Sylva Haralambous

1.1k total citations
19 papers, 943 citations indexed

About

Sylva Haralambous is a scholar working on Oncology, Immunology and Molecular Biology. According to data from OpenAlex, Sylva Haralambous has authored 19 papers receiving a total of 943 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Oncology, 7 papers in Immunology and 5 papers in Molecular Biology. Recurrent topics in Sylva Haralambous's work include Cytokine Signaling Pathways and Interactions (5 papers), Multiple Sclerosis Research Studies (4 papers) and Immunotherapy and Immune Responses (4 papers). Sylva Haralambous is often cited by papers focused on Cytokine Signaling Pathways and Interactions (5 papers), Multiple Sclerosis Research Studies (4 papers) and Immunotherapy and Immune Responses (4 papers). Sylva Haralambous collaborates with scholars based in Greece, Germany and France. Sylva Haralambous's co-authors include George Kollias, Manolis Pasparakis, Lena Alexopoulou, Markus F. Neurath, Ivan J. Fuss, Warren Strober, Karl‐Hermann Meyer zum Büschenfelde, Eleni Douni, Lesley Probert and Era Taoufik and has published in prestigious journals such as The Journal of Immunology, European Journal of Immunology and Journal of Leukocyte Biology.

In The Last Decade

Sylva Haralambous

19 papers receiving 917 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sylva Haralambous Greece 13 350 258 193 188 178 19 943
M. Zaeem Cader United Kingdom 9 365 1.0× 296 1.1× 218 1.1× 169 0.9× 75 0.4× 13 883
Timothy P. LaBranche United States 13 340 1.0× 237 0.9× 280 1.5× 115 0.6× 238 1.3× 19 991
Eva Reali Italy 21 837 2.4× 295 1.1× 137 0.7× 98 0.5× 212 1.2× 50 1.2k
Lina Olsson Sweden 19 809 2.3× 436 1.7× 296 1.5× 188 1.0× 202 1.1× 34 1.4k
Kazuhiko Yamamura Japan 23 475 1.4× 595 2.3× 229 1.2× 200 1.1× 196 1.1× 52 1.7k
Mika Nishihara Japan 7 522 1.5× 292 1.1× 124 0.6× 63 0.3× 246 1.4× 9 996
Yasuto Araki Japan 15 683 2.0× 590 2.3× 253 1.3× 100 0.5× 298 1.7× 31 1.4k
Kouji Matsushima Japan 16 447 1.3× 333 1.3× 104 0.5× 78 0.4× 282 1.6× 21 1.1k
So‐Hee Hong South Korea 18 249 0.7× 381 1.5× 94 0.5× 101 0.5× 118 0.7× 50 931
Kary A. Latham United States 7 522 1.5× 494 1.9× 482 2.5× 80 0.4× 259 1.5× 7 1.4k

Countries citing papers authored by Sylva Haralambous

Since Specialization
Citations

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

Fields of papers citing papers by Sylva Haralambous

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sylva Haralambous

This figure shows the co-authorship network connecting the top 25 collaborators of Sylva Haralambous. A scholar is included among the top collaborators of Sylva Haralambous 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 Sylva Haralambous. Sylva Haralambous is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Grivas, Ioannis, Fabiola Sesti, Era Taoufik, et al.. (2021). Clusterin overexpression in mice exacerbates diabetic phenotypes but suppresses tumor progression in a mouse melanoma model. Aging. 13(5). 6485–6505. 3 indexed citations
2.
Thireou, Trias, Ioannis Grivas, Sylva Haralambous, et al.. (2019). Mapping Interactome Networks of DNAJC11, a Novel Mitochondrial Protein Causing Neuromuscular Pathology in Mice. Journal of Proteome Research. 18(11). 3896–3912. 7 indexed citations
3.
Samara, Pinelopi, Kyriaki Ioannou, Ioannis V. Kostopoulos, et al.. (2019). Antitumor Reactive T-Cell Responses Are Enhanced In Vivo by DAMP Prothymosin Alpha and Its C-Terminal Decapeptide. Cancers. 11(11). 1764–1764. 8 indexed citations
4.
Papazafiri, Panagiota, et al.. (2017). Oxygen and Glucose Deprivation Alter Synaptic Distribution of Tau Protein: The Role of Phosphorylation. Journal of Alzheimer s Disease. 60(2). 593–604. 3 indexed citations
5.
Haralambous, Sylva, et al.. (2016). IFN-β differentially regulates the function of T cell subsets in MS and EAE. Cytokine & Growth Factor Reviews. 30. 47–54. 12 indexed citations
6.
Alé, Albert, Jordi Bruna, Μαρία Καραμίτα, et al.. (2016). Inhibition of the neuronal NFκB pathway attenuates bortezomib-induced neuropathy in a mouse model. NeuroToxicology. 55. 58–64. 21 indexed citations
7.
Evangelidou, Maria, et al.. (2015). IFNAR signaling directly modulates T lymphocyte activity, resulting in milder experimental autoimmune encephalomyelitis development. Journal of Leukocyte Biology. 99(1). 175–188. 10 indexed citations
8.
Mattheolabakis, George, Era Taoufik, Sylva Haralambous, Michael L. Roberts, & Konstantinos Avgoustakis. (2008). In vivo investigation of tolerance and antitumor activity of cisplatin-loaded PLGA-mPEG nanoparticles. European Journal of Pharmaceutics and Biopharmaceutics. 71(2). 190–195. 74 indexed citations
9.
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
10.
Taoufik, Era, et al.. (2007). Positive and Negative Implications of Tumor Necrosis Factor Neutralization for the Pathogenesis of Multiple Sclerosis. Neurodegenerative Diseases. 5(1). 32–37. 16 indexed citations
11.
Tseveleki, Vivian, Jan Bauer, Era Taoufik, et al.. (2004). Cellular FLIP (Long Isoform) Overexpression in T Cells Drives Th2 Effector Responses and Promotes Immunoregulation in Experimental Autoimmune Encephalomyelitis. The Journal of Immunology. 173(11). 6619–6626. 30 indexed citations
12.
Aidinis, Vassilis, David Plows, Sylva Haralambous, et al.. (2003). Functional analysis of an arthritogenic synovial fibroblast. Arthritis Research & Therapy. 5(3). R140–57. 39 indexed citations
13.
14.
Hukkanen, Mika, Louise A. M. Platts, Sylva Haralambous, et al.. (2003). Induction of inducible nitric oxide synthase, argininosuccinate synthase, and GTP cyclohydrolase I in arthritic joints of human tumor necrosis factor-alpha transgenic mice.. PubMed. 30(4). 652–9. 3 indexed citations
15.
Schett, G., Silvia Hayer, M Tohidast-Akrad, et al.. (2001). Adenovirus-based overexpression of tissue inhibitor of metalloproteinases 1 reduces tissue damage in the joints of tumor necrosis factor ? transgenic mice. Arthritis & Rheumatism. 44(12). 2888–2898. 41 indexed citations
16.
Neurath, Markus F., Kai Hildner, Christoph Becker, et al.. (1999). Methotrexate specifically modulates cytokine production by T cells and macrophages in murine collagen-induced arthritis (CIA): a mechanism for methotrexate-mediated immunosuppression. Clinical & Experimental Immunology. 115(1). 42–55. 96 indexed citations
17.
Neurath, Markus F., Ivan J. Fuss, Manolis Pasparakis, et al.. (1997). Predominant pathogenic role of tumor necrosis factor in experimental colitis in mice. European Journal of Immunology. 27(7). 1743–1750. 344 indexed citations
18.
Douni, Eleni, Katerina Akassoglou, Lena Alexopoulou, et al.. (1997). Transgenic and knockout analyses of the role of TNF in immune regulation and disease pathogenesis.. PubMed. 47(1-2). 27–38. 91 indexed citations
19.
Probert, Lesley, Katerina Akassoglou, Lena Alexopoulou, et al.. (1996). Dissection of the pathologies induced by transmembrane and wild-type tumor necrosis factor in transgenic mice. Journal of Leukocyte Biology. 59(4). 518–525. 35 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by M. Zaeem Cader Breakdown of academic impact, for papers by Timothy P. LaBranche Breakdown of academic impact, for papers by Eva Reali Breakdown of academic impact, for papers by Lina Olsson Breakdown of academic impact, for papers by Kazuhiko Yamamura Breakdown of academic impact, for papers by Mika Nishihara Breakdown of academic impact, for papers by Yasuto Araki Breakdown of academic impact, for papers by Kouji Matsushima Breakdown of academic impact, for papers by So‐Hee Hong Breakdown of academic impact, for papers by Kary A. Latham
Rankless by CCL
2026