Kent Jardemark

1.5k total citations
49 papers, 1.1k citations indexed

About

Kent Jardemark is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Kent Jardemark has authored 49 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Cellular and Molecular Neuroscience, 26 papers in Molecular Biology and 12 papers in Psychiatry and Mental health. Recurrent topics in Kent Jardemark's work include Neuroscience and Neuropharmacology Research (23 papers), Neurotransmitter Receptor Influence on Behavior (17 papers) and Ion channel regulation and function (12 papers). Kent Jardemark is often cited by papers focused on Neuroscience and Neuropharmacology Research (23 papers), Neurotransmitter Receptor Influence on Behavior (17 papers) and Ion channel regulation and function (12 papers). Kent Jardemark collaborates with scholars based in Sweden, United States and Denmark. Kent Jardemark's co-authors include Torgny H. Svensson, Monica M. Marcus, Owe Orwar, Åsa Konradsson‐Geuken, Björn Schilström, Ipe Ninan, Ingemar Jacobson, Carl Björkholm, Rex Y. Wang and Xavier Langlois and has published in prestigious journals such as Science, Journal of the American Chemical Society and SHILAP Revista de lepidopterología.

In The Last Decade

Kent Jardemark

47 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kent Jardemark Sweden 21 578 392 239 184 158 49 1.1k
Sandrine Parrot France 23 491 0.8× 454 1.2× 84 0.4× 292 1.6× 36 0.2× 50 1.5k
Gill Anlezark United Kingdom 17 631 1.1× 361 0.9× 328 1.4× 68 0.4× 17 0.1× 29 1.2k
Gabriel M. Belfort United States 11 1.0k 1.8× 433 1.1× 49 0.2× 139 0.8× 81 0.5× 14 1.5k
Richard T. Layer United States 22 1.3k 2.2× 859 2.2× 128 0.5× 36 0.2× 352 2.2× 33 2.0k
Víctor Fernández‐Dueñas Spain 29 1.0k 1.8× 1.2k 3.1× 130 0.5× 42 0.2× 76 0.5× 82 2.2k
Chun-Lei Zhang China 19 494 0.9× 443 1.1× 69 0.3× 65 0.4× 51 0.3× 40 1.2k
I.A. Paterson Canada 25 1.0k 1.8× 594 1.5× 131 0.5× 10 0.1× 109 0.7× 48 1.8k
Leonard T. Meltzer United States 26 1.3k 2.2× 910 2.3× 158 0.7× 22 0.1× 57 0.4× 83 2.5k
Andrea Barberis Italy 25 1.2k 2.1× 819 2.1× 49 0.2× 137 0.7× 25 0.2× 48 1.8k
Jerzy Michaluk Poland 21 801 1.4× 439 1.1× 125 0.5× 11 0.1× 81 0.5× 76 1.3k

Countries citing papers authored by Kent Jardemark

Since Specialization
Citations

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

Fields of papers citing papers by Kent Jardemark

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kent Jardemark

This figure shows the co-authorship network connecting the top 25 collaborators of Kent Jardemark. A scholar is included among the top collaborators of Kent Jardemark 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 Kent Jardemark. Kent Jardemark 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.
Orhan, Funda, Neda Khanlarkhani, Marja Koskuvi, et al.. (2025). Kynurenic Acid and Promotion of Activity-Dependent Synapse Elimination in Schizophrenia. American Journal of Psychiatry. 182(4). 389–400.
2.
Fukutani, Atsuki, Håkan Westerblad, Kent Jardemark, & Joseph D. Bruton. (2024). Ca2+ and force during dynamic contractions in mouse intact skeletal muscle fibers. Scientific Reports. 14(1). 689–689. 2 indexed citations
3.
Youhanna, Sonia, Joseph D. Bruton, Kent Jardemark, Håkan Westerblad, & Volker M. Lauschke. (2023). Calcium measurements in enzymatically dissociated or mechanically microdissected mouse primary skeletal muscle fibers. STAR Protocols. 4(2). 102260–102260. 1 indexed citations
4.
Dutheil, Sophie, et al.. (2022). Lumateperone-mediated effects on prefrontal glutamatergic receptor-mediated neurotransmission: A dopamine D1 receptor dependent mechanism. European Neuropsychopharmacology. 62. 22–35. 27 indexed citations
5.
Ainla, Alar, et al.. (2014). A Multifunctional Pipette for Localized Drug Administration to Brain Slices. Biophysical Journal. 106(2). 191a–191a. 5 indexed citations
6.
Xu, Shijun, Alar Ainla, Kent Jardemark, Aldo Jesorka, & Gavin D. M. Jeffries. (2014). A Heating-Superfusion Platform Technology for the Investigation of Protein Function in Single Cells. Analytical Chemistry. 87(1). 381–387. 7 indexed citations
7.
Björkholm, Carl, Monica M. Marcus, Åsa Konradsson‐Geuken, et al.. (2014). Adjunctive Treatment with Asenapine Augments the Escitalopram-Induced Effects on Monoaminergic Outflow and Glutamatergic Neurotransmission in the Medial Prefrontal Cortex of the Rat. The International Journal of Neuropsychopharmacology. 18(3). pyu068–pyu068. 12 indexed citations
8.
Jansson, Erik T., et al.. (2013). Effect of Cholesterol Depletion on the Pore Dilation of TRPV1. Molecular Pain. 9. 61 indexed citations
9.
Ainla, Alar, Gavin D. M. Jeffries, Holger Wigström, et al.. (2013). A multifunctional pipette for localized drug administration to brain slices. Journal of Neuroscience Methods. 219(2). 292–296. 11 indexed citations
10.
Jansson, Erik T., et al.. (2012). Effect of Cholesterol on the Pore Dilation of TRPV1. Biophysical Journal. 102(3). 342a–342a. 1 indexed citations
11.
Björkholm, Carl, Kent Jardemark, Monica M. Marcus, et al.. (2012). Role of concomitant inhibition of the norepinephrine transporter for the antipsychotic effect of quetiapine. European Neuropsychopharmacology. 23(7). 709–720. 21 indexed citations
13.
Marcus, Monica M., et al.. (2010). Reboxetine Enhances the Olanzapine-Induced Antipsychotic-Like Effect, Cortical Dopamine Outflow and NMDA Receptor-Mediated Transmission. Neuropsychopharmacology. 35(9). 1952–1961. 14 indexed citations
14.
Jardemark, Kent, Åsa Konradsson‐Geuken, Björn Schilström, Monica M. Marcus, & Torgny H. Svensson. (2009). Differential effects of topiramate on prefrontal glutamatergic transmission when combined with raclopride or clozapine. Synapse. 63(10). 913–920. 5 indexed citations
15.
Jardemark, Kent, Monica M. Marcus, Åsa Konradsson‐Geuken, & Torgny H. Svensson. (2005). The combination of nicotine with the D2 antagonist raclopride or the weak D4 antagonist L-745,870 generates a clozapine-like facilitation of NMDA receptor-mediated neurotransmission in pyramidal cells of the rat medial prefrontal cortex. The International Journal of Neuropsychopharmacology. 8(2). 157–162. 12 indexed citations
16.
Marcus, Monica M., et al.. (2005). Combined α2 and D2/3 receptor blockade enhances cortical glutamatergic transmission and reverses cognitive impairment in the rat. The International Journal of Neuropsychopharmacology. 8(3). 315–327. 71 indexed citations
17.
Schilström, Björn, et al.. (2004). Nitric oxide is involved in nicotine-induced burst firing of rat ventral tegmental area dopamine neurons. Neuroscience. 125(4). 957–964. 41 indexed citations
20.
Ryttsén, Frida, Cecilia Farre, Stephen G. Weber, et al.. (2000). Characterization of Single-Cell Electroporation by Using Patch-Clamp and Fluorescence Microscopy. Biophysical Journal. 79(4). 1993–2001. 84 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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