Kaushik Sengupta

2.1k total citations · 1 hit paper
34 papers, 1.6k citations indexed

About

Kaushik Sengupta is a scholar working on Molecular Biology, Cell Biology and Strategy and Management. According to data from OpenAlex, Kaushik Sengupta has authored 34 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 8 papers in Cell Biology and 4 papers in Strategy and Management. Recurrent topics in Kaushik Sengupta's work include Nuclear Structure and Function (23 papers), RNA Research and Splicing (16 papers) and Genomics and Chromatin Dynamics (7 papers). Kaushik Sengupta is often cited by papers focused on Nuclear Structure and Function (23 papers), RNA Research and Splicing (16 papers) and Genomics and Chromatin Dynamics (7 papers). Kaushik Sengupta collaborates with scholars based in India, United States and Philippines. Kaushik Sengupta's co-authors include Robert D. Goldman, Liliana Solimando, Dale K. Shumaker, Takeshi Shimi, Katrin Pfleghaar, Thomas Dechat, Lori S. Cook, Daniel R. Heiser, Stephen A. Adam and Dipak Dasgupta and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Genes & Development.

In The Last Decade

Kaushik Sengupta

33 papers receiving 1.5k citations

Hit Papers

Nuclear lamins: major factors in the structural organizat... 2008 2026 2014 2020 2008 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kaushik Sengupta India 14 1.1k 267 225 182 83 34 1.6k
David P. Cook Canada 20 890 0.8× 171 0.6× 103 0.5× 106 0.6× 88 1.1× 63 1.9k
Susan McCracken Canada 31 3.1k 2.9× 96 0.4× 299 1.3× 167 0.9× 37 0.4× 61 4.4k
David Hollingworth United States 23 966 0.9× 37 0.1× 189 0.8× 245 1.3× 15 0.2× 32 1.5k
Carolin Decker Germany 15 538 0.5× 59 0.2× 50 0.2× 182 1.0× 16 0.2× 35 1.1k
Richard Klein United States 18 723 0.7× 24 0.1× 412 1.8× 421 2.3× 83 1.0× 86 2.1k
Chen‐Ju Lin Taiwan 23 603 0.6× 44 0.2× 35 0.2× 345 1.9× 57 0.7× 89 1.8k
Indu Ramachandran United States 17 354 0.3× 56 0.2× 37 0.2× 186 1.0× 17 0.2× 31 1.6k
Huimin Chung Taiwan 23 266 0.3× 52 0.2× 37 0.2× 284 1.6× 113 1.4× 66 1.9k
Shu Hui Chen United States 14 290 0.3× 139 0.5× 52 0.2× 46 0.3× 19 0.2× 27 777
Herbert E. Longenecker United States 15 322 0.3× 91 0.3× 264 1.2× 41 0.2× 36 0.4× 63 1.6k

Countries citing papers authored by Kaushik Sengupta

Since Specialization
Citations

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

Fields of papers citing papers by Kaushik Sengupta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kaushik Sengupta

This figure shows the co-authorship network connecting the top 25 collaborators of Kaushik Sengupta. A scholar is included among the top collaborators of Kaushik Sengupta 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 Kaushik Sengupta. Kaushik Sengupta 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
2.
Sengupta, Kaushik, et al.. (2024). Lamin A K97E leads to NF‐κB‐mediated dysfunction of inflammatory responses in dilated cardiomyopathy. Biology of the Cell. 116(3). e2300094–e2300094. 2 indexed citations
3.
Sengupta, Kaushik, et al.. (2023). Doing science together: Gaining momentum from long-term explorative university–industry research programs. Drug Discovery Today. 28(9). 103687–103687. 2 indexed citations
4.
Mukhopadhyay, Asima, et al.. (2023). Elevated Levels of Lamin A Promote HR and NHEJ-Mediated Repair Mechanisms in High-Grade Ovarian Serous Carcinoma Cell Line. Cells. 12(5). 757–757. 1 indexed citations
5.
Mukherjee, C. D., et al.. (2022). Slower diffusion and anomalous association of R453W lamin A protein alter nuclear architecture in AD-EDMD. RSC Advances. 12(49). 32129–32141. 2 indexed citations
6.
Mukhopadhyay, Asima, et al.. (2022). A deep hybrid learning pipeline for accurate diagnosis of ovarian cancer based on nuclear morphology. PLoS ONE. 17(1). e0261181–e0261181. 28 indexed citations
7.
Sengupta, Kaushik, et al.. (2022). Lamin A and telomere maintenance in aging: Two to Tango. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 825. 111788–111788. 8 indexed citations
8.
Mukherjee, C. D., et al.. (2021). Active microrheology using pulsed optical tweezers to probe viscoelasticity of lamin A. Soft Matter. 17(28). 6787–6796. 9 indexed citations
9.
Bhattacharyya, Maitree, et al.. (2018). Skeletal Muscle Dystrophy mutant of lamin A alters the structure and dynamics of the Ig fold domain. Scientific Reports. 8(1). 13793–13793. 13 indexed citations
10.
Bhattacharyya, Maitree, et al.. (2018). Changes in the Nuclear Envelope in Laminopathies. Advances in experimental medicine and biology. 1112. 31–38. 6 indexed citations
11.
Chattoraj, Shyamtanu, Shekhar Saha, Alakesh Das, et al.. (2017). Differential role of nonmuscle myosin II isoforms during blebbing of MCF-7 cells. Molecular Biology of the Cell. 28(8). 1034–1042. 9 indexed citations
12.
Dasgupta, Dipak, et al.. (2017). DCM associated LMNA mutations cause distortions in lamina structure and assembly. Biochimica et Biophysica Acta (BBA) - General Subjects. 1861(11). 2598–2608. 17 indexed citations
13.
Sengupta, Kaushik, et al.. (2015). Novel linkage of LMNA Single Nucleotide Polymorphism with Dilated Cardiomyopathy in an Indian case study. IJC Heart & Vasculature. 7. 99–105. 1 indexed citations
14.
Sengupta, Kaushik, et al.. (2015). Hsp70 clears misfolded kinases that partitioned into distinct quality-control compartments. Molecular Biology of the Cell. 26(9). 1583–1600. 10 indexed citations
15.
Krishnaswamy, Rema, et al.. (2013). Viscoelastic Behavior of Human Lamin A Proteins in the Context of Dilated Cardiomyopathy. PLoS ONE. 8(12). e83410–e83410. 31 indexed citations
16.
Cook, Lori S., Daniel R. Heiser, & Kaushik Sengupta. (2011). The moderating effect of supply chain role on the relationship between supply chain practices and performance. International Journal of Physical Distribution & Logistics Management. 41(2). 104–134. 97 indexed citations
17.
Adam, Stephen A., Kaushik Sengupta, & Robert D. Goldman. (2008). Regulation of Nuclear Lamin Polymerization by Importin α. Journal of Biological Chemistry. 283(13). 8462–8468. 41 indexed citations
18.
Dechat, Thomas, Katrin Pfleghaar, Kaushik Sengupta, et al.. (2008). Nuclear lamins: major factors in the structural organization and function of the nucleus and chromatin. Genes & Development. 22(7). 832–853. 752 indexed citations breakdown →
19.
Buda, Richard, et al.. (2006). Employee and Organizational Perspectives of Service Quality: A Cross-Cultural Study in Kuwait, United States and Saudi Arabia. 23(3). 430. 8 indexed citations
20.
Pristovšek, Primož, Kaushik Sengupta, Frank Löhr, et al.. (2003). Structural Analysis of the DNA-binding Domain of theErwinia amylovora RcsB Protein and Its Interaction with the RcsAB Box. Journal of Biological Chemistry. 278(20). 17752–17759. 58 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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