Juan M. Zapata

7.5k total citations · 1 hit paper
81 papers, 6.2k citations indexed

About

Juan M. Zapata is a scholar working on Molecular Biology, Immunology and Cancer Research. According to data from OpenAlex, Juan M. Zapata has authored 81 papers receiving a total of 6.2k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 35 papers in Immunology and 24 papers in Cancer Research. Recurrent topics in Juan M. Zapata's work include Cell death mechanisms and regulation (28 papers), NF-κB Signaling Pathways (22 papers) and Chronic Lymphocytic Leukemia Research (16 papers). Juan M. Zapata is often cited by papers focused on Cell death mechanisms and regulation (28 papers), NF-κB Signaling Pathways (22 papers) and Chronic Lymphocytic Leukemia Research (16 papers). Juan M. Zapata collaborates with scholars based in United States, Spain and Germany. Juan M. Zapata's co-authors include John C. Reed, Shinichi Kitada, Stanisław Krajewski, Maryla Krajewska, Michael Andreeff, Hong‐Gang Wang, Shinichi Takayama, Ahmed Shabaik, Randy D. Gascoyne and Kate Welsh and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and The Journal of Cell Biology.

In The Last Decade

Juan M. Zapata

81 papers receiving 6.1k citations

Hit Papers

Expression of Apoptosis-Regulating Proteins in Chronic Ly... 1998 2026 2007 2016 1998 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
Juan M. Zapata United States 44 4.0k 1.8k 1.4k 1.2k 1.0k 81 6.2k
Domenico Delia Italy 43 4.2k 1.1× 950 0.5× 2.5k 1.8× 1.2k 1.0× 447 0.4× 125 6.9k
David T. Weaver United States 49 6.5k 1.6× 1.4k 0.7× 2.6k 1.9× 1.3k 1.1× 437 0.4× 150 9.0k
Elizabeth W. Newcomb United States 43 3.4k 0.9× 1000 0.6× 2.6k 1.8× 1.5k 1.2× 1.9k 1.9× 81 6.5k
Luisa Lanfrancone Italy 38 4.9k 1.2× 1.2k 0.7× 1.6k 1.1× 813 0.7× 325 0.3× 95 7.8k
Ralph Schwall United States 48 6.1k 1.5× 1.4k 0.8× 2.7k 1.9× 1.2k 1.0× 402 0.4× 85 10.2k
Dan Grandér Sweden 50 3.9k 1.0× 1.4k 0.8× 1.7k 1.2× 1.9k 1.5× 670 0.7× 125 6.5k
Karen E. Pollok United States 38 2.7k 0.7× 1.6k 0.9× 1.7k 1.2× 671 0.5× 677 0.7× 142 5.6k
Simon N. Willis Australia 24 4.9k 1.2× 2.0k 1.1× 1.7k 1.2× 626 0.5× 351 0.3× 36 7.2k
Kurt Bommert Germany 35 3.1k 0.8× 1.2k 0.7× 1.8k 1.3× 1.0k 0.8× 323 0.3× 65 5.1k
Jonas A. Nilsson Sweden 38 5.5k 1.4× 1.5k 0.8× 2.0k 1.4× 2.1k 1.7× 319 0.3× 110 7.8k

Countries citing papers authored by Juan M. Zapata

Since Specialization
Citations

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

Fields of papers citing papers by Juan M. Zapata

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Juan M. Zapata. 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 Juan M. Zapata. The network helps show where Juan M. Zapata may publish in the future.

Co-authorship network of co-authors of Juan M. Zapata

This figure shows the co-authorship network connecting the top 25 collaborators of Juan M. Zapata. A scholar is included among the top collaborators of Juan M. Zapata 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 Juan M. Zapata. Juan M. Zapata 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.
Rosa, Juan Vladimir de la, Carlos Tabraue, Zhiqiang Huang, et al.. (2024). Reprogramming of the LXRα Transcriptome Sustains Macrophage Secondary Inflammatory Responses. Advanced Science. 11(20). e2307201–e2307201. 2 indexed citations
2.
Glez‐Vaz, Javier, Arantza Azpilikueta, María C. Ochoa, et al.. (2023). CD137 (4-1BB) requires physically associated cIAPs for signal transduction and antitumor effects. Science Advances. 9(33). eadf6692–eadf6692. 6 indexed citations
3.
Domı́nguez, Juan Manuel, Gema Pérez-Chacón, María José Guillén, et al.. (2020). CD13 as a new tumor target for antibody-drug conjugates: validation with the conjugate MI130110. Journal of Hematology & Oncology. 13(1). 32–32. 19 indexed citations
4.
Pérez-Chacón, Gema, Carolina Martínez‐Laperche, Beatriz Somovilla-Crespo, et al.. (2015). Indole-3-Carbinol Synergizes with and Restores Fludarabine Sensitivity in Chronic Lymphocytic Leukemia Cells Irrespective of p53 Activity and Treatment Resistances. Clinical Cancer Research. 22(1). 134–145. 7 indexed citations
5.
Lorenzo, Claudia De, et al.. (2015). Efficient expression of bioactive murine IL12 as a self-processing P2A polypeptide driven by inflammation-regulated promoters in tumor cell lines. Cancer Gene Therapy. 22(11). 542–551. 3 indexed citations
6.
Pérez-Chacón, Gema, Carolina Martínez‐Laperche, Beatriz Somovilla-Crespo, et al.. (2014). 39 Phytochemical indole-3-carbinol synergizes strongly with fludarabine and induces p53-dependent and -independent cell death in chronic lymphocytic leukemia cells irrespective of their IGHV mutation state and treatment resistances. European Journal of Cancer. 50. 18–18. 1 indexed citations
7.
Pérez-Chacón, Gema, Cristóbal de los Rı́os, & Juan M. Zapata. (2014). Indole-3-carbinol induces cMYC and IAP-family downmodulation and promotes apoptosis of Epstein–Barr virus (EBV)-positive but not of EBV-negative Burkitt's lymphoma cell lines. Pharmacological Research. 89. 46–56. 15 indexed citations
8.
Somovilla-Crespo, Beatriz, Manuel Alfonso-Pérez, Carlos Cuesta‐Mateos, et al.. (2013). Anti-CCR7 therapy exerts a potent anti-tumor activity in a xenograft model of human mantle cell lymphoma. Journal of Hematology & Oncology. 6(1). 89–89. 30 indexed citations
9.
Zapata, Juan M., David Llobet‐Navàs, Maryla Krajewska, et al.. (2008). Lymphocyte-specific TRAF3 transgenic mice have enhanced humoral responses and develop plasmacytosis, autoimmunity, inflammation, and cancer. Blood. 113(19). 4595–4603. 40 indexed citations
10.
Bailly‐Maitre, Béatrice, Emilie A. Bard-Chapeau, Frédéric Luciano, et al.. (2007). Mice Lacking bi-1 Gene Show Accelerated Liver Regeneration. Cancer Research. 67(4). 1442–1450. 25 indexed citations
11.
Zapata, Juan M., Sophie Lefebvre, & John C. Reed. (2007). Targeting TRAFs for Therapeutic Intervention. Advances in experimental medicine and biology. 597. 188–201. 32 indexed citations
12.
Fukushima, Toru, Juan M. Zapata, Netai C. Singha, et al.. (2006). Critical Function for SIP, a Ubiquitin E3 Ligase Component of the β-Catenin Degradation Pathway, for Thymocyte Development and G1 Checkpoint. Immunity. 24(1). 29–39. 49 indexed citations
13.
Reed, John C., Kutbuddin S. Doctor, Ana M. Rojas, et al.. (2003). Comparative Analysis of Apoptosis and Inflammation Genes of Mice and Humans. Genome Research. 13(6b). 1376–1388. 97 indexed citations
14.
Zapata, Juan M., Maryla Krajewska, Stanisław Krajewski, et al.. (2000). TNFR-Associated Factor Family Protein Expression in Normal Tissues and Lymphoid Malignancies. The Journal of Immunology. 165(9). 5084–5096. 118 indexed citations
15.
Kitada, Shinichi, Juan M. Zapata, Michael Andreeff, & John C. Reed. (2000). Protein kinase inhibitors flavopiridol and 7-hydroxy-staurosporine down-regulate antiapoptosis proteins in B-cell chronic lymphocytic leukemia. Blood. 96(2). 393–397. 172 indexed citations
16.
Ye, Xin, Patrick Mehlen, Shahrooz Rabizadeh, et al.. (1999). TRAF Family Proteins Interact with the Common Neurotrophin Receptor and Modulate Apoptosis Induction. Journal of Biological Chemistry. 274(42). 30202–30208. 158 indexed citations
17.
Kitada, Shinichi, Maryla Krajewska, Xianhui Zhang, et al.. (1998). Expression and location of pro-apoptotic Bcl-2 family protein BAD in normal human tissues and tumor cell lines.. Europe PMC (PubMed Central). 152(1). 51–61. 96 indexed citations
18.
Takayama, Shinichi, S Krajewski, Maryla Krajewska, et al.. (1998). Expression and location of Hsp70/Hsc-binding anti-apoptotic protein BAG-1 and its variants in normal tissues and tumor cell lines.. PubMed. 58(14). 3116–31. 193 indexed citations
19.
Zapata, Juan M., Maryla Krajewska, Stanisław Krajewski, et al.. (1998). Expression of multiple apoptosis-regulatory genes in human breast cancer cell lines and primary tumors. Breast Cancer Research and Treatment. 47(2). 129–140. 98 indexed citations
20.
Krajewski, Stanisław, Juan M. Zapata, Maryla Krajewska, et al.. (1997). Immunohistochemical analysis of in vivo patterns of TRAF-3 expression, a member of the TNF receptor-associated factor family. The Journal of Immunology. 159(12). 5841–5852. 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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