Alfredo Cáceres

10.3k total citations · 2 hit papers
103 papers, 8.7k citations indexed

About

Alfredo Cáceres is a scholar working on Cell Biology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Alfredo Cáceres has authored 103 papers receiving a total of 8.7k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Cell Biology, 52 papers in Molecular Biology and 36 papers in Cellular and Molecular Neuroscience. Recurrent topics in Alfredo Cáceres's work include Microtubule and mitosis dynamics (43 papers), Cellular transport and secretion (27 papers) and Neurogenesis and neuroplasticity mechanisms (23 papers). Alfredo Cáceres is often cited by papers focused on Microtubule and mitosis dynamics (43 papers), Cellular transport and secretion (27 papers) and Neurogenesis and neuroplasticity mechanisms (23 papers). Alfredo Cáceres collaborates with scholars based in Argentina, United States and Chile. Alfredo Cáceres's co-authors include Cecı́lia Conde, Adriana Ferreira, Oswald Steward, Kenneth S. Kosik, Kenneth S. Kosik, Santiago Quiroga, Gabriela Paglini, Michael R. Payne, Lester I. Binder and Jorge Busciglio 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

Alfredo Cáceres

103 papers receiving 8.6k citations

Hit Papers

Microtubule assembly, organization and d... 1990 2026 2002 2014 2009 1990 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alfredo Cáceres Argentina 56 4.4k 3.7k 3.4k 1.6k 1.4k 103 8.7k
Peter W. Baas United States 63 5.1k 1.2× 6.8k 1.8× 3.4k 1.0× 1.1k 0.7× 1.6k 1.1× 163 10.6k
Harish C. Pant United States 54 4.6k 1.0× 2.9k 0.8× 2.7k 0.8× 1.7k 1.0× 1.0k 0.7× 183 9.0k
J. H. Pate Skene United States 40 4.1k 0.9× 1.8k 0.5× 4.5k 1.3× 1.2k 0.7× 1.7k 1.2× 57 8.3k
Yoshio Goshima Japan 53 4.0k 0.9× 2.5k 0.7× 6.6k 1.9× 926 0.6× 1.8k 1.3× 280 9.8k
Barbara Ranscht United States 48 4.2k 1.0× 1.7k 0.4× 2.5k 0.7× 851 0.5× 1.5k 1.1× 78 7.5k
Frank S. Walsh United Kingdom 62 8.2k 1.8× 2.3k 0.6× 5.6k 1.6× 1.5k 0.9× 2.5k 1.8× 169 13.1k
Oleg Shupliakov Sweden 46 5.1k 1.1× 3.7k 1.0× 3.9k 1.1× 844 0.5× 1.4k 1.0× 114 8.6k
Alexander Dityatev Germany 57 4.8k 1.1× 2.4k 0.6× 5.6k 1.6× 807 0.5× 1.9k 1.4× 170 10.2k
Franck Polleux United States 52 5.5k 1.3× 1.8k 0.5× 4.2k 1.2× 853 0.5× 2.5k 1.7× 93 9.5k
Robert G. Kalb United States 49 4.0k 0.9× 1.5k 0.4× 4.2k 1.2× 925 0.6× 1.0k 0.7× 112 8.4k

Countries citing papers authored by Alfredo Cáceres

Since Specialization
Citations

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

Fields of papers citing papers by Alfredo Cáceres

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alfredo Cáceres. 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 Alfredo Cáceres. The network helps show where Alfredo Cáceres may publish in the future.

Co-authorship network of co-authors of Alfredo Cáceres

This figure shows the co-authorship network connecting the top 25 collaborators of Alfredo Cáceres. A scholar is included among the top collaborators of Alfredo Cáceres 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 Alfredo Cáceres. Alfredo Cáceres 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.
Wojnacki, José, Gonzalo Quassollo, Nicolás Unsain, et al.. (2024). Dual spatio-temporal regulation of axon growth and microtubule dynamics by RhoA signaling pathways. Journal of Cell Science. 137(14). 4 indexed citations
2.
Gastaldi, Laura, Lucas J. Sosa, Gonzalo Quassollo, et al.. (2022). BARS Influences Neuronal Development by Regulation of Post-Golgi Trafficking. Cells. 11(8). 1320–1320. 3 indexed citations
3.
Lukin, Jerónimo, David J. Williamson, Nicolás Unsain, et al.. (2021). Three-dimensional total-internal reflection fluorescence nanoscopy with nanometric axial resolution by photometric localization of single molecules. Nature Communications. 12(1). 517–517. 25 indexed citations
4.
Wilson, Carlos, et al.. (2020). The Histone Methyltransferase G9a Controls Axon Growth by Targeting the RhoA Signaling Pathway. Cell Reports. 31(6). 107639–107639. 19 indexed citations
5.
Bisbal, Mariano, et al.. (2018). Rotenone inhibits axonogenesis via an Lfc/RhoA/ROCK pathway in cultured hippocampal neurons. Journal of Neurochemistry. 146(5). 570–584. 19 indexed citations
6.
Quassollo, Gonzalo, José Wojnacki, Daniela Salas, et al.. (2015). A RhoA Signaling Pathway Regulates Dendritic Golgi Outpost Formation. Current Biology. 25(8). 971–982. 78 indexed citations
7.
Conde, Cecı́lia, Aiqun Li, Masaki Saito, et al.. (2010). Evidence for the Involvement of Lfc and Tctex-1 in Axon Formation. Journal of Neuroscience. 30(19). 6793–6800. 34 indexed citations
8.
Dupraz, Sebastián, Diego Grassi, María Eugenia Bernis, et al.. (2009). The TC10–Exo70 Complex Is Essential for Membrane Expansion and Axonal Specification in Developing Neurons. Journal of Neuroscience. 29(42). 13292–13301. 89 indexed citations
9.
Salvarezza, Susana, Sylvie Deborde, Ryan Schreiner, et al.. (2008). LIM Kinase 1 and Cofilin Regulate Actin Filament Population Required for Dynamin-dependent Apical Carrier Fission from theTrans-Golgi Network. Molecular Biology of the Cell. 20(1). 438–451. 82 indexed citations
10.
Abu-Elneel, Kawther, Tomoyo Ochiishi, Miguel Medina, et al.. (2008). A δ-Catenin Signaling Pathway Leading to Dendritic Protrusions. Journal of Biological Chemistry. 283(47). 32781–32791. 53 indexed citations
11.
Sachdev, Perminder S., Santosh T. Menon, David B. Kastner, et al.. (2007). G protein βγ subunit interaction with the dynein light‐chain component Tctex‐1 regulates neurite outgrowth. The EMBO Journal. 26(11). 2621–2632. 56 indexed citations
12.
Rosso, Silvana B., Flavia Bollati, Mariano Bisbal, et al.. (2004). LIMK1 Regulates Golgi Dynamics, Traffic of Golgi-derived Vesicles, and Process Extension in Primary Cultured Neurons. Molecular Biology of the Cell. 15(7). 3433–3449. 109 indexed citations
13.
González‐Billault, Christian, Eva M. Jiménez‐Mateos, Alfredo Cáceres, et al.. (2003). Microtubule‐associated protein 1B function during normal development, regeneration, and pathological conditions in the nervous system. Journal of Neurobiology. 58(1). 48–59. 83 indexed citations
14.
González‐Billault, Christian, Michael Engelke, Eva M. Jiménez‐Mateos, et al.. (2002). Participation of structural microtubule‐associated proteins (MAPs) in the development of neuronal polarity. Journal of Neuroscience Research. 67(6). 713–719. 62 indexed citations
15.
González‐Billault, Christian, Jesús Ávila, & Alfredo Cáceres. (2001). Evidence for the Role of MAP1B in Axon Formation. Molecular Biology of the Cell. 12(7). 2087–2098. 123 indexed citations
16.
Aon, Miguel A., Alfredo Cáceres, & Sonia Cortassa. (1996). Heterogeneous distribution and organization of cytoskeletal proteins drive differential modulation of metabolic fluxes. Journal of Cellular Biochemistry. 60(2). 271–278. 8 indexed citations
17.
Cambiasso, María Julia, et al.. (1995). Neuritogenic effect of estradiol on rat ventromedial hypothalamic neurons co‐cultured with homotopic or heterotopic glia. Journal of Neuroscience Research. 42(5). 700–709. 30 indexed citations
18.
Feiguin, Fabián, et al.. (1994). Microfilament‐associated growth cone component depends upon Tau for its intracellular localization. Cell Motility and the Cytoskeleton. 29(2). 117–130. 64 indexed citations
19.
Morfini, Gerardo, et al.. (1994). Neurotrophin‐3 enhances neurite outgrowth in cultured hippocampal pyramidal neurons. Journal of Neuroscience Research. 39(2). 219–232. 52 indexed citations
20.
Ferreira, Adriana & Alfredo Cáceres. (1992). Expression of the Class III β‐tubulin isotype in developing neurons in culture. Journal of Neuroscience Research. 32(4). 516–529. 108 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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