Joan S. Brugge

55.4k total citations · 20 hit papers
259 papers, 41.9k citations indexed

About

Joan S. Brugge is a scholar working on Molecular Biology, Oncology and Cell Biology. According to data from OpenAlex, Joan S. Brugge has authored 259 papers receiving a total of 41.9k indexed citations (citations by other indexed papers that have themselves been cited), including 163 papers in Molecular Biology, 82 papers in Oncology and 54 papers in Cell Biology. Recurrent topics in Joan S. Brugge's work include Cell Adhesion Molecules Research (52 papers), Virus-based gene therapy research (41 papers) and Cancer Cells and Metastasis (35 papers). Joan S. Brugge is often cited by papers focused on Cell Adhesion Molecules Research (52 papers), Virus-based gene therapy research (41 papers) and Cancer Cells and Metastasis (35 papers). Joan S. Brugge collaborates with scholars based in United States, Canada and Japan. Joan S. Brugge's co-authors include Edwin Clark, Sheila Μ. Thomas, Jayanta Debnath, Senthil K. Muthuswamy, Raymond L. Erikson, Sanford J. Shattil, Cindy K. Miranti, Michael Overholtzer, Gordon B. Mills and Richard Sever and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Joan S. Brugge

256 papers receiving 40.5k citations

Hit Papers

Integrins and Signal Transduction Pathways: the Road Taken 1977 2026 1993 2009 1995 1997 2003 1992 2005 500 1000 1.5k 2.0k 2.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joan S. Brugge United States 111 25.6k 10.2k 9.5k 7.4k 5.2k 259 41.9k
J. Silvio Gutkind United States 121 33.7k 1.3× 11.5k 1.1× 7.8k 0.8× 3.8k 0.5× 6.9k 1.3× 582 52.2k
David A. Cheresh United States 109 28.3k 1.1× 10.3k 1.0× 7.6k 0.8× 18.3k 2.5× 6.5k 1.3× 245 48.7k
Meenhard Herlyn United States 110 26.4k 1.0× 17.1k 1.7× 6.7k 0.7× 3.9k 0.5× 8.6k 1.7× 545 42.8k
Anne J. Ridley United Kingdom 95 26.0k 1.0× 5.7k 0.6× 16.4k 1.7× 7.2k 1.0× 6.3k 1.2× 304 43.9k
Lena Claesson‐Welsh Sweden 87 22.2k 0.9× 6.9k 0.7× 4.8k 0.5× 3.5k 0.5× 3.5k 0.7× 256 32.3k
Mina J. Bissell United States 113 22.8k 0.9× 20.1k 2.0× 10.4k 1.1× 7.0k 0.9× 4.3k 0.8× 372 48.1k
Alan Hall United Kingdom 88 32.4k 1.3× 5.9k 0.6× 20.4k 2.1× 6.6k 0.9× 5.7k 1.1× 162 48.7k
Channing J. Der United States 111 36.2k 1.4× 12.7k 1.2× 10.6k 1.1× 2.9k 0.4× 4.4k 0.8× 406 48.3k
Jean Paul Thiery France 108 34.1k 1.3× 19.4k 1.9× 9.5k 1.0× 5.2k 0.7× 4.5k 0.9× 553 55.8k
Brian Seed United States 77 17.8k 0.7× 5.0k 0.5× 4.5k 0.5× 5.2k 0.7× 11.8k 2.3× 155 33.2k

Countries citing papers authored by Joan S. Brugge

Since Specialization
Citations

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

Fields of papers citing papers by Joan S. Brugge

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joan S. Brugge

This figure shows the co-authorship network connecting the top 25 collaborators of Joan S. Brugge. A scholar is included among the top collaborators of Joan S. Brugge 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 Joan S. Brugge. Joan S. Brugge 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.
Silvestri, F, Michael Oliphant, Dennis P. Orgill, et al.. (2024). Breast organoid suspension cultures maintain long-term estrogen receptor expression and responsiveness. npj Breast Cancer. 10(1). 107–107. 3 indexed citations
2.
Gray, G. Kenneth, Li Ren Kong, Komal Gupta, et al.. (2023). A transcriptional response to replication stress selectively expands a subset of Brca2-mutant mammary epithelial cells. Nature Communications. 14(1). 5206–5206. 3 indexed citations
3.
Takahashi, Nobuaki, Hsing‐Yu Chen, Isaac S. Harris, et al.. (2018). Cancer Cells Co-opt the Neuronal Redox-Sensing Channel TRPA1 to Promote Oxidative-Stress Tolerance. Cancer Cell. 33(6). 985–1003.e7. 201 indexed citations
4.
Muranen, Taru, Marcin Iwanicki, Natasha Curry, et al.. (2017). Starved epithelial cells uptake extracellular matrix for survival. Nature Communications. 8(1). 13989–13989. 86 indexed citations
5.
Stover, Daniel G., Jonathan L. Coloff, William T. Barry, et al.. (2016). The Role of Proliferation in Determining Response to Neoadjuvant Chemotherapy in Breast Cancer: A Gene Expression–Based Meta-Analysis. Clinical Cancer Research. 22(24). 6039–6050. 43 indexed citations
6.
Muranen, Taru, Laura M. Selfors, Julie Hwang, et al.. (2016). ERK and p38 MAPK Activities Determine Sensitivity to PI3K/mTOR Inhibition via Regulation of MYC and YAP. Cancer Research. 76(24). 7168–7180. 53 indexed citations
7.
Godinho, Susana A., Remigio Picone, Mithila Burute, et al.. (2014). Oncogene-like induction of cellular invasion from centrosome amplification. Nature. 510(7503). 167–171. 306 indexed citations
8.
Vakifahmetoglu-Norberg, Helin, Minsu Kim, Hongguang Xia, et al.. (2013). Chaperone-mediated autophagy degrades mutant p53. Genes & Development. 27(15). 1718–1730. 168 indexed citations
9.
Ng, Mei Rosa, Achim Besser, Gaudenz Danuser, & Joan S. Brugge. (2012). Substrate stiffness regulates cadherin-dependent collective migration through myosin-II contractility. The Journal of Cell Biology. 199(3). 545–563. 244 indexed citations
10.
Grassian, Alexandra, Christian M. Metallo, Jonathan L. Coloff, Gregory Stephanopoulos, & Joan S. Brugge. (2011). Erk regulation of pyruvate dehydrogenase flux through PDK4 modulates cell proliferation. Genes & Development. 25(16). 1716–1733. 146 indexed citations
11.
Iwanicki, Marcin, Rachel A. Davidowitz, Mei Rosa Ng, et al.. (2011). Ovarian Cancer Spheroids Use Myosin-Generated Force to Clear the Mesothelium. Cancer Discovery. 1(2). 144–157. 246 indexed citations
12.
Xian, Wa, Leontios Pappas, Laura M. Selfors, et al.. (2009). Fibroblast Growth Factor Receptor 1–Transformed Mammary Epithelial Cells Are Dependent on RSK Activity for Growth and Survival. Cancer Research. 69(6). 2244–2251. 61 indexed citations
13.
Simpson, Kaylene J., Laura M. Selfors, James T. Bui, et al.. (2008). Identification of genes that regulate epithelial cell migration using an siRNA screening approach. Nature Cell Biology. 10(9). 1027–1038. 327 indexed citations
14.
Mouneimne, Ghassan & Joan S. Brugge. (2007). Tensins: A New Switch in Cell Migration. Developmental Cell. 13(3). 317–319. 17 indexed citations
15.
Reginato, Mauricio J., et al.. (2004). Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is required for induction of autophagy during lumen formation in vitro. Proceedings of the National Academy of Sciences. 101(10). 3438–3443. 210 indexed citations
16.
Seton-Rogers, Sarah, Yu Lu, Lisa M. Hines, et al.. (2004). Cooperation of the ErbB2 receptor and transforming growth factor β in induction of migration and invasion in mammary epithelial cells. Proceedings of the National Academy of Sciences. 101(5). 1257–1262. 184 indexed citations
17.
Arias‐Salgado, Elena G., et al.. (2003). Src kinase activation by direct interaction with the integrin β cytoplasmic domain. Proceedings of the National Academy of Sciences. 100(23). 13298–13302. 448 indexed citations
18.
Debnath, Jayanta, et al.. (2002). The Role of Apoptosis in Creating and Maintaining Luminal Space within Normal and Oncogene-Expressing Mammary Acini. Cell. 111(1). 29–40. 624 indexed citations breakdown →
19.
Rivera, Victor M. & Joan S. Brugge. (1995). Clustering of Syk Is Sufficient To Induce Tyrosine Phosphorylation and Release of Allergic Mediators from Rat Basophilic Leukemia Cells. Molecular and Cellular Biology. 15(3). 1582–1590. 60 indexed citations
20.
Weng, Zhigang, Richard J. Rickles, Sibo Feng, et al.. (1995). Structure-Function Analysis of SH3 Domains: SH3 Binding Specificity Altered by Single Amino Acid Substitutions. Molecular and Cellular Biology. 15(10). 5627–5634. 111 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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