Ines Matos

1.9k total citations · 2 hit papers
15 papers, 1.3k citations indexed

About

Ines Matos is a scholar working on Immunology, Oncology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Ines Matos has authored 15 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Immunology, 3 papers in Oncology and 2 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Ines Matos's work include Immunotherapy and Immune Responses (11 papers), T-cell and B-cell Immunology (7 papers) and Immune Cell Function and Interaction (6 papers). Ines Matos is often cited by papers focused on Immunotherapy and Immune Responses (11 papers), T-cell and B-cell Immunology (7 papers) and Immune Cell Function and Interaction (6 papers). Ines Matos collaborates with scholars based in United States, Switzerland and Germany. Ines Matos's co-authors include Ralph M. Steinman, Juliana Idoyaga, M. Paula Longhi, Christine Trumpfheller, Marina Caskey, Marco Colonna, Andres Μ. Salazar, Cheolho Cheong, Chae Gyu Park and Jae‐Hoon Choi and has published in prestigious journals such as Cell, The Journal of Experimental Medicine and The Journal of Immunology.

In The Last Decade

Ines Matos

14 papers receiving 1.2k citations

Hit Papers

Dendritic cells require a systemic type I interferon resp... 2009 2026 2014 2020 2009 2010 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ines Matos United States 9 1.1k 283 140 133 99 15 1.3k
Marco Frentsch Germany 17 684 0.6× 210 0.7× 228 1.6× 146 1.1× 157 1.6× 34 1.1k
Ramon Roozendaal Netherlands 15 867 0.8× 246 0.9× 252 1.8× 156 1.2× 104 1.1× 29 1.3k
Alexey Y. Karulin United States 18 792 0.7× 220 0.8× 105 0.8× 144 1.1× 85 0.9× 32 1.1k
Lauren B. Rodda United States 9 707 0.7× 275 1.0× 159 1.1× 259 1.9× 181 1.8× 13 1.2k
Hansjörg Schild Germany 13 805 0.7× 356 1.3× 179 1.3× 110 0.8× 63 0.6× 13 1.0k
Marie J. Estcourt Australia 13 617 0.6× 228 0.8× 197 1.4× 227 1.7× 93 0.9× 25 927
Laurent Malherbe United States 19 1.0k 0.9× 220 0.8× 211 1.5× 198 1.5× 94 0.9× 42 1.3k
Traci Zell United States 12 1.5k 1.4× 250 0.9× 230 1.6× 147 1.1× 115 1.2× 13 1.8k
Hans Hengartner Switzerland 11 949 0.9× 226 0.8× 111 0.8× 131 1.0× 67 0.7× 11 1.2k
Joanne Pooley Australia 9 2.1k 1.9× 369 1.3× 198 1.4× 114 0.9× 48 0.5× 11 2.2k

Countries citing papers authored by Ines Matos

Since Specialization
Citations

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

Fields of papers citing papers by Ines Matos

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ines Matos

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

All Works

15 of 15 papers shown
1.
Antsiferova, Maria, Marco Berrera, Claudio Murgia, et al.. (2025). Novel immunodominant neoepitope in a KPC mouse model of pancreatic cancer allowing identification of tumor-specific T cells. OncoImmunology. 14(1). 2489815–2489815.
2.
Schlenker, Ramona, Petra Schwalie, Steffen Dettling, et al.. (2024). Myeloid-T cell interplay and cell state transitions associated with checkpoint inhibitor response in melanoma. Med. 5(7). 759–779.e7. 5 indexed citations
3.
Schwalie, Petra, Tamara Hüsser, Caroline Waltzinger, et al.. (2022). Combinations of Toll-like receptor 8 agonist TL8-506 activate human tumor-derived dendritic cells. Journal for ImmunoTherapy of Cancer. 10(6). e004268–e004268. 13 indexed citations
4.
Mayoux, Maud, Marieke F. Fransen, Andreas Roller, et al.. (2017). Abstract 3658: Dendritic cells dictate the responsiveness of PD-L1 blockade in cancer. Cancer Research. 77(13_Supplement). 3658–3658. 2 indexed citations
5.
Mollah, Shamim, et al.. (2014). Correction to: “Flt3L Dependence Helps Define an Uncharacterized Subset of Murine Cutaneous Dendritic Cells”. Journal of Investigative Dermatology. 134(11). 2850–2851. 1 indexed citations
6.
Ghosh, Hiyaa S., Michele Ceribelli, Ines Matos, et al.. (2014). ETO family protein Mtg16 regulates the balance of dendritic cell subsets by repressing Id2. The Journal of Experimental Medicine. 211(8). 1623–1635. 38 indexed citations
7.
Anandasabapathy, Niroshana, Shamim Mollah, Sze‐Wah Tse, et al.. (2014). Classical Flt3L-dependent dendritic cells control immunity to protein vaccine. The Journal of Experimental Medicine. 211(9). 1875–1891. 79 indexed citations
8.
Mollah, Shamim, Sze‐Wah Tse, Ines Matos, et al.. (2013). Flt3L Dependence Helps Define an Uncharacterized Subset of Murine Cutaneous Dendritic Cells. Journal of Investigative Dermatology. 134(5). 1265–1275. 27 indexed citations
9.
Matos, Ines, Olga Mizenina, Ashira Lubkin, Ralph M. Steinman, & Juliana Idoyaga. (2013). Targeting Leishmania major Antigens to Dendritic Cells In Vivo Induces Protective Immunity. PLoS ONE. 8(6). e67453–e67453. 35 indexed citations
10.
Matos, Ines, Olga Mizenina, Ashira Lubkin, Ralph M. Steinman, & Juliana Idoyaga. (2013). Correction: Targeting Leishmania major Antigens to Dendritic Cells In Vivo Induces Protective Immunity. PLoS ONE. 8(9). 7 indexed citations
11.
Hemmi, Hiroaki, Neeha Zaidi, Bei Wang, et al.. (2011). Treml4, an Ig Superfamily Member, Mediates Presentation of Several Antigens to T Cells In Vivo, Including Protective Immunity to HER2 Protein. The Journal of Immunology. 188(3). 1147–1155. 32 indexed citations
12.
Cheong, Cheolho, Ines Matos, Jae‐Hoon Choi, et al.. (2010). New monoclonal anti-mouse DC-SIGN antibodies reactive with acetone-fixed cells. Journal of Immunological Methods. 360(1-2). 66–75. 14 indexed citations
13.
Cheong, Cheolho, Ines Matos, Jae‐Hoon Choi, et al.. (2010). Microbial Stimulation Fully Differentiates Monocytes to DC-SIGN/CD209+ Dendritic Cells for Immune T Cell Areas. Cell. 143(3). 416–429. 467 indexed citations breakdown →
14.
Cheong, Cheolho, Ines Matos, Jae‐Hoon Choi, et al.. (2010). Microbial stimulation fully differentiates monocytes to DC-SIGN/CD209(+) dendritic cells for immune T cell areas. Digital Commons - RU (Rockefeller University). 143(3). 416–429. 1 indexed citations
15.
Longhi, M. Paula, Christine Trumpfheller, Juliana Idoyaga, et al.. (2009). Dendritic cells require a systemic type I interferon response to mature and induce CD4+ Th1 immunity with poly IC as adjuvant. The Journal of Experimental Medicine. 206(7). 1589–1602. 536 indexed citations breakdown →

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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