Barbara Camisa

4.6k total citations · 1 hit paper
27 papers, 2.6k citations indexed

About

Barbara Camisa is a scholar working on Oncology, Immunology and Genetics. According to data from OpenAlex, Barbara Camisa has authored 27 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Oncology, 14 papers in Immunology and 8 papers in Genetics. Recurrent topics in Barbara Camisa's work include CAR-T cell therapy research (21 papers), Virus-based gene therapy research (7 papers) and Immune Cell Function and Interaction (7 papers). Barbara Camisa is often cited by papers focused on CAR-T cell therapy research (21 papers), Virus-based gene therapy research (7 papers) and Immune Cell Function and Interaction (7 papers). Barbara Camisa collaborates with scholars based in Italy, United States and United Kingdom. Barbara Camisa's co-authors include Attilio Bondanza, Fabio Ciceri, Chiara Bonini, Claudio Bordignon, Monica Casucci, Laura Falcone, Margherita Norelli, Maurilio Ponzoni, Catia Traversari and Claudio Doglioni and has published in prestigious journals such as Nature Medicine, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Barbara Camisa

27 papers receiving 2.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Monocyte-derived IL-1 and IL-6 are differentially required for cytokine-release syndrome and neurotoxicity due to CAR T cells

2018 997 citations Margherita Norelli, Barbara Camisa et al. Nature Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Barbara Camisa Italy	13	1.8k	1.2k	598	533	518	27	2.6k
Jinjuan Wang China	12	1.6k 0.9×	657 0.6×	462 0.8×	557 1.0×	508 1.0×	32	1.8k
Bruria Shalmon Israel	17	1.1k 0.6×	834 0.7×	339 0.6×	214 0.4×	66 0.1×	31	1.6k
Aurore Saudemont United Kingdom	25	1.8k 1.0×	2.0k 1.7×	695 1.2×	260 0.5×	138 0.3×	55	3.0k
Guitta Maki France	19	1.2k 0.7×	1.6k 1.4×	412 0.7×	126 0.2×	67 0.1×	24	2.3k
Deborah J. Burt United Kingdom	17	985 0.6×	655 0.6×	368 0.6×	143 0.3×	203 0.4×	24	1.6k
Sid P. Kerkar United States	19	2.1k 1.2×	1.6k 1.3×	628 1.1×	637 1.2×	418 0.8×	36	2.7k
Keichiro Mihara Japan	21	1.2k 0.7×	645 0.5×	914 1.5×	340 0.6×	278 0.5×	70	2.4k
Joseph J. Skitzki United States	22	928 0.5×	752 0.6×	461 0.8×	85 0.2×	254 0.5×	74	1.9k
Liza B. John Australia	16	1.7k 1.0×	1.2k 1.1×	612 1.0×	399 0.7×	389 0.8×	27	2.4k
Jonathan D. Fish United States	17	985 0.6×	476 0.4×	467 0.8×	362 0.7×	290 0.6×	32	1.6k

Countries citing papers authored by Barbara Camisa

Since Specialization

Citations

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

Fields of papers citing papers by Barbara Camisa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barbara Camisa

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

All Works

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20 of 20 papers shown

Doglio, Matteo, Alessio Ugolini, Barbara Camisa, et al.. (2024). Regulatory T cells expressing CD19-targeted chimeric antigen receptor restore homeostasis in Systemic Lupus Erythematosus. Nature Communications. 15(1). 2542–2542. 42 indexed citations

Cianciotti, Beatrice Claudia, Zulma Magnani, Barbara Camisa, et al.. (2024). TIM-3, LAG-3, or 2B4 gene disruptions increase the anti-tumor response of engineered T cells. Frontiers in Immunology. 15. 1315283–1315283. 12 indexed citations

Arcangeli, Silvia, Laura Falcone, Barbara Camisa, et al.. (2023). CD4 CAR-T cells targeting CD19 play a key role in exacerbating cytokine release syndrome, while maintaining long-term responses. Journal for ImmunoTherapy of Cancer. 11(1). e005878–e005878. 30 indexed citations

Camisa, Barbara, Laura Falcone, Francesca Sanvito, et al.. (2023). 1242 Mouse model of CAR-related ICANS development after treatment with human CD19 CAR-T cells. SHILAP Revista de lepidopterología. A1372–A1372. 1 indexed citations

Arcangeli, Silvia, Laura Falcone, Barbara Camisa, et al.. (2020). Next-Generation Manufacturing Protocols Enriching TSCM CAR T Cells Can Overcome Disease-Specific T Cell Defects in Cancer Patients. Frontiers in Immunology. 11. 1217–1217. 96 indexed citations

Brunetto, Emanuela, Lucia De Monte, Gianpaolo Balzano, et al.. (2019). The IL-1/IL-1 receptor axis and tumor cell released inflammasome adaptor ASC are key regulators of TSLP secretion by cancer associated fibroblasts in pancreatic cancer. Journal for ImmunoTherapy of Cancer. 7(1). 45–45. 65 indexed citations

Casucci, Monica, Laura Falcone, Barbara Camisa, et al.. (2018). Extracellular NGFR Spacers Allow Efficient Tracking and Enrichment of Fully Functional CAR-T Cells Co-Expressing a Suicide Gene. Frontiers in Immunology. 9. 507–507. 72 indexed citations

Norelli, Margherita, Barbara Camisa, Giulia Barbiera, et al.. (2018). Monocyte-derived IL-1 and IL-6 are differentially required for cytokine-release syndrome and neurotoxicity due to CAR T cells. Nature Medicine. 24(6). 739–748. 997 indexed citations breakdown →

Gréco, Béatrice, Barbara Camisa, Laura Falcone, et al.. (2018). Combining De-Glycosylating Agents with CAR-T Cells for Targeting Solid Tumors and Reducing Toxicity. Blood. 132(Supplement 1). 4544–4544. 3 indexed citations

10.

Escobar, Giulia, Luigi Barbarossa, Giulia Barbiera, et al.. (2018). Interferon gene therapy reprograms the leukemia microenvironment inducing protective immunity to multiple tumor antigens. Nature Communications. 9(1). 2896–2896. 43 indexed citations

11.

Andolfi, Grazia, Fabio Russo, Antonello E. Spinelli, et al.. (2017). IL-10-Engineered Human CD4+ Tr1 Cells Eliminate Myeloid Leukemia in an HLA Class I-Dependent Mechanism. Molecular Therapy. 25(10). 2254–2269. 41 indexed citations

12.

Norelli, Margherita, Barbara Camisa, & Attilio Bondanza. (2016). Modeling Human Graft-Versus-Host Disease in Immunocompromised Mice. Methods in molecular biology. 1393. 127–132. 2 indexed citations

13.

Casucci, Monica, Serena Perna, Laura Falcone, et al.. (2013). Graft-versus-leukemia Effect of HLA-haploidentical Central-memory T-cells Expanded With Leukemic APCs and Modified With a Suicide Gene. Molecular Therapy. 21(2). 466–475. 17 indexed citations

14.

Casucci, Monica, Benedetta Nicolis di Robilant, Laura Falcone, et al.. (2013). CD44v6-targeted T cells mediate potent antitumor effects against acute myeloid leukemia and multiple myeloma. Blood. 122(20). 3461–3472. 290 indexed citations

15.

Robilant, Benedetta Nicolis di, Monica Casucci, Laura Falcone, et al.. (2013). CD44v6 Is Required For In Vivo Tumorigenesis Of Human AML and MM Cells: Role Of Microenvironmental Signals and Therapeutic Implications. Blood. 122(21). 605–605. 6 indexed citations

16.

Viganò, Paola, Davide Gentilini, Barbara Camisa, et al.. (2012). The selective vitamin D receptor agonist, elocalcitol, reduces endometriosis development in a mouse model by inhibiting peritoneal inflammation. Human Reproduction. 27(7). 2010–2019. 84 indexed citations

17.

Cieri, Nicoletta, Barbara Camisa, Fabienne Cocchiarella, et al.. (2012). IL-7 and IL-15 instruct the generation of human memory stem T cells from naive precursors. Blood. 121(4). 573–584. 455 indexed citations

18.

Casucci, Monica, Benedetta Nicolis di Robilant, Laura Falcone, et al.. (2012). Co-Expression of a Suicide Gene in CAR-Redirected T Cells Enables the Safe Targeting of CD44v6 for Leukemia and Myeloma Eradication. Blood. 120(21). 949–949. 5 indexed citations

19.

Bacci, Monica, Annalisa Capobianco, Antonella Monno, et al.. (2009). Macrophages Are Alternatively Activated in Patients with Endometriosis and Required for Growth and Vascularization of Lesions in a Mouse Model of Disease. American Journal Of Pathology. 175(2). 547–556. 351 indexed citations

20.

Camisa, Barbara, et al.. (2008). Inter-species differences in sensitivity to the calcemic activity of the novel 1,25-dihydroxyvitamin D3 analog BXL746. Regulatory Toxicology and Pharmacology. 52(3). 332–341. 5 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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