Éva M. Szegő

2.9k total citations
38 papers, 1.8k citations indexed

About

Éva M. Szegő is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Éva M. Szegő has authored 38 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Cellular and Molecular Neuroscience, 18 papers in Neurology and 12 papers in Molecular Biology. Recurrent topics in Éva M. Szegő's work include Parkinson's Disease Mechanisms and Treatments (18 papers), Nerve injury and regeneration (9 papers) and Estrogen and related hormone effects (6 papers). Éva M. Szegő is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (18 papers), Nerve injury and regeneration (9 papers) and Estrogen and related hormone effects (6 papers). Éva M. Szegő collaborates with scholars based in Germany, Hungary and United Kingdom. Éva M. Szegő's co-authors include Tiago F. Outeiro, Ellen Gerhardt, Gábor Juhász, István M. Ábrahám, Paul Lingor, Mathias Bähr, Lars Tönges, Jan Christoph Koch, Lars Tatenhorst and Klaudia Barabás and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Journal of Neuroscience.

In The Last Decade

Éva M. Szegő

36 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Éva M. Szegő Germany 22 670 578 512 480 302 38 1.8k
Rita M. Cowell United States 30 1.0k 1.5× 669 1.2× 822 1.6× 622 1.3× 588 1.9× 59 2.5k
Susan C. Su United States 14 1.8k 2.6× 250 0.4× 640 1.3× 594 1.2× 226 0.7× 15 2.7k
Merina Varghese United States 23 707 1.1× 266 0.5× 351 0.7× 472 1.0× 243 0.8× 51 1.8k
Christian Néri France 28 1.8k 2.7× 345 0.6× 1.0k 2.0× 628 1.3× 158 0.5× 71 3.1k
Selma Kanazir Serbia 25 909 1.4× 185 0.3× 667 1.3× 506 1.1× 261 0.9× 87 2.2k
Marta Barrachina Spain 30 1.3k 1.9× 720 1.2× 651 1.3× 706 1.5× 484 1.6× 45 2.8k
Iddo Magen Israel 24 598 0.9× 840 1.5× 617 1.2× 402 0.8× 215 0.7× 38 2.0k
Shawn Hayley Canada 18 664 1.0× 721 1.2× 712 1.4× 290 0.6× 327 1.1× 30 1.8k
Francesca L’Episcopo Italy 23 951 1.4× 526 0.9× 850 1.7× 204 0.4× 449 1.5× 29 2.0k
Kengo Uemura Japan 31 911 1.4× 312 0.5× 559 1.1× 979 2.0× 329 1.1× 58 2.1k

Countries citing papers authored by Éva M. Szegő

Since Specialization
Citations

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

Fields of papers citing papers by Éva M. Szegő

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Éva M. Szegő. 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 Éva M. Szegő. The network helps show where Éva M. Szegő may publish in the future.

Co-authorship network of co-authors of Éva M. Szegő

This figure shows the co-authorship network connecting the top 25 collaborators of Éva M. Szegő. A scholar is included among the top collaborators of Éva M. Szegő 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 Éva M. Szegő. Éva M. Szegő 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.
Szegő, Éva M., Anna Antoniou, Elisabeth Dinter, et al.. (2025). Intermittent fasting reduces alpha-synuclein pathology and functional decline in a mouse model of Parkinson’s disease. Nature Communications. 16(1). 4470–4470. 1 indexed citations
2.
Luksch, Hella, David Sprott, Éva M. Szegő, et al.. (2025). Tissue inflammation induced by constitutively active STING is mediated by enhanced TNF signaling. eLife. 14.
3.
Szegő, Éva M., et al.. (2024). Evaluation of the Effect of β-Wrapin AS69 in a Mouse Model Based on Alpha-Synuclein Overexpression. Biomolecules. 14(7). 756–756. 1 indexed citations
4.
Vitola, Pietro La, Éva M. Szegő, Rita Pinto‐Costa, et al.. (2024). Mitochondrial oxidant stress promotes α-synuclein aggregation and spreading in mice with mutated glucocerebrosidase. npj Parkinson s Disease. 10(1). 233–233. 5 indexed citations
5.
6.
Szegő, Éva M., et al.. (2021). Maturing Autophagosomes are Transported Towards the Cell Periphery. Cellular and Molecular Neurobiology. 42(1). 155–171. 12 indexed citations
7.
Szegő, Éva M., et al.. (2021). Rab7 reduces α-synuclein toxicity in rats and primary neurons. Experimental Neurology. 347. 113900–113900. 14 indexed citations
8.
Szegő, Éva M., Andrei Leonov, Eva Benito, et al.. (2019). Translocator Protein Ligand Protects against Neurodegeneration in the MPTP Mouse Model of Parkinsonism. Journal of Neuroscience. 39(19). 3752–3769. 55 indexed citations
9.
Paiva, Isabel, Gaurav Jain, Diana F. Lázaro, et al.. (2018). Alpha-synuclein deregulates the expression of COL4A2 and impairs ER-Golgi function. Neurobiology of Disease. 119. 121–135. 46 indexed citations
10.
Paiva, Isabel, Raquel Pinho, Maria Angeliki S. Pavlou, et al.. (2017). Sodium butyrate rescues dopaminergic cells from alpha-synuclein-induced transcriptional deregulation and DNA damage. Human Molecular Genetics. 26(12). 2231–2246. 138 indexed citations
11.
Lemos, Vera, Rita Machado de Oliveira, Luana Naia, et al.. (2017). The NAD+-dependent deacetylase SIRT2 attenuates oxidative stress and mitochondrial dysfunction and improves insulin sensitivity in hepatocytes. Human Molecular Genetics. 26(21). 4105–4117. 71 indexed citations
12.
Tatenhorst, Lars, Lars Tönges, Kim‐Ann Saal, et al.. (2014). Rho Kinase Inhibition by Fasudil in the Striatal 6-Hydroxydopamine Lesion Mouse Model of Parkinson Disease. Journal of Neuropathology & Experimental Neurology. 73(8). 770–779. 45 indexed citations
13.
Yin, Guowei, Tomás Lopes da Fonseca, Ane Martín Anduaga, et al.. (2014). α-Synuclein interacts with the switch region of Rab8a in a Ser129 phosphorylation-dependent manner. Neurobiology of Disease. 70. 149–161. 77 indexed citations
14.
Saal, Kim‐Ann, Jan Christoph Koch, Lars Tatenhorst, et al.. (2014). AAV.shRNA-mediated downregulation of ROCK2 attenuates degeneration of dopaminergic neurons in toxin-induced models of Parkinson's disease in vitro and in vivo. Neurobiology of Disease. 73. 150–162. 55 indexed citations
15.
Szegő, Éva M., Tiago F. Outeiro, Pawel Kermer, & Jörg B. Schulz. (2012). Impairment of the septal cholinergic neurons in MPTP-treated A30P α-synuclein mice. Neurobiology of Aging. 34(2). 589–601. 14 indexed citations
16.
Gerhardt, Ellen, Éva M. Szegő, Nicoleta Moisoi, et al.. (2011). Idebenone and Resveratrol Extend Lifespan and Improve Motor Function of HtrA2 Knockout Mice. PLoS ONE. 6(12). e28855–e28855. 40 indexed citations
17.
Sárvári, Miklós, Éva M. Szegő, Klaudia Barabás, et al.. (2009). Genistein Induces Phosphorylation of cAMP Response Element‐binding Protein in Neonatal Hypothalamus In Vivo. Journal of Neuroendocrinology. 21(12). 1024–1028. 7 indexed citations
18.
Ábrahám, István M., et al.. (2009). Action of estrogen on survival of basal forebrain cholinergic neurons: Promoting amelioration. Psychoneuroendocrinology. 34. S104–S112. 26 indexed citations
19.
Szegő, Éva M., Klaudia Barabás, Júlia Balog, et al.. (2006). Estrogen Induces Estrogen Receptor α-Dependent cAMP Response Element-Binding Protein Phosphorylation via Mitogen Activated Protein Kinase Pathway in Basal Forebrain Cholinergic NeuronsIn Vivo. Journal of Neuroscience. 26(15). 4104–4110. 103 indexed citations
20.
Kovács, Zsolt, Katalin A. Kékesi, Nóra Szilágyi, et al.. (2006). Facilitation of spike-wave discharge activity by lipopolysaccharides in Wistar Albino Glaxo/Rijswijk rats. Neuroscience. 140(2). 731–742. 62 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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