Géza Szűcs

958 total citations
34 papers, 807 citations indexed

About

Géza Szűcs is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Sensory Systems. According to data from OpenAlex, Géza Szűcs has authored 34 papers receiving a total of 807 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 16 papers in Cellular and Molecular Neuroscience and 13 papers in Sensory Systems. Recurrent topics in Géza Szűcs's work include Ion channel regulation and function (17 papers), Neuroscience and Neuropharmacology Research (14 papers) and Hearing, Cochlea, Tinnitus, Genetics (12 papers). Géza Szűcs is often cited by papers focused on Ion channel regulation and function (17 papers), Neuroscience and Neuropharmacology Research (14 papers) and Hearing, Cochlea, Tinnitus, Genetics (12 papers). Géza Szűcs collaborates with scholars based in Hungary, Australia and Germany. Géza Szűcs's co-authors include Zoltán Rusznák, Ian D. Forsythe, Matthew Barker, Balázs Pál, Paul D. Dodson, Brian Billups, László Csernoch, Stephan Heinke, Bernd Nilius and Csaba Harasztosi and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Physiology and Brain Research.

In The Last Decade

Géza Szűcs

33 papers receiving 801 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Géza Szűcs Hungary 16 523 329 200 132 88 34 807
Astrid Kollewe Germany 11 425 0.8× 293 0.9× 123 0.6× 22 0.2× 58 0.7× 12 635
Valérie Friend France 9 933 1.8× 194 0.6× 365 1.8× 55 0.4× 27 0.3× 11 1.2k
Clinton J. Doering Canada 18 851 1.6× 603 1.8× 64 0.3× 29 0.2× 112 1.3× 25 986
Ana E. Vázquez United States 14 570 1.1× 189 0.6× 260 1.3× 71 0.5× 410 4.7× 20 861
Xintong Dong United States 19 498 1.0× 260 0.8× 74 0.4× 29 0.2× 123 1.4× 27 1.3k
Tadashi Inui Japan 14 341 0.7× 334 1.0× 103 0.5× 89 0.7× 12 0.1× 35 670
Erik Smedler Sweden 13 283 0.5× 164 0.5× 38 0.2× 57 0.4× 22 0.3× 23 604
Claudia F. Beck United States 9 759 1.5× 486 1.5× 128 0.6× 24 0.2× 142 1.6× 13 893
Shengwei Zou United States 15 659 1.3× 259 0.8× 28 0.1× 20 0.2× 49 0.6× 19 876
Anna Boccaccio Italy 22 656 1.3× 706 2.1× 533 2.7× 50 0.4× 94 1.1× 40 1.3k

Countries citing papers authored by Géza Szűcs

Since Specialization
Citations

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

Fields of papers citing papers by Géza Szűcs

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Géza Szűcs

This figure shows the co-authorship network connecting the top 25 collaborators of Géza Szűcs. A scholar is included among the top collaborators of Géza Szűcs 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 Géza Szűcs. Géza Szűcs 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.
Gyáni, Károly, et al.. (2017). A nyelőcső óriás inflammatorikus fibroid polipja. Magyar Sebészet (Hungarian Journal of Surgery). 70(1). 69–73. 1 indexed citations
2.
Nagy, D. L., Mónika Gönczi, B. Dienes, et al.. (2014). Silencing the KCNK9 potassium channel (TASK-3) gene disturbs mitochondrial function, causes mitochondrial depolarization, and induces apoptosis of human melanoma cells. Archives of Dermatological Research. 306(10). 885–902. 35 indexed citations
3.
Szűcs, Géza, et al.. (2012). Three-dimensional reconstruction and quantitative morphometric analysis of pyramidal and giant neurons of the rat dorsal cochlear nucleus. Brain Structure and Function. 218(5). 1279–1292. 4 indexed citations
4.
Szabó, Miklós, et al.. (2012). Chylothorax as a complication of coronary artery bypass grafting operation. Orvosi Hetilap. 153(14). 553–558. 1 indexed citations
5.
Vincze, János, Zoltán Rusznák, YuHong Fu, et al.. (2012). Activation of muscarinic receptors increases the activity of the granule neurones of the rat dorsal cochlear nucleus—a calcium imaging study. Pflügers Archiv - European Journal of Physiology. 463(6). 829–844. 14 indexed citations
6.
Tóth, Imre, Géza Szűcs, & Tamás F. Molnár. (2012). Mediastinoscope-controlled parasternal fenestration of the pericardium: definitive surgical palliation of malignant pericardial effusion. Journal of Cardiothoracic Surgery. 7(1). 56–56. 10 indexed citations
7.
Rusznák, Zoltán, D. L. Nagy, Zsuzsanna Nagy, et al.. (2011). Inhibition of TASK-3 (KCNK9) channel biosynthesis changes cell morphology and decreases both DNA content and mitochondrial function of melanoma cells maintained in cell culture. Melanoma Research. 21(4). 308–322. 36 indexed citations
8.
Pál, Balázs, et al.. (2009). Purkinje-like cells of the rat cochlear nucleus: A combined functional and morphological study. Brain Research. 1297. 57–69. 5 indexed citations
9.
10.
Rusznák, Zoltán & Géza Szűcs. (2008). Spiral ganglion neurones: an overview of morphology, firing behaviour, ionic channels and function. Pflügers Archiv - European Journal of Physiology. 457(6). 1303–1325. 51 indexed citations
12.
Rusznák, Zoltán, et al.. (2008). Voltage-gated Potassium Channel (Kv) Subunits Expressed in the Rat Cochlear Nucleus. Journal of Histochemistry & Cytochemistry. 56(5). 443–465. 22 indexed citations
13.
Rusznák, Zoltán, et al.. (2005). Presence and distribution of three calcium binding proteins in projection neurons of the adult rat cochlear nucleus. Brain Research. 1039(1-2). 63–74. 30 indexed citations
14.
Kecskeméti, Valéria, Zoltán Rusznák, Pál Riba, et al.. (2005). Norfluoxetine and fluoxetine have similar anticonvulsant and Ca2+ channel blocking potencies. Brain Research Bulletin. 67(1-2). 126–132. 30 indexed citations
15.
Szappanos, Henrietta Cserné, Gyula P. Szigeti, Balázs Pál, et al.. (2005). The Penicillium chrysogenum-derived antifungal peptide shows no toxic effects on mammalian cells in the intended therapeutic concentration. Naunyn-Schmiedeberg s Archives of Pharmacology. 371(2). 122–132. 40 indexed citations
16.
Pál, Balázs, et al.. (2004). Voltage-gated and background K+ channel subunits expressed by the bushy cells of the rat cochlear nucleus. Hearing Research. 199(1-2). 57–70. 20 indexed citations
17.
Dodson, Paul D., Brian Billups, Zoltán Rusznák, et al.. (2003). Presynaptic Rat Kv1.2 Channels Suppress Synaptic Terminal Hyperexcitability Following Action Potential Invasion. The Journal of Physiology. 550(1). 27–33. 134 indexed citations
18.
Harasztosi, Csaba, Ian D. Forsythe, Géza Szűcs, Peter Stanfield, & Zoltán Rusznák. (1999). Possible modulatory role of voltage-activated Ca2+ currents determining the membrane properties of isolated pyramidal neurones of the rat dorsal cochlear nucleus. Brain Research. 839(1). 109–119. 15 indexed citations
19.
Nilius, Bernd, Volker Gerke, Jean Prenen, et al.. (1996). Annexin II Modulates Volume-activated Chloride Currents in Vascular Endothelial Cells. Journal of Biological Chemistry. 271(48). 30631–30636. 63 indexed citations
20.
Csernoch, László, Gonzalo Pizarro, Jesús Garcı́a, et al.. (1992). Effects of Calcium Release from the Sarcoplasmic Reticulum on Intramembrane Charge Movement in Skeletal Muscle. Advances in experimental medicine and biology. 311. 137–148. 3 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026