Elek Molnár

8.2k total citations · 2 hit papers
98 papers, 6.7k citations indexed

About

Elek Molnár is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Elek Molnár has authored 98 papers receiving a total of 6.7k indexed citations (citations by other indexed papers that have themselves been cited), including 73 papers in Cellular and Molecular Neuroscience, 58 papers in Molecular Biology and 18 papers in Cognitive Neuroscience. Recurrent topics in Elek Molnár's work include Neuroscience and Neuropharmacology Research (67 papers), Ion channel regulation and function (22 papers) and Neuroinflammation and Neurodegeneration Mechanisms (16 papers). Elek Molnár is often cited by papers focused on Neuroscience and Neuropharmacology Research (67 papers), Ion channel regulation and function (22 papers) and Neuroinflammation and Neurodegeneration Mechanisms (16 papers). Elek Molnár collaborates with scholars based in United Kingdom, United States and Japan. Elek Molnár's co-authors include Graham L. Collingridge, Péter Somogyi, Jeremy M. Henley, Jacques Noël, Zoltán Nusser, R. A. Jeffrey McIlhinney, Anikó Váradi, Lisa Pickard, Rafael Luján and Zafar I. Bashir and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Neuron and Journal of Neuroscience.

In The Last Decade

Elek Molnár

97 papers receiving 6.6k citations

Hit Papers

Cell Type and Pathway Dependence of Synaptic AMPA Recepto... 1998 2026 2007 2016 1998 2004 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elek Molnár United Kingdom 41 4.9k 3.6k 1.6k 846 672 98 6.7k
P. H. Seeburg Germany 25 5.8k 1.2× 5.8k 1.6× 1.1k 0.7× 889 1.1× 654 1.0× 37 9.0k
David J. A. Wyllie United Kingdom 46 4.5k 0.9× 4.3k 1.2× 1.3k 0.8× 770 0.9× 392 0.6× 100 6.9k
Robert T. Fremeau United States 37 5.7k 1.2× 4.8k 1.3× 1.3k 0.8× 397 0.5× 801 1.2× 61 9.0k
Farrukh A. Chaudhry Norway 38 4.9k 1.0× 3.1k 0.9× 948 0.6× 743 0.9× 829 1.2× 73 7.4k
Heng‐Ye Man United States 44 3.9k 0.8× 4.0k 1.1× 1.2k 0.7× 881 1.0× 717 1.1× 107 7.7k
Claudio Rivera Finland 40 6.2k 1.3× 4.3k 1.2× 1.6k 1.0× 651 0.8× 462 0.7× 85 8.6k
Kogo Takamiya United States 38 3.6k 0.7× 3.1k 0.9× 1.3k 0.8× 680 0.8× 779 1.2× 69 5.8k
Richard J. Reimer United States 31 3.9k 0.8× 3.2k 0.9× 918 0.6× 497 0.6× 868 1.3× 53 6.7k
Thomas W. Rosahl United States 28 3.7k 0.7× 2.9k 0.8× 1.1k 0.7× 471 0.6× 1.4k 2.1× 55 5.7k
Tak Pan Wong Canada 35 3.9k 0.8× 2.6k 0.7× 1.4k 0.8× 916 1.1× 518 0.8× 73 6.2k

Countries citing papers authored by Elek Molnár

Since Specialization
Citations

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

Fields of papers citing papers by Elek Molnár

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elek Molnár

This figure shows the co-authorship network connecting the top 25 collaborators of Elek Molnár. A scholar is included among the top collaborators of Elek Molnár 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 Elek Molnár. Elek Molnár 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.
Watts, W. E., John L. Crompton, Kate J. Heesom, et al.. (2025). Brief transcranial focused ultrasound stimulation causes lasting modifications to the synaptic circuitry of the hippocampus. Brain stimulation. 18(5). 1587–1599.
2.
Jepson, Mark A., Kate J. Heesom, Eunju Shin, et al.. (2023). Ultrasound modulates neuronal potassium currents via ionotropic glutamate receptors. Brain stimulation. 16(2). 540–552. 18 indexed citations
3.
Jane, David E., et al.. (2018). Assembly and Trafficking of Homomeric and Heteromeric Kainate Receptors with Impaired Ligand Binding Sites. Neurochemical Research. 44(3). 585–599. 5 indexed citations
4.
Rajatileka, Shavanthi, David Odd, Matthew T. Robinson, et al.. (2017). Variants of the EAAT2 Glutamate Transporter Gene Promoter Are Associated with Cerebral Palsy in Preterm Infants. Molecular Neurobiology. 55(3). 2013–2024. 16 indexed citations
5.
Borbély, Sándor, et al.. (2015). Repeated Application of 4-Aminopyridine Provoke an Increase in Entorhinal Cortex Excitability and Rearrange AMPA and Kainate Receptors. Neurotoxicity Research. 27(4). 441–452. 6 indexed citations
6.
Brozzi, Flora, Frédérique Diraison, Shavanthi Rajatileka, et al.. (2012). MyRIP interaction with MyoVa on secretory granules is controlled by the cAMP-PKA pathway. Molecular Biology of the Cell. 23(22). 4444–4455. 17 indexed citations
7.
Collingridge, Graham L., Arturas Volianskis, Neil Bannister, et al.. (2012). The NMDA receptor as a target for cognitive enhancement. Neuropharmacology. 64. 13–26. 188 indexed citations
8.
Fernández‐Alacid, Laura, Masahiko Watanabe, Elek Molnár, Kevin Wickman, & Rafael Luján. (2011). Developmental regulation of G protein‐gated inwardly‐rectifying K+(GIRK/Kir3) channel subunits in the brain. European Journal of Neuroscience. 34(11). 1724–1736. 60 indexed citations
9.
Jane, David E., et al.. (2010). Mapping the Ligand Binding Sites of Kainate Receptors: Molecular Determinants of Subunit-Selective Binding of the Antagonist [3H]UBP310. Molecular Pharmacology. 78(6). 1036–1045. 16 indexed citations
10.
Molnár, Elek, et al.. (2010). Assembly and intracellular distribution of kainate receptors is determined by RNA editing and subunit composition. Journal of Neurochemistry. 114(6). 1805–1818. 31 indexed citations
11.
Tarusawa, Etsuko, Ko Matsui, Timotheus Budisantoso, et al.. (2009). Input-Specific Intrasynaptic Arrangements of Ionotropic Glutamate Receptors and Their Impact on Postsynaptic Responses. Journal of Neuroscience. 29(41). 12896–12908. 92 indexed citations
12.
Molnár, Elek. (2008). Handbook of Neurochemistry and Molecular Neurobiology: Neurotransmitter Systems. Springer US. 18 indexed citations
13.
Masugi-Tokita, Miwako, Etsuko Tarusawa, Masahiko Watanabe, et al.. (2007). Number and Density of AMPA Receptors in Individual Synapses in the Rat Cerebellum as Revealed by SDS-Digested Freeze-Fracture Replica Labeling. Journal of Neuroscience. 27(8). 2135–2144. 137 indexed citations
14.
Molnár, Elek, et al.. (2007). Metabotropic glutamate receptor-mediated long-term depression involves AMPA receptor redistribution triggered by protein tyrosine phosphatases. Proceedings of The Physiological Society. 7 indexed citations
15.
Tanaka, Junichi, M Matsuzaki, Etsuko Tarusawa, et al.. (2005). Number and Density of AMPA Receptors in Single Synapses in Immature Cerebellum. Journal of Neuroscience. 25(4). 799–807. 131 indexed citations
16.
Luyt, Karen, Anikó Váradi, Christopher Halfpenny, Neil Scolding, & Elek Molnár. (2004). Metabotropic glutamate receptors are expressed in adult human glial progenitor cells. Biochemical and Biophysical Research Communications. 319(1). 120–129. 24 indexed citations
17.
Gallyas, Ferenc, et al.. (2003). Assembly and cell surface expression of KA‐2 subunit‐containing kainate receptors. Journal of Neurochemistry. 86(6). 1414–1427. 46 indexed citations
18.
Molnár, Elek, et al.. (1999). Alpha4 but not alpha3 nicotinic acetylcholine receptor subunits are lost from the temporal cortex in Alzheimer's disease. Fundamental and Clinical Pharmacology. 17 indexed citations
19.
Gurd, James W., Nankie Bissoon, Nicolas Tricaud, et al.. (1998). Identification of Lectin‐Purified Neural Glycoproteins, GPs 180, 116, and 110, with NMDA and AMPA Receptor Subunits: Conservation of Glycosylation at the Synapse. Journal of Neurochemistry. 70(6). 2594–2605. 51 indexed citations
20.
Nemcsók, J., et al.. (1992). Different sensitivity of the sarcoplasmic reticulum Ca2+-ATPase enzyme to fluorescein-isothiocyanate in rabbit and carp muscles. Comparative Biochemistry and Physiology Part B Comparative Biochemistry. 102(1). 19–23. 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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