Santosh Karnewar

2.0k total citations
27 papers, 1.5k citations indexed

About

Santosh Karnewar is a scholar working on Molecular Biology, Organic Chemistry and Immunology. According to data from OpenAlex, Santosh Karnewar has authored 27 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Organic Chemistry and 7 papers in Immunology. Recurrent topics in Santosh Karnewar's work include Synthesis and biological activity (6 papers), Atherosclerosis and Cardiovascular Diseases (5 papers) and Sirtuins and Resveratrol in Medicine (3 papers). Santosh Karnewar is often cited by papers focused on Synthesis and biological activity (6 papers), Atherosclerosis and Cardiovascular Diseases (5 papers) and Sirtuins and Resveratrol in Medicine (3 papers). Santosh Karnewar collaborates with scholars based in India, United States and Netherlands. Santosh Karnewar's co-authors include Srigiridhar Kotamraju, Anantha Koteswararao Kanugula, Sathish Babu Vasamsetti, Jerald Mahesh Kumar, Praveen Neeli, Gary K. Owens, Paradesi Naidu Gollavilli, Mahesh Kumar Jerald, Raja Gopoju and Gabriel F. Alencar and has published in prestigious journals such as Circulation, PLoS ONE and Diabetes.

In The Last Decade

Santosh Karnewar

27 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Santosh Karnewar India 19 718 367 191 189 177 27 1.5k
Yijun Deng United States 18 1.0k 1.4× 344 0.9× 175 0.9× 174 0.9× 191 1.1× 31 1.7k
Michael Y. Bonner United States 20 720 1.0× 205 0.6× 79 0.4× 211 1.1× 141 0.8× 36 1.5k
Helga Reicher Austria 25 751 1.0× 350 1.0× 245 1.3× 182 1.0× 53 0.3× 37 1.6k
Hong‐Ye Zhao China 21 878 1.2× 112 0.3× 189 1.0× 280 1.5× 112 0.6× 82 1.5k
Bogdan G. Gugiu United States 14 886 1.2× 349 1.0× 133 0.7× 211 1.1× 85 0.5× 18 1.4k
Tillmann Cyrus United States 23 551 0.8× 552 1.5× 473 2.5× 122 0.6× 112 0.6× 28 2.0k
Johannes Kreuzer United States 15 801 1.1× 242 0.7× 140 0.7× 188 1.0× 203 1.1× 25 1.5k
Ying Sun China 24 1.1k 1.5× 162 0.4× 124 0.6× 392 2.1× 222 1.3× 93 2.1k
Stephen A. Whelan United States 21 1.1k 1.6× 404 1.1× 104 0.5× 123 0.7× 386 2.2× 37 1.5k
Steven S. Mundt United States 15 375 0.5× 353 1.0× 398 2.1× 119 0.6× 95 0.5× 23 1.4k

Countries citing papers authored by Santosh Karnewar

Since Specialization
Citations

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

Fields of papers citing papers by Santosh Karnewar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Santosh Karnewar

This figure shows the co-authorship network connecting the top 25 collaborators of Santosh Karnewar. A scholar is included among the top collaborators of Santosh Karnewar 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 Santosh Karnewar. Santosh Karnewar 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.
Karnewar, Santosh, Rebecca A. Deaton, Laura S. Shankman, et al.. (2024). IL-1β Inhibition Partially Negates the Beneficial Effects of Diet-Induced Atherosclerosis Regression in Mice. Arteriosclerosis Thrombosis and Vascular Biology. 44(6). 1379–1392. 5 indexed citations
2.
Aherrahrou, Rédouane, Ferheen Baig, Konstantinos Theofilatos, et al.. (2024). Secreted Protein Profiling of Human Aortic Smooth Muscle Cells Identifies Vascular Disease Associations. Arteriosclerosis Thrombosis and Vascular Biology. 44(4). 898–914. 6 indexed citations
3.
Neeli, Praveen, et al.. (2022). DOT1L regulates MTDH ‐mediated angiogenesis in triple‐negative breast cancer: intermediacy of NF‐κB‐HIF1α axis. FEBS Journal. 290(2). 502–520. 16 indexed citations
4.
5.
Newman, Alexandra, Vlad Serbulea, Richard A. Baylis, et al.. (2021). Multiple cell types contribute to the atherosclerotic lesion fibrous cap by PDGFRβ and bioenergetic mechanisms. Nature Metabolism. 3(2). 166–181. 100 indexed citations
6.
Alencar, Gabriel F., Katherine Owsiany, Santosh Karnewar, et al.. (2020). Stem Cell Pluripotency Genes Klf4 and Oct4 Regulate Complex SMC Phenotypic Changes Critical in Late-Stage Atherosclerotic Lesion Pathogenesis. Circulation. 142(21). 2045–2059. 234 indexed citations
7.
8.
Karnewar, Santosh, Praveen Neeli, K. Sasikumar, et al.. (2018). Metformin regulates mitochondrial biogenesis and senescence through AMPK mediated H3K79 methylation: Relevance in age-associated vascular dysfunction. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1864(4). 1115–1128. 117 indexed citations
9.
Karnewar, Santosh, et al.. (2017). Mitochondria‐targeted esculetin inhibits PAI‐1 levels by modulating STAT3 activation and miR‐19b via SIRT3: Role in acute coronary artery syndrome. Journal of Cellular Physiology. 233(1). 214–225. 26 indexed citations
10.
Vasamsetti, Sathish Babu, Santosh Karnewar, Raja Gopoju, et al.. (2016). Resveratrol attenuates monocyte-to-macrophage differentiation and associated inflammation via modulation of intracellular GSH homeostasis: Relevance in atherosclerosis. Free Radical Biology and Medicine. 96. 392–405. 59 indexed citations
11.
Karnewar, Santosh, Sathish Babu Vasamsetti, Raja Gopoju, et al.. (2016). Mitochondria-targeted esculetin alleviates mitochondrial dysfunction by AMPK-mediated nitric oxide and SIRT3 regulation in endothelial cells: potential implications in atherosclerosis. Scientific Reports. 6(1). 24108–24108. 57 indexed citations
12.
Karnewar, Santosh, et al.. (2015). Novel Bioactive Wild Medicinal Mushroom-Xylaria sp. R006 (Ascomycetes) against Multidrug Resistant Human Bacterial Pathogens and Human Cancer Cell Lines. International journal of medicinal mushrooms. 17(10). 1005–1017. 12 indexed citations
13.
Gollavilli, Paradesi Naidu, et al.. (2015). AMPK inhibits MTDH expression via GSK3β and SIRT1 activation: potential role in triple negative breast cancer cell proliferation. FEBS Journal. 282(20). 3971–3985. 47 indexed citations
14.
Kesharwani, Rajesh K., et al.. (2015). Synthesis, biological activity evaluation and molecular docking studies of novel coumarin substituted thiazolyl-3-aryl-pyrazole-4-carbaldehydes. Bioorganic & Medicinal Chemistry Letters. 25(24). 5797–5803. 68 indexed citations
15.
Venkateswarlu, Somepalli, Trimurtulu Golakoti, Anantha Koteswararao Kanugula, et al.. (2014). Mitochondrial-Targeted Curcuminoids: A Strategy to Enhance Bioavailability and Anticancer Efficacy of Curcumin. PLoS ONE. 9(3). e89351–e89351. 91 indexed citations
16.
Kamal, Ähmed, Vangala Santhosh Reddy, Santosh Karnewar, et al.. (2014). Synthesis of imidazo[2,1-b][1,3,4]thiadiazole–chalcones as apoptosis inducing anticancer agents. MedChemComm. 5(11). 1718–1723. 28 indexed citations
17.
Kumar, Rakesh, C. Kurumurthy, P. Shanthan Rao, et al.. (2014). Synthesis of Novel Pyrido[3′,2′:4,5]furo[3,2‐d]pyrimidine Derivatives and Their Cytotoxic Activity. Journal of Heterocyclic Chemistry. 51(5). 1531–1535. 1 indexed citations
18.
Kamal, Ähmed, Vangala Santhosh Reddy, Santosh Karnewar, et al.. (2013). Synthesis and Biological Evaluation of Imidazopyridine–Oxindole Conjugates as Microtubule‐Targeting Agents. ChemMedChem. 8(12). 2015–2025. 36 indexed citations
19.
Khatua, Tarak Nath, Raju Padiya, Santosh Karnewar, et al.. (2012). Garlic provides protection to mice heart against isoproterenol-induced oxidative damage: Role of nitric oxide. Nitric Oxide. 27(1). 9–17. 31 indexed citations
20.
Thangamuthu, Madasamy, Pandiaraj Manickam, Murugesan Balamurugan, et al.. (2012). Virtual electrochemical nitric oxide analyzer using copper, zinc superoxide dismutase immobilized on carbon nanotubes in polypyrrole matrix. Talanta. 100. 168–174. 20 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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