José R. Bayascas

3.1k total citations · 1 hit paper
46 papers, 2.4k citations indexed

About

José R. Bayascas is a scholar working on Molecular Biology, Global and Planetary Change and Cell Biology. According to data from OpenAlex, José R. Bayascas has authored 46 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 11 papers in Global and Planetary Change and 6 papers in Cell Biology. Recurrent topics in José R. Bayascas's work include PI3K/AKT/mTOR signaling in cancer (12 papers), Marine Ecology and Invasive Species (11 papers) and Planarian Biology and Electrostimulation (10 papers). José R. Bayascas is often cited by papers focused on PI3K/AKT/mTOR signaling in cancer (12 papers), Marine Ecology and Invasive Species (11 papers) and Planarian Biology and Electrostimulation (10 papers). José R. Bayascas collaborates with scholars based in Spain, United Kingdom and United States. José R. Bayascas's co-authors include Dario R. Alessi, Kei Sakamoto, Joan X. Comella, Emili Saló, Vı́ctor J. Yuste, Mario Encinas, Xavier Dolcet, Estela Castillo, Jordi García‐Fernàndez and Ana M Muñoz‐Mármol and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Neuroscience and The Journal of Cell Biology.

In The Last Decade

José R. Bayascas

46 papers receiving 2.4k citations

Hit Papers

LKB1-Dependent Signaling Pathways 2006 2026 2012 2019 2006 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
José R. Bayascas Spain 27 1.8k 286 269 255 251 46 2.4k
Mario Looso Germany 31 2.2k 1.2× 160 0.6× 369 1.4× 245 1.0× 307 1.2× 84 3.0k
Bingyu Mao China 22 2.8k 1.5× 211 0.7× 218 0.8× 437 1.7× 380 1.5× 88 3.5k
Rachid Safi United States 23 1.2k 0.7× 220 0.8× 567 2.1× 576 2.3× 171 0.7× 31 2.6k
B. Boilly France 25 1.6k 0.9× 407 1.4× 236 0.9× 350 1.4× 382 1.5× 73 2.4k
Momoki Hirai Japan 30 1.8k 1.0× 173 0.6× 301 1.1× 210 0.8× 269 1.1× 92 3.1k
Timothy C. Grammer United States 20 1.7k 0.9× 161 0.6× 210 0.8× 526 2.1× 291 1.2× 20 2.4k
Oliver Wessely United States 30 2.9k 1.6× 226 0.8× 613 2.3× 411 1.6× 429 1.7× 71 4.3k
Zhan Yin China 27 1.4k 0.8× 96 0.3× 204 0.8× 230 0.9× 215 0.9× 93 2.5k
Jeremy M. Simon United States 29 2.1k 1.2× 126 0.4× 452 1.7× 279 1.1× 132 0.5× 80 2.9k
Frédéric Flamant France 35 1.6k 0.9× 303 1.1× 133 0.5× 150 0.6× 96 0.4× 107 3.7k

Countries citing papers authored by José R. Bayascas

Since Specialization
Citations

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

Fields of papers citing papers by José R. Bayascas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by José R. Bayascas. 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 José R. Bayascas. The network helps show where José R. Bayascas may publish in the future.

Co-authorship network of co-authors of José R. Bayascas

This figure shows the co-authorship network connecting the top 25 collaborators of José R. Bayascas. A scholar is included among the top collaborators of José R. Bayascas 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 José R. Bayascas. José R. Bayascas 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.
Diéguez-Martínez, Nora, Guillermo Yoldi, Héctor Perez‐Montoyo, et al.. (2022). The ERK5/NF-κB signaling pathway targets endometrial cancer proliferation and survival. Cellular and Molecular Life Sciences. 79(10). 524–524. 21 indexed citations
2.
Zhang, Yuan, Yuling Chen, Zhao Zhang, et al.. (2022). Acox2 is a regulator of lysine crotonylation that mediates hepatic metabolic homeostasis in mice. Cell Death and Disease. 13(3). 279–279. 38 indexed citations
4.
Bayascas, José R., et al.. (2021). Sex-Dependent Signatures, Time Frames and Longitudinal Fine-Tuning of the Marble Burying Test in Normal and AD-Pathological Aging Mice. Biomedicines. 9(8). 994–994. 12 indexed citations
5.
Sánchez‐Osuna, María, Alejandro Sánchez‐Chardi, Salvio Suárez–García, et al.. (2021). Gossypol Treatment Restores Insufficient Apoptotic Function of DFF40/CAD in Human Glioblastoma Cells. Cancers. 13(21). 5579–5579. 3 indexed citations
6.
Vilardell, Jordi, Christian Borgo, Eduard Sarró, et al.. (2020). Effects of CK2β subunit down-regulation on Akt signalling in HK-2 renal cells. PLoS ONE. 15(1). e0227340–e0227340. 11 indexed citations
7.
Erazo, Tatiana, Mar Lorente, Patricia Fernández‐Nogueira, et al.. (2015). The New Antitumor Drug ABTL0812 Inhibits the Akt/mTORC1 Axis by Upregulating Tribbles-3 Pseudokinase. Clinical Cancer Research. 22(10). 2508–2519. 59 indexed citations
8.
Zhou, Xiangyu, et al.. (2014). Fine-tuning the intensity of the PKB/Akt signal enables diverse physiological responses. Cell Cycle. 13(20). 3164–3168. 17 indexed citations
9.
Waugh, Caryll, Linda V. Sinclair, David K. Finlay, José R. Bayascas, & Doreen A. Cantrell. (2009). Phosphoinositide (3,4,5)-Triphosphate Binding to Phosphoinositide-Dependent Kinase 1 Regulates a Protein Kinase B/Akt Signaling Threshold That Dictates T-Cell Migration, Not Proliferation. Molecular and Cellular Biology. 29(21). 5952–5962. 67 indexed citations
10.
Bayascas, José R.. (2008). Dissecting the role of the 3-phosphoinositide-dependent protein kinase-1 (PDK1) signalling pathways. Cell Cycle. 7(19). 2978–2982. 79 indexed citations
11.
Yuste, Vı́ctor J., Carme Solé, Rana S. Moubarak, et al.. (2005). The Contribution of Apoptosis-inducing Factor, Caspase-activated DNase, and Inhibitor of Caspase-activated DNase to the Nuclear Phenotype and DNA Degradation during Apoptosis. Journal of Biological Chemistry. 280(42). 35670–35683. 76 indexed citations
12.
Yuste, Vı́ctor J., et al.. (2001). The Absence of Oligonucleosomal DNA Fragmentation during Apoptosis of IMR-5 Neuroblastoma Cells. Journal of Biological Chemistry. 276(25). 22323–22331. 61 indexed citations
13.
Soler, Rosa M., Xavier Dolcet, Mario Encinas, et al.. (1999). Receptors of the Glial Cell Line-Derived Neurotrophic Factor Family of Neurotrophic Factors Signal Cell Survival through the Phosphatidylinositol 3-Kinase Pathway in Spinal Cord Motoneurons. Journal of Neuroscience. 19(21). 9160–9169. 148 indexed citations
14.
Bayascas, José R., Estela Castillo, Ana M Muñoz‐Mármol, Jaume Baguñà, & Emili Saló. (1998). Synchronous and early activation of planarian Hox genes and the re-specification of body axes during regeneration in Dugesia (G.) tigrina (Turbellaria; Tricladida). Hydrobiologia. 383(1-3). 125–130. 5 indexed citations
15.
Muñoz‐Mármol, Ana M, Andreu Casali, David Bueno, et al.. (1998). Characterization of Platyhelminth POU domain genes: ubiquitous and specific anterior nerve cell expression of different epitopes of GtPOU-1. Mechanisms of Development. 76(1-2). 127–140. 10 indexed citations
16.
Bayascas, José R., Estela Castillo, & Emili Saló. (1998). Platyhelminthes have a Hox code differentially activated during regeneration, with genes closely related to those of spiralian protostomes. Development Genes and Evolution. 208(8). 467–473. 44 indexed citations
17.
Bayascas, José R., Estela Castillo, Ana M Muñoz‐Mármol, & Emili Saló. (1997). Planarian Hox genes: novel patterns of expression during regeneration. Development. 124(1). 141–148. 64 indexed citations
18.
Bueno, David, Estela Castillo, Francesc Cebrià, et al.. (1997). New protocol to visualize gene expression in intact and regenerating adult planarians by whole-mount in situhybridization. 2(1). 164–166. 3 indexed citations
19.
Bayascas, José R., et al.. (1996). Hox genes disobey colinearity and do not distinguish head from tail during planarian regeneration. The International Journal of Developmental Biology. 40(S1). S173–S174. 2 indexed citations
20.
Baguñà, Jaume, Emili Saló, Rafael Romero, et al.. (1994). REGENERATION AND PATTERN FORMATION IN PLANARIANS : CELLS, MOLECULES AND GENES. ZOOLOGICAL SCIENCE. 11(6). 781–795. 76 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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