Mala Chakraborty

4.0k total citations · 1 hit paper
33 papers, 3.1k citations indexed

About

Mala Chakraborty is a scholar working on Immunology, Radiology, Nuclear Medicine and Imaging and Oncology. According to data from OpenAlex, Mala Chakraborty has authored 33 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Immunology, 12 papers in Radiology, Nuclear Medicine and Imaging and 11 papers in Oncology. Recurrent topics in Mala Chakraborty's work include Immunotherapy and Immune Responses (17 papers), Immune Cell Function and Interaction (11 papers) and Monoclonal and Polyclonal Antibodies Research (10 papers). Mala Chakraborty is often cited by papers focused on Immunotherapy and Immune Responses (17 papers), Immune Cell Function and Interaction (11 papers) and Monoclonal and Polyclonal Antibodies Research (10 papers). Mala Chakraborty collaborates with scholars based in United States, Netherlands and France. Mala Chakraborty's co-authors include James W. Hodge, Kevin Camphausen, Jeffrey Schlom, Scott I. Abrams, Elizabeth K. Wansley, Elly Mesman, Tom A. Groothuis, Eric A. Reits, Rosalie M. Luiten and Jacques Neefjes and has published in prestigious journals such as The Journal of Experimental Medicine, Journal of Clinical Oncology and The Journal of Cell Biology.

In The Last Decade

Mala Chakraborty

33 papers receiving 3.1k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Radiation modulates the peptide repertoire, enhances MHC class I expression, and induces successful antitumor immunotherapy

2006 1.3k citations Eric A. Reits, James W. Hodge et al. The Journal of Experimental Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mala Chakraborty United States	21	2.1k	2.0k	564	499	462	33	3.1k
Andrew J. Long United States	8	2.9k 1.3×	2.8k 1.4×	688 1.2×	481 1.0×	195 0.4×	11	4.6k
Jon M. Wigginton United States	32	2.1k 1.0×	2.0k 1.1×	823 1.5×	376 0.8×	203 0.4×	100	3.5k
Fumiya Hirano Japan	9	4.2k 2.0×	3.4k 1.8×	781 1.4×	688 1.4×	221 0.5×	21	5.5k
Francine M. Foss United States	32	1.0k 0.5×	1.7k 0.9×	775 1.4×	132 0.3×	187 0.4×	128	3.7k
Leopoldo Luistro United States	15	1.0k 0.5×	1.1k 0.6×	777 1.4×	183 0.4×	281 0.6×	28	2.2k
Masanori Noguchi Japan	31	1.3k 0.6×	1.7k 0.9×	1.1k 1.9×	1.2k 2.3×	346 0.7×	125	3.2k
Kwong Y. Tsang United States	38	3.1k 1.5×	3.5k 1.8×	1.5k 2.6×	818 1.6×	577 1.2×	109	5.2k
Mark P. Rubinstein United States	32	2.1k 1.0×	3.4k 1.8×	817 1.4×	177 0.4×	165 0.4×	76	4.6k
R. K. Oldham United States	26	869 0.4×	892 0.5×	497 0.9×	244 0.5×	543 1.2×	77	2.1k
Kavita M. Dhodapkar United States	29	2.0k 0.9×	2.6k 1.4×	999 1.8×	237 0.5×	393 0.9×	73	4.0k

Countries citing papers authored by Mala Chakraborty

Since Specialization

Citations

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

Fields of papers citing papers by Mala Chakraborty

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mala Chakraborty

This figure shows the co-authorship network connecting the top 25 collaborators of Mala Chakraborty. A scholar is included among the top collaborators of Mala Chakraborty 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 Mala Chakraborty. Mala Chakraborty is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Clara, Joseph, Emily R. Levy, Robert Reger, et al.. (2022). High-affinity CD16 integration into a CRISPR/Cas9-edited CD38 locus augments CD38-directed antitumor activity of primary human natural killer cells. Journal for ImmunoTherapy of Cancer. 10(2). e003804–e003804. 25 indexed citations

Allan, David, et al.. (2021). Systematic improvements in lentiviral transduction of primary human natural killer cells undergoing ex vivo expansion. Molecular Therapy — Methods & Clinical Development. 20. 559–571. 42 indexed citations

Allan, David, Mala Chakraborty, Emily R. Levy, et al.. (2017). High-Efficiency Lentiviral Genetic Modification of Primary Human Natural Killer Cells. Blood. 130. 5566–5566. 2 indexed citations

Proctor, William R., Mala Chakraborty, Aaron Fullerton, et al.. (2014). Thymic stromal lymphopoietin and interleukin-4 mediate the pathogenesis of halothane-induced liver injury in mice. Hepatology. 60(5). 1741–1752. 14 indexed citations

Proctor, William R., Mala Chakraborty, Julia D. Berkson, et al.. (2012). Eosinophils mediate the pathogenesis of halothane-induced liver injury in mice. Hepatology. 57(5). 2026–2036. 44 indexed citations

Chakraborty, Mala, Alexander Gelbard, Jorge A. Carrasquillo, et al.. (2008). Use of radiolabeled monoclonal antibody to enhance vaccine-mediated antitumor effects. Cancer Immunology Immunotherapy. 57(8). 1173–1183. 36 indexed citations

Wansley, Elizabeth K., Mala Chakraborty, Kenneth W. Hance, et al.. (2007). Vaccination of CEA-transgenic mice with a recombinant Saccharomyces cerevisiae-CEA vaccine breaks immune tolerance and elicits therapeutic antitumor responses. Molecular Cancer Therapeutics. 6. 1 indexed citations

Chakraborty, Mala, Jeffrey Schlom, & James W. Hodge. (2007). The combined activation of positive costimulatory signals with modulation of a negative costimulatory signal for the enhancement of vaccine-mediated T-cell responses. Cancer Immunology Immunotherapy. 56(9). 1471–1484. 24 indexed citations

Reits, Eric A., James W. Hodge, Carla Herberts, et al.. (2006). Radiation modulates the peptide repertoire, enhances MHC class I expression, and induces successful antitumor immunotherapy. The Journal of Experimental Medicine. 203(5). 1259–1271. 1346 indexed citations breakdown →

10.

Wansley, Elizabeth K., Mala Chakraborty, Jorge A. Carrasquillo, et al.. (2006). Use of Samarium-153 (Quadramet) to modulate phenotype and enhance killing of tumor cells. Cancer Research. 66. 1032–1032. 2 indexed citations

11.

Chakraborty, Mala, Alexander Gelbard, Jorge A. Carrasquillo, et al.. (2006). Systemic radioimmunotherapy in synergy with vaccine renders antitumor effects in a preclinical model. Cancer Research. 66. 275–275. 3 indexed citations

12.

Reits, Eric A., James W. Hodge, Carla Herberts, et al.. (2006). Radiation modulates the peptide repertoire, enhances MHC class I expression, and induces successful antitumor immunotherapy. The Journal of Cell Biology. 173(4). i6–i6. 65 indexed citations

13.

Hodge, James W., Mala Chakraborty, Chie Kudo‐Saito, Charlie Garnett‐Benson, & Jeffrey Schlom. (2005). Multiple costimulatory modalities enhance CTL avidity. The Journal of Immunology. 174(12). 8220–8220. 4 indexed citations

14.

Garnett‐Benson, Charlie, John W. Greiner, Chie Kudo‐Saito, et al.. (2005). TRICOM Vector Based Cancer Vaccines. Current Pharmaceutical Design. 12(3). 351–361. 32 indexed citations

15.

Chakraborty, Mala, Scott I. Abrams, Kevin Camphausen, et al.. (2003). Irradiation of Tumor Cells Up-Regulates Fas and Enhances CTL Lytic Activity and CTL Adoptive Immunotherapy. The Journal of Immunology. 170(12). 6338–6347. 373 indexed citations

16.

Chatterjee, Sunil K., et al.. (2000). Counterpoint. Cancer vaccines: single-epitope anti-idiotype vaccine versus multiple-epitope antigen vaccine. Cancer Immunology Immunotherapy. 49(3). 133–141. 34 indexed citations

17.

Foon, Kenneth A., William J. John, Mala Chakraborty, et al.. (1999). Clinical and Immune Responses in Resected Colon Cancer Patients Treated With Anti-Idiotype Monoclonal Antibody Vaccine That Mimics the Carcinoembryonic Antigen. Journal of Clinical Oncology. 17(9). 2889–2889. 123 indexed citations

18.

Sen, Goutam, Mala Chakraborty, Kenneth A. Foon, Ralph A. Reisfeld, & Malaya Bhattacharya‐Chatterjee. (1998). Induction of IgG Antibodies by an Anti-Idiotype Antibody Mimicking Disialoganglioside GD2. Journal of Immunotherapy. 21(1). 75–83. 32 indexed citations

19.

Chakraborty, Mala, Kenneth A. Foon, Heinz Köhler, & Malaya Bhattacharya‐Chatterjee. (1995). Preclinical Evaluation in Nonhuman Primates of an Anti-Idiotypic Antibody that Mimicks the Carcinoembryonic Antigen. Journal of Immunotherapy. 18(2). 95–103. 14 indexed citations

20.

Chakraborty, Mala, et al.. (1993). Immuno-suppressive Effect of Human Alphafetoprotein: A Cross Species Study. Immunological Investigations. 22(5). 329–339. 18 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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