Egle Solito

7.3k total citations
111 papers, 5.4k citations indexed

About

Egle Solito is a scholar working on Molecular Biology, Immunology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Egle Solito has authored 111 papers receiving a total of 5.4k indexed citations (citations by other indexed papers that have themselves been cited), including 80 papers in Molecular Biology, 46 papers in Immunology and 17 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Egle Solito's work include S100 Proteins and Annexins (71 papers), Immune Response and Inflammation (29 papers) and Neonatal Respiratory Health Research (17 papers). Egle Solito is often cited by papers focused on S100 Proteins and Annexins (71 papers), Immune Response and Inflammation (29 papers) and Neonatal Respiratory Health Research (17 papers). Egle Solito collaborates with scholars based in United Kingdom, Italy and France. Egle Solito's co-authors include Mauro Perretti, Luca Parente, Magdalena Sastre, Roderick J. Flower, Helen Christian, Françoise Russo‐Marie, Julia C. Buckingham, Simon McArthur, Catherine de Coupade and Stéfano Marullo and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Medicine.

In The Last Decade

Egle Solito

111 papers receiving 5.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Egle Solito United Kingdom 42 3.5k 2.1k 772 760 650 111 5.4k
Susumu Ishida Japan 52 3.2k 0.9× 881 0.4× 708 0.9× 355 0.5× 638 1.0× 402 9.6k
Yoshiyuki Rikitake Japan 40 3.3k 0.9× 916 0.4× 955 1.2× 510 0.7× 464 0.7× 111 6.2k
Fumikazu Okajima Japan 59 7.1k 2.0× 1.2k 0.6× 1.6k 2.1× 301 0.4× 480 0.7× 197 9.9k
Felicity N. E. Gavins United Kingdom 33 1.9k 0.5× 1.2k 0.6× 243 0.3× 384 0.5× 338 0.5× 85 3.4k
Sawsan Youssef United States 30 1.4k 0.4× 2.4k 1.2× 315 0.4× 242 0.3× 495 0.8× 46 5.2k
Jaroslaw W. Zmijewski United States 40 2.1k 0.6× 1.6k 0.8× 618 0.8× 963 1.3× 191 0.3× 70 5.1k
Harald Esterbauer Austria 41 2.7k 0.8× 841 0.4× 1.6k 2.1× 183 0.2× 273 0.4× 94 5.5k
Anu Srinivasan United States 37 4.5k 1.3× 738 0.4× 935 1.2× 144 0.2× 682 1.0× 52 7.3k
Yoshihide Kanaoka United States 49 2.5k 0.7× 2.0k 1.0× 2.4k 3.1× 672 0.9× 176 0.3× 93 6.8k

Countries citing papers authored by Egle Solito

Since Specialization
Citations

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

Fields of papers citing papers by Egle Solito

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Egle Solito

This figure shows the co-authorship network connecting the top 25 collaborators of Egle Solito. A scholar is included among the top collaborators of Egle Solito 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 Egle Solito. Egle Solito 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.
Pontifex, Matthew G., Emily Connell, Gwénaëlle Le Gall, et al.. (2024). Cerebrovascular damage caused by the gut microbe/host co-metabolite p -cresol sulfate is prevented by blockade of the EGF receptor. Gut Microbes. 16(1). 2431651–2431651. 7 indexed citations
2.
Amato, Felice, R. de Franchis, Speranza Esposito, et al.. (2023). The Immune Response to SARS-CoV-2 Vaccine in a Cohort of Family Pediatricians from Southern Italy. Cells. 12(11). 1447–1447. 6 indexed citations
3.
Callender, Lauren A., et al.. (2019). Mitochondrial mass governs the extent of human T cell senescence. Aging Cell. 19(2). e13067–e13067. 120 indexed citations
4.
Rocha, Gustavo Henrique Oliveira da, et al.. (2019). Control of expression and activity of peroxisome proliferated‐activated receptor γ by Annexin A1 on microglia during efferocytosis. Cell Biochemistry and Function. 37(7). 560–568. 19 indexed citations
5.
Montague-Cardoso, Karli, et al.. (2019). Changes in vascular permeability in the spinal cord contribute to chemotherapy-induced neuropathic pain. Brain Behavior and Immunity. 83. 248–259. 26 indexed citations
6.
McArthur, Simon, et al.. (2012). ER[beta] and GPR30 mediate distinct and opposite oestrogenic influences on microglial phagocytosis of apoptotic neuronal cells. 28. 1 indexed citations
7.
Kamal, Ahmad M., Richard Hayhoe, Dianne Cooper, et al.. (2006). Antiflammin-2 Activates the Human Formyl-Peptide Receptor Like 1. The Scientific World JOURNAL. 6. 1375–1384. 20 indexed citations
8.
Payne, John A., et al.. (2005). Modulators of the SUR2B/Kir6.1 ATP-sensitive K+ channel regulate annexin 1 release in the TtT/GF folliculostellate cell line. 9. 3 indexed citations
9.
Solito, Egle, et al.. (2004). Characterization of formylated peptide receptor expression in murine brain, pituitary and adrenal tissue. 8(11). 1156–62. 1 indexed citations
10.
Buckingham, Julia C., Egle Solito, Christopher John, et al.. (2003). Annexin 1: a paracrine/juxtacrine mediator of glucorticoid action in the neuroendocrine system. Cell Biochemistry and Function. 21(3). 217–221. 18 indexed citations
11.
Solito, Egle, Kristina E. Froud, Helen Christian, J Morris, & J Buckingham. (2003). Opposite effects of dexamethasone and oestardiol on annexin 1 expression. 6. 2 indexed citations
12.
Solito, Egle, et al.. (2002). USE OF MUTAGENESIS TO STUDY THE TRANSLOCATION OF ANNEXIN 1 ACROSS THE CELL MEMBRANE. 4. 2 indexed citations
13.
Mulla, Abeda, et al.. (2001). ANNEXIN 1 EXPRESSION IN PERIPHERAL BLOOD LEUKOCYTES (PBLs) FROM PATIENTS WITH ENDOCRINE DISEASES CORRELATES WITH THE SERUM CORTISOL. 2. 2 indexed citations
14.
Smith, Sue, et al.. (2001). An annexin 1 (ANXA1)‐derived peptide inhibits prototype antigen‐driven human T cell Th1 and Th2 responses in vitro. Clinical & Experimental Allergy. 31(7). 1116–1125. 35 indexed citations
15.
Canaider, Silvia, Egle Solito, Catherine de Coupade, et al.. (2000). Increased apoptosis in U937 cells over-expressing lipocortin 1 (annexin I). Life Sciences. 66(18). PL265–PL270. 30 indexed citations
16.
Solito, Egle, Ignacio A. Romero, Stéfano Marullo, Françoise Russo‐Marie, & Babette B. Weksler. (2000). Annexin 1 Binds to U937 Monocytic Cells and Inhibits Their Adhesion to Microvascular Endothelium: Involvement of the α4β1 Integrin. The Journal of Immunology. 165(3). 1573–1581. 70 indexed citations
17.
18.
Hirst, Warren D., et al.. (1999). De novo expression of lipocortin-1 in reactive microglia and astrocytes in kainic acid lesioned rat cerebellum. Glia. 26(4). 333–343. 33 indexed citations
19.
Raugei, Giovanni, Donatella Degl’Innocenti, Paola Chiarugi, et al.. (1999). Preferential accumulation of muscle type acylphosphatase in the nucleus during differentiation. IUBMB Life. 47(1). 127–136. 6 indexed citations
20.
Palla, Emanuela, Adriana Mirtella, Cesira L. Galeotti, et al.. (1996). Synthetic Alleles at Position 121 Define a Functional Domain of Human Interleukin‐1β. European Journal of Biochemistry. 238(2). 308–316. 5 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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