Natalia Ramírez

2.1k total citations · 1 hit paper
32 papers, 1.7k citations indexed

About

Natalia Ramírez is a scholar working on Immunology, Epidemiology and Oncology. According to data from OpenAlex, Natalia Ramírez has authored 32 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Immunology, 14 papers in Epidemiology and 13 papers in Oncology. Recurrent topics in Natalia Ramírez's work include Immune Cell Function and Interaction (12 papers), Cytomegalovirus and herpesvirus research (12 papers) and T-cell and B-cell Immunology (7 papers). Natalia Ramírez is often cited by papers focused on Immune Cell Function and Interaction (12 papers), Cytomegalovirus and herpesvirus research (12 papers) and T-cell and B-cell Immunology (7 papers). Natalia Ramírez collaborates with scholars based in Spain, United Kingdom and United States. Natalia Ramírez's co-authors include Eva Bandrés, Ruth Zárate, Jesús García‐Foncillas, Xabier Agirre, Nerea Bitarte, I. Moreno, Mariano Monzó, Alfons Navarro, Elena Cubedo and Raquel Malumbres and has published in prestigious journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and Clinical Cancer Research.

In The Last Decade

Natalia Ramírez

30 papers receiving 1.7k citations

Hit Papers

Identification by Real-time PCR of 13 mature microRNAs di... 2006 2026 2012 2019 2006 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
Natalia Ramírez Spain 14 1.3k 1.3k 230 158 104 32 1.7k
Michael Lam United States 5 1.1k 0.8× 790 0.6× 231 1.0× 249 1.6× 65 0.6× 12 1.4k
Geert Harms Netherlands 19 1.0k 0.8× 846 0.7× 216 0.9× 358 2.3× 60 0.6× 25 1.6k
Wenjin Xi China 17 970 0.7× 685 0.5× 236 1.0× 235 1.5× 56 0.5× 36 1.3k
Bi-Jun Huang China 20 900 0.7× 597 0.5× 283 1.2× 163 1.0× 58 0.6× 29 1.2k
Chang–Gong Liu United States 11 2.0k 1.5× 1.9k 1.5× 273 1.2× 125 0.8× 93 0.9× 13 2.5k
Qunying Yang China 11 731 0.6× 538 0.4× 191 0.8× 373 2.4× 96 0.9× 35 1.3k
Jung‐Joo Choi South Korea 24 830 0.6× 508 0.4× 316 1.4× 386 2.4× 191 1.8× 41 1.5k
Ma-Yan Huang China 9 1.3k 1.0× 1.1k 0.9× 225 1.0× 96 0.6× 29 0.3× 9 1.6k
Guoen Fang China 16 945 0.7× 856 0.7× 278 1.2× 214 1.4× 146 1.4× 33 1.5k
Melanie Winkle Netherlands 10 1.2k 0.9× 992 0.8× 69 0.3× 90 0.6× 86 0.8× 13 1.4k

Countries citing papers authored by Natalia Ramírez

Since Specialization
Citations

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

Fields of papers citing papers by Natalia Ramírez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Natalia Ramírez

This figure shows the co-authorship network connecting the top 25 collaborators of Natalia Ramírez. A scholar is included among the top collaborators of Natalia Ramírez 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 Natalia Ramírez. Natalia Ramírez 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.
Arasanz, Hugo, Ana E. Huerta, Natália Castro, et al.. (2025). CAR-T Therapy for the Treatment of Colorectal Cancer. Discovery Medicine. 37(195). 618–618. 1 indexed citations
2.
Kwon, Mi, Laura Solán, Rebeca Bailén, et al.. (2022). Risk prediction of CMV reactivation after allogeneic stem cell transplantation using five non-HLA immunogenetic polymorphisms. Annals of Hematology. 101(7). 1567–1576. 6 indexed citations
3.
Ramírez, Natalia, et al.. (2021). Meningitis bacteriana aguda del adulto adquirida en la comunidad. SHILAP Revista de lepidopterología. 37(1 Supl 1). 55–63. 2 indexed citations
4.
Soria, Elena, et al.. (2019). Telomerase-specific attenuated viruses, a definitive strategy or just one more in circulating tumor cells detection anthology?. Cancer Letters. 469. 490–497. 5 indexed citations
5.
Mansilla, Cristina, et al.. (2018). Combined Selection System to Lower the Cutoff for Plasma Cell Enrichment Applied to iFISH Analysis in Multiple Myeloma. Translational Oncology. 11(3). 647–652.
6.
Mansilla, Cristina, Elena Soria, & Natalia Ramírez. (2018). The identification and isolation of CTCs: A biological Rubik’s cube. Critical Reviews in Oncology/Hematology. 126. 129–134. 20 indexed citations
7.
Viúdez, A., Ana De Jesus‐Acosta, Filipe L.F. Carvalho, et al.. (2016). Pancreatic neuroendocrine tumors: Challenges in an underestimated disease. Critical Reviews in Oncology/Hematology. 101. 193–206. 15 indexed citations
8.
Mansilla, Cristina, et al.. (2015). Assessment of the effector function of CMV-specific CTLs isolated using MHC-multimers from granulocyte-colony stimulating factor mobilized peripheral blood. Journal of Translational Medicine. 13(1). 165–165. 2 indexed citations
9.
Viúdez, A., et al.. (2014). Nab-paclitaxel: A flattering facelift. Critical Reviews in Oncology/Hematology. 92(3). 166–180. 32 indexed citations
10.
Ramírez, Natalia & Eduardo Olavarría. (2013). Viral-specific adoptive immunotherapy after allo-SCT: the role of multimer-based selection strategies. Bone Marrow Transplantation. 48(10). 1265–1270. 13 indexed citations
11.
Liechtenstein, Thérèse, Christopher Bricogne, Alessio Lanna, et al.. (2013). Immune modulation by genetic modification of dendritic cells with lentiviral vectors. Virus Research. 176(1-2). 1–15. 18 indexed citations
12.
Zárate, Ruth, Javier Rodríguez, Eva Bandrés, et al.. (2010). Oxaliplatin, irinotecan and capecitabine as first-line therapy in metastatic colorectal cancer (mCRC): a dose-finding study and pharmacogenomic analysis. British Journal of Cancer. 102(6). 987–994. 40 indexed citations
13.
Bandrés, Eva, Nerea Bitarte, Fernando Arias, et al.. (2009). microRNA-451 Regulates Macrophage Migration Inhibitory Factor Production and Proliferation of Gastrointestinal Cancer Cells. Clinical Cancer Research. 15(7). 2281–2290. 302 indexed citations
14.
Bandrés, Eva, Xabier Agirre, Nerea Bitarte, et al.. (2009). Epigenetic regulation of microRNA expression in colorectal cancer. International Journal of Cancer. 125(11). 2737–2743. 369 indexed citations
15.
Ramírez, Natalia. (2008). Centralización de la tesorería: un caso práctico. 46–54.
16.
Ramírez, Natalia, Eva Bandrés, Alfons Navarro, et al.. (2008). Epigenetic events in normal colonic mucosa surrounding colorectal cancer lesions. European Journal of Cancer. 44(17). 2689–2695. 28 indexed citations
17.
Bandrés, Eva, Xabier Agirre, Natalia Ramírez, Ruth Zárate, & Jesús García‐Foncillas. (2007). MicroRNAs as Cancer Players: Potential Clinical and Biological Effects. DNA and Cell Biology. 26(5). 273–282. 57 indexed citations
18.
Merino-Torres, Juan Francisco, Natalia Ramírez, Cristina Moreno, et al.. (2007). BY55/CD160 cannot be considered a cytotoxic marker in cytomegalovirus-specific human CD8+ T cells. Clinical & Experimental Immunology. 149(1). 87–96. 10 indexed citations
19.
Bandrés, Eva, Elena Cubedo, Xabier Agirre, et al.. (2006). Identification by Real-time PCR of 13 mature microRNAs differentially expressed in colorectal cancer and non-tumoral tissues.. Molecular Cancer. 5(1). 29–29. 706 indexed citations breakdown →
20.
Merino, Juana, et al.. (2004). Lipopolysaccharide needs soluble CD14 to interact with TLR4 in human monocytes depleted of membrane CD14. Microbes and Infection. 6(11). 990–995. 24 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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