Tarek Boussetta

1.0k total citations
16 papers, 838 citations indexed

About

Tarek Boussetta is a scholar working on Molecular Biology, Immunology and Physiology. According to data from OpenAlex, Tarek Boussetta has authored 16 papers receiving a total of 838 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 10 papers in Immunology and 2 papers in Physiology. Recurrent topics in Tarek Boussetta's work include Neutrophil, Myeloperoxidase and Oxidative Mechanisms (8 papers), Immune Response and Inflammation (5 papers) and Signaling Pathways in Disease (4 papers). Tarek Boussetta is often cited by papers focused on Neutrophil, Myeloperoxidase and Oxidative Mechanisms (8 papers), Immune Response and Inflammation (5 papers) and Signaling Pathways in Disease (4 papers). Tarek Boussetta collaborates with scholars based in France, Algeria and United States. Tarek Boussetta's co-authors include Jamel El‐Benna, Marie‐Anne Gougerot‐Pocidalo, Houssam Raad, Pham My‐Chan Dang, Yolande Kroviarski, Fathi Driss, Sahra Amel Belambri, Karama Makni‐Maalej, Françoise Morel and Rafik Bachoual and has published in prestigious journals such as Journal of Clinical Investigation, Blood and The Journal of Immunology.

In The Last Decade

Tarek Boussetta

16 papers receiving 827 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tarek Boussetta France 13 391 291 178 97 81 16 838
Lotte F. Hansen United States 11 615 1.6× 326 1.1× 84 0.5× 99 1.0× 16 0.2× 13 1.2k
Houssam Raad France 13 372 1.0× 359 1.2× 105 0.6× 150 1.5× 53 0.7× 16 844
Jean‐François Mirjolet France 11 258 0.7× 397 1.4× 58 0.3× 192 2.0× 78 1.0× 21 1.1k
Yeong Seok Kim South Korea 20 236 0.6× 408 1.4× 118 0.7× 37 0.4× 19 0.2× 51 907
Hyunkeun Song South Korea 21 443 1.1× 380 1.3× 61 0.3× 62 0.6× 24 0.3× 38 1.1k
Tingting Long China 18 157 0.4× 350 1.2× 52 0.3× 49 0.5× 148 1.8× 56 988
Emmanuelle Rollet‐Labelle Canada 18 386 1.0× 544 1.9× 26 0.1× 95 1.0× 52 0.6× 27 1.0k
Feng Tian China 16 192 0.5× 351 1.2× 43 0.2× 57 0.6× 41 0.5× 41 828
Zhiqiang Zheng China 18 89 0.2× 569 2.0× 146 0.8× 92 0.9× 43 0.5× 49 1.0k
Kaiyu Jiang United States 20 396 1.0× 378 1.3× 34 0.2× 41 0.4× 46 0.6× 60 1.1k

Countries citing papers authored by Tarek Boussetta

Since Specialization
Citations

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

Fields of papers citing papers by Tarek Boussetta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tarek Boussetta

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

All Works

16 of 16 papers shown
1.
Boussetta, Tarek, Houssam Raad, Marie‐Anne Gougerot‐Pocidalo, et al.. (2024). The peptidyl-prolyl isomerase Pin1 controls GM-CSF-induced priming of NADPH oxidase in human neutrophils and priming at inflammatory sites. International Immunopharmacology. 137. 112425–112425. 6 indexed citations
2.
Belambri, Sahra Amel, Viviana Marzaioli, Margarita Hurtado-Nédelec, et al.. (2022). Impaired p47phox phosphorylation in neutrophils from patients with p67phox-deficient chronic granulomatous disease. Blood. 139(16). 2512–2522. 12 indexed citations
3.
Liu, Min, et al.. (2021). Prolyl-Isomerase Pin1 Controls Key fMLP-Induced Neutrophil Functions. Biomedicines. 9(9). 1130–1130. 9 indexed citations
4.
Raad, Houssam, Hamad Hassan, Tarek Boussetta, et al.. (2020). The protein kinase A negatively regulates reactive oxygen species production by phosphorylating gp91phox/NOX2 in human neutrophils. Free Radical Biology and Medicine. 160. 19–27. 17 indexed citations
5.
Boussetta, Tarek, Sahra Amel Belambri, Viviana Marzaioli, et al.. (2016). Vasoactive intestinal peptide dampens formyl-peptide-induced ROS production and inflammation by targeting a MAPK-p47phox phosphorylation pathway in monocytes. Mucosal Immunology. 10(2). 332–340. 21 indexed citations
6.
Makni‐Maalej, Karama, Viviana Marzaioli, Tarek Boussetta, et al.. (2015). TLR8, but not TLR7, induces the priming of the NADPH oxidase activation in human neutrophils. Journal of Leukocyte Biology. 97(6). 1081–1087. 24 indexed citations
7.
Mkaddem, Sanae Ben, Gilles Hayem, Friederike Jönsson, et al.. (2014). Shifting FcγRIIA-ITAM from activation to inhibitory configuration ameliorates arthritis. Journal of Clinical Investigation. 124(9). 3945–3959. 78 indexed citations
8.
Hurtado-Nédelec, Margarita, Tarek Boussetta, Sahra Amel Belambri, et al.. (2013). Increased reactive oxygen species production and p47phox phosphorylation in neutrophils from myeloproliferative disorders patients with JAK2 (V617F) mutation. Haematologica. 98(10). 1517–1524. 51 indexed citations
9.
Liu, Miao, Tarek Boussetta, Karama Makni‐Maalej, et al.. (2013). Protectin DX, a Double Lipoxygenase Product of DHA, Inhibits Both ROS Production in Human Neutrophils and Cyclooxygenase Activities. Lipids. 49(1). 49–57. 62 indexed citations
10.
Aloulou, Meryem, Sanae Ben Mkaddem, Martine Biarnes‐Pelicot, et al.. (2012). IgG1 and IVIg induce inhibitory ITAM signaling through FcγRIII controlling inflammatory responses. Blood. 119(13). 3084–3096. 78 indexed citations
11.
Makni‐Maalej, Karama, Tarek Boussetta, Margarita Hurtado-Nédelec, et al.. (2012). The TLR7/8 Agonist CL097 Primes N-Formyl-Methionyl-Leucyl-Phenylalanine–Stimulated NADPH Oxidase Activation in Human Neutrophils: Critical Role of p47phox Phosphorylation and the Proline Isomerase Pin1. The Journal of Immunology. 189(9). 4657–4665. 39 indexed citations
12.
Dang, Pham My‐Chan, Houssam Raad, Tarek Boussetta, et al.. (2011). The NADPH oxidase cytosolic component p67phox is constitutively phosphorylated in human neutrophils: Regulation by a protein tyrosine kinase, MEK1/2 and phosphatases 1/2A. Biochemical Pharmacology. 82(9). 1145–1152. 26 indexed citations
13.
Bachoual, Rafik, et al.. (2011). An aqueous pomegranate peel extract inhibits neutrophil myeloperoxidase in vitro and attenuates lung inflammation in mice. Food and Chemical Toxicology. 49(6). 1224–1228. 87 indexed citations
14.
Boussetta, Tarek, Marie‐Anne Gougerot‐Pocidalo, Gilles Hayem, et al.. (2010). The prolyl isomerase Pin1 acts as a novel molecular switch for TNF-α–induced priming of the NADPH oxidase in human neutrophils. Blood. 116(26). 5795–5802. 82 indexed citations
15.
Boussetta, Tarek, Houssam Raad, Philippe Lettéron, et al.. (2009). Punicic Acid a Conjugated Linolenic Acid Inhibits TNFα-Induced Neutrophil Hyperactivation and Protects from Experimental Colon Inflammation in Rats. PLoS ONE. 4(7). e6458–e6458. 106 indexed citations
16.
Raad, Houssam, Tarek Boussetta, Yolande Kroviarski, et al.. (2008). Regulation of the phagocyte NADPH oxidase activity: phosphorylation of gp91 phox /NOX2 by protein kinase C enhances its diaphorase activity and binding to Rac2, p67 phox , and p47 phox. The FASEB Journal. 23(4). 1011–1022. 140 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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