László Détári

2.3k total citations
48 papers, 1.8k citations indexed

About

László Détári is a scholar working on Cognitive Neuroscience, Cellular and Molecular Neuroscience and Endocrine and Autonomic Systems. According to data from OpenAlex, László Détári has authored 48 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Cognitive Neuroscience, 32 papers in Cellular and Molecular Neuroscience and 20 papers in Endocrine and Autonomic Systems. Recurrent topics in László Détári's work include Neuroscience and Neuropharmacology Research (23 papers), Sleep and Wakefulness Research (23 papers) and Circadian rhythm and melatonin (17 papers). László Détári is often cited by papers focused on Neuroscience and Neuropharmacology Research (23 papers), Sleep and Wakefulness Research (23 papers) and Circadian rhythm and melatonin (17 papers). László Détári collaborates with scholars based in Hungary, United States and Netherlands. László Détári's co-authors include Johanna H. Meijer, Tom Deboer, Jeroen Schaap, C.H. Vanderwolf, Douglas D. Rasmusson, Kazue Semba, H. Albus, Mariska J. Vansteensel, László Záborszky and T Kukorelli and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Neuroscience and Nature Neuroscience.

In The Last Decade

László Détári

48 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
László Détári Hungary 21 1.2k 1.0k 909 300 219 48 1.8k
Teresa L. Steininger United States 19 1.4k 1.1× 928 0.9× 1.2k 1.3× 601 2.0× 294 1.3× 37 2.3k
Romain Goutagny France 25 1.6k 1.3× 1.1k 1.0× 787 0.9× 351 1.2× 215 1.0× 37 2.1k
Lynda Mainville Canada 22 2.1k 1.7× 1.5k 1.5× 1.1k 1.3× 543 1.8× 388 1.8× 24 2.8k
Kristi A. Kohlmeier Denmark 21 974 0.8× 606 0.6× 781 0.9× 566 1.9× 398 1.8× 104 1.8k
Birendra Nath Mallick India 31 2.0k 1.6× 1.2k 1.2× 1.0k 1.1× 777 2.6× 392 1.8× 116 2.7k
Glenda C. Harris United States 12 1.5k 1.2× 1.0k 1.0× 1.2k 1.3× 717 2.4× 450 2.1× 17 2.4k
Pablo Torterolo Uruguay 28 1.6k 1.3× 567 0.5× 1.1k 1.2× 515 1.7× 112 0.5× 128 2.1k
William J. Giardino United States 16 705 0.6× 625 0.6× 526 0.6× 307 1.0× 294 1.3× 28 1.4k
Stephen R. Morairty United States 20 1.1k 0.8× 663 0.6× 820 0.9× 652 2.2× 415 1.9× 34 1.7k
N. Upton United Kingdom 24 826 0.7× 916 0.9× 758 0.8× 452 1.5× 492 2.2× 38 2.2k

Countries citing papers authored by László Détári

Since Specialization
Citations

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

Fields of papers citing papers by László Détári

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of László Détári

This figure shows the co-authorship network connecting the top 25 collaborators of László Détári. A scholar is included among the top collaborators of László Détári 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 László Détári. László Détári 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.
Tóth, Attila, et al.. (2024). Sleep and local field potential effect of the D2 receptor agonist bromocriptine during the estrus cycle and postpartum period in female rats. Pharmacology Biochemistry and Behavior. 239. 173754–173754. 2 indexed citations
2.
3.
Borbély, Sándor, et al.. (2017). Sleep deprivation decreases neuronal excitability and responsiveness in rats both in vivo and ex vivo. Brain Research Bulletin. 137. 166–177. 18 indexed citations
4.
Tóth, Attila, et al.. (2016). Sleep loss and recovery after administration of drugs related to different arousal systems in rats. Physiology International. 103(3). 271–289. 7 indexed citations
5.
Tóth, Attila, et al.. (2013). Characteristic changes in the slow cortical waves after a 6-h sleep deprivation in rat. Brain Research. 1501. 1–11. 15 indexed citations
6.
Tóth, Attila, et al.. (2011). Cholinergic modulation of slow cortical rhythm in urethane-anesthetized rats. Brain Research Bulletin. 87(1). 117–129. 9 indexed citations
7.
Tóth, Attila, et al.. (2007). Effect of basal forebrain neuropeptide Y administration on sleep and spontaneous behavior in freely moving rats. Brain Research Bulletin. 72(4-6). 293–301. 31 indexed citations
8.
Balatoni, Balázs, et al.. (2006). Effect of cortical spreading depression on basal forebrain neurons. Experimental Brain Research. 169(2). 261–265. 5 indexed citations
9.
Borbély, Sándor, Katalin Halasy, Zoltán Somogyvári, László Détári, & Ildikó Világi. (2005). Laminar analysis of initiation and spread of epileptiform discharges in three in vitro models. Brain Research Bulletin. 69(2). 161–167. 17 indexed citations
10.
Borbély, Sándor, Ildikó Világi, László Détári, et al.. (2005). Lateral entorhinal cortex lesions rearrange afferents, glutamate receptors, increase seizure latency and suppress seizure‐induced c‐fosexpression in the hippocampus of adult rat. Journal of Neurochemistry. 95(1). 111–124. 24 indexed citations
11.
Schaap, Jeroen, H. Albus, Henk Tjebbe vanderLeest, et al.. (2003). Heterogeneity of rhythmic suprachiasmatic nucleus neurons: Implications for circadian waveform and photoperiodic encoding. Proceedings of the National Academy of Sciences. 100(26). 15994–15999. 172 indexed citations
12.
Deboer, Tom, Mariska J. Vansteensel, László Détári, & Johanna H. Meijer. (2003). Sleep states alter activity of suprachiasmatic nucleus neurons. Nature Neuroscience. 6(10). 1086–1090. 242 indexed citations
13.
Dóczi, Judit, Hana Kubová, László Détári, et al.. (2003). Long-term changes of activity of cortical neurons after status epilepticus induced at early developmental stages in rats. Neuroscience Letters. 352(2). 125–128. 4 indexed citations
14.
Détári, László, et al.. (2002). Nerve conduction velocity and spinal reflexes may change in rats after fumonisin B1exposure. Acta Biologica Hungarica. 53(4). 413–422. 7 indexed citations
15.
Gulyás-Kovács, Attila, et al.. (2002). Comparison of spontaneous and evoked epileptiform activity in three in vitro epilepsy models. Brain Research. 945(2). 174–180. 35 indexed citations
16.
Duque, Alvaro, Balázs Balatoni, László Détári, & László Záborszky. (2000). EEG Correlation of the Discharge Properties of Identified Neurons in the Basal Forebrain. Journal of Neurophysiology. 84(3). 1627–1635. 135 indexed citations
17.
Détári, László, Douglas D. Rasmusson, & Kazue Semba. (1997). Phasic relationship between the activity of basal forebrain neurons and cortical EEG in urethane-anesthetized rat. Brain Research. 759(1). 112–121. 45 indexed citations
18.
Meijer, Johanna H., Kazuto Watanabe, László Détári, et al.. (1996). Chapter 12 Light entrainment of the mammalian biological clock. Progress in brain research. 111. 175–190. 13 indexed citations
19.
Meijer, Johanna H., Kazuto Watanabe, László Détári, & Jeroen Schaap. (1996). Circadian rhythm in light response in suprachiasmatic nucleus neurons of freely moving rats. Brain Research. 741(1-2). 352–355. 39 indexed citations
20.
Kukorelli, T, et al.. (1986). Effect of glutaurine on sleep-wakefulness cycle and aggressive behaviour in the cat.. PubMed. 67(1). 31–5. 7 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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