity mechanisms (18 papers), Nerve injury and regeneration (10 papers) and Neuroscience and Neuropharmacology Research (8 papers). David Lutz collaborates with scholars based in Germany, United States and China. David Lutz's co-authors include Ralf Kleene, Melitta Schachner, Gabriele Loers, Hardeep Kataria, Gerrit Wolters‐Eisfeld, Melitta Schachner, Michael Frotscher, Harshita Chaudhary, Irina I. Stoyanova and Igor Jakovčevski and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and Journal of Neuroscience.

In The Last Decade

David Lutz

36 papers receiving 759 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David Lutz Germany 19 372 334 231 116 79 36 767
Hidemasa Kato Japan 17 318 0.9× 699 2.1× 236 1.0× 122 1.1× 86 1.1× 34 1.1k
Jin-Chong Xu United States 10 235 0.6× 277 0.8× 116 0.5× 86 0.7× 73 0.9× 11 575
Verónica T. Cheli United States 19 346 0.9× 377 1.1× 231 1.0× 108 0.9× 122 1.5× 28 943
Thomas W. Gould United States 19 477 1.3× 535 1.6× 182 0.8× 95 0.8× 127 1.6× 37 1.1k
Takao Hikita Japan 17 285 0.8× 600 1.8× 124 0.5× 206 1.8× 67 0.8× 28 1.0k
Xiuxin Liu China 14 490 1.3× 540 1.6× 446 1.9× 83 0.7× 78 1.0× 33 1.2k
Claire Sauvageot United States 8 296 0.8× 507 1.5× 216 0.9× 97 0.8× 40 0.5× 9 863
Dina N. Arvanitis France 15 365 1.0× 438 1.3× 131 0.6× 221 1.9× 175 2.2× 30 882
Nathalie Doerflinger France 11 349 0.9× 753 2.3× 247 1.1× 127 1.1× 72 0.9× 13 1.2k
Carol Charniga United States 15 353 0.9× 484 1.4× 108 0.5× 66 0.6× 95 1.2× 17 798

Countries citing papers authored by David Lutz

Since Specialization
Citations

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

Fields of papers citing papers by David Lutz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Lutz

This figure shows the co-authorship network connecting the top 25 collaborators of David Lutz. A scholar is included among the top collaborators of David Lutz 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 David Lutz. David Lutz 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.
Hausrat, Torben J., Philipp Christoph Janiesch, Petra Breiden, et al.. (2022). Disruption of tubulin-alpha4a polyglutamylation prevents aggregation of hyper-phosphorylated tau and microglia activation in mice. Nature Communications. 13(1). 4192–4192. 14 indexed citations
2.
Lutz, David, et al.. (2022). Melatonin signalling in Schwann cells during neuroregeneration. Frontiers in Cell and Developmental Biology. 10. 999322–999322. 9 indexed citations
3.
Jakovčevski, Igor, Melitta Schachner, Monika von Düring, et al.. (2021). Mice lacking perforin have improved regeneration of the injured femoral nerve. Neural Regeneration Research. 17(8). 1802–1802. 2 indexed citations
4.
Stoyanova, Irina I. & David Lutz. (2021). Ghrelin-Mediated Regeneration and Plasticity After Nervous System Injury. Frontiers in Cell and Developmental Biology. 9. 595914–595914. 11 indexed citations
5.
Lutz, David, Elisabeth Petrasch‐Parwez, Jan Claudius Schwitalla, et al.. (2020). Reelin signaling modulates GABAB receptor function in the neocortex. Journal of Neurochemistry. 156(5). 589–603. 16 indexed citations
6.
Lombino, Franco L., Mary Muhia, Jeffrey Lopez‐Rojas, et al.. (2019). The Microtubule Severing Protein Katanin Regulates Proliferation of Neuronal Progenitors in Embryonic and Adult Neurogenesis. Scientific Reports. 9(1). 15940–15940. 10 indexed citations
7.
Kleene, Ralf, et al.. (2018). A fragment of adhesion molecule L1 is imported into mitochondria, and regulates mitochondrial metabolism and trafficking. Journal of Cell Science. 131(9). 24 indexed citations
8.
Kleene, Ralf, Ingke Braren, Hardeep Kataria, et al.. (2018). A Fragment of Adhesion Molecule L1 Binds to Nuclear Receptors to Regulate Synaptic Plasticity and Motor Coordination. Molecular Neurobiology. 55(9). 7164–7178. 18 indexed citations
9.
Grüner, F., Michelle S. Bradbury, Ulrich Wiesner, et al.. (2018). Localising functionalised gold-nanoparticles in murine spinal cords by X-ray fluorescence imaging and background-reduction through spatial filtering for human-sized objects. Scientific Reports. 8(1). 16561–16561. 29 indexed citations
10.
Brunne, Bianka, Shanting Zhao, Xuejun Chai, et al.. (2017). Trajectory Analysis Unveils Reelin's Role in the Directed Migration of Granule Cells in the Dentate Gyrus. Journal of Neuroscience. 38(1). 137–148. 22 indexed citations
11.
Lee, Sang Hun, et al.. (2017). Presenilins regulate synaptic plasticity and mitochondrial calcium homeostasis in the hippocampal mossy fiber pathway. Molecular Neurodegeneration. 12(1). 48–48. 26 indexed citations
12.
Lutz, David, Ahmed Sharaf, Dagmar Drexler, et al.. (2017). Proteolytic cleavage of transmembrane cell adhesion molecule L1 by extracellular matrix molecule Reelin is important for mouse brain development. Scientific Reports. 7(1). 15268–15268. 17 indexed citations
13.
Loers, Gabriele, et al.. (2017). Generation and intracellular trafficking of a polysialic acid-carrying fragment of the neural cell adhesion molecule NCAM to the cell nucleus. Scientific Reports. 7(1). 8622–8622. 11 indexed citations
14.
Lutz, David, et al.. (2016). The polysialic acid mimetics 5-nonyloxytryptamine and vinorelbine facilitate nervous system repair. Scientific Reports. 6(1). 26927–26927. 27 indexed citations
15.
Lutz, David, Gabriele Loers, Ralf Kleene, et al.. (2014). Myelin Basic Protein Cleaves Cell Adhesion Molecule L1 and Promotes Neuritogenesis and Cell Survival. Journal of Biological Chemistry. 289(19). 13503–13518. 50 indexed citations
16.
Strekalova, Elena, Nevena Djogo, Gabriele Loers, et al.. (2013). Generation of Amyloid-β Is Reduced by the Interaction of Calreticulin with Amyloid Precursor Protein, Presenilin and Nicastrin. PLoS ONE. 8(4). e61299–e61299. 12 indexed citations
17.
Schulz, Florian, David Lutz, Neus G. Bastús, et al.. (2013). Gold nanoparticles functionalized with a fragment of the neural cell adhesion molecule L1 stimulate L1-mediated functions. Nanoscale. 5(21). 10605–10605. 23 indexed citations
18.
Wurm, M., et al.. (2010). Microtechnology meets systems biology: The small molecules of metabolome as next big targets. Journal of Biotechnology. 149(1-2). 33–51. 19 indexed citations
19.
Johnson, Steve A., N. Thin Luu, Richard J. Knapp, et al.. (1999). Synergistic Interactions between Ampakines and Antipsychotic Drugs. Journal of Pharmacology and Experimental Therapeutics. 289(1). 392–397. 66 indexed citations
20.
Pettit, Hugh O., David Lutz, Carlos Enrique Gutierrez, & David Eveleth. (1994). I.c.v. infusions of ACPD(1S,3R) attenuate learning in a Morris water maze paradigm. Neuroscience Letters. 178(1). 43–46. 21 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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