Shampa Chatterjee

4.3k total citations
85 papers, 2.8k citations indexed

About

Shampa Chatterjee is a scholar working on Physiology, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Shampa Chatterjee has authored 85 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Physiology, 36 papers in Molecular Biology and 21 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Shampa Chatterjee's work include Nitric Oxide and Endothelin Effects (31 papers), Neutrophil, Myeloperoxidase and Oxidative Mechanisms (15 papers) and Redox biology and oxidative stress (12 papers). Shampa Chatterjee is often cited by papers focused on Nitric Oxide and Endothelin Effects (31 papers), Neutrophil, Myeloperoxidase and Oxidative Mechanisms (15 papers) and Redox biology and oxidative stress (12 papers). Shampa Chatterjee collaborates with scholars based in United States, India and Germany. Shampa Chatterjee's co-authors include Aron B. Fisher, Chandra Dodia, Sheldon I. Feinstein, Elena M. Sorokina, Kris DeBolt, Melpo Christofidou‐Solomidou, T.S. Srivastava, Alessandra Caporale, Evguenia Arguiri and Félix W. Wehrli and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Scientific Reports.

In The Last Decade

Shampa Chatterjee

83 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shampa Chatterjee United States 33 1.2k 796 554 373 352 85 2.8k
Edith Tzeng United States 31 1.5k 1.3× 1.0k 1.3× 374 0.7× 362 1.0× 573 1.6× 87 3.2k
Balu K. Chacko United States 36 2.0k 1.7× 870 1.1× 309 0.6× 549 1.5× 353 1.0× 66 4.0k
Nicoletta Gagliano Italy 31 1.2k 1.0× 279 0.4× 463 0.8× 309 0.8× 365 1.0× 115 3.2k
Angela Lombardi Italy 35 2.1k 1.7× 526 0.7× 346 0.6× 371 1.0× 516 1.5× 109 4.7k
Ben‐Ami Sela Israel 36 1.4k 1.2× 519 0.7× 273 0.5× 331 0.9× 419 1.2× 148 4.2k
Eva Nozik‐Grayck United States 35 1.2k 1.0× 632 0.8× 1.7k 3.1× 350 0.9× 634 1.8× 125 3.8k
Jean‐Loup Bascands France 35 1.9k 1.6× 313 0.4× 420 0.8× 536 1.4× 452 1.3× 155 4.7k
Stanislovas S. Jankauskas United States 29 1.7k 1.4× 485 0.6× 198 0.4× 361 1.0× 399 1.1× 89 3.7k
Paul O’Connor United States 32 1.2k 1.0× 420 0.5× 354 0.6× 146 0.4× 329 0.9× 76 3.1k
Benito Yard Germany 40 1.3k 1.1× 1.1k 1.4× 661 1.2× 820 2.2× 1.1k 3.2× 190 5.0k

Countries citing papers authored by Shampa Chatterjee

Since Specialization
Citations

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

Fields of papers citing papers by Shampa Chatterjee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shampa Chatterjee

This figure shows the co-authorship network connecting the top 25 collaborators of Shampa Chatterjee. A scholar is included among the top collaborators of Shampa Chatterjee 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 Shampa Chatterjee. Shampa Chatterjee 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.
Jain, Nikita, Natalia Louneva, Kathleen T. Montone, et al.. (2024). Reactive oxygen species in endothelial signaling in COVID-19: Protective role of the novel peptide PIP-2. PLoS ONE. 19(5). e0289854–e0289854. 1 indexed citations
2.
Litzky, Leslie A., Michael D. Feldman, Kathleen T. Montone, et al.. (2022). Pulmonary vascular inflammation with fatal coronavirus disease 2019 (COVID-19): possible role for the NLRP3 inflammasome. Respiratory Research. 23(1). 25–25. 18 indexed citations
3.
Greenwood, John C., David H. Jang, Jacob T. Gutsche, et al.. (2020). Severe Impairment of Microcirculatory Perfused Vessel Density Is Associated With Postoperative Lactate and Acute Organ Injury After Cardiac Surgery. Journal of Cardiothoracic and Vascular Anesthesia. 35(1). 106–115. 28 indexed citations
4.
Pourfathi, M., Stephen Kadlecek, Shampa Chatterjee, & Rahim R. Rizi. (2020). Metabolic Imaging and Biological Assessment: Platforms to Evaluate Acute Lung Injury and Inflammation. Frontiers in Physiology. 11. 937–937. 9 indexed citations
5.
Chatterjee, Shampa. (2018). Endothelial Mechanotransduction, Redox Signaling and the Regulation of Vascular Inflammatory Pathways. Frontiers in Physiology. 9. 524–524. 135 indexed citations
6.
Li, Haitao, Suiping Zhou, Chandra Dodia, et al.. (2015). Critical role of peroxiredoxin 6 in the repair of peroxidized cell membranes following oxidative stress. Free Radical Biology and Medicine. 87. 356–365. 66 indexed citations
7.
Chatterjee, Shampa, Keigi Fujiwara, Néstor G. Pérez, Masuko Ushio‐Fukai, & Aron B. Fisher. (2015). Mechanosignaling in the vasculature: emerging concepts in sensing, transduction and physiological responses. American Journal of Physiology-Heart and Circulatory Physiology. 308(12). H1451–H1462. 35 indexed citations
8.
Wojtovich, Andrew P., William R. Urciuoli, Shampa Chatterjee, et al.. (2013). Kir6.2 is not the mitochondrial K ATP channel but is required for cardioprotection by ischemic preconditioning. American Journal of Physiology-Heart and Circulatory Physiology. 304(11). H1439–H1445. 39 indexed citations
9.
Chatterjee, Shampa, et al.. (2013). Letters to the Editor. Endocrine Practice. 19(3). 558–560. 4 indexed citations
10.
Wang, Hui, Nankang Hong, Kevin Yu, et al.. (2013). Mechanotransduction Drives Post Ischemic Revascularization Through K ATP Channel Closure and Production of Reactive Oxygen Species. Antioxidants and Redox Signaling. 20(6). 872–886. 26 indexed citations
11.
Lee, James, Stathis Kanterakis, Shampa Chatterjee, et al.. (2009). Dietary flaxseed prevents radiation-induced oxidative lung damage, inflammation and fibrosis in a mouse model of thoracic radiation injury. Cancer Biology & Therapy. 8(1). 47–53. 88 indexed citations
12.
Chatterjee, Shampa, Kenneth E. Chapman, & Aron B. Fisher. (2008). Lung Ischemia: A Model for Endothelial Mechanotransduction. Cell Biochemistry and Biophysics. 52(3). 125–138. 36 indexed citations
13.
Zhang, Qunwei, Shampa Chatterjee, Zhihua Wei, Weidong Liu, & Aron B. Fisher. (2007). Rac and PI3 Kinase Mediate Endothelial Cell–Reactive Oxygen Species Generation During Normoxic Lung Ischemia. Antioxidants and Redox Signaling. 10(4). 679–690. 36 indexed citations
14.
Milovanova, Tatyana N., Shampa Chatterjee, Yefim Manevich, et al.. (2005). Lung endothelial cell proliferation with decreased shear stress is mediated by reactive oxygen species. American Journal of Physiology-Cell Physiology. 290(1). C66–C76. 55 indexed citations
15.
Matsuzaki, Ikuo, Shampa Chatterjee, Kris DeBolt, et al.. (2004). Membrane depolarization and NADPH oxidase activation in aortic endothelium during ischemia reflect altered mechanotransduction. American Journal of Physiology-Heart and Circulatory Physiology. 288(1). H336–H343. 51 indexed citations
16.
Noack, Heiko, Heiko Possel, Shampa Chatterjee, Gerburg Keilhoff, & Gerald Wolf. (2000). Nitrosative stress in primary glial cultures after induction of the inducible isoform of nitric oxide synthase (i-NOS). Toxicology. 148(2-3). 133–142. 7 indexed citations
17.
Chatterjee, Shampa, et al.. (1999). The Expression ofproUKinEscherichia coli: ThevgbPromoter Replaces IPTG and Coexpression ofargUCompensates for Rare Codons in a Hypoxic Induction Model. Bioscience Biotechnology and Biochemistry. 63(12). 2097–2101. 2 indexed citations
18.
19.
Chatterjee, Shampa, T.S. Srivastava, Jayashree P. Kamat, & T.P.A. Devasagayam. (1997). Lipid peroxidation induced by meso-tetrakis[3,4-bis(carboxymethyleneoxy)phenyl]porphyrin on photosensitization in hepatic and tumor microsomes. Chemico-Biological Interactions. 108(1-2). 27–37. 9 indexed citations
20.
Chatterjee, Shampa, J.P. Kamat, Shankar J. Shetty, T.S. Srivastava, & T.P.A. Devasagayam. (1997). Oxidative damage induced by a novel porphyrin on rat brain mitochondria and its possible implications in therapy. Redox Report. 3(3). 183–188. 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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