Raul E. Guzman

757 total citations
20 papers, 553 citations indexed

About

Raul E. Guzman is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Raul E. Guzman has authored 20 papers receiving a total of 553 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 11 papers in Cellular and Molecular Neuroscience and 7 papers in Cell Biology. Recurrent topics in Raul E. Guzman's work include Ion channel regulation and function (15 papers), Neuroscience and Neuropharmacology Research (9 papers) and Cellular transport and secretion (7 papers). Raul E. Guzman is often cited by papers focused on Ion channel regulation and function (15 papers), Neuroscience and Neuropharmacology Research (9 papers) and Cellular transport and secretion (7 papers). Raul E. Guzman collaborates with scholars based in Germany, China and Venezuela. Raul E. Guzman's co-authors include Christoph Fahlke, Alexi K. Alekov, Arne Franzen, Magalie Martineau, Jürgen Klingauf, Dieter Bruns, Yvonne Schwarz, Jens Rettig, Patricia Hidalgo and Marc Freichel and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and Journal of Neuroscience.

In The Last Decade

Raul E. Guzman

19 papers receiving 552 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Raul E. Guzman Germany 12 366 240 135 89 68 20 553
Seth Malmersjö Sweden 13 551 1.5× 341 1.4× 131 1.0× 197 2.2× 76 1.1× 16 870
Astrid Kollewe Germany 11 425 1.2× 293 1.2× 80 0.6× 123 1.4× 46 0.7× 12 635
Laura Fedrizzi Italy 10 423 1.2× 216 0.9× 54 0.4× 76 0.9× 105 1.5× 12 634
Michael Kirmiz United States 7 348 1.0× 200 0.8× 115 0.9× 41 0.5× 52 0.8× 9 509
Elías Leiva‐Salcedo Chile 13 313 0.9× 169 0.7× 39 0.3× 144 1.6× 56 0.8× 36 601
Shengjie Feng United States 11 557 1.5× 242 1.0× 64 0.5× 254 2.9× 118 1.7× 14 834
William E. McIntire United States 17 787 2.2× 299 1.2× 95 0.7× 51 0.6× 150 2.2× 29 969
Oscar Vivas United States 14 553 1.5× 271 1.1× 234 1.7× 111 1.2× 142 2.1× 33 835
Alexander Haupt Germany 8 517 1.4× 360 1.5× 128 0.9× 38 0.4× 63 0.9× 9 674
Hidetada Matsuoka Japan 14 276 0.8× 172 0.7× 67 0.5× 92 1.0× 26 0.4× 38 487

Countries citing papers authored by Raul E. Guzman

Since Specialization
Citations

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

Fields of papers citing papers by Raul E. Guzman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Raul E. Guzman. 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 Raul E. Guzman. The network helps show where Raul E. Guzman may publish in the future.

Co-authorship network of co-authors of Raul E. Guzman

This figure shows the co-authorship network connecting the top 25 collaborators of Raul E. Guzman. A scholar is included among the top collaborators of Raul E. Guzman 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 Raul E. Guzman. Raul E. Guzman 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.
2.
Sahly, Ahmed N., Arne Franzen, Chantal Poulin, et al.. (2024). Genotype-phenotype correlation in CLCN4-related developmental and epileptic encephalopathy. Human Genetics. 143(5). 667–681. 3 indexed citations
3.
He, Hailan, Arne Franzen, Hongwei Zhang, et al.. (2024). Expanding the genetic and phenotypic relevance of CLCN4 variants in neurodevelopmental condition: 13 new patients. Journal of Neurology. 271(8). 4933–4948. 3 indexed citations
4.
Kortzak, Daniel, et al.. (2023). Vesicular glutamate transporters are H+-anion exchangers that operate at variable stoichiometry. Nature Communications. 14(1). 9 indexed citations
5.
Willuweit, Antje, et al.. (2022). ClC-3 regulates the excitability of nociceptive neurons and is involved in inflammatory processes within the spinal sensory pathway. Frontiers in Cellular Neuroscience. 16. 920075–920075. 4 indexed citations
6.
Guzman, Raul E., et al.. (2022). Functional Characterization of CLCN4 Variants Associated With X-Linked Intellectual Disability and Epilepsy. Frontiers in Molecular Neuroscience. 15. 872407–872407. 11 indexed citations
7.
He, Hailan, Raul E. Guzman, Dezhi Cao, et al.. (2021). The molecular and phenotypic spectrum of CLCN4‐related epilepsy. Epilepsia. 62(6). 1401–1415. 19 indexed citations
8.
Guzman, Raul E., et al.. (2020). Metabolic energy sensing by mammalian CLC anion/proton exchangers. EMBO Reports. 21(6). e47872–e47872. 8 indexed citations
9.
10.
Guzman, Raul E., et al.. (2017). Preferential association with ClC-3 permits sorting of ClC-4 into endosomal compartments. Journal of Biological Chemistry. 292(46). 19055–19065. 21 indexed citations
11.
Kollewe, Astrid, Jörg Pohle, Ilka Mathar, et al.. (2017). Heteromeric channels formed by TRPC 1, TRPC 4 and TRPC 5 define hippocampal synaptic transmission and working memory. The EMBO Journal. 36(18). 2770–2789. 92 indexed citations
12.
Martineau, Magalie, Raul E. Guzman, Christoph Fahlke, & Jürgen Klingauf. (2017). VGLUT1 functions as a glutamate/proton exchanger with chloride channel activity in hippocampal glutamatergic synapses. Nature Communications. 8(1). 2279–2279. 71 indexed citations
13.
Guzman, Raul E., et al.. (2015). Neuronal ClC-3 Splice Variants Differ in Subcellular Localizations, but Mediate Identical Transport Functions. Journal of Biological Chemistry. 290(43). 25851–25862. 44 indexed citations
14.
Stölting, Gabriel, Raul E. Guzman, Silke Schmidt, et al.. (2014). Direct Interaction of CaVβ with Actin Up-regulates L-type Calcium Currents in HL-1 Cardiomyocytes. Journal of Biological Chemistry. 290(8). 4561–4572. 31 indexed citations
15.
Ewers, David, et al.. (2014). The N-terminal Domain Tethers the Voltage-gated Calcium Channel β2e-subunit to the Plasma Membrane via Electrostatic and Hydrophobic Interactions. Journal of Biological Chemistry. 289(15). 10387–10398. 28 indexed citations
16.
Guzman, Raul E., Alexi K. Alekov, Mikhail A Filippov, Jan Hegermann, & Christoph Fahlke. (2014). Involvement of ClC-3 chloride/proton exchangers in controlling glutamatergic synaptic strength in cultured hippocampal neurons. Frontiers in Cellular Neuroscience. 8. 143–143. 31 indexed citations
17.
Matti, Ulf, Varsha Pattu, Mahantappa Halimani, et al.. (2013). Synaptobrevin2 is the v-SNARE required for cytotoxic T-lymphocyte lytic granule fusion. Nature Communications. 4(1). 1439–1439. 48 indexed citations
18.
Guzman, Raul E., et al.. (2013). ClC-3 Is an Intracellular Chloride/Proton Exchanger with Large Voltage-Dependent Nonlinear Capacitance. ACS Chemical Neuroscience. 4(6). 994–1003. 69 indexed citations
19.
Guzman, Raul E., Yvonne Schwarz, Jens Rettig, & Dieter Bruns. (2010). SNARE Force Synchronizes Synaptic Vesicle Fusion and Controls the Kinetics of Quantal Synaptic Transmission. Journal of Neuroscience. 30(31). 10272–10281. 39 indexed citations
20.
Guzman, Raul E., Pura Bolaños, Héctor Rojas, et al.. (2006). Depolymerisation and rearrangement of actin filaments during exocytosis in rat peritoneal mast cells: involvement of ryanodine-sensitive calcium stores. Pflügers Archiv - European Journal of Physiology. 454(1). 131–141. 12 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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