Subhasree Basu

2.2k total citations
22 papers, 1.1k citations indexed

About

Subhasree Basu is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, Subhasree Basu has authored 22 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 8 papers in Oncology and 6 papers in Cancer Research. Recurrent topics in Subhasree Basu's work include Cancer-related Molecular Pathways (8 papers), Connexins and lens biology (6 papers) and Epigenetics and DNA Methylation (5 papers). Subhasree Basu is often cited by papers focused on Cancer-related Molecular Pathways (8 papers), Connexins and lens biology (6 papers) and Epigenetics and DNA Methylation (5 papers). Subhasree Basu collaborates with scholars based in United States, India and United Kingdom. Subhasree Basu's co-authors include Maureen E. Murphy, Che-Pei Kung, A. Sue Menko, Anna Budina-Kolomets, Thibaut Barnoud, Keerthana Gnanapradeepan, Qin Liu, Julia I-Ju Leu, Donna L. George and Sakina Khaku and has published in prestigious journals such as Journal of Biological Chemistry, Genes & Development and Cancer Research.

In The Last Decade

Subhasree Basu

22 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Subhasree Basu United States 14 782 445 330 275 167 22 1.1k
Peter Schirmacher Germany 11 390 0.5× 320 0.7× 241 0.7× 188 0.7× 135 0.8× 21 849
Nadire Duru United States 19 802 1.0× 522 1.2× 170 0.5× 407 1.5× 140 0.8× 26 1.4k
Shanshan Liu China 17 599 0.8× 211 0.5× 265 0.8× 276 1.0× 178 1.1× 36 1.1k
Gregory Dyson United States 20 577 0.7× 326 0.7× 142 0.4× 304 1.1× 160 1.0× 74 1.1k
Won Kyu Kim South Korea 18 359 0.5× 212 0.5× 122 0.4× 236 0.9× 74 0.4× 39 787
Barry Jutten Netherlands 17 442 0.6× 266 0.6× 106 0.3× 209 0.8× 192 1.1× 19 804
Zhanjun Guo China 21 903 1.2× 433 1.0× 123 0.4× 180 0.7× 175 1.0× 94 1.3k
Abdirashid M. Shire United States 16 537 0.7× 157 0.4× 89 0.3× 161 0.6× 170 1.0× 26 1.0k
Jocelyn S. Kasper United States 10 615 0.8× 246 0.6× 188 0.6× 305 1.1× 70 0.4× 12 843
Alessandro Marra Germany 19 815 1.0× 603 1.4× 484 1.5× 442 1.6× 70 0.4× 42 1.5k

Countries citing papers authored by Subhasree Basu

Since Specialization
Citations

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

Fields of papers citing papers by Subhasree Basu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Subhasree Basu

This figure shows the co-authorship network connecting the top 25 collaborators of Subhasree Basu. A scholar is included among the top collaborators of Subhasree Basu 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 Subhasree Basu. Subhasree Basu 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.
Gnanapradeepan, Keerthana, Julia I-Ju Leu, Subhasree Basu, et al.. (2020). Increased mTOR activity and metabolic efficiency in mouse and human cells containing the African-centric tumor-predisposing p53 variant Pro47Ser. eLife. 9. 12 indexed citations
2.
Barnoud, Thibaut, Anna Budina-Kolomets, Subhasree Basu, et al.. (2018). Tailoring Chemotherapy for the African-Centric S47 Variant of TP53. Cancer Research. 78(19). 5694–5705. 6 indexed citations
3.
Basu, Subhasree, Keerthana Gnanapradeepan, Thibaut Barnoud, et al.. (2018). Mutant p53 controls tumor metabolism and metastasis by regulating PGC-1α. Genes & Development. 32(3-4). 230–243. 77 indexed citations
4.
Gnanapradeepan, Keerthana, Subhasree Basu, Thibaut Barnoud, et al.. (2018). The p53 Tumor Suppressor in the Control of Metabolism and Ferroptosis. Frontiers in Endocrinology. 9. 124–124. 148 indexed citations
5.
Basu, Subhasree, et al.. (2016). PUMA-dependent apoptosis in NSCLC cancer cells by a dimeric β-carboline. Bioorganic & Medicinal Chemistry Letters. 26(20). 4884–4887. 6 indexed citations
6.
Kung, Che-Pei, Julia I-Ju Leu, Subhasree Basu, et al.. (2016). The P72R Polymorphism of p53 Predisposes to Obesity and Metabolic Dysfunction. Cell Reports. 14(10). 2413–2425. 91 indexed citations
7.
Basu, Subhasree & Maureen E. Murphy. (2016). Genetic Modifiers of the p53 Pathway. Cold Spring Harbor Perspectives in Medicine. 6(4). a026302–a026302. 49 indexed citations
8.
Jennis, Matthew, Che-Pei Kung, Subhasree Basu, et al.. (2016). An African-specific polymorphism in the TP53 gene impairs p53 tumor suppressor function in a mouse model. Genes & Development. 30(8). 918–930. 293 indexed citations
9.
Basu, Subhasree & Maureen E. Murphy. (2016). p53 family members regulate cancer stem cells. Cell Cycle. 15(11). 1403–1404. 9 indexed citations
10.
Kung, Che-Pei, Subhasree Basu, & Maureen E. Murphy. (2016). A link between TP53 polymorphisms and metabolism. Molecular & Cellular Oncology. 3(4). e1173769–e1173769. 12 indexed citations
11.
Basu, Subhasree, et al.. (2016). The African-specific S47 polymorphism of p53 alters chemosensitivity. Cell Cycle. 15(19). 2557–2560. 20 indexed citations
12.
Basu, Subhasree, et al.. (2015). Design, synthesis, and biological evaluation of β-carboline dimers based on the structure of neokauluamine. Tetrahedron Letters. 56(23). 3515–3517. 15 indexed citations
13.
14.
Basu, Subhasree, et al.. (2014). α6 Integrin Transactivates Insulin-like Growth Factor Receptor-1 (IGF-1R) to Regulate Caspase-3-mediated Lens Epithelial Cell Differentiation Initiation. Journal of Biological Chemistry. 289(7). 3842–3855. 17 indexed citations
15.
Basu, Subhasree, et al.. (2014). Endogenous hydrogen peroxide production in the epithelium of the developing embryonic lens.. PubMed. 20. 458–67. 21 indexed citations
16.
Chauss, Daniel, Subhasree Basu, Zhiwei Ma, et al.. (2014). Differentiation State-Specific Mitochondrial Dynamic Regulatory Networks Are Revealed by Global Transcriptional Analysis of the Developing Chicken Lens. G3 Genes Genomes Genetics. 4(8). 1515–1527. 41 indexed citations
17.
Costello, M. Joseph, Lisa Brennan, Subhasree Basu, et al.. (2013). Autophagy and mitophagy participate in ocular lens organelle degradation. Experimental Eye Research. 116. 141–150. 120 indexed citations
18.
Lou, Marjorie F., Subhasree Basu, Yibo Yu, Hongli Wu, & A. Sue Menko. (2012). Glutaredoxin (Grx2) Gene Knockout Suppresses Fiber Cell Differentiation and Delays De-nucleation of the Mouse Lens. Investigative Ophthalmology & Visual Science. 53(14). 5592–5592. 3 indexed citations
19.
20.
Basu, Subhasree, et al.. (2001). Impact of questionnaires and telephone screening on attendance for ambulatory surgery.. PubMed. 83(5). 329–31. 17 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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