Rosa M. Guasch

1.5k total citations
27 papers, 1.2k citations indexed

About

Rosa M. Guasch is a scholar working on Molecular Biology, Cell Biology and Oncology. According to data from OpenAlex, Rosa M. Guasch has authored 27 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 10 papers in Cell Biology and 5 papers in Oncology. Recurrent topics in Rosa M. Guasch's work include Protein Kinase Regulation and GTPase Signaling (10 papers), Microtubule and mitosis dynamics (5 papers) and Cellular Mechanics and Interactions (5 papers). Rosa M. Guasch is often cited by papers focused on Protein Kinase Regulation and GTPase Signaling (10 papers), Microtubule and mitosis dynamics (5 papers) and Cellular Mechanics and Interactions (5 papers). Rosa M. Guasch collaborates with scholars based in Spain, United Kingdom and France. Rosa M. Guasch's co-authors include Anne J. Ridley, Kirsi Riento, Consuelo Guerri, Ritu Garg, Boquan Jin, Priam Villalonga, Gareth E. Jones, Peter Scambler, Rebeca Miñambres and Jaime Renau‐Piqueras and has published in prestigious journals such as Journal of Biological Chemistry, The EMBO Journal and PLoS ONE.

In The Last Decade

Rosa M. Guasch

27 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rosa M. Guasch Spain 16 847 395 197 150 124 27 1.2k
Kristin Roovers United States 6 966 1.1× 284 0.7× 310 1.6× 96 0.6× 139 1.1× 7 1.3k
Olivier Féraud France 20 1.4k 1.7× 224 0.6× 182 0.9× 113 0.8× 199 1.6× 53 1.9k
Pengcheng Zhou China 19 1.0k 1.2× 343 0.9× 316 1.6× 139 0.9× 198 1.6× 34 1.6k
Olga A. Agapova United States 23 914 1.1× 155 0.4× 232 1.2× 138 0.9× 145 1.2× 29 1.8k
Mimi Tamamori‐Adachi Japan 21 1.0k 1.2× 171 0.4× 306 1.6× 66 0.4× 192 1.5× 41 1.5k
Claudio Raimondi United Kingdom 18 841 1.0× 207 0.5× 233 1.2× 140 0.9× 234 1.9× 27 1.2k
Hideyuki Yokote Japan 19 589 0.7× 149 0.4× 249 1.3× 215 1.4× 96 0.8× 59 1.3k
Josema Torres Spain 17 1.7k 2.0× 173 0.4× 318 1.6× 113 0.8× 225 1.8× 25 2.0k
Oxana M. Tsygankova United States 16 965 1.1× 130 0.3× 208 1.1× 118 0.8× 101 0.8× 19 1.2k
Coralie Poizat United States 19 1.0k 1.2× 159 0.4× 178 0.9× 69 0.5× 90 0.7× 34 1.5k

Countries citing papers authored by Rosa M. Guasch

Since Specialization
Citations

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

Fields of papers citing papers by Rosa M. Guasch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rosa M. Guasch. 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 Rosa M. Guasch. The network helps show where Rosa M. Guasch may publish in the future.

Co-authorship network of co-authors of Rosa M. Guasch

This figure shows the co-authorship network connecting the top 25 collaborators of Rosa M. Guasch. A scholar is included among the top collaborators of Rosa M. Guasch 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 Rosa M. Guasch. Rosa M. Guasch 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.
Mocholí, Enric, Susana González-Granero, Sabina Sánchez-Hernández, et al.. (2022). Rnd3 Expression is Necessary to Maintain Mitochondrial Homeostasis but Dispensable for Autophagy. Frontiers in Cell and Developmental Biology. 10. 834561–834561. 8 indexed citations
2.
González-Granero, Susana, Enric Mocholí, Enric Poch, et al.. (2014). RhoE deficiency alters postnatal subventricular zone development and the number of calbindin-expressing neurons in the olfactory bulb of mouse. Brain Structure and Function. 220(6). 3113–3130. 12 indexed citations
3.
Georgess, Dan, M. Mazzorana, José Terrado, et al.. (2013). Comparative transcriptomics reveals RhoE as a novel regulator of actin dynamics in bone-resorbing osteoclasts. Molecular Biology of the Cell. 25(3). 380–396. 35 indexed citations
4.
Poch, Enric, Enric Mocholí, Carmen Ivorra, et al.. (2013). The Rho Family Member RhoE Interacts with Skp2 and Is Degraded at the Proteasome during Cell Cycle Progression. Journal of Biological Chemistry. 288(43). 30872–30882. 17 indexed citations
5.
González-Granero, Susana, José Manuel García‐Verdugo, Ignacio Pérez‐Roger, et al.. (2012). Neuronal polarization is impaired in mice lacking RhoE expression. Journal of Neurochemistry. 121(6). 903–914. 23 indexed citations
6.
Mocholí, Enric, Glòria Arqué, Enric Poch, et al.. (2011). RhoE Deficiency Produces Postnatal Lethality, Profound Motor Deficits and Neurodevelopmental Delay in Mice. PLoS ONE. 6(4). e19236–e19236. 38 indexed citations
7.
Taléns‐Visconti, Raquel, et al.. (2009). RhoE stimulates neurite‐like outgrowth in PC12 cells through inhibition of the RhoA/ROCK‐I signalling. Journal of Neurochemistry. 112(4). 1074–1087. 18 indexed citations
8.
Poch, Enric, et al.. (2009). RhoE is spatiotemporally regulated in the postnatal mouse CNS. Neuroscience. 163(2). 586–593. 11 indexed citations
9.
Guasch, Rosa M., et al.. (2007). RhoE participates in the stimulation of the inflammatory response induced by ethanol in astrocytes. Experimental Cell Research. 313(17). 3779–3788. 24 indexed citations
10.
Miñambres, Rebeca, et al.. (2006). The RhoA/ROCK-I/MLC pathway is involved in the ethanol-induced apoptosis by anoikis in astrocytes. Journal of Cell Science. 119(2). 271–282. 82 indexed citations
11.
Poch, Enric, Rebeca Miñambres, Enric Mocholí, et al.. (2006). RhoE interferes with Rb inactivation and regulates the proliferation and survival of the U87 human glioblastoma cell line. Experimental Cell Research. 313(4). 719–731. 55 indexed citations
12.
Riento, Kirsi, Nick Totty, Priam Villalonga, et al.. (2005). RhoE function is regulated by ROCK I‐mediated phosphorylation. The EMBO Journal. 24(6). 1170–1180. 135 indexed citations
13.
Villalonga, Priam, Rosa M. Guasch, Kirsi Riento, & Anne J. Ridley. (2004). RhoE Inhibits Cell Cycle Progression and Ras-Induced Transformation. Molecular and Cellular Biology. 24(18). 7829–7840. 97 indexed citations
14.
Guasch, Rosa M., Mónica Tomás, Rebeca Miñambres, et al.. (2003). RhoA and lysophosphatidic acid are involved in the actin cytoskeleton reorganization of astrocytes exposed to ethanol. Journal of Neuroscience Research. 72(4). 487–502. 60 indexed citations
15.
Vallés, Soraya L., Ana María Andrés Blanco, Inmaculada Azorı́n, et al.. (2003). Chronic Ethanol Consumption Enhances Interleukin‐1‐Mediated Signal Transduction in Rat Liver and in Cultured Hepatocytes. Alcoholism Clinical and Experimental Research. 27(12). 1979–1986. 55 indexed citations
16.
Guasch, Rosa M., Peter Scambler, Gareth E. Jones, & Anne J. Ridley. (1998). RhoE Regulates Actin Cytoskeleton Organization and Cell Migration. Molecular and Cellular Biology. 18(8). 4761–4771. 185 indexed citations
17.
Guasch, Rosa M., Consuelo Guerri, & José‐Enrique O’Connor. (1995). Study of surface carbohydrates on isolated Golgi subfractions by fluorescent‐lectin binding and flow cytometry. Cytometry. 19(2). 112–118. 15 indexed citations
18.
Guasch, Rosa M., Consuelo Guerri, & José‐Enrique O’Connor. (1993). Flow Cytometric Analysis of Concanavalin A Binding to Isolated Golgi Fractions from Rat Liver. Experimental Cell Research. 207(1). 136–141. 14 indexed citations
19.
Guasch, Rosa M., Jaime Renau‐Piqueras, & Consuelo Guerri. (1992). Chronic Ethanol Consumption Induces Accumulation of Proteins in the Liver Golgi Apparatus and Decreases Galactosyltransferase Activity. Alcoholism Clinical and Experimental Research. 16(5). 942–948. 49 indexed citations
20.
Portolés, Manuel, et al.. (1989). Effect of caffeine on urea biosynthesis and some related processes, ketone bodies, ATP and liver amino acids. Biochemical Pharmacology. 38(16). 2727–2732. 9 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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