Mario Perro

5.6k total citations · 1 hit paper
27 papers, 1.5k citations indexed

About

Mario Perro is a scholar working on Immunology, Oncology and Molecular Biology. According to data from OpenAlex, Mario Perro has authored 27 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Immunology, 10 papers in Oncology and 8 papers in Molecular Biology. Recurrent topics in Mario Perro's work include CAR-T cell therapy research (8 papers), Immunotherapy and Immune Responses (7 papers) and Monoclonal and Polyclonal Antibodies Research (7 papers). Mario Perro is often cited by papers focused on CAR-T cell therapy research (8 papers), Immunotherapy and Immune Responses (7 papers) and Monoclonal and Polyclonal Antibodies Research (7 papers). Mario Perro collaborates with scholars based in United States, Switzerland and United Kingdom. Mario Perro's co-authors include Ulrich H. von Andrian, David Álvarez, John N. Wood, Silke Paust, Aude Thiriot, Lorena Riol‐Blanco, José Ordovás-Montañés, Bodo Grimbacher, Mamoun Elawad and Erik‐Oliver Glocker and has published in prestigious journals such as Nature, Science and The Lancet.

In The Last Decade

Mario Perro

26 papers receiving 1.5k citations

Hit Papers

Nociceptive sensory neurons drive interleukin-23-mediated... 2014 2026 2018 2022 2014 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mario Perro United States 17 903 333 324 171 161 27 1.5k
Gudrun F. Debes United States 21 1.9k 2.1× 268 0.8× 546 1.7× 129 0.8× 207 1.3× 34 2.6k
Nathalie Cools Belgium 29 1.4k 1.5× 708 2.1× 360 1.1× 169 1.0× 63 0.4× 91 2.5k
Takaji Matsutani Japan 23 1.3k 1.4× 331 1.0× 421 1.3× 145 0.8× 201 1.2× 62 2.2k
François Van Laethem United States 24 1.5k 1.6× 581 1.7× 507 1.6× 100 0.6× 80 0.5× 34 2.1k
Anna M. Hansen United States 17 1.1k 1.2× 349 1.0× 350 1.1× 127 0.7× 86 0.5× 24 2.0k
Steven M. Kerfoot Canada 22 1.2k 1.4× 407 1.2× 264 0.8× 87 0.5× 40 0.2× 39 2.1k
Katia De Filippo United Kingdom 12 975 1.1× 440 1.3× 232 0.7× 81 0.5× 37 0.2× 12 1.6k
Giorgio Trinchieri United States 8 1.1k 1.2× 237 0.7× 396 1.2× 136 0.8× 75 0.5× 8 1.5k
Leonid Izikson United States 15 801 0.9× 203 0.6× 504 1.6× 98 0.6× 338 2.1× 23 1.8k
Catherine J. McMahan United States 18 1.9k 2.1× 825 2.5× 511 1.6× 184 1.1× 65 0.4× 30 2.7k

Countries citing papers authored by Mario Perro

Since Specialization
Citations

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

Fields of papers citing papers by Mario Perro

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mario Perro

This figure shows the co-authorship network connecting the top 25 collaborators of Mario Perro. A scholar is included among the top collaborators of Mario Perro 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 Mario Perro. Mario Perro 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
2.
Stoltzfus, Caleb, Ramya Sivakumar, Leo Kunz, et al.. (2021). Multi-Parameter Quantitative Imaging of Tumor Microenvironments Reveals Perivascular Immune Niches Associated With Anti-Tumor Immunity. Frontiers in Immunology. 12. 726492–726492. 22 indexed citations
3.
Cremasco, Floriana, Elena Menietti, Johannes Sam, et al.. (2021). Cross-linking of T cell to B cell lymphoma by the T cell bispecific antibody CD20-TCB induces IFNγ/CXCL10-dependent peripheral T cell recruitment in humanized murine model. PLoS ONE. 16(1). e0241091–e0241091. 24 indexed citations
4.
Doucey, Marie‐Agnès, Thierry Monney, Riccardo Turrini, et al.. (2021). ISB 1342: A first-in-class CD38 T cell engager for the treatment of relapsed refractory multiple myeloma.. Journal of Clinical Oncology. 39(15_suppl). 8044–8044. 16 indexed citations
5.
Stoltzfus, Caleb, Benjamin H. Gern, Brandy Olin, et al.. (2020). CytoMAP: A Spatial Analysis Toolbox Reveals Features of Myeloid Cell Organization in Lymphoid Tissues. Cell Reports. 31(3). 107523–107523. 136 indexed citations
6.
Sam, Johannes, Sara Colombetti, Tanja Fauti, et al.. (2020). Combination of T-Cell Bispecific Antibodies With PD-L1 Checkpoint Inhibition Elicits Superior Anti-Tumor Activity. Frontiers in Oncology. 10. 575737–575737. 38 indexed citations
7.
Perro, Mario, Matteo Iannacone, Ulrich H. von Andrian, & António Peixoto. (2020). Role of LFA-1 integrin in the control of a lymphocytic choriomeningitis virus (LCMV) infection. Virulence. 11(1). 1640–1655. 3 indexed citations
8.
Stoltzfus, Caleb, Benjamin H. Gern, Brandy Olin, et al.. (2019). CytoMAP: A Spatial Analysis Toolbox Reveals Features of Myeloid Cell Organization in Lymphoid Tissues. SSRN Electronic Journal. 1 indexed citations
9.
Grandjean, Capucine L., Susanna Celli, David Michonneau, et al.. (2016). Intravital imaging reveals improved Kupffer cell-mediated phagocytosis as a mode of action of glycoengineered anti-CD20 antibodies. Scientific Reports. 6(1). 34382–34382. 47 indexed citations
10.
Stary, Georg, Andrew J. Olive, Aleksandar F. Radovic‐Moreno, et al.. (2015). A mucosal vaccine against Chlamydia trachomatis generates two waves of protective memory T cells. Science. 348(6241). aaa8205–aaa8205. 290 indexed citations
11.
Olive, Andrew J., Aleksandar F. Radovic‐Moreno, David Gondek, et al.. (2015). A mucosal vaccine against Chlamydia trachomatis generates two waves of protective memory T cells. DSpace@MIT (Massachusetts Institute of Technology). 16 indexed citations
12.
Riol‐Blanco, Lorena, José Ordovás-Montañés, Mario Perro, et al.. (2014). Nociceptive sensory neurons drive interleukin-23-mediated psoriasiform skin inflammation. Nature. 510(7503). 157–161. 409 indexed citations breakdown →
13.
Pang, Paul, Xiaohua Jin, Brandon M. Proctor, et al.. (2014). RGS4 inhibits angiotensin II signaling and macrophage localization during renal reperfusion injury independent of vasospasm. Kidney International. 87(4). 771–783. 13 indexed citations
14.
Henrickson, Sarah E., Mario Perro, Scott Loughhead, et al.. (2013). Antigen Availability Determines CD8+ T Cell-Dendritic Cell Interaction Kinetics and Memory Fate Decisions. Immunity. 39(3). 496–507. 115 indexed citations
15.
Martini, Hélène, Mario Perro, Sarita Workman, et al.. (2011). Importance of B cell co-stimulation in CD4+ T cell differentiation: X-linked agammaglobulinaemia, a human model. Clinical & Experimental Immunology. 164(3). 381–387. 32 indexed citations
16.
Perro, Mario, Julia Y. Tsang, David Escors, et al.. (2010). Generation of multi-functional antigen-specific human T-cells by lentiviral TCR gene transfer. Gene Therapy. 17(6). 721–732. 32 indexed citations
17.
Glocker, Erik‐Oliver, Natalie Frede, Mario Perro, et al.. (2010). Infant colitis—it's in the genes. The Lancet. 376(9748). 1272–1272. 183 indexed citations
18.
Lorenzato, Annalisa, Martina Olivero, Mario Perro, et al.. (2007). A cancer‐predisposing “hot spot” mutation of the fumarase gene creates a dominant negative protein. International Journal of Cancer. 122(4). 947–951. 16 indexed citations
19.
Stauss, Hans J., Sharyn Thomas, Michela Cesco-Gaspere, et al.. (2007). WT1-specific T cell receptor gene therapy: Improving TCR function in transduced T cells. Blood Cells Molecules and Diseases. 40(1). 113–116. 43 indexed citations
20.
Stauss, Hans J., Michela Cesco-Gaspere, Sharyn Thomas, et al.. (2007). Monoclonal T-Cell Receptors: New Reagents for Cancer Therapy. Molecular Therapy. 15(10). 1744–1750. 40 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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