Iván Soltész

19.6k total citations · 2 hit papers
195 papers, 13.1k citations indexed

About

Iván Soltész is a scholar working on Cellular and Molecular Neuroscience, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Iván Soltész has authored 195 papers receiving a total of 13.1k indexed citations (citations by other indexed papers that have themselves been cited), including 157 papers in Cellular and Molecular Neuroscience, 110 papers in Cognitive Neuroscience and 44 papers in Molecular Biology. Recurrent topics in Iván Soltész's work include Neuroscience and Neuropharmacology Research (144 papers), Neural dynamics and brain function (69 papers) and Memory and Neural Mechanisms (49 papers). Iván Soltész is often cited by papers focused on Neuroscience and Neuropharmacology Research (144 papers), Neural dynamics and brain function (69 papers) and Memory and Neural Mechanisms (49 papers). Iván Soltész collaborates with scholars based in United States, Hungary and United Kingdom. Iván Soltész's co-authors include Caren Armstrong, Esther Krook‐Magnuson, István Módy, Vijayalakshmi Santhakumar, Mikko Oijala, Csaba Varga, Csaba Földy, Robert J. Morgan, Marianne Bezaire and Vincenzo Crunelli and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Iván Soltész

193 papers receiving 12.9k citations

Hit Papers

Bridging the cleft at GABA synapses in the brain 1994 2026 2004 2015 1994 2013 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Iván Soltész United States 68 9.9k 6.5k 3.1k 1.4k 1.2k 195 13.1k
Yuchio Yanagawa Japan 64 8.3k 0.8× 4.3k 0.7× 5.0k 1.6× 811 0.6× 2.1k 1.7× 321 14.6k
John R. Huguenard United States 72 12.7k 1.3× 8.6k 1.3× 7.5k 2.4× 1.7k 1.2× 1.4k 1.2× 191 19.0k
Grażyna Rajkowska United States 50 4.9k 0.5× 3.2k 0.5× 2.5k 0.8× 2.0k 1.5× 1.5k 1.2× 112 12.9k
Peter L. Carlen Canada 63 8.5k 0.9× 4.2k 0.7× 5.2k 1.7× 1.4k 1.0× 640 0.5× 359 13.8k
Chris J. McBain United States 65 12.7k 1.3× 5.5k 0.9× 7.9k 2.6× 684 0.5× 2.1k 1.7× 135 16.8k
Kai Kaila Finland 75 12.8k 1.3× 5.8k 0.9× 9.0k 2.9× 2.1k 1.6× 1.4k 1.2× 209 19.4k
David A. Prince United States 76 14.0k 1.4× 7.5k 1.2× 6.9k 2.2× 2.9k 2.2× 826 0.7× 182 17.0k
Juha Voipio Finland 46 6.8k 0.7× 3.2k 0.5× 4.4k 1.4× 1.1k 0.8× 785 0.6× 89 10.0k
Douglas A. Coulter United States 62 7.7k 0.8× 2.5k 0.4× 4.4k 1.4× 2.7k 2.0× 915 0.8× 116 10.8k
Walter E. Kaufmann United States 66 2.9k 0.3× 7.7k 1.2× 5.9k 1.9× 1.7k 1.3× 851 0.7× 193 16.7k

Countries citing papers authored by Iván Soltész

Since Specialization
Citations

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

Fields of papers citing papers by Iván Soltész

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Iván Soltész

This figure shows the co-authorship network connecting the top 25 collaborators of Iván Soltész. A scholar is included among the top collaborators of Iván Soltész 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 Iván Soltész. Iván Soltész 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.
Jamiolkowski, Ryan M., Quynh-Anh Nguyen, Jordan S. Farrell, et al.. (2024). The fasciola cinereum of the hippocampal tail as an interventional target in epilepsy. Nature Medicine. 30(5). 1292–1299. 18 indexed citations
2.
Dudok, Barna, Diana Zala, Mariana Tasso, et al.. (2024). Presynaptic nanoscale components of retrograde synaptic signaling. Science Advances. 10(22). eado0077–eado0077. 8 indexed citations
3.
Liao, Zhenrui, Satoshi Terada, Ivan Raikov, et al.. (2024). Inhibitory plasticity supports replay generalization in the hippocampus. Nature Neuroscience. 27(10). 1987–1998. 4 indexed citations
4.
Dudok, Barna, Linlin Z. Fan, Jordan S. Farrell, et al.. (2024). Retrograde endocannabinoid signaling at inhibitory synapses in vivo. Science. 383(6686). 967–970. 16 indexed citations
5.
Alaghband, Yasaman, Peter Klein, Enikö A. Kramár, et al.. (2023). Galactic cosmic radiation exposure causes multifaceted neurocognitive impairments. Cellular and Molecular Life Sciences. 80(1). 29–29. 18 indexed citations
6.
Gschwind, Tilo, Ayman Zeine, Ivan Raikov, et al.. (2023). Hidden behavioral fingerprints in epilepsy. Neuron. 111(9). 1440–1452.e5. 18 indexed citations
7.
Milstein, Aaron D., et al.. (2022). Offline memory replay in recurrent neuronal networks emerges from constraints on online dynamics. The Journal of Physiology. 601(15). 3241–3264. 6 indexed citations
8.
Szabó, Gergely, Jordan S. Farrell, Barna Dudok, et al.. (2022). Ripple-selective GABAergic projection cells in the hippocampus. Neuron. 110(12). 1959–1977.e9. 22 indexed citations
9.
Dudok, Barna, Miklos Szoboszlay, Anirban Paul, et al.. (2021). Recruitment and inhibitory action of hippocampal axo-axonic cells during behavior. Neuron. 109(23). 3838–3850.e8. 49 indexed citations
10.
Farrell, Jordan S., Matthew Lovett-Barron, Peter Klein, et al.. (2021). Supramammillary regulation of locomotion and hippocampal activity. Science. 374(6574). 1492–1496. 40 indexed citations
11.
Klein, Peter, Yasaman Alaghband, Ning Ru, et al.. (2021). Acute, Low-Dose Neutron Exposures Adversely Impact Central Nervous System Function. International Journal of Molecular Sciences. 22(16). 9020–9020. 7 indexed citations
12.
Chen, Ritchie, Felicity Gore, Quynh-Anh Nguyen, et al.. (2020). Deep brain optogenetics without intracranial surgery. Nature Biotechnology. 39(2). 161–164. 150 indexed citations
13.
Farrell, Jordan S., Roberto Colangeli, Barna Dudok, et al.. (2020). In vivo assessment of mechanisms underlying the neurovascular basis of postictal amnesia. Scientific Reports. 10(1). 14992–14992. 21 indexed citations
14.
Bui, Anh, Theresa Nguyen, Charles Limouse, et al.. (2018). Dentate gyrus mossy cells control spontaneous convulsive seizures and spatial memory. Science. 359(6377). 787–790. 158 indexed citations
15.
Tõkés, Anna‐Mária, Attila Marcell Szász, István Kenessey, et al.. (2015). Expression of proliferation markers Ki67, cyclin A, geminin and aurora-kinase A in primary breast carcinomas and corresponding distant metastases. Journal of Clinical Pathology. 68(4). 274–282. 21 indexed citations
16.
Ewell, Laura A., Liang Liang, Caren Armstrong, et al.. (2015). Brain State Is a Major Factor in Preseizure Hippocampal Network Activity and Influences Success of Seizure Intervention. Journal of Neuroscience. 35(47). 15635–15648. 36 indexed citations
17.
Winterer, Jochen, A. Vanessa Stempel, Tamar Dugladze, et al.. (2011). Cell-Type-Specific Modulation of Feedback Inhibition by Serotonin in the Hippocampus. Journal of Neuroscience. 31(23). 8464–8475. 22 indexed citations
18.
Morgan, Robert J., Vijayalakshmi Santhakumar, & Iván Soltész. (2007). Modeling the dentate gyrus. Progress in brain research. 163. 639–658. 37 indexed citations
19.
Spampanato, Jay, Jennifer A. Kearney, Gerald de Haan, et al.. (2004). A Novel Epilepsy Mutation in the Sodium ChannelSCN1AIdentifies a Cytoplasmic Domain for β Subunit Interaction. Journal of Neuroscience. 24(44). 10022–10034. 128 indexed citations
20.
Tóth, Zsuzsanna, et al.. (1998). Rapid increase in the excitatory glutamatergic drive to dentate interneurons following head trauma. The Society for Neuroscience Abstracts. 24. 322. 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.

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