Eliver Ghosn

3.9k total citations
50 papers, 2.2k citations indexed

About

Eliver Ghosn is a scholar working on Immunology, Infectious Diseases and Molecular Biology. According to data from OpenAlex, Eliver Ghosn has authored 50 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Immunology, 14 papers in Infectious Diseases and 14 papers in Molecular Biology. Recurrent topics in Eliver Ghosn's work include T-cell and B-cell Immunology (10 papers), Immune cells in cancer (9 papers) and Immunotherapy and Immune Responses (8 papers). Eliver Ghosn is often cited by papers focused on T-cell and B-cell Immunology (10 papers), Immune cells in cancer (9 papers) and Immunotherapy and Immune Responses (8 papers). Eliver Ghosn collaborates with scholars based in United States, Brazil and Japan. Eliver Ghosn's co-authors include Leonore A. Herzenberg, Leonard A. Herzenberg, Sandro Rogério de Almeida, Karina Ramalho Bortoluci, Yang Yang, Takeshi Fukuhara, Gregory Govoni, Yang Yang, Denise M. Monack and James W. Tung and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and The Journal of Immunology.

In The Last Decade

Eliver Ghosn

50 papers receiving 2.2k citations

Peers

Eliver Ghosn
Georg Varga Germany
Zhuo Zhou China
Gregory L. Szeto United States
Suk‐Jo Kang South Korea
Su Metcalfe United Kingdom
Mark Kühnel Germany
Alain C. Tissot Switzerland
Georg Varga Germany
Eliver Ghosn
Citations per year, relative to Eliver Ghosn Eliver Ghosn (= 1×) peers Georg Varga

Countries citing papers authored by Eliver Ghosn

Since Specialization
Citations

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

Fields of papers citing papers by Eliver Ghosn

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eliver Ghosn

This figure shows the co-authorship network connecting the top 25 collaborators of Eliver Ghosn. A scholar is included among the top collaborators of Eliver Ghosn 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 Eliver Ghosn. Eliver Ghosn 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.
Tkachev, Sasha, Florian Georgescauld, Tyler Levy, et al.. (2025). Lifting the curse from high-dimensional data: automated projection pursuit clustering for a variety of biological data modalities. GigaScience. 14. 2 indexed citations
2.
Kosters, Astrid, Victoria Murray, Gurjot Gill, et al.. (2024). Transient anti-interferon autoantibodies in the airways are associated with recovery from COVID-19. Science Translational Medicine. 16(772). eadq1789–eadq1789. 5 indexed citations
3.
Chen, Zhihong, Gonzalo Piñero, Bruno Giotti, et al.. (2023). Monocyte depletion enhances neutrophil influx and proneural to mesenchymal transition in glioblastoma. Nature Communications. 14(1). 1839–1839. 32 indexed citations
4.
Kosters, Astrid, Dalia Arafat, Meixue Duan, et al.. (2023). Profiling the peripheral immune response to ex vivo TNF stimulation in untreated juvenile idiopathic arthritis using single cell RNA sequencing. Pediatric Rheumatology. 21(1). 17–17. 6 indexed citations
5.
Kolachala, Vasantha L., Suresh Venkateswaran, Anne Dodd, et al.. (2022). Assessing Cellular and Transcriptional Diversity of Ileal Mucosa Among Treatment-Naïve and Treated Crohn’s Disease. Inflammatory Bowel Diseases. 29(2). 274–285. 17 indexed citations
6.
Bassit, Leda, Joshua D. Chandler, Natalie S. Haddad, et al.. (2022). Inactivation of SARS-CoV-2 and COVID-19 Patient Samples for Contemporary Immunology and Metabolomics Studies. ImmunoHorizons. 6(2). 144–155. 5 indexed citations
7.
Xu, Congmin, et al.. (2022). Comprehensive multi-omics single-cell data integration reveals greater heterogeneity in the human immune system. iScience. 25(10). 105123–105123. 7 indexed citations
8.
Yang, Junkai, Astrid Kosters, Ximo Pechuan-Jorge, et al.. (2022). Transcriptional reprogramming of infiltrating neutrophils drives lung pathology in severe COVID-19 despite low viral load. Blood Advances. 7(5). 778–799. 19 indexed citations
9.
Dobosh, Brian, Keivan Zandi, Junkai Yang, et al.. (2022). Baricitinib attenuates the proinflammatory phase of COVID-19 driven by lung-infiltrating monocytes. Cell Reports. 39(11). 110945–110945. 11 indexed citations
10.
Ma, Tongcui, Heeju Ryu, Matthew McGregor, et al.. (2021). Protracted yet Coordinated Differentiation of Long-Lived SARS-CoV-2-Specific CD8+ T Cells during Convalescence. The Journal of Immunology. 207(5). 1344–1356. 9 indexed citations
11.
Kosters, Astrid, Jeffrey Waters, Koshika Yadava, et al.. (2021). Hematopoietic Stem Cell Requirement for Macrophage Regeneration Is Tissue Specific. The Journal of Immunology. 207(12). 3028–3037. 3 indexed citations
12.
Neidleman, Jason, Xiaoyu Luo, Ashley F. George, et al.. (2021). Distinctive features of SARS-CoV-2-specific T cells predict recovery from severe COVID-19. Cell Reports. 36(3). 109414–109414. 58 indexed citations
13.
Kobayashi, Michihiro, Yang Lin, Akansha Mishra, et al.. (2020). Bmi1 Maintains the Self-Renewal Property of Innate-like B Lymphocytes. The Journal of Immunology. 204(12). 3262–3272. 12 indexed citations
14.
Neidleman, Jason, Xiaoyu Luo, Julie Frouard, et al.. (2020). SARS-CoV-2-Specific T Cells Exhibit Phenotypic Features of Helper Function, Lack of Terminal Differentiation, and High Proliferation Potential. Cell Reports Medicine. 1(6). 100081–100081. 126 indexed citations
15.
Parks, David R., Justin Youngyunpipatkul, Leonore A. Herzenberg, et al.. (2019). Automated subset identification and characterization pipeline for multidimensional flow and mass cytometry data clustering and visualization. Communications Biology. 2(1). 229–229. 9 indexed citations
16.
Ghosn, Eliver, Momoko Yoshimoto, Hiromitsu Nakauchi, Irving L. Weissman, & Leonore A. Herzenberg. (2019). Hematopoietic stem cell-independent hematopoiesis and the origins of innate-like B lymphocytes. Development. 146(15). 44 indexed citations
17.
Ghosn, Eliver, Jeffrey Waters, Ryō Yamamoto, et al.. (2015). Fetal Hematopoietic Stem Cell Transplantation Fails to Fully Regenerate the B-Lymphocyte Compartment. Stem Cell Reports. 6(1). 137–149. 52 indexed citations
18.
Ghosn, Eliver, Robert C. Axtell, Katja Herges, et al.. (2012). Reversal of Paralysis and Reduced Inflammation from Peripheral Administration of β-Amyloid in T H 1 and T H 17 Versions of Experimental Autoimmune Encephalomyelitis. Science Translational Medicine. 4(145). 145ra105–145ra105. 80 indexed citations
19.
Yang, Yang, Eliver Ghosn, Leah E. Cole, et al.. (2012). Antigen-specific antibody responses in B-1a and their relationship to natural immunity. Proceedings of the National Academy of Sciences. 109(14). 5382–5387. 45 indexed citations
20.
Cassado, Alexandra dos Anjos, José Antônio Tavares de Albuquerque, Luiz Roberto Sardinha, et al.. (2011). Cellular Renewal and Improvement of Local Cell Effector Activity in Peritoneal Cavity in Response to Infectious Stimuli. PLoS ONE. 6(7). e22141–e22141. 49 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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