Jesse Haramati

467 total citations
27 papers, 343 citations indexed

About

Jesse Haramati is a scholar working on Immunology, Molecular Biology and Oncology. According to data from OpenAlex, Jesse Haramati has authored 27 papers receiving a total of 343 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Immunology, 9 papers in Molecular Biology and 8 papers in Oncology. Recurrent topics in Jesse Haramati's work include Immune Cell Function and Interaction (10 papers), Immunotherapy and Immune Responses (5 papers) and Liver Disease Diagnosis and Treatment (4 papers). Jesse Haramati is often cited by papers focused on Immune Cell Function and Interaction (10 papers), Immunotherapy and Immune Responses (5 papers) and Liver Disease Diagnosis and Treatment (4 papers). Jesse Haramati collaborates with scholars based in Mexico, United States and Germany. Jesse Haramati's co-authors include Susana del Toro‐Arreola, Martha Cecilia Téllez‐Bañuelos, Nehla Banu, Miriam Ruth Bueno‐Topete, Sandeep Surendra Panikar, Blanca Estela Bastidas‐Ramírez, Adriana Aguilar‐Lemarroy, Pablo Cesar Ortiz‐Lazareno, Luis Felipe Jave‐Suárez and Ana Laura Pereira-Suárez and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Controlled Release and Neuroscience & Biobehavioral Reviews.

In The Last Decade

Jesse Haramati

24 papers receiving 339 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jesse Haramati Mexico 13 133 119 95 43 31 27 343
Matthias Schröder Germany 12 115 0.9× 154 1.3× 57 0.6× 18 0.4× 28 0.9× 28 325
Olga Will Germany 11 56 0.4× 138 1.2× 87 0.9× 44 1.0× 32 1.0× 27 352
Zbigniew Korwek Poland 11 109 0.8× 180 1.5× 67 0.7× 19 0.4× 14 0.5× 14 398
Qiu Tu China 10 48 0.4× 210 1.8× 84 0.9× 61 1.4× 14 0.5× 16 465
Chaoyu Zhang China 9 31 0.2× 119 1.0× 48 0.5× 37 0.9× 23 0.7× 14 304
Suhe Dong China 13 67 0.5× 184 1.5× 42 0.4× 68 1.6× 77 2.5× 26 402
Jinkun Liu China 9 37 0.3× 135 1.1× 58 0.6× 15 0.3× 55 1.8× 28 317
Jinbao Zong China 12 183 1.4× 189 1.6× 100 1.1× 19 0.4× 9 0.3× 26 416
Giulia Cerrato France 9 148 1.1× 142 1.2× 102 1.1× 18 0.4× 17 0.5× 17 346

Countries citing papers authored by Jesse Haramati

Since Specialization
Citations

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

Fields of papers citing papers by Jesse Haramati

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jesse Haramati

This figure shows the co-authorship network connecting the top 25 collaborators of Jesse Haramati. A scholar is included among the top collaborators of Jesse Haramati 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 Jesse Haramati. Jesse Haramati 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
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Bastidas‐Ramírez, Blanca Estela, Martha Cecilia Téllez‐Bañuelos, Pablo Cesar Ortiz‐Lazareno, et al.. (2024). New Advances in the Study of CMTM6, a Focus on Its Novel Non-Canonical Cellular Locations, and Functions beyond Its Role as a PD-L1 Stabilizer. Cancers. 16(18). 3126–3126.
3.
Montoya‐Buelna, Margarita, et al.. (2024). Contribution of extracellular vesicles to steatosis-related liver disease and their therapeutic potential. World Journal of Hepatology. 16(9). 1211–1228. 2 indexed citations
4.
Ortiz‐Lazareno, Pablo Cesar, et al.. (2023). A Modified Method for the Quantification of Immune Checkpoint Ligands on Exosomes from Human Serum using Flow Cytometry. Technology in Cancer Research & Treatment. 22. 2213892212–2213892212. 4 indexed citations
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Bueno‐Topete, Miriam Ruth, Natali Vega‐Magaña, Blanca Estela Bastidas‐Ramírez, et al.. (2022). Non‐fitness status of peripheral NK cells defined by decreased NKp30 and perforin, and increased soluble B7H6, in cervical cancer patients. Immunology. 168(3). 538–553. 6 indexed citations
7.
Panikar, Sandeep Surendra, Nehla Banu, Jesse Haramati, et al.. (2021). Nanobodies as efficient drug-carriers: Progress and trends in chemotherapy. Journal of Controlled Release. 334. 389–412. 41 indexed citations
8.
Téllez‐Bañuelos, Martha Cecilia, Georgina Hernández‐Flores, Alejandro Bravo‐Cuéllar, et al.. (2020). Differential effects of alliin and allicin on apoptosis and senescence in luminal A and triple‐negative breast cancer: Caspase, ΔΨm, and pro‐apoptotic gene involvement. Fundamental and Clinical Pharmacology. 34(6). 671–686. 29 indexed citations
9.
Ortiz‐Lazareno, Pablo Cesar, Blanca Estela Bastidas‐Ramírez, Abraham Zepeda‐Moreno, et al.. (2020). Immune checkpoint expression on peripheral cytotoxic lymphocytes in cervical cancer patients: moving beyond the PD-1/PD-L1 axis. Clinical & Experimental Immunology. 204(1). 78–95. 18 indexed citations
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Minjarez, Benito, et al.. (2017). Behavioral changes in models of chemoconvulsant-induced epilepsy: A review. Neuroscience & Biobehavioral Reviews. 83. 373–380. 19 indexed citations
13.
Hernández‐Gutiérrez, Rodolfo, Miriam Ruth Bueno‐Topete, Jesse Haramati, et al.. (2017). Characterization of B7H6, an endogenous ligand for the NK cell activating receptor NKp30, reveals the identity of two different soluble isoforms during normal human pregnancy. Immunobiology. 223(1). 57–63. 16 indexed citations
14.
Bueno‐Topete, Miriam Ruth, Luis Felipe Jave‐Suárez, Eduardo Gómez-Bañuelos, et al.. (2017). Loss of CD28 within CD4+ T cell subsets from cervical cancer patients is accompanied by the acquisition of intracellular perforin, and is further enhanced by NKG2D expression. Immunology Letters. 182. 30–38. 21 indexed citations
15.
Nuño, J., Susana del Toro‐Arreola, Natali Vega‐Magaña, et al.. (2016). Expression of ADAM10, Fas, FasL and Soluble FasL in Patients with Oral Squamous Cell Carcinoma (OSCC) and their Association with Clinical-Pathological Parameters. Pathology & Oncology Research. 23(2). 345–353. 10 indexed citations
16.
Téllez‐Bañuelos, Martha Cecilia, et al.. (2016). Chronic exposure to endosulfan induces inflammation in murine colon via β-catenin expression and IL-6 production. Journal of Immunotoxicology. 13(6). 842–849. 14 indexed citations
17.
García‐Chagollán, Mariel, Luis Felipe Jave‐Suárez, Jesse Haramati, et al.. (2015). An approach to the immunophenotypic features of circulating CD4+NKG2D+ T cells in invasive cervical carcinoma. Journal of Biomedical Science. 22(1). 91–91. 12 indexed citations
18.
García‐Chagollán, Mariel, Luis Felipe Jave‐Suárez, Jesse Haramati, et al.. (2013). Substantial increase in the frequency of circulating CD4+NKG2D+ T cells in patients with cervical intraepithelial neoplasia grade 1. Journal of Biomedical Science. 20(1). 60–60. 13 indexed citations
19.
Toro‐Arreola, Susana del, Adriana Aguilar‐Lemarroy, Ángel Cid-Arregui, et al.. (2011). MHC class I-related chain A and B ligands are differentially expressed in human cervical cancer cell lines. Cancer Cell International. 11(1). 15–15. 17 indexed citations
20.
Haramati, Jesse, et al.. (2007). A Rapid Method for Skin Grafting in Mice That Greatly Enhances Graft and Recipient Survival. Transplantation. 84(10). 1364–1367. 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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