Jan Kitajewski

22.6k total citations · 4 hit papers
180 papers, 17.7k citations indexed

About

Jan Kitajewski is a scholar working on Molecular Biology, Oncology and Neurology. According to data from OpenAlex, Jan Kitajewski has authored 180 papers receiving a total of 17.7k indexed citations (citations by other indexed papers that have themselves been cited), including 134 papers in Molecular Biology, 24 papers in Oncology and 20 papers in Neurology. Recurrent topics in Jan Kitajewski's work include Developmental Biology and Gene Regulation (45 papers), Angiogenesis and VEGF in Cancer (40 papers) and Wnt/β-catenin signaling in development and cancer (34 papers). Jan Kitajewski is often cited by papers focused on Developmental Biology and Gene Regulation (45 papers), Angiogenesis and VEGF in Cancer (40 papers) and Wnt/β-catenin signaling in development and cancer (34 papers). Jan Kitajewski collaborates with scholars based in United States, Russia and Japan. Jan Kitajewski's co-authors include Carrie J. Shawber, Yasuhiro Funahashi, Hendrik Uyttendaele, Ian Tattersall, Guangyu Wu, David Sassoon, Martin A. Julius, Kevin L. Stark, John R. Shutter and Marina Vorontchikhina and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Jan Kitajewski

175 papers receiving 17.4k citations

Hit Papers

Stromal Elements Act to R... 2000 2026 2008 2017 2014 2000 2010 2012 500 1000 1.5k

Author Peers

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

Author Last Decade Papers Cites
Jan Kitajewski 11.6k 3.6k 2.3k 2.3k 1.9k 180 17.7k
Masahide Takahashi 8.9k 0.8× 3.3k 0.9× 1.6k 0.7× 1.7k 0.7× 1.9k 1.0× 367 16.0k
Hellmut G. Augustin 11.0k 0.9× 4.3k 1.2× 2.7k 1.1× 3.4k 1.5× 1.9k 1.0× 206 19.0k
Shigeki Higashiyama 8.2k 0.7× 4.4k 1.2× 2.1k 0.9× 2.0k 0.9× 1.6k 0.8× 279 15.6k
Freddy Radtke 12.7k 1.1× 3.9k 1.1× 5.4k 2.3× 2.2k 1.0× 2.0k 1.0× 178 21.7k
M. Luisa Iruela‐Arispe 12.5k 1.1× 3.1k 0.9× 2.8k 1.2× 5.0k 2.2× 2.0k 1.0× 202 21.4k
Charles D. Stiles 11.0k 0.9× 3.0k 0.8× 2.0k 0.9× 3.1k 1.4× 1.1k 0.6× 139 18.0k
Catherine M. Verfaillie 10.4k 0.9× 3.7k 1.0× 4.0k 1.7× 1.8k 0.8× 5.3k 2.7× 481 25.2k
Lieve Moons 9.9k 0.9× 2.6k 0.7× 1.9k 0.8× 5.5k 2.4× 1.8k 0.9× 270 19.5k
Jack Lawler 11.8k 1.0× 2.9k 0.8× 2.3k 1.0× 4.7k 2.1× 1.5k 0.8× 206 20.2k
Raphael Kopan 17.5k 1.5× 2.7k 0.8× 2.4k 1.0× 1.9k 0.8× 1.5k 0.8× 163 25.2k

Countries citing papers authored by Jan Kitajewski

Since Specialization
Citations

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

Fields of papers citing papers by Jan Kitajewski

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jan Kitajewski

This figure shows the co-authorship network connecting the top 25 collaborators of Jan Kitajewski. A scholar is included among the top collaborators of Jan Kitajewski 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 Jan Kitajewski. Jan Kitajewski 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.
Anwar, Mumtaz, Prerak Gupta, Mark A. Sanborn, et al.. (2024). Notch transcriptional target tmtc1 maintains vascular homeostasis. Cellular and Molecular Life Sciences. 81(1). 370–370.
2.
Naiche, L.A., et al.. (2023). CLIC4 Regulates Endothelial Barrier Control by Mediating PAR1 Signaling via RhoA. Arteriosclerosis Thrombosis and Vascular Biology. 43(8). 1441–1454. 13 indexed citations
3.
Naiche, L.A., et al.. (2023). Abstract 3618: The role of endothelial ACKR1 in triple-negative breast cancer metastasis. Cancer Research. 83(7_Supplement). 3618–3618.
4.
Phillips, Evan H., Vytautas P. Bindokas, Jan Kitajewski, et al.. (2023). Three‐dimensional spatial quantitative analysis of cardiac lymphatics in the mouse heart. Microcirculation. 30(7). e12826–e12826. 3 indexed citations
5.
Qiu, Wanglong, Richard A. Friedman, Iok In Christine Chio, et al.. (2022). Inactivation of Notch4 Attenuated Pancreatic Tumorigenesis in Mice. Cancer Research Communications. 2(12). 1601–1616. 2 indexed citations
6.
Delgado, Ana C., Angel R. Maldonado‐Soto, Violeta Silva-Vargas, et al.. (2021). Release of stem cells from quiescence reveals gliogenic domains in the adult mouse brain. Science. 372(6547). 1205–1209. 51 indexed citations
7.
Swaminathan, Bhairavi, Hideru Obinata, Yulia Komarova, et al.. (2021). CLIC1 and CLIC4 mediate endothelial S1P receptor signaling to facilitate Rac1 and RhoA activity and function. Science Signaling. 14(679). 18 indexed citations
8.
Muley, Ajit, Minji K. Uh, Bhairavi Swaminathan, et al.. (2021). Unique functions for Notch4 in murine embryonic lymphangiogenesis. Angiogenesis. 25(2). 205–224. 17 indexed citations
9.
Marchetto, Nicole M., et al.. (2020). Endothelial Jagged1 Antagonizes Dll4/Notch Signaling in Decidual Angiogenesis during Early Mouse Pregnancy. International Journal of Molecular Sciences. 21(18). 6477–6477. 14 indexed citations
10.
Tian, Wen, Stanley G. Rockson, Xinguo Jiang, et al.. (2017). Leukotriene B4antagonism ameliorates experimental lymphedema. Science Translational Medicine. 9(389). 127 indexed citations
11.
Banerjee, Debarshi, Sonia L. Hernandez, Alejandro J. Garcia, et al.. (2015). Notch Suppresses Angiogenesis and Progression of Hepatic Metastases. Cancer Research. 75(8). 1592–1602. 43 indexed citations
12.
Kangsamaksin, Thaned, Aino Murtomäki, Natalie Kofler, et al.. (2014). NOTCH Decoys That Selectively Block DLL/NOTCH or JAG/NOTCH Disrupt Angiogenesis by Unique Mechanisms to Inhibit Tumor Growth. Cancer Discovery. 5(2). 182–197. 121 indexed citations
13.
Rhim, Andrew D., Paul E. Oberstein, Dafydd Thomas, et al.. (2014). Stromal Elements Act to Restrain, Rather Than Support, Pancreatic Ductal Adenocarcinoma. Cancer Cell. 25(6). 735–747. 1513 indexed citations breakdown →
14.
Xu, Haixia, Jimmy Zhu, Sinéad M. Smith, et al.. (2012). Notch–RBP-J signaling regulates the transcription factor IRF8 to promote inflammatory macrophage polarization. Nature Immunology. 13(7). 642–650. 353 indexed citations
15.
Quante, Michael, Govind Bhagat, Julian A. Abrams, et al.. (2012). Bile Acid and Inflammation Activate Gastric Cardia Stem Cells in a Mouse Model of Barrett-Like Metaplasia. Cancer Cell. 21(1). 36–51. 357 indexed citations breakdown →
16.
Funahashi, Yasuhiro, Sonia L. Hernandez, Indranil Das, et al.. (2008). A Notch1 Ectodomain Construct Inhibits Endothelial Notch Signaling, Tumor Growth, and Angiogenesis. Cancer Research. 68(12). 4727–4735. 128 indexed citations
17.
Shawber, Carrie J. & Jan Kitajewski. (2008). Arterial Regulators Taken Up by Lymphatics. Lymphatic Research and Biology. 6(3-4). 139–143. 3 indexed citations
18.
Young, C. S. H., Marina Kitamura, Stephen Hardy, & Jan Kitajewski. (1998). Wnt-1 Induces Growth, Cytosolic β-Catenin, and Tcf/Lef Transcriptional Activation in Rat-1 Fibroblasts. Molecular and Cellular Biology. 18(5). 2474–2485. 141 indexed citations
19.
Münsterberg, Andrea, Jan Kitajewski, David Bumcrot, Andrew P. McMahon, & Andrew B. Lassar. (1995). Combinatorial signaling by Sonic hedgehog and Wnt family members induces myogenic bHLH gene expression in the somite.. Genes & Development. 9(23). 2911–2922. 437 indexed citations
20.
Mason, John O., Jan Kitajewski, & Harold Varmus. (1992). Mutational analysis of mouse Wnt-1 identifies two temperature-sensitive alleles and attributes of Wnt-1 protein essential for transformation of a mammary cell line.. Molecular Biology of the Cell. 3(5). 521–533. 91 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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