Sunil K. Raghav

5.2k total citations · 1 hit paper
71 papers, 2.2k citations indexed

About

Sunil K. Raghav is a scholar working on Molecular Biology, Immunology and Infectious Diseases. According to data from OpenAlex, Sunil K. Raghav has authored 71 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 26 papers in Immunology and 8 papers in Infectious Diseases. Recurrent topics in Sunil K. Raghav's work include Immunotherapy and Immune Responses (12 papers), Immune Cell Function and Interaction (9 papers) and Immune Response and Inflammation (8 papers). Sunil K. Raghav is often cited by papers focused on Immunotherapy and Immune Responses (12 papers), Immune Cell Function and Interaction (9 papers) and Immune Response and Inflammation (8 papers). Sunil K. Raghav collaborates with scholars based in India, Switzerland and United States. Sunil K. Raghav's co-authors include Bart Deplancke, Bhawna Gupta, Hasi R. Das, Lukas Baitsch, Hanifa Bouzourène, Sébastien Wieckowski, Nathalie Rufer, Daniel E. Speiser, Leticia Barba and Estelle Devêvre and has published in prestigious journals such as Journal of Clinical Investigation, Nature Communications and The EMBO Journal.

In The Last Decade

Sunil K. Raghav

64 papers receiving 2.2k citations

Hit Papers

Exhaustion of tumor-specific CD8+ T cells in metastases f... 2011 2026 2016 2021 2011 200 400 600
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.

  1. Exhaustion of tumor-specific CD8+ T cells in metastases from melanoma patients
    2011 650 citations Lukas Baitsch, Petra Baumgaertner et al. Journal of Clinical Investigation profile →

Peers

Sunil K. Raghav
Divya Singh India
Patrick J. Duriez United Kingdom
Yu‐Li Chen Taiwan
Carl L. Manthey United States
Can Cui China
Thomas A. Mace United States
Pablo Cesar Ortiz‐Lazareno Mexico
Xiaorong Zhou China
Patrice Decker France
Divya Singh India
Sunil K. Raghav
Citations per year, relative to Sunil K. Raghav Sunil K. Raghav (= 1×) peers Divya Singh

Countries citing papers authored by Sunil K. Raghav

Since Specialization
Citations

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

Fields of papers citing papers by Sunil K. Raghav

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sunil K. Raghav

This figure shows the co-authorship network connecting the top 25 collaborators of Sunil K. Raghav. A scholar is included among the top collaborators of Sunil K. Raghav 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 Sunil K. Raghav. Sunil K. Raghav 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.
Panda, Alok Kumar, Ayon Chakraborty, Rahul Modak, et al.. (2024). Lysine acetylation of Hsp16.3: Effect on its structure, chaperone function and influence towards the growth of Mycobacterium tuberculosis. International Journal of Biological Macromolecules. 268(Pt 2). 131763–131763. 2 indexed citations
2.
Mamidi, Prabhudutta, Baijayantimala Mishra, Soma Chattopadhyay, et al.. (2024). Identification of a novel Indian clade of Coxsackievirus A16 in Hand, Foot and Mouth disease outbreak in 2022. Future Virology. 19(5). 161–172. 1 indexed citations
3.
4.
Ghosh, Arup, et al.. (2024). Impact of vaccination on SARS-CoV-2 evolution and immune escape variants. Vaccine. 42(21). 126153–126153. 2 indexed citations
5.
Raghav, Sunil K., et al.. (2024). Novel Mutations in Acute Erythroid Leukemia–A Case Report with Review of Literature. Indian Journal of Hematology and Blood Transfusion. 41(2). 383–387.
6.
7.
Sen, Kaushik, Abdul Ahad, Arup Ghosh, et al.. (2023). NCoR1 controls Mycobacterium tuberculosis growth in myeloid cells by regulating the AMPK-mTOR-TFEB axis. PLoS Biology. 21(8). e3002231–e3002231. 6 indexed citations
8.
Mishra, Gyan P., Kaushik Sen, Shuchi Smita, et al.. (2022). SMRT and NCoR1 fine-tune inflammatory versus tolerogenic balance in dendritic cells by differentially regulating STAT3 signaling. Frontiers in Immunology. 13. 910705–910705. 8 indexed citations
9.
Sen, Kaushik, et al.. (2022). NCoR1 controls immune tolerance in conventional dendritic cells by fine-tuning glycolysis and fatty acid oxidation. Redox Biology. 59. 102575–102575. 31 indexed citations
10.
Sen, Kaushik, et al.. (2022). Epigenomics of conventional type-I dendritic cells depicted preferential control of TLR9 versus TLR3 response by NCoR1 through differential IRF3 activation. Cellular and Molecular Life Sciences. 79(8). 429–429. 3 indexed citations
11.
Horváth, Attila, Gergely Nagy, Szilárd Póliska, et al.. (2022). A Multi-Omics Approach Reveals Features That Permit Robust and Widespread Regulation of IFN-Inducible Antiviral Effectors. The Journal of Immunology. 209(10). 1930–1941. 2 indexed citations
12.
Dash, Pujarini, Jyotirmayee Turuk, Santosh Kumar Behera, et al.. (2021). Sequence analysis of Indian SARS-CoV-2 isolates shows a stronger interaction of mutant receptor-binding domain with ACE2. International Journal of Infectious Diseases. 104. 491–500. 6 indexed citations
13.
Khanna, Shweta, et al.. (2020). Differential mitochondrial genome in patients with Rheumatoid Arthritis. Autoimmunity. 54(1). 1–12. 9 indexed citations
14.
Chen, Wanze, Petra Schwalie, Carine Gubelmann, et al.. (2019). ZFP30 promotes adipogenesis through the KAP1-mediated activation of a retrotransposon-derived Pparg2 enhancer. Nature Communications. 10(1). 1809–1809. 26 indexed citations
15.
Schmid, Adrien W., Paola A. Gilardoni, Benjamin Zoller, et al.. (2013). Absolute quantification of transcription factors during cellular differentiation using multiplexed targeted proteomics. Nature Methods. 10(6). 570–576. 71 indexed citations
16.
Raghav, Sunil K., Sebastian M. Waszak, Carine Gubelmann, et al.. (2012). Integrative Genomics Identifies the Corepressor SMRT as a Gatekeeper of Adipogenesis through the Transcription Factors C/EBPβ and KAISO. Molecular Cell. 46(3). 335–350. 70 indexed citations
17.
Baitsch, Lukas, Petra Baumgaertner, Estelle Devêvre, et al.. (2011). Exhaustion of tumor-specific CD8+ T cells in metastases from melanoma patients. Journal of Clinical Investigation. 121(6). 2350–2360. 650 indexed citations breakdown →
18.
Elo, Laura L., Soile Tuomela, Sunil K. Raghav, et al.. (2010). Genome-wide Profiling of Interleukin-4 and STAT6 Transcription Factor Regulation of Human Th2 Cell Programming. Immunity. 32(6). 852–862. 124 indexed citations
19.
Rautajoki, Kirsi J., et al.. (2008). An insight into molecular mechanisms of human T helper cell differentiation. Annals of Medicine. 40(5). 322–335. 63 indexed citations
20.
AHLUWALIA, V. K., et al.. (1988). Acid catalyzed condensation of isoprene with hydroxypropiophenones synthesis of 2 2 dimethylchromans and some new 2 amino and 2 mercapto 4 aryl 5 methylthiazoles. Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry. 27(7). 629–632. 1 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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