Rupesh Chaturvedi

3.7k total citations
61 papers, 2.9k citations indexed

About

Rupesh Chaturvedi is a scholar working on Surgery, Immunology and Molecular Biology. According to data from OpenAlex, Rupesh Chaturvedi has authored 61 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Surgery, 23 papers in Immunology and 19 papers in Molecular Biology. Recurrent topics in Rupesh Chaturvedi's work include Helicobacter pylori-related gastroenterology studies (32 papers), Galectins and Cancer Biology (12 papers) and Veterinary medicine and infectious diseases (6 papers). Rupesh Chaturvedi is often cited by papers focused on Helicobacter pylori-related gastroenterology studies (32 papers), Galectins and Cancer Biology (12 papers) and Veterinary medicine and infectious diseases (6 papers). Rupesh Chaturvedi collaborates with scholars based in United States, India and France. Rupesh Chaturvedi's co-authors include Keith T. Wilson, M. Kay Washington, Richard M. Peek, Mohammad Asim, D. Brent Polk, Fang Yan, Hanwei Cao, Daniel P. Barry, M. Blanca Piazuelo and Kshipra Singh and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Rupesh Chaturvedi

59 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rupesh Chaturvedi United States	31	1.3k	896	787	405	320	61	2.9k
Kazuko Shichijo Japan	18	961 0.7×	520 0.6×	609 0.8×	396 1.0×	682 2.1×	64	2.5k
Yuji Ikeda Japan	13	785 0.6×	458 0.5×	584 0.7×	274 0.7×	665 2.1×	83	2.2k
Jie Zhou China	34	1.2k 0.9×	313 0.3×	1.4k 1.8×	448 1.1×	104 0.3×	135	3.3k
Shahid Umar United States	32	1.6k 1.3×	386 0.4×	388 0.5×	736 1.8×	362 1.1×	96	3.3k
Andy Wullaert Belgium	26	2.2k 1.7×	437 0.5×	1.6k 2.0×	364 0.9×	496 1.6×	45	3.9k
Pedro A. Ruiz Switzerland	23	1.0k 0.8×	345 0.4×	637 0.8×	196 0.5×	389 1.2×	56	2.5k
David G. Besselsen United States	32	1.2k 0.9×	365 0.4×	341 0.4×	609 1.5×	562 1.8×	83	3.0k
Daniel P. Barry United States	25	1.0k 0.8×	603 0.7×	760 1.0×	257 0.6×	176 0.6×	53	2.0k
Tadao Bamba Japan	33	1.3k 1.0×	1.0k 1.1×	1.1k 1.4×	665 1.6×	1.1k 3.5×	160	4.2k
Keiko Kataoka Japan	35	1.5k 1.2×	278 0.3×	399 0.5×	133 0.3×	220 0.7×	158	3.5k

Countries citing papers authored by Rupesh Chaturvedi

Since Specialization

Citations

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

Fields of papers citing papers by Rupesh Chaturvedi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rupesh Chaturvedi

This figure shows the co-authorship network connecting the top 25 collaborators of Rupesh Chaturvedi. A scholar is included among the top collaborators of Rupesh Chaturvedi 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 Rupesh Chaturvedi. Rupesh Chaturvedi 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

Kumar, Sanjay, Md. Zubbair Malik, Marzia Di Donato, et al.. (2025). siRNA-based therapeutic candidate targeting PRDM2 for inhibition of lung cancer progression. Biomedicine & Pharmacotherapy. 193. 118807–118807.

Kushwaha, Hemant R., et al.. (2024). Oncogenic potential of SARS-CoV-2—targeting hallmarks of cancer pathways. Cell Communication and Signaling. 22(1). 447–447. 10 indexed citations

Jindal, S., et al.. (2024). Linking COVID-19 and cancer: Underlying mechanism. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1871(1). 167563–167563. 3 indexed citations

Sharma, Shilpa, Md. Zubbair Malik, Ankita Rai, et al.. (2024). Plasma Virome of HIV-infected Subjects on Suppressive AntiretroviralTherapy Reveals Association of Differentially Abundant Viruses withDistinct T-cell Phenotypes and Inflammation. Current Genomics. 25(2). 105–119. 4 indexed citations

Pandey, Achyut, Shruti Mishra, Anupam Patra, et al.. (2023). Role of curcumin's phenolic –OH group in the inhibition of Helicobacter pylori CagA phosphorylation. Journal of Molecular Structure. 1296. 136763–136763. 3 indexed citations

Pandey, Achyut, et al.. (2022). Oxidative Products of Curcumin Rather Than Curcumin Bind to Helicobacter Pylori Virulence Factor VacA and Are Required to Inhibit Its Vacuolation Activity. Molecules. 27(19). 6727–6727. 12 indexed citations

Venkatesh, Vimala, et al.. (2019). Helicobacter pylori Reactivates Human Immunodeficiency Virus-1 in Latently Infected Monocytes with Increased Expression of IL-1β and CXCL8. Current Genomics. 20(8). 556–568. 2 indexed citations

Shet, Anita, et al.. (2018). High Abundance of genus Prevotella in the gut of perinatally HIV-infected children is associated with IP-10 levels despite therapy. Scientific Reports. 8(1). 17679–17679. 47 indexed citations

Chaturvedi, Rupesh, Mohammad Asim, M. Blanca Piazuelo, et al.. (2014). Activation of EGFR and ERBB2 by Helicobacter pylori Results in Survival of Gastric Epithelial Cells With DNA Damage. Gastroenterology. 146(7). 1739–1751.e14. 77 indexed citations

10.

Barrett, Caitlyn W., Ning Wei, Xi Chen, et al.. (2012). Tumor Suppressor Function of the Plasma Glutathione Peroxidase Gpx3 in Colitis-Associated Carcinoma. Cancer Research. 73(3). 1245–1255. 154 indexed citations

11.

Wang, Lihong, Liping Liu, Yan Shi, et al.. (2012). Berberine Induces Caspase-Independent Cell Death in Colon Tumor Cells through Activation of Apoptosis-Inducing Factor. PLoS ONE. 7(5). e36418–e36418. 110 indexed citations

12.

Gobert, Alain P., Thomas G. Verriere, Thibaut de Sablet, et al.. (2012). Haem oxygenase-1 inhibits phosphorylation of theHelicobacter pylorioncoprotein CagA in gastric epithelial cells. Cellular Microbiology. 15(1). 145–156. 24 indexed citations

13.

Barrett, Caitlyn W., Barbara Fingleton, Ning Wei, et al.. (2011). MTGR1 Is Required for Tumorigenesis in the Murine AOM/DSS Colitis-Associated Carcinoma Model. Cancer Research. 71(4). 1302–1312. 31 indexed citations

14.

Chaturvedi, Rupesh, Mohammad Asim, Judith Romero–Gallo, et al.. (2011). Spermine Oxidase Mediates the Gastric Cancer Risk Associated With Helicobacter pylori CagA. Gastroenterology. 141(5). 1696–1708.e2. 161 indexed citations

15.

Dhawan, Punita, Rizwan Ahmad, Rupesh Chaturvedi, et al.. (2011). Claudin-2 expression increases tumorigenicity of colon cancer cells: role of epidermal growth factor receptor activation. Oncogene. 30(29). 3234–3247. 130 indexed citations

16.

Barry, Daniel P., Mohammad Asim, David A. Leiman, et al.. (2011). Difluoromethylornithine Is a Novel Inhibitor of Helicobacter pylori Growth, CagA Translocation, and Interleukin-8 Induction. PLoS ONE. 6(2). e17510–e17510. 33 indexed citations

17.

Lewis, Nuruddeen D., Mohammad Asim, Daniel P. Barry, et al.. (2010). Arginase II Restricts Host Defense to Helicobacter pylori by Attenuating Inducible Nitric Oxide Synthase Translation in Macrophages. The Journal of Immunology. 184(5). 2572–2582. 80 indexed citations

18.

Singh, Kshipra, Rupesh Chaturvedi, Mohammad Asim, et al.. (2008). The Apolipoprotein E-mimetic Peptide COG112 Inhibits the Inflammatory Response to Citrobacter rodentium in Colonic Epithelial Cells by Preventing NF-κB Activation. Journal of Biological Chemistry. 283(24). 16752–16761. 46 indexed citations

19.

O’Brien, D., Judith Romero–Gallo, Barbara Schneider, et al.. (2008). Regulation of the Helicobacter pylori Cellular Receptor Decay-accelerating Factor. Journal of Biological Chemistry. 283(35). 23922–23930. 19 indexed citations

20.

Chaturvedi, Rupesh, Mohammad Asim, Nuruddeen D. Lewis, Françoise I. Bussière, & Keith T. Wilson. (2006). O25. Arginine availability is critical to the innate immune response to Helicobacter pylori by regulation of iNOS translation. Nitric Oxide. 14(4). 8–8. 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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