Nathalie Rufer

10.5k total citations · 4 hit papers
114 papers, 8.2k citations indexed

About

Nathalie Rufer is a scholar working on Immunology, Oncology and Molecular Biology. According to data from OpenAlex, Nathalie Rufer has authored 114 papers receiving a total of 8.2k indexed citations (citations by other indexed papers that have themselves been cited), including 98 papers in Immunology, 42 papers in Oncology and 22 papers in Molecular Biology. Recurrent topics in Nathalie Rufer's work include Immunotherapy and Immune Responses (62 papers), T-cell and B-cell Immunology (59 papers) and Immune Cell Function and Interaction (56 papers). Nathalie Rufer is often cited by papers focused on Immunotherapy and Immune Responses (62 papers), T-cell and B-cell Immunology (59 papers) and Immune Cell Function and Interaction (56 papers). Nathalie Rufer collaborates with scholars based in Switzerland, United States and Belgium. Nathalie Rufer's co-authors include Daniel E. Speiser, Pedro Romero, Eddy Roosnek, Peter M. Lansdorp, Petra Baumgaertner, Estelle Devêvre, Jean‐Charles Cerottini, Donata Rimoldi, Tim H. Brümmendorf and Danielle Líénard and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Nathalie Rufer

114 papers receiving 8.1k citations

Hit Papers

Exhaustion of tumor-specific CD8+ T cells in met... 1999 2026 2008 2017 2011 2002 1999 2005 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nathalie Rufer Switzerland 42 5.6k 3.1k 1.9k 1.3k 1.2k 114 8.2k
William Vermi Italy 54 8.5k 1.5× 3.4k 1.1× 2.2k 1.2× 999 0.8× 569 0.5× 157 12.3k
Richard A. Kroczek Germany 54 9.2k 1.7× 2.2k 0.7× 2.1k 1.1× 975 0.8× 635 0.5× 103 12.5k
Shixin Qin United States 37 6.4k 1.2× 2.9k 0.9× 1.2k 0.6× 631 0.5× 921 0.7× 49 9.1k
Carola G. Vinuesa Australia 54 11.2k 2.0× 1.7k 0.6× 2.9k 1.5× 992 0.8× 646 0.5× 117 14.8k
Richard J. Armitage United States 45 7.1k 1.3× 1.8k 0.6× 1.6k 0.9× 835 0.7× 405 0.3× 75 9.3k
Helmut Jonuleit Germany 44 10.8k 1.9× 2.8k 0.9× 2.8k 1.5× 632 0.5× 583 0.5× 107 12.8k
Otto Majdic Austria 59 6.8k 1.2× 1.9k 0.6× 2.5k 1.3× 648 0.5× 717 0.6× 192 10.5k
M P Beckmann United States 33 3.8k 0.7× 1.7k 0.5× 1.9k 1.0× 583 0.5× 515 0.4× 44 6.9k
Masaki Yasukawa Japan 47 4.0k 0.7× 2.6k 0.8× 2.0k 1.0× 1.3k 1.0× 310 0.3× 249 8.1k
Lishan Su United States 48 3.5k 0.6× 1.3k 0.4× 3.4k 1.8× 1.9k 1.5× 817 0.7× 184 8.8k

Countries citing papers authored by Nathalie Rufer

Since Specialization
Citations

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

Fields of papers citing papers by Nathalie Rufer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nathalie Rufer

This figure shows the co-authorship network connecting the top 25 collaborators of Nathalie Rufer. A scholar is included among the top collaborators of Nathalie Rufer 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 Nathalie Rufer. Nathalie Rufer 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.
Croce, Giancarlo, Sara Bobisse, Maiia E. Bragina, et al.. (2025). Phage display enables machine learning discovery of cancer antigen–specific TCRs. Science Advances. 11(24). eads5589–eads5589. 2 indexed citations
2.
Gachoud, David, Trestan Pillonel, Γεράσιμος Τσιλιμιδός, et al.. (2022). Antibody response and intra‐host viral evolution after plasma therapy in COVID ‐19 patients pre‐exposed or not to B‐cell‐depleting agents. British Journal of Haematology. 199(4). 549–559. 5 indexed citations
3.
Martínez-Usatorre, Amaia, Lorenzo F. Sempere, Santiago J. Carmona, et al.. (2019). MicroRNA-155 Expression Is Enhanced by T-cell Receptor Stimulation Strength and Correlates with Improved Tumor Control in Melanoma. Cancer Immunology Research. 7(6). 1013–1024. 33 indexed citations
4.
Gannon, Philippe O., Petra Baumgaertner, Alexandre Huber, et al.. (2016). Rapid and Continued T-Cell Differentiation into Long-term Effector and Memory Stem Cells in Vaccinated Melanoma Patients. Clinical Cancer Research. 23(13). 3285–3296. 19 indexed citations
5.
Hebeisen, Michaël, Julien Schmidt, Philippe Guillaume, et al.. (2015). Identification of Rare High-Avidity, Tumor-Reactive CD8+ T Cells by Monomeric TCR–Ligand Off-Rates Measurements on Living Cells. Cancer Research. 75(10). 1983–1991. 38 indexed citations
6.
Marraco, Silvia A. Fuertes, Charlotte Soneson, Laurène Cagnon, et al.. (2015). Long-lasting stem cell–like memory CD8 + T cells with a naïve-like profile upon yellow fever vaccination. Science Translational Medicine. 7(282). 282ra48–282ra48. 149 indexed citations
7.
Legat, Amandine, Hélène Maby–El Hajjami, Petra Baumgaertner, et al.. (2015). Vaccination with LAG-3Ig (IMP321) and Peptides Induces Specific CD4 and CD8 T-Cell Responses in Metastatic Melanoma Patients—Report of a Phase I/IIa Clinical Trial. Clinical Cancer Research. 22(6). 1330–1340. 76 indexed citations
8.
Baitsch, Lukas, Petra Baumgaertner, Estelle Devêvre, et al.. (2011). Exhaustion of tumor-specific CD8+ T cells in metastases from melanoma patients. Journal of Clinical Investigation. 121(6). 2350–2360. 650 indexed citations breakdown →
9.
Jandus, Camilla, Gilles Bioley, Danijel Dojcinovic, et al.. (2009). Tumor Antigen–Specific FOXP3+ CD4 T Cells Identified in Human Metastatic Melanoma: Peptide Vaccination Results in Selective Expansion of Th1-like Counterparts. Cancer Research. 69(20). 8085–8093. 34 indexed citations
10.
Iancu, Emanuela M., Patricia Corthésy, Petra Baumgaertner, et al.. (2009). Clonotype Selection and Composition of Human CD8 T Cells Specific for Persistent Herpes Viruses Varies with Differentiation but Is Stable Over Time. The Journal of Immunology. 183(1). 319–331. 58 indexed citations
11.
Appay, Victor, Andreas Bosio, Christian Biervert, et al.. (2007). Sensitive Gene Expression Profiling of Human T Cell Subsets Reveals Parallel Post-Thymic Differentiation for CD4+ and CD8+ Lineages. The Journal of Immunology. 179(11). 7406–7414. 35 indexed citations
12.
Barbey, Catherine, Petra Baumgaertner, Estelle Devêvre, et al.. (2007). IL-12 Controls Cytotoxicity of a Novel Subset of Self-Antigen-Specific Human CD28+ Cytolytic T Cells. The Journal of Immunology. 178(6). 3566–3574. 14 indexed citations
13.
Migliaccio, Marco, Pedro M. Sousa Alves, Pedro Romero, & Nathalie Rufer. (2006). Distinct Mechanisms Control Human Naive and Antigen-Experienced CD8+ T Lymphocyte Proliferation. The Journal of Immunology. 176(4). 2173–2182. 16 indexed citations
14.
Colombetti, Sara, Petra Baumgärtner, Laurence Chapatte, et al.. (2006). Impact of Orthologous Melan-A Peptide Immunizations on the Anti-Self Melan-A/HLA-A2 T Cell Cross-Reactivity. The Journal of Immunology. 176(11). 6560–6567. 6 indexed citations
15.
Migliaccio, Marco, et al.. (2006). Mechanisms Regulating the Proliferative Potential of Human CD8+ T Lymphocytes Overexpressing Telomerase. The Journal of Immunology. 177(6). 3657–3668. 28 indexed citations
16.
Speiser, Daniel E., Danielle Líénard, Nathalie Rufer, et al.. (2005). Rapid and strong human CD8+ T cell responses to vaccination with peptide, IFA, and CpG oligodeoxynucleotide 7909. Journal of Clinical Investigation. 115(3). 739–746. 36 indexed citations
17.
Speiser, Daniel E., Danielle Líénard, Nathalie Rufer, et al.. (2005). Rapid and strong human CD8+ T cell responses to vaccination with peptide, IFA, and CpG oligodeoxynucleotide 7909. Journal of Clinical Investigation. 115(3). 739–746. 514 indexed citations breakdown →
18.
Migliaccio, Marco, et al.. (2005). Mechanisms That Limit the In Vitro Proliferative Potential of Human CD8+ T Lymphocytes. The Journal of Immunology. 174(6). 3335–3343. 25 indexed citations
19.
Zippelius, Alfred, Gilles Bioley, Frédérique‐Anne Le Gal, et al.. (2004). Human Thymus Exports Naive CD8 T Cells That Can Home to Nonlymphoid Tissues. The Journal of Immunology. 172(5). 2773–2777. 19 indexed citations
20.
Brümmendorf, Tim H., Peter M. Lansdorp, & Nathalie Rufer. (2000). Telomere Length Dynamics in Normal and Malignant Hematopoiesis. 3(4). 397–409. 2 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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