Lesley Probert

9.3k total citations · 1 hit paper
101 papers, 7.4k citations indexed

About

Lesley Probert is a scholar working on Immunology, Molecular Biology and Neurology. According to data from OpenAlex, Lesley Probert has authored 101 papers receiving a total of 7.4k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Immunology, 30 papers in Molecular Biology and 26 papers in Neurology. Recurrent topics in Lesley Probert's work include Neuroinflammation and Neurodegeneration Mechanisms (26 papers), Immune Response and Inflammation (21 papers) and Multiple Sclerosis Research Studies (18 papers). Lesley Probert is often cited by papers focused on Neuroinflammation and Neurodegeneration Mechanisms (26 papers), Immune Response and Inflammation (21 papers) and Multiple Sclerosis Research Studies (18 papers). Lesley Probert collaborates with scholars based in Greece, United Kingdom and United States. Lesley Probert's co-authors include George Kollias, Katerina Akassoglou, D Kioussis, Spiros Georgopoulos, Manolis Pasparakis, George Kontogeorgos, Hans Lassmann, George Kassiotis, Era Taoufik and Vivian Tseveleki and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Journal of Experimental Medicine.

In The Last Decade

Lesley Probert

100 papers receiving 7.3k citations

Hit Papers

Transgenic mice expressing human tumour necrosis factor: ... 1991 2026 2002 2014 1991 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lesley Probert Greece 44 2.3k 2.2k 1.3k 1.3k 1.2k 101 7.4k
Neil Scolding United Kingdom 52 1.3k 0.6× 2.2k 1.0× 1.2k 0.9× 897 0.7× 665 0.6× 218 7.9k
Mohsen Khademi Sweden 47 2.5k 1.1× 1.7k 0.8× 901 0.7× 825 0.6× 1.0k 0.9× 130 6.7k
Oded Abramsky Israel 49 1.7k 0.7× 1.8k 0.8× 896 0.7× 893 0.7× 654 0.6× 197 8.0k
Jia Newcombe United Kingdom 56 3.2k 1.4× 2.7k 1.2× 2.4k 1.8× 650 0.5× 1.3k 1.1× 102 9.6k
Rhonda R. Voskuhl United States 53 3.6k 1.6× 1.5k 0.7× 1.7k 1.3× 1.1k 0.9× 1.2k 1.0× 117 9.0k
Masahide Asano Japan 56 3.8k 1.7× 4.8k 2.2× 966 0.7× 590 0.5× 1.4k 1.2× 169 11.0k
Klaus V. Toyka Germany 50 1.8k 0.8× 2.1k 0.9× 1.3k 1.0× 534 0.4× 755 0.6× 144 8.7k
Martin Stangel Germany 50 1.9k 0.8× 2.3k 1.0× 2.5k 2.0× 585 0.5× 889 0.8× 283 9.1k
M. L. Cuzner United Kingdom 52 2.7k 1.2× 2.7k 1.2× 2.6k 2.1× 575 0.4× 1.1k 1.0× 133 9.2k
Christine D. Dijkstra Netherlands 55 4.0k 1.8× 2.6k 1.2× 2.6k 2.0× 492 0.4× 1.0k 0.9× 132 9.7k

Countries citing papers authored by Lesley Probert

Since Specialization
Citations

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

Fields of papers citing papers by Lesley Probert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lesley Probert

This figure shows the co-authorship network connecting the top 25 collaborators of Lesley Probert. A scholar is included among the top collaborators of Lesley Probert 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 Lesley Probert. Lesley Probert 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.
Papadopoulos, Dimitrios, Roberta Magliozzi, Lesley Probert, et al.. (2025). Accelerated Cellular Senescence in Progressive Multiple Sclerosis: A Histopathological Study. Annals of Neurology. 97(6). 1074–1087. 3 indexed citations
3.
Boziki, Marina, Charis Styliadis, Christos Bakirtzis, et al.. (2021). A National Representative, Cross-Sectional Study by the Hellenic Academy of NeuroImmunology (HEL.A.NI.) on COVID-19 and Multiple Sclerosis: Overall Impact and Willingness Toward Vaccination. Frontiers in Neurology. 12. 757038–757038. 5 indexed citations
4.
Swanson, Kathryn A., et al.. (2020). Inflammation and Oxidative Stress in Multiple Sclerosis: Consequences for Therapy Development. Oxidative Medicine and Cellular Longevity. 2020. 1–19. 117 indexed citations
5.
Probert, Lesley, et al.. (2020). Characterization of Asparagine Deamidation in Immunodominant Myelin Oligodendrocyte Glycoprotein Peptide Potential Immunotherapy for the Treatment of Multiple Sclerosis. International Journal of Molecular Sciences. 21(20). 7566–7566. 6 indexed citations
6.
Probert, Lesley. (2015). TNF and its receptors in the CNS: The essential, the desirable and the deleterious effects. Neuroscience. 302. 2–22. 370 indexed citations
7.
Tseveleki, Vivian, Theodore Tselios, Olga S. Koutsoni, et al.. (2014). Mannan-conjugated myelin peptides prime non-pathogenic Th1 and Th17 cells and ameliorate experimental autoimmune encephalomyelitis. Experimental Neurology. 267. 254–267. 29 indexed citations
8.
Tseveleki, Vivian, Renee Rubio, Sotirios–Spyridon Vamvakas, et al.. (2010). Comparative gene expression analysis in mouse models for multiple sclerosis, Alzheimer's disease and stroke for identifying commonly regulated and disease-specific gene changes. Genomics. 96(2). 82–91. 69 indexed citations
9.
Taoufik, Era, Vivian Tseveleki, Sotirios–Spyridon Vamvakas, et al.. (2009). Neuronal IκB Kinase β Protects Mice from Autoimmune Encephalomyelitis by Mediating Neuroprotective and Immunosuppressive Effects in the Central Nervous System. The Journal of Immunology. 183(12). 7877–7889. 28 indexed citations
10.
Quinones, Marlon P., Yogeshwar Kalkonde, Carlos A. Estrada, et al.. (2007). Role of astrocytes and chemokine systems in acute TNFα induced demyelinating syndrome: CCR2-dependent signals promote astrocyte activation and survival via NF-κB and Akt. Molecular and Cellular Neuroscience. 37(1). 96–109. 47 indexed citations
11.
Mastronardi, Fabrizio G., D. D. Wood, Mei Jiang, et al.. (2006). Increased Citrullination of Histone H3 in Multiple Sclerosis Brain and Animal Models of Demyelination: A Role for Tumor Necrosis Factor-Induced Peptidylarginine Deiminase 4 Translocation. Journal of Neuroscience. 26(44). 11387–11396. 188 indexed citations
12.
Akassoglou, Katerina, Eleni Douni, Jan Bauer, et al.. (2003). Exclusive tumor necrosis factor (TNF) signaling by the p75TNF receptor triggers inflammatory ischemia in the CNS of transgenic mice. Proceedings of the National Academy of Sciences. 100(2). 709–714. 70 indexed citations
13.
Tselios, Theodore, Ioanna Daliani, Lesley Probert, et al.. (2000). Treatment of experimental allergic encephalomyelitis (EAE) induced by guinea pig myelin basic protein epitope 72–85 with a Human MBP87–99 analogue and effects of cyclic peptides. Bioorganic & Medicinal Chemistry. 8(8). 1903–1909. 32 indexed citations
14.
Kassiotis, George, Jan Bauer, Katerina Akassoglou, et al.. (1999). A tumor necrosis factor-induced model of human primary demyelinating diseases develops in immunodeficient mice. European Journal of Immunology. 29(3). 912–917. 32 indexed citations
15.
Kassiotis, George, Jan Bauer, Katerina Akassoglou, et al.. (1999). A tumor necrosis factor-induced model of human primary demyelinating diseases develops in immunodeficient mice. European Journal of Immunology. 29(3). 912–917. 2 indexed citations
16.
Kassiotis, George, Manolis Pasparakis, George Kollias, & Lesley Probert. (1999). TNF accelerates the onset but does not alter the incidence and severity of myelin basic protein-induced experimental autoimmune encephalomyelitis. European Journal of Immunology. 29(3). 774–780. 82 indexed citations
17.
Fiore, Marco, Enrico Alleva, Lesley Probert, et al.. (1998). Exploratory and Displacement Behavior in Transgenic Mice Expressing High Levels of Brain TNF-α. Physiology & Behavior. 63(4). 571–576. 46 indexed citations
18.
Cope, Andrew P., Roland Liblau, Xiaodong Yang, et al.. (1997). Chronic Tumor Necrosis Factor Alters T Cell Responses by Attenuating T Cell Receptor Signaling. The Journal of Experimental Medicine. 185(9). 1573–1584. 259 indexed citations
19.
Akassoglou, Katerina, Lesley Probert, George Kontogeorgos, & George Kollias. (1997). Astrocyte-specific but not neuron-specific transmembrane TNF triggers inflammation and degeneration in the central nervous system of transgenic mice. The Journal of Immunology. 158(1). 438–445. 217 indexed citations
20.
Terenghi, G., J. M. Polak, Lesley Probert, et al.. (1982). Mapping, quantitative distribution and origin of substance P- and VIP-containing nerves in the Uvea of guinea pig eye. Histochemistry. 75(3). 399–417. 89 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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