Sumit K. Chanda

30.0k total citations · 3 hit papers
82 papers, 13.8k citations indexed

About

Sumit K. Chanda is a scholar working on Molecular Biology, Immunology and Virology. According to data from OpenAlex, Sumit K. Chanda has authored 82 papers receiving a total of 13.8k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 28 papers in Immunology and 23 papers in Virology. Recurrent topics in Sumit K. Chanda's work include HIV Research and Treatment (23 papers), interferon and immune responses (16 papers) and Immune Cell Function and Interaction (9 papers). Sumit K. Chanda is often cited by papers focused on HIV Research and Treatment (23 papers), interferon and immune responses (16 papers) and Immune Cell Function and Interaction (9 papers). Sumit K. Chanda collaborates with scholars based in United States, Germany and Switzerland. Sumit K. Chanda's co-authors include Lars Pache, Yingyao Zhou, Bin Zhou, Christopher Benner, Max W. Chang, Olga Tanaseichuk, Alireza Hadj Khodabakhshi, Anthony P. Orth, Renate König and Serge Batalov and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Sumit K. Chanda

81 papers receiving 13.7k citations

Hit Papers

Metascape provides a biologist-o... 2008 2026 2014 2020 2019 2008 2021 2.5k 5.0k 7.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sumit K. Chanda United States 36 8.2k 2.5k 2.0k 1.7k 1.4k 82 13.8k
Yingyao Zhou United States 33 7.0k 0.9× 2.6k 1.1× 1.8k 0.9× 1.4k 0.8× 1.4k 1.0× 62 13.2k
Lars Pache United States 18 5.5k 0.7× 1.7k 0.7× 1.6k 0.8× 1.2k 0.7× 1.4k 0.9× 27 9.9k
Max W. Chang United States 23 6.4k 0.8× 1.7k 0.7× 1.7k 0.9× 1.2k 0.7× 1.4k 1.0× 40 11.8k
Glynn Dennis United States 12 7.5k 0.9× 1.6k 0.7× 2.0k 1.0× 1.1k 0.6× 950 0.7× 13 12.3k
Michael R. Green United States 68 15.3k 1.9× 1.8k 0.7× 1.3k 0.7× 1.5k 0.9× 458 0.3× 177 19.2k
Frank J. T. Staal Netherlands 55 5.6k 0.7× 3.2k 1.3× 932 0.5× 1.6k 0.9× 577 0.4× 188 11.0k
Robert M. Stephens United States 64 13.3k 1.6× 1.8k 0.7× 5.9k 3.0× 1.7k 1.0× 1.1k 0.8× 151 19.1k
Zichen Wang United States 32 9.2k 1.1× 2.2k 0.9× 2.4k 1.2× 1.6k 0.9× 1.3k 0.9× 90 15.4k
Yi Liu China 45 5.2k 0.6× 1.5k 0.6× 1.1k 0.6× 1.3k 0.8× 569 0.4× 247 8.4k
William L. Farrar United States 71 6.8k 0.8× 5.7k 2.3× 2.2k 1.1× 4.7k 2.7× 1.0k 0.7× 212 15.5k

Countries citing papers authored by Sumit K. Chanda

Since Specialization
Citations

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

Fields of papers citing papers by Sumit K. Chanda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sumit K. Chanda. 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 Sumit K. Chanda. The network helps show where Sumit K. Chanda may publish in the future.

Co-authorship network of co-authors of Sumit K. Chanda

This figure shows the co-authorship network connecting the top 25 collaborators of Sumit K. Chanda. A scholar is included among the top collaborators of Sumit K. Chanda 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 Sumit K. Chanda. Sumit K. Chanda 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.
Chen, Hao, Frederick J. King, Bin Zhou, et al.. (2024). Drug target prediction through deep learning functional representation of gene signatures. Nature Communications. 15(1). 1853–1853. 34 indexed citations
2.
Pal, Lipika R., Kuoyuan Cheng, Nishanth Ulhas Nair, et al.. (2022). Synthetic lethality-based prediction of anti-SARS-CoV-2 targets. iScience. 25(5). 104311–104311. 5 indexed citations
3.
Cheng, Kuoyuan, Laura Martin‐Sancho, Lipika R. Pal, et al.. (2021). Genome‐scale metabolic modeling reveals SARS‐CoV‐2‐induced metabolic changes and antiviral targets. Molecular Systems Biology. 17(11). e10260–e10260. 29 indexed citations
4.
Kallol, Sampada, Laura Martin‐Sancho, Donald Pizzo, et al.. (2021). Potential Risk of Infection of First Trimester Placentas by SARS-CoV2. Reproductive Sciences. 28. 1 indexed citations
5.
Pache, Lars, Matthew D. Marsden, Peter Teriete, et al.. (2020). Pharmacological Activation of Non-canonical NF-κB Signaling Activates Latent HIV-1 Reservoirs In Vivo. Cell Reports Medicine. 1(3). 100037–100037. 38 indexed citations
6.
Du, Yushen, Judd F. Hultquist, Quan Zhou, et al.. (2020). mRNA display with library of even-distribution reveals cellular interactors of influenza virus NS1. Nature Communications. 11(1). 2449–2449. 13 indexed citations
7.
Langer, Simon, Christian Hammer, Lukas Klein, et al.. (2019). HIV-1 Vpu is a potent transcriptional suppressor of NF-κB-elicited antiviral immune responses. eLife. 8. 53 indexed citations
8.
Rodríguez-Frandsen, Ariel, Laura Martin‐Sancho, Anshu P. Gounder, et al.. (2019). Viral Determinants in H5N1 Influenza A Virus Enable Productive Infection of HeLa Cells. Journal of Virology. 94(4). 3 indexed citations
9.
Zhou, Yingyao, Bin Zhou, Lars Pache, et al.. (2019). Metascape provides a biologist-oriented resource for the analysis of systems-level datasets. Nature Communications. 10(1). 1523–1523. 8740 indexed citations breakdown →
10.
Chen, Bo-Rui, Anagha Deshpande, Maria Kleppe, et al.. (2018). Genomic and Proteomic Profiling of AF10-Fusion Oncoproteins Reveal Mechanisms of Leukemogenesis and Actionable Targets. Blood. 132(Supplement 1). 544–544. 2 indexed citations
11.
Jiang, Dan, Peng Qin, Yuelin Zhang, et al.. (2017). Inhibition of NUCKS Facilitates Corneal Recovery Following Alkali Burn. Scientific Reports. 7(1). 41224–41224. 20 indexed citations
12.
Pohl, Marie O., Ariel Rodríguez-Frandsen, Emilio Yángüez, et al.. (2017). Identification of Polo-like kinases as potential novel drug targets for influenza A virus. Scientific Reports. 7(1). 8629–8629. 14 indexed citations
13.
Emig-Agius, Dorothea, Kevin C. Olivieri, Lars Pache, et al.. (2014). An Integrated Map of HIV-Human Protein Complexes that Facilitate Viral Infection. PLoS ONE. 9(5). e96687–e96687. 11 indexed citations
14.
Opaluch, Amanda M., Monika Schneider, Chih-Yuan Chiang, et al.. (2014). Positive Regulation of TRAF6-Dependent Innate Immune Responses by Protein Phosphatase PP1-γ. PLoS ONE. 9(2). e89284–e89284. 14 indexed citations
15.
Peng, Tao, et al.. (2010). Determining the distribution of probes between different subcellular locations through automated unmixing of subcellular patterns. Proceedings of the National Academy of Sciences. 107(7). 2944–2949. 31 indexed citations
16.
Bandyopadhyay, Sourav, Chih-Yuan Chiang, Jyoti Srivastava, et al.. (2010). A human MAP kinase interactome. Nature Methods. 7(10). 801–805. 157 indexed citations
17.
Gómez-Ferrerı́a, Marı́a Ana, Uttama Rath, Daniel W. Buster, et al.. (2007). Human Cep192 Is Required for Mitotic Centrosome and Spindle Assembly. Current Biology. 17(22). 1960–1966. 166 indexed citations
18.
Yu, Fuqu, Josephine N. Harada, Helen Brown, et al.. (2007). Systematic Identification of Cellular Signals Reactivating Kaposi Sarcoma–Associated Herpesvirus. PLoS Pathogens. 3(3). e44–e44. 84 indexed citations
19.
Huang, Qihong, Ángel Raya, Paul DeJesus, et al.. (2004). Identification of p53 regulators by genome-wide functional analysis. Proceedings of the National Academy of Sciences. 101(10). 3456–3461. 118 indexed citations
20.
Smith, Kevin S., Sumit K. Chanda, Douglas T. Ross, et al.. (2003). Bmi-1 Regulation of INK4A-ARF Is a Downstream Requirement for Transformation of Hematopoietic Progenitors by E2a-Pbx1. Molecular Cell. 12(2). 393–400. 75 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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