Joe W. Ramos

3.3k total citations
67 papers, 2.7k citations indexed

About

Joe W. Ramos is a scholar working on Molecular Biology, Cell Biology and Immunology and Allergy. According to data from OpenAlex, Joe W. Ramos has authored 67 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 17 papers in Cell Biology and 17 papers in Immunology and Allergy. Recurrent topics in Joe W. Ramos's work include Protein Kinase Regulation and GTPase Signaling (19 papers), Cell Adhesion Molecules Research (17 papers) and Melanoma and MAPK Pathways (14 papers). Joe W. Ramos is often cited by papers focused on Protein Kinase Regulation and GTPase Signaling (19 papers), Cell Adhesion Molecules Research (17 papers) and Melanoma and MAPK Pathways (14 papers). Joe W. Ramos collaborates with scholars based in United States, Japan and France. Joe W. Ramos's co-authors include Mark H. Ginsberg, Florian J. Sulzmaier, Douglas W. DeSimone, Paul E. Hughes, Csilla A. Fenczik, Michelle L. Matter, Hema Vaidyanathan, Tariq Sethi, Hervé Chneiweiss and Marı́a Contel and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Joe W. Ramos

67 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
Joe W. Ramos United States 27 1.8k 536 520 417 298 67 2.7k
Xin-Yun Huang United States 24 2.2k 1.2× 480 0.9× 553 1.1× 231 0.6× 335 1.1× 27 3.4k
Andreas Gschwind Germany 9 1.6k 0.9× 1.1k 2.1× 202 0.4× 277 0.7× 137 0.5× 10 2.7k
Yasuhisa Fukui Japan 35 3.4k 1.9× 801 1.5× 1.1k 2.1× 366 0.9× 160 0.5× 85 4.5k
Erica Werner United States 23 1.5k 0.8× 334 0.6× 490 0.9× 192 0.5× 78 0.3× 44 2.6k
Jiing‐Dwan Lee United States 21 2.1k 1.2× 472 0.9× 450 0.9× 88 0.2× 141 0.5× 26 2.7k
Motoko Shibanuma Japan 31 2.2k 1.3× 367 0.7× 543 1.0× 536 1.3× 63 0.2× 67 3.3k
Esther Zwick Germany 11 2.3k 1.3× 1.2k 2.2× 297 0.6× 332 0.8× 132 0.4× 12 3.7k
Hwan Geun Choi South Korea 32 2.8k 1.6× 1.1k 2.0× 411 0.8× 108 0.3× 438 1.5× 77 4.2k
Francisco Cruzalegui France 25 2.0k 1.1× 472 0.9× 399 0.8× 92 0.2× 166 0.6× 51 2.9k
William J. Pitts United States 20 2.4k 1.4× 673 1.3× 304 0.6× 195 0.5× 965 3.2× 34 4.4k

Countries citing papers authored by Joe W. Ramos

Since Specialization
Citations

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

Fields of papers citing papers by Joe W. Ramos

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joe W. Ramos. 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 Joe W. Ramos. The network helps show where Joe W. Ramos may publish in the future.

Co-authorship network of co-authors of Joe W. Ramos

This figure shows the co-authorship network connecting the top 25 collaborators of Joe W. Ramos. A scholar is included among the top collaborators of Joe W. Ramos 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 Joe W. Ramos. Joe W. Ramos 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.
Yamaguchi, Masayoshi, Tomiyasu Murata, & Joe W. Ramos. (2022). Overexpression of regucalcin blocks the migration, invasion, and bone metastatic activity of human prostate cancer cells: Crosstalk between cancer cells and bone cells. The Prostate. 82(10). 1025–1039. 5 indexed citations
2.
Tabrizi, Leila, Won Seok Yang, Chetan Chintha, et al.. (2021). Gold(I) Complexes with a Quinazoline Carboxamide Alkynyl Ligand: Synthesis, Cytotoxicity, and Mechanistic Studies. European Journal of Inorganic Chemistry. 2021(20). 1921–1928. 9 indexed citations
3.
Rochford, Justin J., et al.. (2021). Phosphoprotein enriched in astrocytes (PEA)-15 is a novel regulator of adipose tissue expansion. Scientific Reports. 11(1). 6949–6949. 3 indexed citations
4.
Yamaguchi, Masayoshi, Tomiyasu Murata, & Joe W. Ramos. (2020). The calcium channel agonist Bay K 8644 promotes the growth of human liver cancer HepG2 cells in vitro: suppression with overexpressed regucalcin. Molecular and Cellular Biochemistry. 472(1-2). 173–185. 4 indexed citations
5.
Yamaguchi, Masayoshi, Satoru Osuka, Tomiyasu Murata, & Joe W. Ramos. (2020). Progression-free survival of prostate cancer patients is prolonged with a higher regucalcin expression in the tumor tissues: Overexpressed regucalcin suppresses the growth and bone activity in human prostate cancer cells. Translational Oncology. 14(1). 100955–100955. 9 indexed citations
6.
Wakefield, Devin L., Ottavia Golfetto, Joe W. Ramos, et al.. (2016). Molecular signatures of mu opioid receptor and somatostatin receptor 2 in pancreatic cancer. Molecular Biology of the Cell. 27(22). 3659–3672. 26 indexed citations
7.
Peer, Cody J., Zhenwu Li, Sima Hayavi, et al.. (2016). Synthesis of a stable and orally bioavailable englerin analogue. Bioorganic & Medicinal Chemistry Letters. 26(11). 2641–2644. 10 indexed citations
8.
Griffiths, Genevieve S., Mayumi Jijiwa, Michelle de la Vega, et al.. (2015). Bit-1 is an essential regulator of myogenic differentiation. Journal of Cell Science. 128(9). 1707–17. 15 indexed citations
9.
Sharma, Amrish, Cynthia Rajani, Yuka Endo, et al.. (2014). Targeted deletion of RasGRP1 impairs skin tumorigenesis. Carcinogenesis. 35(5). 1084–1091. 18 indexed citations
10.
Sulzmaier, Florian J., et al.. (2012). Phosphorylation is the switch that turns PEA-15 from tumor suppressor to tumor promoter. Small GTPases. 3(3). 173–177. 33 indexed citations
11.
Sulzmaier, Florian J., et al.. (2012). Englerin A Selectively Induces Necrosis in Human Renal Cancer Cells. PLoS ONE. 7(10). e48032–e48032. 36 indexed citations
12.
Sulzmaier, Florian J., Deirdre A. Nelson, Dirk Geerts, et al.. (2011). PEA-15 potentiates H-Ras-mediated epithelial cell transformation through phospholipase D. Oncogene. 31(30). 3547–3560. 29 indexed citations
13.
Ramos, Joe W., et al.. (2009). Deletion of PEA-15 in mice is associated with specific impairments of spatial learning abilities. BMC Neuroscience. 10(1). 134–134. 11 indexed citations
14.
Ramos, Joe W.. (2008). The regulation of extracellular signal-regulated kinase (ERK) in mammalian cells. The International Journal of Biochemistry & Cell Biology. 40(12). 2707–2719. 384 indexed citations
15.
Renault-Mihara, François, Frédéric Beuvon, Xavier Iturrioz, et al.. (2006). Phosphoprotein Enriched in Astrocytes-15 kDa Expression Inhibits Astrocyte Migration by a Protein Kinase Cδ-dependent Mechanism. Molecular Biology of the Cell. 17(12). 5141–5152. 40 indexed citations
16.
Vaidyanathan, Hema & Joe W. Ramos. (2003). RSK2 Activity Is Regulated by Its Interaction with PEA-15. Journal of Biological Chemistry. 278(34). 32367–32372. 54 indexed citations
17.
Ramos, Joe W., Paul E. Hughes, Mark W. Renshaw, et al.. (2000). Death Effector Domain Protein PEA-15 Potentiates Ras Activation of Extracellular Signal Receptor-activated Kinase by an Adhesion-independent Mechanism. Molecular Biology of the Cell. 11(9). 2863–2872. 62 indexed citations
18.
Zhang, Yue, Olga E. Redina, Yelena M. Altshuller, et al.. (2000). Regulation of Expression of Phospholipase D1 and D2 by PEA-15, a Novel Protein That Interacts with Them. Journal of Biological Chemistry. 275(45). 35224–35232. 52 indexed citations
19.
Ramos, Joe W., et al.. (1998). The Death Effector Domain of PEA-15 Is Involved in Its Regulation of Integrin Activation. Journal of Biological Chemistry. 273(51). 33897–33900. 82 indexed citations
20.
Fenczik, Csilla A., Tariq Sethi, Joe W. Ramos, Paul E. Hughes, & Mark H. Ginsberg. (1997). Complementation of dominant suppression implicates CD98 in integrin activation. Nature. 390(6655). 81–85. 245 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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