Devendra Parmar

1.7k total citations
76 papers, 1.3k citations indexed

About

Devendra Parmar is a scholar working on Pharmacology, Oncology and Molecular Biology. According to data from OpenAlex, Devendra Parmar has authored 76 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Pharmacology, 19 papers in Oncology and 18 papers in Molecular Biology. Recurrent topics in Devendra Parmar's work include Pharmacogenetics and Drug Metabolism (23 papers), Carcinogens and Genotoxicity Assessment (14 papers) and Pesticide Exposure and Toxicity (10 papers). Devendra Parmar is often cited by papers focused on Pharmacogenetics and Drug Metabolism (23 papers), Carcinogens and Genotoxicity Assessment (14 papers) and Pesticide Exposure and Toxicity (10 papers). Devendra Parmar collaborates with scholars based in India, United States and Japan. Devendra Parmar's co-authors include Alok Dhawan, Prahlad K. Seth, P.K. Seth, Rakesh Shukla, Neeraj Mathur, Mohan C. Pant, Parag P. Shah, Poonam Kakkar, D. Kar Chowdhuri and R.C. Srimal and has published in prestigious journals such as SHILAP Revista de lepidopterología, Free Radical Biology and Medicine and International Journal of Radiation Oncology*Biology*Physics.

In The Last Decade

Devendra Parmar

73 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Devendra Parmar India 21 383 321 281 270 207 76 1.3k
Seon‐Hee Oh South Korea 27 977 2.6× 219 0.7× 194 0.7× 205 0.8× 176 0.9× 65 2.1k
Liang Zheng China 22 519 1.4× 120 0.4× 157 0.6× 239 0.9× 95 0.5× 65 1.6k
Yannick Morel France 12 573 1.5× 288 0.9× 212 0.8× 185 0.7× 191 0.9× 21 1.4k
Tzuu‐Huei Ueng Taiwan 21 330 0.9× 281 0.9× 355 1.3× 164 0.6× 146 0.7× 77 1.3k
Cihan Gür Türkiye 27 502 1.3× 329 1.0× 352 1.3× 53 0.2× 289 1.4× 77 1.8k
Hong Xie China 24 502 1.3× 409 1.3× 69 0.2× 232 0.9× 177 0.9× 51 1.5k
Shohda A. El‐Maraghy Egypt 20 421 1.1× 103 0.3× 89 0.3× 169 0.6× 128 0.6× 40 1.1k
Xiance Sun China 28 882 2.3× 443 1.4× 171 0.6× 165 0.6× 160 0.8× 66 2.0k
Jieshu Wu China 26 1000 2.6× 212 0.7× 111 0.4× 363 1.3× 124 0.6× 61 1.8k
Xin Yan China 25 523 1.4× 313 1.0× 105 0.4× 123 0.5× 127 0.6× 55 1.8k

Countries citing papers authored by Devendra Parmar

Since Specialization
Citations

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

Fields of papers citing papers by Devendra Parmar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Devendra Parmar

This figure shows the co-authorship network connecting the top 25 collaborators of Devendra Parmar. A scholar is included among the top collaborators of Devendra Parmar 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 Devendra Parmar. Devendra Parmar 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
2.
Pandey, Rashmi, et al.. (2021). An update on the diagnostic biomarkers for asthma. Journal of Family Medicine and Primary Care. 10(3). 1139–1148. 8 indexed citations
3.
Srivastava, Meenu, et al.. (2021). Expression of Antimicrobial Peptides and Cytokines in Human Omentum Following Abdominal Surgery. Cureus. 13(8). e17477–e17477. 2 indexed citations
4.
Daiwile, Atul P., Prashant Tarale, Saravanadevi Sivanesan, et al.. (2018). Role of fluoride induced epigenetic alterations in the development of skeletal fluorosis. Ecotoxicology and Environmental Safety. 169. 410–417. 45 indexed citations
5.
Gandhi, Ajeet Kumar, Madhup Rastogi, M L B Bhatt, et al.. (2017). Evaluation of XRCC-1 Gene Polymorphism as a Biomarker in Head and Neck Cancer Patients Undergoing Chemoradiation Therapy. International Journal of Radiation Oncology*Biology*Physics. 99(2). S236–S236. 3 indexed citations
6.
Singh, Anshuman, et al.. (2017). Role of matrix metalloproteinase 13 gene expression in the evaluation of radiation response in oral squamous cell carcinoma. Journal of Carcinogenesis. 16(1). 2–2. 6 indexed citations
7.
Chandra, Abhijit, et al.. (2016). Polymorphism and Expression Profile of Cholecystokinin Type A Receptor in Relation to Gallstone Disease Susceptibility. Biochemical Genetics. 54(5). 665–675. 1 indexed citations
8.
Srivastava, Shikha, et al.. (2015). Effect of prenatal exposure of lindane on alterations in the expression of cerebral cytochrome P450s and neurotransmitter receptors in brain regions. Food and Chemical Toxicology. 77. 74–81. 6 indexed citations
9.
Chandra, Abhijit, et al.. (2014). Expression of survivin mRNA in gallbladder cancer: a diagnostic and prognostic marker?. Tumor Biology. 35(9). 9241–9246. 22 indexed citations
10.
Chandra, Abhijit, et al.. (2013). Prognostic Significance of K-<b><i>ras</i></b> Codon 12 Mutation in Patients with Resected Gallbladder Cancer. Digestive Surgery. 30(3). 233–239. 18 indexed citations
11.
Joshi, Chaitanya G., et al.. (2012). Effect of IGF-I gene polymorphism on various economic traits of synthetic White Leghorn. Indian Journal of Poultry Science. 47(1). 10–13.
13.
Shah, Parag P., et al.. (2009). Evidence for increased cytochrome P450 1A1 expression in blood lymphocytes of lung cancer patients. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 670(1-2). 74–78. 70 indexed citations
14.
Sharma, Amit, et al.. (2009). Polycyclic aromatic hydrocarbon metabolizing cytochrome P450s in freshly prepared uncultured rat blood lymphocytes. Biochemical Pharmacology. 79(8). 1182–1188. 19 indexed citations
15.
Bajpayee, Mahima, Alok K. Pandey, Javed Musarrat, et al.. (2006). DNA damage and mutagenicity induced by endosulfan and its metabolites. Environmental and Molecular Mutagenesis. 47(9). 682–692. 72 indexed citations
16.
Chowdhuri, D. Kar, Devendra Parmar, Poonam Kakkar, et al.. (2002). Antistress effects of bacosides of Bacopa monnieri: modulation of Hsp70 expression, superoxide dismutase and cytochrome P450 activity in rat brain. Phytotherapy Research. 16(7). 639–645. 128 indexed citations
17.
Parmar, Devendra, et al.. (2002). Effect of pretreatment of cytochrome P450 (P450) modifiers on neurobehavioral toxicity induced by deltamethrin. Food and Chemical Toxicology. 41(3). 431–437. 35 indexed citations
18.
Dey, Aparajit Ballav, Devendra Parmar, Alok Dhawan, Debabrata Dash, & P.K. Seth. (2002). Cytochrome P450 2E1 dependent catalytic activity and lipid peroxidation in rat blood lymphocytes. Life Sciences. 71(21). 2509–2519. 23 indexed citations
20.
Parmar, Devendra & Leo T. Burka. (1993). Studies on the interaction of furan with hepatic cytochrome P‐450. Journal of Biochemical Toxicology. 8(1). 1–9. 36 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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