Joaquín de Navascués

2.6k total citations · 1 hit paper
27 papers, 2.0k citations indexed

About

Joaquín de Navascués is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Joaquín de Navascués has authored 27 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 6 papers in Cell Biology. Recurrent topics in Joaquín de Navascués's work include RNA Research and Splicing (5 papers), Neurobiology and Insect Physiology Research (4 papers) and Ubiquitin and proteasome pathways (4 papers). Joaquín de Navascués is often cited by papers focused on RNA Research and Splicing (5 papers), Neurobiology and Insect Physiology Research (4 papers) and Ubiquitin and proteasome pathways (4 papers). Joaquín de Navascués collaborates with scholars based in Spain, United Kingdom and Germany. Joaquín de Navascués's co-authors include François‐Michel Boisvert, Angus I. Lamond, Silvana van Koningsbruggen, Miguel Lafarga, Marı́a T. Berciano, Íñigo Casafont, Juan Modolell, Benjamin D. Simons, Allison J. Bardin and Carmen Pérez‐Rontomé and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Reviews Molecular Cell Biology and The EMBO Journal.

In The Last Decade

Joaquín de Navascués

25 papers receiving 2.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The multifunctional nucleolus

2007 1.2k citations François‐Michel Boisvert, Silvana van Koningsbruggen et al. Nature Reviews Molecular Cell Biology profile →

Peers

Joaquín de Navascués

ONCOL

GENET

Serge Urbach France

Dierk Niessing Germany

Wang L. Cheung United States

Zhigang Jin China

Michael Sheets United States

Mônica Beltrame Italy

Andrew J. Saurin France

Erich Brunner Switzerland

Saskia Hutten Germany

Marc Gentzel Germany

Serge Urbach France

Joaquín de Navascués

1.4k ×0.9

410 ×1.7

277 ×1.1

213 ×1.0

ONCOL

132 ×0.8

GENET

Citations per year, relative to Joaquín de Navascués Joaquín de Navascués (= 1×) peers Serge Urbach

Countries citing papers authored by Joaquín de Navascués

Since Specialization

Citations

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

Fields of papers citing papers by Joaquín de Navascués

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joaquín de Navascués. 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 Joaquín de Navascués. The network helps show where Joaquín de Navascués may publish in the future.

Co-authorship network of co-authors of Joaquín de Navascués

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

All Works

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20 of 20 papers shown

Edgar, Bruce A., et al.. (2025). A bHLH interaction code controls bipotential differentiation and self-renewal in the Drosophila gut. Cell Reports. 44(3). 115398–115398.

Martinez-Corral, Rosa, et al.. (2017). Diversity of fate outcomes in cell pairs under lateral inhibition. Development. 144(7). 1177–1186. 32 indexed citations

Porazinski, Sean, Joaquín de Navascués, Yuta Yako, et al.. (2016). EphA2 Drives the Segregation of Ras-Transformed Epithelial Cells from Normal Neighbors. Current Biology. 26(23). 3220–3229. 56 indexed citations

Navascués, Joaquín de, et al.. (2016). α-Catenin stabilises Cadherin–Catenin complexes and modulates actomyosin dynamics to allow pulsatile apical contraction. Journal of Cell Science. 129(24). 4496–4508. 31 indexed citations

Alfonso, Pilar, Joaquín de Navascués, Silvia Navarro, et al.. (2013). Characterization of Variants in the Glucosylceramide Synthase Gene and their Association with Type 1 Gaucher Disease Severity. Human Mutation. 34(10). 1396–1403. 10 indexed citations

Muñoz‐Descalzo, Silvia, Joaquín de Navascués, & Alfonso Martínez Arias. (2012). Wnt‐Notch signalling: An integrated mechanism regulating transitions between cell states. BioEssays. 34(2). 110–118. 32 indexed citations

Clemente, Maria R., Pilar Bustos‐Sanmamed, Jorge Loscos, et al.. (2012). Thiol synthetases of legumes: immunogold localization and differential gene regulation by phytohormones. Journal of Experimental Botany. 63(10). 3923–3934. 15 indexed citations

Navascués, Joaquín de, Carolina N. Perdigoto, Yu Bian, et al.. (2012). Drosophila midgut homeostasis involves neutral competition between symmetrically dividing intestinal stem cells. The EMBO Journal. 31(11). 2473–2485. 124 indexed citations

Navascués, Joaquín de, Carmen Pérez‐Rontomé, Diego H. Sánchez, et al.. (2011). Oxidative stress is a consequence, not a cause, of aluminum toxicity in the forage legume Lotus corniculatus. New Phytologist. 193(3). 625–636. 63 indexed citations

10.

Navascués, Joaquín de & Juan Modolell. (2010). The pronotum LIM-HD gene tailup is both a positive and a negative regulator of the proneural genes achaete and scute of Drosophila. Mechanisms of Development. 127(9-12). 393–406. 13 indexed citations

11.

Navascués, Joaquín de, Rocío Bengoechea, O. Tapia, et al.. (2008). SUMO-1 transiently localizes to Cajal bodies in mammalian neurons. Journal of Structural Biology. 163(2). 137–146. 38 indexed citations

12.

Boisvert, François‐Michel, Silvana van Koningsbruggen, Joaquín de Navascués, & Angus I. Lamond. (2007). The multifunctional nucleolus. Nature Reviews Molecular Cell Biology. 8(7). 574–585. 1247 indexed citations breakdown →

13.

Casafont, Íñigo, et al.. (2007). The giant fibrillar center: A nucleolar structure enriched in upstream binding factor (UBF) that appears in transcriptionally more active sensory ganglia neurons. Journal of Structural Biology. 159(3). 451–461. 27 indexed citations

14.

Navascués, Joaquín de, Rocío Bengoechea, O. Tapia, et al.. (2007). Characterization of a new SUMO-1 nuclear body (SNB) enriched in pCREB, CBP, c-Jun in neuron-like UR61 cells. Chromosoma. 116(5). 441–451. 17 indexed citations

15.

Casafont, Íñigo, et al.. (2006). Nuclear organization and dynamics of transcription sites in rat sensory ganglia neurons detected by incorporation of 5′-fluorouridine into nascent RNA. Neuroscience. 140(2). 453–462. 47 indexed citations

16.

Villagrá, Nuria T., Joaquín de Navascués, Íñigo Casafont, et al.. (2005). The PML-nuclear inclusion of human supraoptic neurons: a new compartment with SUMO-1- and ubiquitin–proteasome-associated domains. Neurobiology of Disease. 21(1). 181–193. 20 indexed citations

17.

Navascués, Joaquín de, Íñigo Casafont, Nuria T. Villagrá, Miguel Lafarga, & Marı́a T. Berciano. (2004). Reorganization of nuclear compartments of type A neurons of trigeminal ganglia in response to inflammatory injury of peripheral nerve endings. Journal of Neurocytology. 33(4). 393–405. 7 indexed citations

18.

Villagrá, Nuria T., José Berciano, Joaquín de Navascués, et al.. (2004). PML bodies in reactive sensory ganglion neurons of the Guillain–Barré syndrome. Neurobiology of Disease. 16(1). 158–168. 20 indexed citations

19.

Navascués, Joaquín de, et al.. (2004). Targeting SMN to Cajal bodies and nuclear gems during neuritogenesis. Chromosoma. 112(8). 398–409. 43 indexed citations

20.

Berciano, Marı́a T., et al.. (2002). Structural and functional compartmentalization of the cell nucleus in supraoptic neurons. Microscopy Research and Technique. 56(2). 132–142. 19 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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