Ralph Lucius

3.4k total citations
82 papers, 2.6k citations indexed

About

Ralph Lucius is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Oncology. According to data from OpenAlex, Ralph Lucius has authored 82 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 19 papers in Cellular and Molecular Neuroscience and 12 papers in Oncology. Recurrent topics in Ralph Lucius's work include Nerve injury and regeneration (9 papers), Retinal Diseases and Treatments (8 papers) and Cell Adhesion Molecules Research (8 papers). Ralph Lucius is often cited by papers focused on Nerve injury and regeneration (9 papers), Retinal Diseases and Treatments (8 papers) and Cell Adhesion Molecules Research (8 papers). Ralph Lucius collaborates with scholars based in Germany, France and Denmark. Ralph Lucius's co-authors include Janka Held‐Feindt, Jobst Sievers, Rolf Mentlein, Philip Rosenstiel, Stefan Gallinat, Kirsten Hattermann, Thomas Unger, Thomas Herdegen, Friederike Knerlich‐Lukoschus and H. Maximilian Mehdorn and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Experimental Medicine and Blood.

In The Last Decade

Ralph Lucius

81 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ralph Lucius Germany 27 923 456 439 413 321 82 2.6k
Ludwig Wagner Austria 29 1.2k 1.3× 385 0.8× 347 0.8× 373 0.9× 378 1.2× 124 2.9k
Mitsuru Kuwamura Japan 32 1.5k 1.6× 688 1.5× 375 0.9× 325 0.8× 425 1.3× 307 4.2k
Annie Schmid‐Alliana France 33 1.4k 1.5× 594 1.3× 457 1.0× 597 1.4× 355 1.1× 60 2.7k
Marion Gröger Austria 33 1.0k 1.1× 1.0k 2.2× 190 0.4× 467 1.1× 286 0.9× 68 3.1k
Peter Schratzberger Austria 28 1.1k 1.2× 440 1.0× 673 1.5× 307 0.7× 451 1.4× 57 2.7k
Toshihiko Matsuo Japan 33 1.3k 1.4× 578 1.3× 365 0.8× 358 0.9× 437 1.4× 258 4.9k
Uh‐Hyun Kim South Korea 37 2.0k 2.2× 479 1.1× 211 0.5× 408 1.0× 405 1.3× 114 4.0k
Qi Xiang China 33 1.3k 1.4× 558 1.2× 298 0.7× 333 0.8× 278 0.9× 131 3.6k
Kimiyoshi Arimura Japan 38 1.2k 1.3× 1.2k 2.5× 762 1.7× 323 0.8× 369 1.1× 190 4.7k
Christos D. Katsetos United States 36 1.8k 2.0× 471 1.0× 442 1.0× 775 1.9× 605 1.9× 101 4.3k

Countries citing papers authored by Ralph Lucius

Since Specialization
Citations

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

Fields of papers citing papers by Ralph Lucius

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ralph Lucius

This figure shows the co-authorship network connecting the top 25 collaborators of Ralph Lucius. A scholar is included among the top collaborators of Ralph Lucius 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 Ralph Lucius. Ralph Lucius 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.
Schröder, Katja, Sebastian Heinzel, Annika Kluge, et al.. (2025). Evaluation of an antibody panel for alpha-synuclein detection in FFPE rectal biopsies in Parkinson’s disease. IBRO Neuroscience Reports. 19. 844–853. 1 indexed citations
2.
Boni, Sébastien, Katja Schröder, Stefanie Küerten, et al.. (2025). SOX10-Mediated Regulation of Enteric Glial Phenotype in vitro and its Relevance for Neuroinflammatory Disorders. Journal of Molecular Neuroscience. 75(1). 26–26. 1 indexed citations
3.
Cossais, François, et al.. (2024). Resveratrol Alleviates the Early Challenges of Implant-Based Drug Delivery in a Human Glial Cell Model. International Journal of Molecular Sciences. 25(4). 2078–2078.
4.
Will, Olga, Fabian Schütt, Ralph Lucius, et al.. (2023). Establishment of a Rodent Glioblastoma Partial Resection Model for Chemotherapy by Local Drug Carriers—Sharing Experience. Biomedicines. 11(6). 1518–1518. 1 indexed citations
5.
Li, Wenjia, Alice Drobny, Christoph Becker‐Pauly, et al.. (2023). Proteolysis of CD44 at the cell surface controls a downstream protease network. Frontiers in Molecular Biosciences. 10. 1026810–1026810. 15 indexed citations
6.
Schmitt, Christina, Regina Scherließ, Ralph Lucius, et al.. (2020). Macroscopic Silicone Microchannel Matrix for Tailored Drug Release and Localized Glioblastoma Therapy. ACS Biomaterials Science & Engineering. 6(6). 3388–3397. 12 indexed citations
8.
Lucius, Ralph, et al.. (2020). Interaction of inflammatorily activated retinal pigment epithelium with retinal microglia and neuronal cells. Experimental Eye Research. 199. 108167–108167. 22 indexed citations
9.
Schmitt, Christina, Rainer Adelung, Ralph Lucius, et al.. (2019). Establishment of a glioblastoma in vitro (in)complete resection dual co-culture model suitable for drug testing. Annals of Anatomy - Anatomischer Anzeiger. 228. 151440–151440. 12 indexed citations
10.
Fritsch, Jürgen, et al.. (2018). A toolbox for the immunomagnetic purification of signaling organelles. Traffic. 20(3). 246–258. 8 indexed citations
11.
Schneppenheim, Janna, Michaela Schweizer, Renate Lüllmann‐Rauch, et al.. (2017). The Influence of MHC Class II on B Cell Defects Induced by Invariant Chain/CD74 N-Terminal Fragments. The Journal of Immunology. 199(1). 172–185. 11 indexed citations
12.
Kuehne, Andreas, Hila Emmert, Joern Soehle, et al.. (2015). Acute Activation of Oxidative Pentose Phosphate Pathway as First-Line Response to Oxidative Stress in Human Skin Cells. Molecular Cell. 59(3). 359–371. 300 indexed citations
13.
Speck, Nancy A., Corinna Brandsch, Nadine Schmidt, et al.. (2015). The Antiatherogenic Effect of Fish Oil in Male Mice Is Associated with a Diminished Release of Endothelial ADAM17 and ADAM10 Substrates. Journal of Nutrition. 145(6). 1218–1226. 13 indexed citations
14.
Egbert, Megan, et al.. (2013). The matricellular protein periostin contributes to proper collagen function and is downregulated during skin aging. Journal of Dermatological Science. 73(1). 40–48. 61 indexed citations
15.
Birkenfeld, Falk, Martin Steiner, Matthias Kern, et al.. (2011). Forces Charging the Orbital Floor After Fractures. Journal of Craniofacial Surgery. 22(5). 1641–1646. 6 indexed citations
16.
Hattermann, Kirsten, Janka Held‐Feindt, Ralph Lucius, et al.. (2010). The Chemokine Receptor CXCR7 Is Highly Expressed in Human Glioma Cells and Mediates Antiapoptotic Effects. Cancer Research. 70(8). 3299–3308. 239 indexed citations
17.
Brandenburg, Lars‐Ove, Sandra Jansen, Christoph Jan Wruck, Ralph Lucius, & Thomas Pufe. (2010). Antimicrobial peptide rCRAMP induced glial cell activation through P2Y receptor signalling pathways. Molecular Immunology. 47(10). 1905–1913. 39 indexed citations
18.
Birkenfeld, Falk, et al.. (2010). Changes in human mandibular bone morphology after heat application. Annals of Anatomy - Anatomischer Anzeiger. 192(4). 227–231. 9 indexed citations
19.
Meybohm, Patrick, Matthias Gruenewald, Martin Albrecht, et al.. (2009). Hypothermia and Postconditioning after Cardiopulmonary Resuscitation Reduce Cardiac Dysfunction by Modulating Inflammation, Apoptosis and Remodeling. PLoS ONE. 4(10). e7588–e7588. 63 indexed citations
20.
Rosenstiel, Philip, Stephan Hellmig, Jochen Hampe, et al.. (2006). Influence of polymorphisms in the NOD1/CARD4 and NOD2/CARD15 genes on the clinical outcome of Helicobacter pylori infection. Cellular Microbiology. 8(7). 1188–1198. 96 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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