Christopher S. Stipp

4.6k total citations
49 papers, 3.7k citations indexed

About

Christopher S. Stipp is a scholar working on Immunology and Allergy, Molecular Biology and Cell Biology. According to data from OpenAlex, Christopher S. Stipp has authored 49 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Immunology and Allergy, 26 papers in Molecular Biology and 24 papers in Cell Biology. Recurrent topics in Christopher S. Stipp's work include Cell Adhesion Molecules Research (27 papers), Platelet Disorders and Treatments (13 papers) and Caveolin-1 and cellular processes (12 papers). Christopher S. Stipp is often cited by papers focused on Cell Adhesion Molecules Research (27 papers), Platelet Disorders and Treatments (13 papers) and Caveolin-1 and cellular processes (12 papers). Christopher S. Stipp collaborates with scholars based in United States, Russia and Australia. Christopher S. Stipp's co-authors include Martin E. Hemler, Tatiana V. Kolesnikova, Christoph Claas, Arthur D. Lander, Xiuwei H. Yang, Mary E. Herndon, Gregory J. Carven, Ilaria Potolicchio, Xiaonan Xu and Laura Santambrogio and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Cell Biology and Blood.

In The Last Decade

Christopher S. Stipp

49 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
Christopher S. Stipp United States 33 2.0k 1.6k 1.3k 574 562 49 3.7k
Jaewon Han United States 24 2.1k 1.0× 1.7k 1.0× 1.6k 1.2× 347 0.6× 811 1.4× 32 3.9k
Chungho Kim South Korea 21 1.4k 0.7× 1.6k 1.0× 1.0k 0.8× 450 0.8× 511 0.9× 53 3.0k
Susan J. Monkley United Kingdom 33 2.5k 1.3× 1.8k 1.1× 1.9k 1.4× 486 0.8× 1.0k 1.8× 53 5.3k
Magdalena Chrzanowska‐Wodnicka United States 33 3.2k 1.6× 2.0k 1.2× 3.0k 2.3× 445 0.8× 565 1.0× 62 6.3k
Kyle R. Legate Germany 18 1.6k 0.8× 1.8k 1.1× 1.5k 1.2× 231 0.4× 606 1.1× 24 3.7k
José M. de Pereda Spain 29 2.0k 1.0× 2.0k 1.2× 2.2k 1.7× 403 0.7× 479 0.9× 58 4.2k
Martin Pfaff Germany 19 1.6k 0.8× 2.1k 1.3× 1.2k 0.9× 365 0.6× 448 0.8× 24 3.4k
Janet A. Askari United Kingdom 30 1.5k 0.8× 2.2k 1.4× 1.6k 1.2× 247 0.4× 535 1.0× 43 3.6k
Jari Ylänne Finland 37 2.1k 1.0× 2.2k 1.3× 1.8k 1.4× 850 1.5× 529 0.9× 75 4.8k
Bing‐Hao Luo United States 18 1.4k 0.7× 2.1k 1.3× 872 0.7× 501 0.9× 817 1.5× 38 3.3k

Countries citing papers authored by Christopher S. Stipp

Since Specialization
Citations

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

Fields of papers citing papers by Christopher S. Stipp

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher S. Stipp. 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 Christopher S. Stipp. The network helps show where Christopher S. Stipp may publish in the future.

Co-authorship network of co-authors of Christopher S. Stipp

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher S. Stipp. A scholar is included among the top collaborators of Christopher S. Stipp 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 Christopher S. Stipp. Christopher S. Stipp 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.
Herndon, Mary E., Katherine N. Gibson‐Corley, Michael K. Wendt, et al.. (2024). The highly metastatic 4T1 breast carcinoma model possesses features of a hybrid epithelial/mesenchymal phenotype. Disease Models & Mechanisms. 17(9). 5 indexed citations
2.
Stipp, Christopher S., et al.. (2024). Single-cell genomics analysis reveals complex genetic interactions in an in vivo model of acquired BRAF inhibitor resistance. NAR Cancer. 6(1). zcad061–zcad061. 1 indexed citations
3.
Moose, Devon L., et al.. (2023). Abl kinases can function as suppressors of tumor progression and metastasis. Frontiers in Oncology. 13. 1241056–1241056. 2 indexed citations
4.
Gutierrez, Wade R., Andrew P. Voigt, Vickie Knepper-Adrian, et al.. (2022). PRC2 loss drives MPNST metastasis and matrix remodeling. JCI Insight. 7(20). 11 indexed citations
5.
Zhao, Lei, Kathleen H. Holt, Mohammed Milhem, et al.. (2020). Functional Genomic Screening Independently Identifies CUL3 as a Mediator of Vemurafenib Resistance via Src-Rac1 Signaling Axis. Frontiers in Oncology. 10. 442–442. 18 indexed citations
6.
Voigt, Andrew P., et al.. (2019). Src-Dependent DBL Family Members Drive Resistance to Vemurafenib in Human Melanoma. Cancer Research. 79(19). 5074–5087. 15 indexed citations
7.
Ma, Deqin, et al.. (2016). α3β1 Integrin Suppresses Prostate Cancer Metastasis via Regulation of the Hippo Pathway. Cancer Research. 76(22). 6577–6587. 53 indexed citations
8.
Zhou, Bo, Katherine N. Gibson‐Corley, Mary E. Herndon, et al.. (2013). Integrin α3β1 Can Function to Promote Spontaneous Metastasis and Lung Colonization of Invasive Breast Carcinoma. Molecular Cancer Research. 12(1). 143–154. 58 indexed citations
9.
10.
Esser, Alison K., Michael R. Miller, Qin Huang, et al.. (2012). Loss of LARGE2 Disrupts Functional Glycosylation of α-Dystroglycan in Prostate Cancer. Journal of Biological Chemistry. 288(4). 2132–2142. 33 indexed citations
11.
Herndon, Mary E., et al.. (2009). Expression of α5 integrin rescues fibronectin responsiveness in NT2N CNS neuronal cells. Journal of Neuroscience Research. 88(1). 222–232. 9 indexed citations
12.
Potolicchio, Ilaria, Gregory J. Carven, Xiaonan Xu, et al.. (2005). Proteomic Analysis of Microglia-Derived Exosomes: Metabolic Role of the Aminopeptidase CD13 in Neuropeptide Catabolism. The Journal of Immunology. 175(4). 2237–2243. 318 indexed citations
13.
Yang, Xiuwei H., Oleg Kovalenko, Wei Tang, et al.. (2004). Palmitoylation supports assembly and function of integrin–tetraspanin complexes. The Journal of Cell Biology. 167(6). 1231–1240. 183 indexed citations
14.
Hemler, Martin E., et al.. (2004). Dynamic Regulation of a GPCR-Tetraspanin-G Protein Complex on Intact Cells: Central Role of CD81 in Facilitating GPR56-Gαq/11Association. Molecular Biology of the Cell. 15(5). 2375–2387. 168 indexed citations
15.
Zhang, Xin A., et al.. (2002). Function of the Tetraspanin CD151–α6β1 Integrin Complex during Cellular Morphogenesis. Molecular Biology of the Cell. 13(1). 1–11. 110 indexed citations
16.
Stipp, Christopher S., Tatiana V. Kolesnikova, & Martin E. Hemler. (2001). EWI-2 Is a Major CD9 and CD81 Partner and Member of a Novel Ig Protein Subfamily. Journal of Biological Chemistry. 276(44). 40545–40554. 185 indexed citations
17.
Zhang, Xin A., Christopher S. Stipp, Stine‐Kathrein Kraeft, et al.. (2001). Phosphorylation of a Conserved Integrin α3 QPSXXE Motif Regulates Signaling, Motility, and Cytoskeletal Engagement. Molecular Biology of the Cell. 12(2). 351–365. 50 indexed citations
18.
Claas, Christoph, Christopher S. Stipp, & Martin E. Hemler. (2001). Evaluation of Prototype Transmembrane 4 Superfamily Protein Complexes and Their Relation to Lipid Rafts. Journal of Biological Chemistry. 276(11). 7974–7984. 262 indexed citations
19.
Ivins, Jonathan K., E. David Litwack, Asli Kumbasar, Christopher S. Stipp, & Arthur D. Lander. (1997). Cerebroglycan, a Developmentally Regulated Cell-Surface Heparan Sulfate Proteoglycan, Is Expressed on Developing Axons and Growth Cones. Developmental Biology. 184(2). 320–332. 60 indexed citations
20.
Lander, Arthur D., et al.. (1996). The glypican family of heparan sulfate proteoglycans: major cell-surface proteoglycans of the developing nervous system.. PubMed. 3(4). 347–58. 65 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Jaewon Han Breakdown of academic impact, for papers by Chungho Kim Breakdown of academic impact, for papers by Susan J. Monkley Breakdown of academic impact, for papers by Magdalena Chrzanowska‐Wodnicka Breakdown of academic impact, for papers by Kyle R. Legate Breakdown of academic impact, for papers by José M. de Pereda Breakdown of academic impact, for papers by Martin Pfaff Breakdown of academic impact, for papers by Janet A. Askari Breakdown of academic impact, for papers by Jari Ylänne Breakdown of academic impact, for papers by Bing‐Hao Luo
Rankless by CCL
2026