Carlos M. Luque

1.1k total citations
17 papers, 899 citations indexed

About

Carlos M. Luque is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Carlos M. Luque has authored 17 papers receiving a total of 899 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Cell Biology and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Carlos M. Luque's work include Hippo pathway signaling and YAP/TAZ (4 papers), Developmental Biology and Gene Regulation (4 papers) and Neurobiology and Insect Physiology Research (3 papers). Carlos M. Luque is often cited by papers focused on Hippo pathway signaling and YAP/TAZ (4 papers), Developmental Biology and Gene Regulation (4 papers) and Neurobiology and Insect Physiology Research (3 papers). Carlos M. Luque collaborates with scholars based in Spain, Germany and Singapore. Carlos M. Luque's co-authors include Pernille Rørth, Gáspár Jékely, Hsin-Ho Sung, Isabel Correas, Peter Duchek, Lutz Kockel, Katja Brückner, Norbert Perrimon, Minna Poukkula and Juliette Mathieu 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

Carlos M. Luque

17 papers receiving 886 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carlos M. Luque Spain 13 505 431 197 188 86 17 899
Daria E. Siekhaus Austria 18 440 0.9× 309 0.7× 197 1.0× 275 1.5× 42 0.5× 31 885
Erika R. Geisbrecht United States 17 803 1.6× 478 1.1× 208 1.1× 167 0.9× 44 0.5× 38 1.2k
Aparna Ratheesh Australia 12 429 0.8× 522 1.2× 75 0.4× 124 0.7× 42 0.5× 19 825
Yutaka Matsubayashi United Kingdom 12 375 0.7× 298 0.7× 143 0.7× 97 0.5× 30 0.3× 18 754
Jessica K. Sawyer United States 10 500 1.0× 703 1.6× 131 0.7× 70 0.4× 53 0.6× 16 965
Sol Sotillos Spain 16 640 1.3× 417 1.0× 201 1.0× 155 0.8× 21 0.2× 26 961
Søren Prag United Kingdom 14 594 1.2× 434 1.0× 118 0.6× 106 0.6× 40 0.5× 17 1.1k
Catherine Hogan United Kingdom 15 659 1.3× 377 0.9× 122 0.6× 154 0.8× 31 0.4× 25 1.1k
Luis Alberto Baena-López United Kingdom 17 861 1.7× 617 1.4× 179 0.9× 149 0.8× 26 0.3× 30 1.2k
Juliette Mathieu France 15 788 1.6× 611 1.4× 140 0.7× 120 0.6× 74 0.9× 24 1.2k

Countries citing papers authored by Carlos M. Luque

Since Specialization
Citations

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

Fields of papers citing papers by Carlos M. Luque

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carlos M. Luque

This figure shows the co-authorship network connecting the top 25 collaborators of Carlos M. Luque. A scholar is included among the top collaborators of Carlos M. Luque 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 Carlos M. Luque. Carlos M. Luque is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Luque, Carlos M., et al.. (2023). Hunting Drosophila viruses from wild populations: A novel isolation approach and characterisation of viruses. PLoS Pathogens. 19(3). e1010883–e1010883. 6 indexed citations
2.
Molnar, Cristina, et al.. (2021). EGFRAP encodes a new negative regulator of the EGFR acting in both normal and oncogenic EGFR/Ras-driven tissue morphogenesis. PLoS Genetics. 17(8). e1009738–e1009738. 5 indexed citations
3.
Luque, Carlos M., et al.. (2019). A Toggle-Switch and a Feed-Forward Loop Engage in the Control of the Drosophila Retinal Determination Gene Network. Frontiers in Ecology and Evolution. 7. 1 indexed citations
4.
Ramel, Damien, Marganit Farago, Carlos M. Luque, et al.. (2013). The GEF Vav regulates guided cell migration by coupling guidance receptor signalling to local Rac activation. Journal of Cell Science. 126(Pt 10). 2285–93. 34 indexed citations
5.
Cordero, Mario D., Elísabet Alcocer‐Gómez, Manuel de Miguel, et al.. (2011). Coenzyme Q10: A novel therapeutic approach for Fibromyalgia? Case series with 5 patients. Mitochondrion. 11(4). 623–625. 37 indexed citations
6.
Fernández‐Miñán, Ana, et al.. (2008). A role for the chaperone Hsp70 in the regulation of border cell migration in the Drosophila ovary. Mechanisms of Development. 125(11-12). 1048–1058. 23 indexed citations
7.
Bejarano, Fernando, et al.. (2008). A Gain-of-Function Suppressor Screen for Genes Involved in Dorsal–Ventral Boundary Formation in the Drosophila Wing. Genetics. 178(1). 307–323. 30 indexed citations
8.
Bianco, Ambra, Minna Poukkula, Adam Cliffe, et al.. (2007). Two distinct modes of guidance signalling during collective migration of border cells. Nature. 448(7151). 362–365. 235 indexed citations
9.
Luque, Carlos M. & Marco Milán. (2006). Growth control in the proliferative region of the Drosophila eye–head primordium: The elbow–noc gene complex. Developmental Biology. 301(2). 327–339. 14 indexed citations
10.
Jékely, Gáspár, Hsin-Ho Sung, Carlos M. Luque, & Pernille Rørth. (2005). Regulators of Endocytosis Maintain Localized Receptor Tyrosine Kinase Signaling in Guided Migration. Developmental Cell. 9(2). 197–207. 173 indexed citations
11.
Brückner, Katja, Lutz Kockel, Peter Duchek, et al.. (2004). The PDGF/VEGF Receptor Controls Blood Cell Survival in Drosophila. Developmental Cell. 7(1). 73–84. 209 indexed citations
12.
Luque, Carlos M., et al.. (2003). An Alternative Domain Containing a Leucine-rich Sequence Regulates Nuclear Cytoplasmic Localization of Protein 4.1R. Journal of Biological Chemistry. 278(4). 2686–2691. 18 indexed citations
13.
Luque, Carlos M., et al.. (2001). 4.1R Proteins Associate with Interphase Microtubules in Human T Cells. Journal of Biological Chemistry. 276(48). 44785–44791. 24 indexed citations
14.
Luque, Carlos M., et al.. (2001). Overexpression of 4.1R Disturbs Microtubule Organization.. PubMed. 6(2). 225–225. 1 indexed citations
15.
Luque, Carlos M. & Isabel Correas. (2000). A constitutive region is responsible for nuclear targeting of 4.1R: modulation by alternative sequences results in differential intracellular localization. Journal of Cell Science. 113(13). 2485–2495. 29 indexed citations
16.
Luque, Carlos M., et al.. (1999). The N-terminal 209-aa domain of high molecular- weight 4.1R isoforms abrogates 4.1R targeting to the nucleus. Proceedings of the National Academy of Sciences. 96(26). 14925–14930. 19 indexed citations
17.
Luque, Carlos M., et al.. (1998). An Alternative Domain Determines Nuclear Localization in Multifunctional Protein 4.1. Journal of Biological Chemistry. 273(19). 11643–11649. 41 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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