Tanusree Sen

2.8k total citations · 1 hit paper
38 papers, 2.3k citations indexed

About

Tanusree Sen is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, Tanusree Sen has authored 38 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 8 papers in Oncology and 6 papers in Cancer Research. Recurrent topics in Tanusree Sen's work include Mitochondrial Function and Pathology (6 papers), Cancer-related Molecular Pathways (5 papers) and Neuroinflammation and Neurodegeneration Mechanisms (3 papers). Tanusree Sen is often cited by papers focused on Mitochondrial Function and Pathology (6 papers), Cancer-related Molecular Pathways (5 papers) and Neuroinflammation and Neurodegeneration Mechanisms (3 papers). Tanusree Sen collaborates with scholars based in United States, India and Netherlands. Tanusree Sen's co-authors include Nilkantha Sen, Risheng Xu, Solomon H. Snyder, Moataz M. Gadalla, Bindu D. Paul, Seyun Kim, Asif K. Mustafa, Rajaneesh K. Gupta, Pampa Saha and Sasanka Chakrabarti and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Neuron.

In The Last Decade

Tanusree Sen

35 papers receiving 2.2k citations

Hit Papers

Hydrogen Sulfide-Linked Sulfhydration of NF-κB Mediates I... 2012 2026 2016 2021 2012 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tanusree Sen United States 24 1.2k 564 427 214 210 38 2.3k
Douglas R. Moellering United States 32 1.4k 1.1× 447 0.8× 812 1.9× 124 0.6× 295 1.4× 58 3.2k
Juan R. Vinã Spain 31 1.2k 1.0× 651 1.2× 553 1.3× 78 0.4× 280 1.3× 88 3.3k
Marinus Durán Netherlands 44 3.0k 2.5× 634 1.1× 1.1k 2.5× 174 0.8× 270 1.3× 102 5.3k
John S. Hothersall United Kingdom 32 1.2k 1.0× 405 0.7× 855 2.0× 97 0.5× 168 0.8× 73 2.9k
Akbar Ahmad United States 27 681 0.6× 518 0.9× 294 0.7× 61 0.3× 203 1.0× 48 2.0k
Robert Langenbach United States 25 946 0.8× 517 0.9× 289 0.7× 369 1.7× 105 0.5× 38 3.5k
Rhéure Alves-Lopes United Kingdom 26 894 0.7× 151 0.3× 595 1.4× 133 0.6× 258 1.2× 70 2.8k
Anna Signorile Italy 38 1.9k 1.5× 135 0.2× 520 1.2× 235 1.1× 328 1.6× 78 3.4k
Yi Chu United States 36 901 0.7× 231 0.4× 750 1.8× 74 0.3× 327 1.6× 79 3.0k
Gino Cortopassi United States 34 2.1k 1.8× 133 0.2× 698 1.6× 173 0.8× 239 1.1× 83 3.4k

Countries citing papers authored by Tanusree Sen

Since Specialization
Citations

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

Fields of papers citing papers by Tanusree Sen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tanusree Sen

This figure shows the co-authorship network connecting the top 25 collaborators of Tanusree Sen. A scholar is included among the top collaborators of Tanusree Sen 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 Tanusree Sen. Tanusree Sen 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.
Sen, Tanusree, et al.. (2024). Clinical profile and underlying causes of recurrent pneumonia in young children. International Journal of Research in Medical Sciences. 13(1). 96–101.
2.
Sen, Tanusree. (2019). MS14.04 Targeting DNA Damage and Repair. Journal of Thoracic Oncology. 14(10). S183–S184. 1 indexed citations
3.
Gupta, Rajaneesh K., Pampa Saha, Tanusree Sen, & Nilkantha Sen. (2019). An augmentation in histone dimethylation at lysine nine residues elicits vision impairment following traumatic brain injury. Free Radical Biology and Medicine. 134. 630–643. 15 indexed citations
4.
Saha, Pampa, Rajaneesh K. Gupta, Tanusree Sen, & Nilkantha Sen. (2019). Histone Deacetylase 4 Downregulation Elicits Post-Traumatic Psychiatric Disorders through Impairment of Neurogenesis. Journal of Neurotrauma. 36(23). 3284–3296. 13 indexed citations
5.
Sen, Tanusree, Rajaneesh K. Gupta, Helen Kaiser, & Nilkantha Sen. (2017). Activation of PERK Elicits Memory Impairment through Inactivation of CREB and Downregulation of PSD95 After Traumatic Brain Injury. Journal of Neuroscience. 37(24). 5900–5911. 94 indexed citations
6.
Sen, Tanusree & Nilkantha Sen. (2016). Isoflurane-induced inactivation of CREB through histone deacetylase 4 is responsible for cognitive impairment in developing brain. Neurobiology of Disease. 96. 12–21. 19 indexed citations
7.
Michailidi, Christina, Masamichi Hayashi, Sayantan Datta, et al.. (2015). Involvement of Epigenetics and EMT-Related miRNA in Arsenic-Induced Neoplastic Transformation and Their Potential Clinical Use. Cancer Prevention Research. 8(3). 208–221. 43 indexed citations
8.
Mir, Sajad Ahmad, Tanusree Sen, & Nilkantha Sen. (2014). Cytokine-Induced GAPDH Sulfhydration Affects PSD95 Degradation and Memory. Molecular Cell. 56(6). 786–795. 57 indexed citations
9.
Xu, Risheng, Anthony V. Serritella, Tanusree Sen, et al.. (2013). Behavioral Effects of Cocaine Mediated by Nitric Oxide-GAPDH Transcriptional Signaling. Neuron. 78(4). 623–630. 24 indexed citations
10.
Sen, Tanusree, Nilkantha Sen, Maartje Noordhuis, et al.. (2012). OGDHL Is a Modifier of AKT-Dependent Signaling and NF-κB Function. PLoS ONE. 7(11). e48770–e48770. 58 indexed citations
11.
Sen, Nilkantha, Bindu D. Paul, Moataz M. Gadalla, et al.. (2012). Hydrogen Sulfide-Linked Sulfhydration of NF-κB Mediates Its Antiapoptotic Actions. Molecular Cell. 45(1). 13–24. 609 indexed citations breakdown →
12.
Chatterjee, Aditi, Tanusree Sen, Xiaofei Chang, & David Sidransky. (2010). Yes-associated protein 1 regulates the stability of ΔNp63α. Cell Cycle. 9(1). 162–167. 16 indexed citations
13.
Sen, Tanusree, Xiaofei Chang, David Sidransky, & Aditi Chatterjee. (2010). Regulation of ΔNp63α by NFκΒ . Cell Cycle. 9(24). 4841–4847. 23 indexed citations
14.
Huang, Yiping, Tanusree Sen, Jatin Nagpal, et al.. (2008). ATM kinase is a master switch for the ΔNp63α phosphorylation/degradation in human head and neck squamous cell carcinoma cells upon DNA damage. Cell Cycle. 7(18). 2846–2855. 43 indexed citations
15.
Sen, Tanusree, et al.. (2007). Depolarization and cardiolipin depletion in aged rat brain mitochondria: Relationship with oxidative stress and electron transport chain activity. Neurochemistry International. 50(5). 719–725. 76 indexed citations
16.
Sen, Tanusree, Sirsendu Jana, Sen Chandra Sreetama, Uttara Chatterjee, & Sasanka Chakrabarti. (2006). Gene-specific oxidative lesions in aged rat brain detected by polymerase chain reaction inhibition assay. Free Radical Research. 41(3). 288–294. 2 indexed citations
17.
Sen, Tanusree, Nilkantha Sen, Gayatri Tripathi, Uttara Chatterjee, & Sasanka Chakrabarti. (2006). Lipid peroxidation associated cardiolipin loss and membrane depolarization in rat brain mitochondria. Neurochemistry International. 49(1). 20–27. 76 indexed citations
18.
Sen, Nilkantha, et al.. (2006). Leishmania donovani: Intracellular ATP level regulates apoptosis-like death in luteolin induced dyskinetoplastid cells. Experimental Parasitology. 114(3). 204–214. 25 indexed citations
19.
Sen, Tanusree, et al.. (2005). Inhibition of rat brain mitochondrial electron transport chain activity by dopamine oxidation products during extended in vitro incubation: Implications for Parkinson's disease. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1741(1-2). 65–74. 76 indexed citations
20.
Sen, Nilkantha, Benu Brata Das, Anirban Ganguly, et al.. (2004). Camptothecin induced mitochondrial dysfunction leading to programmed cell death in unicellular hemoflagellate Leishmania donovani. Cell Death and Differentiation. 11(8). 924–936. 213 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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