Gisèle Alcaraz

2.1k total citations
27 papers, 1.7k citations indexed

About

Gisèle Alcaraz is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Gisèle Alcaraz has authored 27 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 14 papers in Cellular and Molecular Neuroscience and 6 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Gisèle Alcaraz's work include Neuroscience and Neuropharmacology Research (13 papers), Ion channel regulation and function (13 papers) and Monoclonal and Polyclonal Antibodies Research (6 papers). Gisèle Alcaraz is often cited by papers focused on Neuroscience and Neuropharmacology Research (13 papers), Ion channel regulation and function (13 papers) and Monoclonal and Polyclonal Antibodies Research (6 papers). Gisèle Alcaraz collaborates with scholars based in France, United States and Italy. Gisèle Alcaraz's co-authors include Edmond Carlier, H Metzger, Dominique Debanne, Andrzej Bialowas, Emilie Campanac, Jean‐Pierre Kinet, R J Hohman, Victor S. Pribluda, Rodolfo Quarto and François Couraud and has published in prestigious journals such as Journal of Biological Chemistry, Neuron and Journal of Neuroscience.

In The Last Decade

Gisèle Alcaraz

27 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gisèle Alcaraz France 16 788 664 370 364 215 27 1.7k
Eldon E. Geisert United States 29 1.4k 1.7× 779 1.2× 153 0.4× 189 0.5× 210 1.0× 103 2.5k
Betty Haldeman United States 14 1.3k 1.7× 1.1k 1.7× 585 1.6× 76 0.2× 80 0.4× 17 2.8k
Tobias Langenhan Germany 22 1.2k 1.5× 890 1.3× 128 0.3× 170 0.5× 281 1.3× 49 1.8k
Tomáš Mazel Czechia 21 550 0.7× 486 0.7× 132 0.4× 197 0.5× 38 0.2× 27 1.4k
Roman Urfer United States 22 1.1k 1.4× 726 1.1× 185 0.5× 87 0.2× 129 0.6× 28 1.8k
F S Walsh United Kingdom 32 1.8k 2.3× 809 1.2× 143 0.4× 162 0.4× 217 1.0× 56 2.8k
Junya Mitoma Japan 20 1.2k 1.6× 313 0.5× 434 1.2× 89 0.2× 227 1.1× 37 1.8k
Lijin Dong United States 24 1.4k 1.7× 338 0.5× 133 0.4× 161 0.4× 88 0.4× 64 2.0k
Angélique Levoye France 19 838 1.1× 414 0.6× 588 1.6× 96 0.3× 101 0.5× 25 1.9k
H. Nakagawa Japan 16 891 1.1× 203 0.3× 272 0.7× 169 0.5× 289 1.3× 26 1.8k

Countries citing papers authored by Gisèle Alcaraz

Since Specialization
Citations

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

Fields of papers citing papers by Gisèle Alcaraz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gisèle Alcaraz

This figure shows the co-authorship network connecting the top 25 collaborators of Gisèle Alcaraz. A scholar is included among the top collaborators of Gisèle Alcaraz 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 Gisèle Alcaraz. Gisèle Alcaraz 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.
Carlier, Edmond, et al.. (2011). Calmodulin and calcium differentially regulate the neuronal Nav1.1 voltage-dependent sodium channel. Biochemical and Biophysical Research Communications. 411(2). 329–334. 13 indexed citations
2.
Salin, Paul, Gisèle Alcaraz, Francis Castets, et al.. (2007). Nav1.7 and Nav1.3 are the only tetrodotoxin‐sensitive sodium channels expressed by the adult guinea pig enteric nervous system. The Journal of Comparative Neurology. 504(4). 363–378. 23 indexed citations
3.
Martin‐Moutôt, Nicole, Pascal Mansuelle, Gisèle Alcaraz, et al.. (2006). Phoneutria nigriventer Toxin 1: A Novel, State-Dependent Inhibitor of Neuronal Sodium Channels That Interacts with μ Conotoxin Binding Sites. Molecular Pharmacology. 69(6). 1931–1937. 42 indexed citations
4.
Osorio, Nancy, Gisèle Alcaraz, Françoise Padilla, et al.. (2005). Differential targeting and functional specialization of sodium channels in cultured cerebellar granule cells. The Journal of Physiology. 569(3). 801–816. 44 indexed citations
5.
6.
Devaux, Jérôme, Gisèle Alcaraz, Judith B. Grinspan, et al.. (2003). Kv3.1b Is a Novel Component of CNS Nodes. Journal of Neuroscience. 23(11). 4509–4518. 113 indexed citations
7.
Tricaud, Nicolas, Pierre Giraud, Ekaterini Kordeli, et al.. (2002). Interaction of the Nav1.2a Subunit of the Voltage-dependent Sodium Channel with Nodal AnkyrinG. Journal of Biological Chemistry. 277(32). 28996–29004. 45 indexed citations
8.
Alessandri‐Haber, Nicole, Gisèle Alcaraz, Charlotte Deleuze, et al.. (2002). Molecular determinants of emerging excitability in rat embryonic motoneurons. The Journal of Physiology. 541(1). 25–39. 44 indexed citations
9.
Marin, Philippe, Laurent Fagni, Yvette Torrens, et al.. (2001). AMPA receptor activation induces association of G‐beta protein with the alpha subunit of the sodium channel in neurons. European Journal of Neuroscience. 14(12). 1953–1960. 14 indexed citations
10.
Levy‐Mozziconacci, Annie, Gisèle Alcaraz, Pierre Giraud, et al.. (1998). Expression of the mRNA for the β2 subunit of the voltage‐dependent sodium channel in rat CNS. European Journal of Neuroscience. 10(9). 2757–2767. 14 indexed citations
11.
Alcaraz, Gisèle, et al.. (1998). Multiple pathways regulate the expression of genes encoding sodium channel subunits in developing neurons. Molecular Brain Research. 56(1-2). 238–255. 12 indexed citations
12.
Alcaraz, Gisèle, Nicolas Tricaud, Pierre Giraud, et al.. (1997). Down-regulation of voltage-dependent sodium channels coincides with a low expression of αβ1 subunit complexes. Molecular Brain Research. 51(1-2). 143–153. 14 indexed citations
13.
Dargent, Bénédicte, et al.. (1996). Channel activators reduce the expression of sodium channel α-subunit mRNA in developing neurons. Molecular Brain Research. 37(1-2). 116–124. 17 indexed citations
14.
Dargent, Bénédicte, Christophe Paillart, Edmond Carlier, et al.. (1994). Sodium channel internalization in developing neurons. Neuron. 13(3). 683–690. 55 indexed citations
15.
Alcaraz, Gisèle & Christo Goridis. (1991). Biosynthesis and processing of polysialylated NCAM by AtT-20 cells.. PubMed. 55(1). 165–73. 40 indexed citations
16.
Alcaraz, Gisèle, et al.. (1987). Further characterization of the subunits of the receptor with high affinity for immunoglobulin E. Biochemistry. 26(9). 2569–2575. 15 indexed citations
17.
Metzger, H, et al.. (1986). The receptor for immunoglobulin E as a membrane protein.. PubMed. 51. 59–67. 2 indexed citations
18.
19.
Alcaraz, Gisèle, Jacques Marti, Danielle Moinier, & Michel Fougereau. (1981). NH2-terminal sequence of Calf Fetuin. Biochemical and Biophysical Research Communications. 99(1). 30–36. 9 indexed citations
20.
Alcaraz, Gisèle, et al.. (1980). Partial structure of a rat IgD molecule with a deletion in the heavy chain.. PubMed. 131C(3). 363–88. 7 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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