Ashish Banerjee

1.6k total citations
33 papers, 1.3k citations indexed

About

Ashish Banerjee is a scholar working on Immunology, Molecular Biology and Cancer Research. According to data from OpenAlex, Ashish Banerjee has authored 33 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Immunology, 11 papers in Molecular Biology and 11 papers in Cancer Research. Recurrent topics in Ashish Banerjee's work include Immune Cell Function and Interaction (12 papers), NF-κB Signaling Pathways (11 papers) and Immune Response and Inflammation (7 papers). Ashish Banerjee is often cited by papers focused on Immune Cell Function and Interaction (12 papers), NF-κB Signaling Pathways (11 papers) and Immune Response and Inflammation (7 papers). Ashish Banerjee collaborates with scholars based in Australia, United States and India. Ashish Banerjee's co-authors include Steve Gerondakis, Raffi Gugasyan, Raelene J. Grumont, Iwao Isomura, W. Wei‐Lynn Wong, Martin McMahon, George Grigoriadis, Ajithkumar Vasanthakumar, Ranjeny Thomas and Gerard F. Hoyne and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and The Journal of Experimental Medicine.

In The Last Decade

Ashish Banerjee

33 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
Ashish Banerjee Australia 19 794 439 424 211 84 33 1.3k
Vito Ruggiero Italy 14 821 1.0× 415 0.9× 197 0.5× 201 1.0× 109 1.3× 29 1.3k
Kelsey Voss United States 14 500 0.6× 474 1.1× 321 0.8× 308 1.5× 78 0.9× 22 1.2k
Ria Baumgrass Germany 22 838 1.1× 539 1.2× 117 0.3× 330 1.6× 92 1.1× 55 1.7k
Wei Hseun Yeap Singapore 11 623 0.8× 346 0.8× 131 0.3× 296 1.4× 147 1.8× 11 1.2k
Michelle M. Appenheimer United States 14 593 0.7× 443 1.0× 131 0.3× 518 2.5× 62 0.7× 16 1.3k
Olivier Déas France 16 363 0.5× 1.1k 2.4× 584 1.4× 212 1.0× 78 0.9× 40 1.5k
Norihiko Narita Japan 20 462 0.6× 398 0.9× 216 0.5× 379 1.8× 74 0.9× 92 1.4k
Steffen Schmitt Germany 17 1.2k 1.5× 535 1.2× 160 0.4× 358 1.7× 139 1.7× 28 1.9k
Fay J. Dufort United States 13 560 0.7× 503 1.1× 158 0.4× 126 0.6× 128 1.5× 22 1.1k
Ryan Sowell United States 9 979 1.2× 507 1.2× 194 0.5× 394 1.9× 119 1.4× 14 1.4k

Countries citing papers authored by Ashish Banerjee

Since Specialization
Citations

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

Fields of papers citing papers by Ashish Banerjee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ashish Banerjee

This figure shows the co-authorship network connecting the top 25 collaborators of Ashish Banerjee. A scholar is included among the top collaborators of Ashish Banerjee 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 Ashish Banerjee. Ashish Banerjee 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.
West, Alison C., Benjamin P. Martin, Daniel M. Andrews, et al.. (2016). The SMAC mimetic, LCL-161, reduces survival in aggressive MYC-driven lymphoma while promoting susceptibility to endotoxic shock. Oncogenesis. 5(4). e216–e216. 24 indexed citations
2.
Sadler, Anthony J., Bandar A. Suliman, Yu Liang, et al.. (2015). The acetyltransferase HAT1 moderates the NF-κB response by regulating the transcription factor PLZF. Nature Communications. 6(1). 6795–6795. 61 indexed citations
3.
Lancaster, Graeme I., Michael J. Kraakman, Hélène L. Kammoun, et al.. (2014). The Dual-Specificity Phosphatase 2 (DUSP2) Does Not Regulate Obesity-Associated Inflammation or Insulin Resistance in Mice. PLoS ONE. 9(11). e111524–e111524. 8 indexed citations
4.
Banerjee, Ashish, Nicole A. Mifsud, Robert Bird, et al.. (2014). The oral iron chelator deferasirox inhibits NF‐κB mediated gene expression without impacting on proximal activation: implications for myelodysplasia and aplastic anaemia. British Journal of Haematology. 168(4). 576–582. 26 indexed citations
5.
Sidwell, Tom, et al.. (2013). Thymic Regulatory T Cell Development: Role of Signalling Pathways and Transcription Factors. SHILAP Revista de lepidopterología. 2013. 1–8. 15 indexed citations
6.
Lancaster, Graeme I., Greg M. Kowalski, Emma Estévez, et al.. (2012). Tumor Progression Locus 2 (Tpl2) Deficiency Does Not Protect against Obesity-Induced Metabolic Disease. PLoS ONE. 7(6). e39100–e39100. 16 indexed citations
7.
Gerondakis, Steve, Ashish Banerjee, George Grigoriadis, et al.. (2012). NF‐κB subunit specificity in hemopoiesis. Immunological Reviews. 246(1). 272–285. 45 indexed citations
8.
Gugasyan, Raffi, Sarah Kinkel, George Grigoriadis, et al.. (2011). The NF‐κB1 transcription factor prevents the intrathymic development of CD8 T cells with memory properties. The EMBO Journal. 31(3). 692–706. 18 indexed citations
9.
Grigoriadis, George, Ajithkumar Vasanthakumar, Ashish Banerjee, et al.. (2011). c-Rel Controls Multiple Discrete Steps in the Thymic Development of Foxp3+ CD4 Regulatory T Cells. PLoS ONE. 6(10). e26851–e26851. 26 indexed citations
10.
Isomura, Iwao, Raelene J. Grumont, Karen Bunting, et al.. (2010). c-Rel is required for the development of thymic Foxp3(+) CD4 regulatory T cells (vol 206, pg 3001, 2009). The Journal of Experimental Medicine. 207(4). 1 indexed citations
11.
Isomura, Iwao, Raelene J. Grumont, Karen Bunting, et al.. (2010). c-Rel is required for the development of thymic Foxp3+ CD4 regulatory T cells. The Journal of Experimental Medicine. 207(4). 899–899. 4 indexed citations
12.
Shi, Wei, Ashish Banerjee, Matthew E. Ritchie, Steve Gerondakis, & Gordon K. Smyth. (2009). Illumina WG-6 BeadChip strips should be normalized separately. BMC Bioinformatics. 10(1). 372–372. 19 indexed citations
13.
Banerjee, Ashish, Raelene J. Grumont, Raffi Gugasyan, et al.. (2008). NF-κB1 and c-Rel cooperate to promote the survival of TLR4-activated B cells by neutralizing Bim via distinct mechanisms. Blood. 112(13). 5063–5073. 43 indexed citations
14.
Gerondakis, Steve, Raelene J. Grumont, & Ashish Banerjee. (2007). Regulating B‐cell activation and survival in response to TLR signals. Immunology and Cell Biology. 85(6). 471–475. 66 indexed citations
15.
Prasad, Pramod Vishwanath, Shail K. Chaube, Rajesh Chaudhary, et al.. (2006). Molecular dissection of an hCG-β epitope using single-step solid phase radioimmunoassay. Clinica Chimica Acta. 376(1-2). 52–59. 8 indexed citations
16.
Gerondakis, Steve, Raelene J. Grumont, Raffi Gugasyan, et al.. (2006). Unravelling the complexities of the NF-κB signalling pathway using mouse knockout and transgenic models. Oncogene. 25(51). 6781–6799. 240 indexed citations
17.
Banerjee, Ashish, et al.. (2004). Analysis of human chorionic gonadotropin-monoclonal antibody interaction in BIAcore. Journal of Biosciences. 29(1). 57–66. 7 indexed citations
18.
Banerjee, Ashish, et al.. (2002). Determination of thermodynamic parameters of antigen–antibody interaction from real-time kinetic studies. Current Science. 82(12). 1442–1448. 2 indexed citations
19.
Banerjee, Ashish, et al.. (2002). Real-time kinetic analysis of hCG–monoclonal antibody interaction using radiolabeled hCG probe: presence of two forms of Ag–mAb complex as revealed by solid phase dissociation studies. Biochimica et Biophysica Acta (BBA) - General Subjects. 1569(1-3). 21–30. 12 indexed citations
20.
Banerjee, Ashish, et al.. (2002). Thermodynamics of hCG–monoclonal antibody interaction: an analysis of real time kinetics data obtained using radiolabeled hCG probe. Biochimica et Biophysica Acta (BBA) - General Subjects. 1572(1). 31–36. 5 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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