László Siklós

3.8k total citations · 1 hit paper
48 papers, 3.1k citations indexed

About

László Siklós is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, László Siklós has authored 48 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Neurology, 16 papers in Cellular and Molecular Neuroscience and 15 papers in Molecular Biology. Recurrent topics in László Siklós's work include Amyotrophic Lateral Sclerosis Research (25 papers), Parkinson's Disease Mechanisms and Treatments (13 papers) and Neuroinflammation and Neurodegeneration Mechanisms (9 papers). László Siklós is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (25 papers), Parkinson's Disease Mechanisms and Treatments (13 papers) and Neuroinflammation and Neurodegeneration Mechanisms (9 papers). László Siklós collaborates with scholars based in Hungary, United States and Germany. László Siklós's co-authors include Stanley H. Appel, David R. Beers, Jenny S. Henkel, József I. Engelhardt, J. Engelhardt, Scott R. McKercher, Weihua Zhao, Qin Xiao, Jinghong Wang and Albert Yen and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Neurology.

In The Last Decade

László Siklós

47 papers receiving 3.0k citations

Hit Papers

Wild-type microglia extend survival in PU.1 knockout mice... 2006 2026 2012 2019 2006 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
László Siklós Hungary 27 1.7k 1.0k 905 759 603 48 3.1k
Makiko Nagai Japan 27 2.1k 1.2× 788 0.8× 1.2k 1.3× 1.0k 1.3× 803 1.3× 61 3.4k
Patricia Cassina Uruguay 28 1.3k 0.8× 711 0.7× 1.1k 1.3× 624 0.8× 641 1.1× 45 2.9k
Thomas Philips United States 11 1.6k 0.9× 693 0.7× 870 1.0× 858 1.1× 465 0.8× 15 2.5k
Carlos J. Miranda United States 19 1.2k 0.7× 675 0.7× 1.4k 1.5× 693 0.9× 754 1.3× 35 2.8k
Christelle Guégan France 21 1.3k 0.8× 612 0.6× 1.3k 1.4× 457 0.6× 813 1.3× 25 2.8k
Cédric Raoul France 28 1.2k 0.7× 359 0.4× 1.3k 1.4× 664 0.9× 688 1.1× 70 2.7k
Hidefumi Ito Japan 38 1.7k 1.0× 1.0k 1.0× 1.5k 1.6× 564 0.7× 838 1.4× 145 3.9k
Nadia D’Ambrosi Italy 32 757 0.4× 940 0.9× 1.0k 1.1× 280 0.4× 595 1.0× 56 3.2k
Smita Saxena Switzerland 22 1.4k 0.8× 366 0.4× 1.5k 1.7× 774 1.0× 1.1k 1.8× 40 3.6k
Genevíève Gowing United States 27 1.1k 0.6× 1.9k 1.9× 1.3k 1.4× 748 1.0× 881 1.5× 37 4.1k

Countries citing papers authored by László Siklós

Since Specialization
Citations

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

Fields of papers citing papers by László Siklós

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of László Siklós

This figure shows the co-authorship network connecting the top 25 collaborators of László Siklós. A scholar is included among the top collaborators of László Siklós 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 Siklós. László Siklós 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.
Polgár, Tamás F., et al.. (2025). Photobleaching alters the morphometric analysis of fluorescently labeled neurons and microglial cells. Pathology & Oncology Research. 31. 1612087–1612087.
2.
Mészáros, Mária, Lóránd Kiss, Zoltán Kóta, et al.. (2018). Niosomes decorated with dual ligands targeting brain endothelial transporters increase cargo penetration across the blood-brain barrier. European Journal of Pharmaceutical Sciences. 123. 228–240. 44 indexed citations
3.
Patai, Roland, Massimo Tortarolo, Caterina Bendotti, et al.. (2017). Presymptomatically applied AMPA receptor antagonist prevents calcium increase in vulnerable type of motor axon terminals of mice modeling amyotrophic lateral sclerosis. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1863(7). 1739–1748. 6 indexed citations
4.
Patai, Roland, et al.. (2016). Calcium in the pathomechanism of amyotrophic lateral sclerosis – Taking center stage?. Biochemical and Biophysical Research Communications. 483(4). 1031–1039. 17 indexed citations
5.
Baka, Judith, Nikoletta Dobos, László Siklós, et al.. (2016). Stress induces equivalent remodeling of hippocampal spine synapses in a simulated postpartum environment and in a female rat model of major depression. Neuroscience. 343. 384–397. 22 indexed citations
6.
Hoyk, Zsófia, et al.. (2014). Aromatase and estrogen receptor beta expression in the rat olfactory bulb: Neuroestrogen action in the first relay station of the olfactory pathway?. Acta Neurobiologiae Experimentalis. 74(1). 1–14. 15 indexed citations
7.
Tortarolo, Massimo, et al.. (2011). Talampanel reduces the level of motoneuronal calcium in transgenic mutant SOD1 mice only if applied presymptomatically. Amyotrophic Lateral Sclerosis. 12(5). 340–344. 29 indexed citations
8.
Engelhardt, József I., et al.. (2009). Hypoglossal motor neurons display a reduced calcium increase after axotomy in mice with upregulated parvalbumin. The Journal of Comparative Neurology. 518(11). 1946–1961. 8 indexed citations
9.
Hamar, J., et al.. (2006). Capsaicin delays regeneration of the neuromuscular junction of rat extensor digitorum longus muscle after ischemia. Muscle & Nerve. 33(4). 556–567. 1 indexed citations
10.
Smith, R G, et al.. (2005). Sublethal dose of 4-hydroxynonenal reduces intracellular calcium in surviving motor neurons in vivo. Acta Neuropathologica. 109(6). 567–575. 12 indexed citations
11.
Kim, Seung Hyun, Jenny S. Henkel, David R. Beers, et al.. (2003). PARP Expression Is Increased in Astrocytes but Decreased in Motor Neurons in the Spinal Cord of Sporadic ALS Patients. Journal of Neuropathology & Experimental Neurology. 62(1). 88–103. 48 indexed citations
12.
Henkel, Jenny S., J. Engelhardt, László Siklós, et al.. (2003). Presence of dendritic cells, MCP‐1, and activated microglia/macrophages in amyotrophic lateral sclerosis spinal cord tissue. Annals of Neurology. 55(2). 221–235. 439 indexed citations
13.
Adalbert, Róbert, József I. Engelhardt, & László Siklós. (2002). DL -Homocysteic acid application disrupts calcium homeostasis and induces degeneration of spinal motor neurons in vivo. Acta Neuropathologica. 103(5). 428–436. 30 indexed citations
14.
Mosier, Dennis R., László Siklós, Maria E. Alexianu, et al.. (2002). Immunoglobulin Fcγ receptor promotes immunoglobulin uptake, immunoglobulin‐mediated calcium increase, and neurotransmitter release in motor neurons. Journal of Neuroscience Research. 69(1). 110–116. 65 indexed citations
15.
Beers, David R., László Siklós, Maria E. Alexianu, et al.. (2001). Parvalbumin overexpression alters immune‐mediated increases in intracellular calcium, and delays disease onset in a transgenic model of familial amyotrophic lateral sclerosis. Journal of Neurochemistry. 79(3). 499–509. 134 indexed citations
16.
Siklós, László, József I. Engelhardt, Róbert Adalbert, & Stanley H. Appel. (1999). Calcium-containing endosomes at oculomotor terminals in animal models of ALS. Neuroreport. 10(12). 2539–2545. 9 indexed citations
17.
Engelhardt, József I., László Siklós, & Stanley H. Appel. (1997). Altered Calcium Homeostasis and Ultrastructure in Motoneurons of Mice Caused by Passively Transferred Anti-motoneuronal IgG. Journal of Neuropathology & Experimental Neurology. 56(1). 21–39. 32 indexed citations
18.
Siklós, László, József I. Engelhardt, Yadollah Harati, et al.. (1996). Ultrastructural evidence for altered calcium in motor nerve terminals in amyotrophc lateral sclerosis. Annals of Neurology. 39(2). 203–216. 246 indexed citations
20.
Wolff, Joachim, József Toldi, László Siklós, O. Fehér, & Ferenc Joó. (1992). Neonatal enucleation induces correlated modification in sensory responsive areas and pial angioarchitecture of the parietal and occipital cortex of albino rats. The Journal of Comparative Neurology. 317(2). 187–194. 11 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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