Kai Schledzewski

5.1k total citations
60 papers, 3.7k citations indexed

About

Kai Schledzewski is a scholar working on Molecular Biology, Immunology and Cell Biology. According to data from OpenAlex, Kai Schledzewski has authored 60 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 25 papers in Immunology and 12 papers in Cell Biology. Recurrent topics in Kai Schledzewski's work include Cell Adhesion Molecules Research (12 papers), Immune cells in cancer (11 papers) and Liver physiology and pathology (8 papers). Kai Schledzewski is often cited by papers focused on Cell Adhesion Molecules Research (12 papers), Immune cells in cancer (11 papers) and Liver physiology and pathology (8 papers). Kai Schledzewski collaborates with scholars based in Germany, United States and Sweden. Kai Schledzewski's co-authors include Sergij Goerdt, Julia Kzhyshkowska, Alexei Gratchev, Oliver Politz, Pierre Guillot, Ralf R. Mendel, Cyrill Géraud, Astrid Schmieder, Nahid Hakiy and Alexandra Demory and has published in prestigious journals such as Circulation, Journal of Clinical Investigation and Blood.

In The Last Decade

Kai Schledzewski

58 papers receiving 3.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kai Schledzewski Germany 30 1.6k 1.4k 724 487 457 60 3.7k
Yuko Kojima Japan 30 1.5k 1.0× 1.6k 1.1× 763 1.1× 326 0.7× 185 0.4× 68 4.0k
Manfred Blessing Germany 35 1.6k 1.0× 1.7k 1.2× 990 1.4× 295 0.6× 319 0.7× 47 4.9k
Brian J. Nickoloff United States 33 1.1k 0.7× 1.6k 1.2× 859 1.2× 342 0.7× 373 0.8× 49 4.3k
Karen Piper Hanley United Kingdom 44 2.2k 1.4× 1.1k 0.8× 640 0.9× 448 0.9× 320 0.7× 119 5.7k
Tatiana I. Novobrantseva United States 24 1.5k 0.9× 1.4k 1.0× 422 0.6× 252 0.5× 264 0.6× 42 3.3k
Alexei Gratchev Germany 39 2.7k 1.7× 2.0k 1.4× 1.0k 1.4× 380 0.8× 138 0.3× 123 5.4k
Rami Hershkoviz Israel 35 1.2k 0.7× 1.4k 1.0× 548 0.8× 584 1.2× 150 0.3× 98 3.9k
T Sudo Japan 33 2.9k 1.9× 2.1k 1.5× 1.1k 1.6× 552 1.1× 179 0.4× 80 5.6k
Jian Hong China 38 1.3k 0.8× 1.5k 1.1× 841 1.2× 168 0.3× 276 0.6× 120 3.9k
Sònia Tugues Switzerland 25 1.2k 0.8× 1.5k 1.1× 1.1k 1.5× 121 0.2× 386 0.8× 40 3.6k

Countries citing papers authored by Kai Schledzewski

Since Specialization
Citations

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

Fields of papers citing papers by Kai Schledzewski

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kai Schledzewski

This figure shows the co-authorship network connecting the top 25 collaborators of Kai Schledzewski. A scholar is included among the top collaborators of Kai Schledzewski 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 Kai Schledzewski. Kai Schledzewski 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.
Hoffmann, Johannes, Julia Schüler, Carsten Sticht, et al.. (2025). Steatohepatitis-induced vascular niche alterations promote melanoma metastasis. Cancer & Metabolism. 13(1). 5–5.
2.
Winkler, Manuel, Johannes Hoffmann, Julio Cordero, et al.. (2025). Endothelial c-Maf prevents MASLD-like liver fibrosis by regulating chromatin accessibility to suppress pathogenic microvascular cell subsets. JHEP Reports. 7(9). 101475–101475.
4.
Leibing, Thomas, Mirco Friedrich, Hendrik Nolte, et al.. (2022). Targeting of Scavenger Receptors Stabilin-1 and Stabilin-2 Ameliorates Atherosclerosis by a Plasma Proteome Switch Mediating Monocyte/Macrophage Suppression. Circulation. 146(23). 1783–1799. 41 indexed citations
5.
Wohlfeil, Sebastian A., Carsten Sticht, Anna Jauch, et al.. (2022). Angiogenic and molecular diversity determine hepatic melanoma metastasis and response to anti-angiogenic treatment. Journal of Translational Medicine. 20(1). 62–62. 10 indexed citations
6.
Olsavszky, Victor, Carsten Sticht, Christian David Schmid, et al.. (2020). Exploring the transcriptomic network of multi-ligand scavenger receptor Stabilin-1- and Stabilin-2-deficient liver sinusoidal endothelial cells. Gene. 768. 145284–145284. 16 indexed citations
7.
Wohlfeil, Sebastian A., Kai Schledzewski, Manuel Winkler, et al.. (2018). Hepatic Endothelial Notch Activation Protects against Liver Metastasis by Regulating Endothelial-Tumor Cell Adhesion Independent of Angiocrine Signaling. Cancer Research. 79(3). 598–610. 38 indexed citations
8.
Zhang, Xinran, Victor Olsavszky, Kai Schledzewski, et al.. (2018). Hepatic angiocrine HGF signaling plays a vital role in the early stage of liver regeneration after PHx in mice. HPB. 20. S483–S483. 1 indexed citations
9.
Koch, Philipp‐Sebastian, Victor Olsavszky, Carsten Sticht, et al.. (2016). Angiocrine Bmp2 signaling in murine liver controls normal iron homeostasis. Blood. 129(4). 415–419. 119 indexed citations
10.
Schledzewski, Kai, Manuel Winkler, Christian Gorzelanny, et al.. (2016). Leda-1/Pianp is targeted to the basolateral plasma membrane by a distinct intracellular juxtamembrane region and modulates barrier properties and E-Cadherin processing. Biochemical and Biophysical Research Communications. 475(4). 342–349. 6 indexed citations
11.
Schledzewski, Kai, et al.. (2015). Counter-regulation of the ligand-receptor pair Leda-1/Pianp and Pilrα during the LPS-mediated immune response of murine macrophages. Biochemical and Biophysical Research Communications. 464(4). 1078–1083. 10 indexed citations
12.
Michel, Julia, Kai Schledzewski, Carsten Sticht, et al.. (2013). Identification of the novel differentiation marker MS4A8B and its murine homolog MS4A8A in colonic epithelial cells lost during neoplastic transformation in human colon. Cell Death and Disease. 4(1). e469–e469. 17 indexed citations
13.
Weber, J., et al.. (2013). Proteolytic cleavage of LEDA-1/PIANP by furin-like proprotein convertases precedes its plasma membrane localization. Biochemical and Biophysical Research Communications. 434(1). 22–27. 5 indexed citations
14.
Géraud, Cyrill, Beate K. Straub, Wiebke K. Peitsch, et al.. (2012). Unique Cell Type-Specific Junctional Complexes in Vascular Endothelium of Human and Rat Liver Sinusoids. PLoS ONE. 7(4). e34206–e34206. 54 indexed citations
15.
Werno, Christian, Andreas Weigert, Nathalie Dehne, et al.. (2010). Knockout of HIF-1  in tumor-associated macrophages enhances M2 polarization and attenuates their pro-angiogenic responses. Carcinogenesis. 31(10). 1863–1872. 141 indexed citations
16.
Karikoski, Marika, Heikki Irjala, Mikael Maksimow, et al.. (2009). Clever‐1/Stabilin‐1 regulates lymphocyte migration within lymphatics and leukocyte entrance to sites of inflammation. European Journal of Immunology. 39(12). 3477–3487. 75 indexed citations
17.
Klein, Diana, Alexandra Demory, Jens Krøll, et al.. (2008). Wnt2 acts as a cell type–specific, autocrine growth factor in rat hepatic sinusoidal endothelial cells cross-stimulating the VEGF pathway. Hepatology. 47(3). 1018–1031. 83 indexed citations
18.
Hansen, Bettina E., Paola Longati, Kjetil Elvevold, et al.. (2005). Stabilin-1 and stabilin-2 are both directed into the early endocytic pathway in hepatic sinusoidal endothelium via interactions with clathrin/AP-2, independent of ligand binding. Experimental Cell Research. 303(1). 160–173. 114 indexed citations
19.
Gratchev, Alexei, Pierre Guillot, Nahid Hakiy, et al.. (2001). Alternatively Activated Macrophages Differentially Express Fibronectin and Its Splice Variants and the Extracellular Matrix Protein βIG‐H3. Scandinavian Journal of Immunology. 53(4). 386–392. 231 indexed citations
20.
Schledzewski, Kai, Henner Brinkmann, & Ralf R. Mendel. (1999). Phylogenetic Analysis of Components of the Eukaryotic Vesicle Transport System Reveals a Common Origin of Adaptor Protein Complexes 1, 2, and 3 and the F Subcomplex of the Coatomer COPI. Journal of Molecular Evolution. 48(6). 770–778. 101 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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