Srustidhar Das

2.6k total citations
37 papers, 1.7k citations indexed

About

Srustidhar Das is a scholar working on Molecular Biology, Immunology and Oncology. According to data from OpenAlex, Srustidhar Das has authored 37 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 16 papers in Immunology and 15 papers in Oncology. Recurrent topics in Srustidhar Das's work include Glycosylation and Glycoproteins Research (16 papers), Immune Cell Function and Interaction (9 papers) and Cancer Cells and Metastasis (7 papers). Srustidhar Das is often cited by papers focused on Glycosylation and Glycoproteins Research (16 papers), Immune Cell Function and Interaction (9 papers) and Cancer Cells and Metastasis (7 papers). Srustidhar Das collaborates with scholars based in United States, Sweden and Germany. Srustidhar Das's co-authors include Surinder K. Batra, Surinder K. Batra, Moorthy P. Ponnusamy, Satyanarayana Rachagani, Imayavaramban Lakshmanan, Eduardo J. Villablanca, Shantibhusan Senapati, Sara Martina Parigi, Lynette M. Smith and Subhankar Chakraborty and has published in prestigious journals such as Nature Communications, PLoS ONE and Cancer Research.

In The Last Decade

Srustidhar Das

37 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Srustidhar Das United States 25 1.0k 479 448 188 179 37 1.7k
Yue Zhou China 25 1.0k 1.0× 471 1.0× 293 0.7× 197 1.0× 103 0.6× 120 1.9k
Jonathan Lopez France 24 1.5k 1.5× 535 1.1× 514 1.1× 330 1.8× 265 1.5× 89 2.7k
Radosław Zagożdżon Poland 25 792 0.8× 803 1.7× 820 1.8× 213 1.1× 154 0.9× 104 2.2k
Carmen Ruiz‐Ruiz Spain 27 1.6k 1.5× 656 1.4× 592 1.3× 361 1.9× 97 0.5× 54 2.5k
Eliana Abdelhay Brazil 26 1.1k 1.1× 474 1.0× 244 0.5× 452 2.4× 177 1.0× 125 2.0k
Lan Wang China 25 905 0.9× 274 0.6× 367 0.8× 338 1.8× 110 0.6× 74 1.8k
Ming‐Chei Maa Taiwan 22 956 0.9× 378 0.8× 322 0.7× 173 0.9× 74 0.4× 35 1.6k
Xiaohe Yang United States 25 1.8k 1.8× 818 1.7× 341 0.8× 396 2.1× 121 0.7× 51 2.7k
Hwa‐Chain Robert Wang United States 28 1.5k 1.5× 507 1.1× 291 0.6× 297 1.6× 101 0.6× 72 2.4k
Kunitaka Hirose Japan 22 883 0.9× 421 0.9× 574 1.3× 241 1.3× 92 0.5× 34 1.8k

Countries citing papers authored by Srustidhar Das

Since Specialization
Citations

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

Fields of papers citing papers by Srustidhar Das

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Srustidhar Das

This figure shows the co-authorship network connecting the top 25 collaborators of Srustidhar Das. A scholar is included among the top collaborators of Srustidhar Das 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 Srustidhar Das. Srustidhar Das 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.
Monasterio, Gustavo, Rodrigo A. Morales, David Alejandro Bejarano, et al.. (2024). A versatile tissue-rolling technique for spatial-omics analyses of the entire murine gastrointestinal tract. Nature Protocols. 19(10). 3085–3137. 3 indexed citations
2.
Parigi, Sara Martina, Ludvig Larsson, Srustidhar Das, et al.. (2022). The spatial transcriptomic landscape of the healing mouse intestine following damage. Nature Communications. 13(1). 828–828. 63 indexed citations
3.
Diaz, Oscar E., Chiara Sorini, Rodrigo A. Morales, et al.. (2021). Perfluorooctanesulfonic acid modulates barrier function and systemic T-cell homeostasis during intestinal inflammation. Disease Models & Mechanisms. 14(12). 21 indexed citations
4.
Kshirsagar, Prakash, Wade M. Junker, Abhijit Aithal, et al.. (2021). Characterization of recombinant β subunit of human MUC4 mucin (rMUC4β). Scientific Reports. 11(1). 23730–23730. 5 indexed citations
5.
Kaya, Berna, Oscar E. Diaz, Rodrigo A. Morales, et al.. (2020). Lysophosphatidic Acid-Mediated GPR35 Signaling in CX3CR1+ Macrophages Regulates Intestinal Homeostasis. Cell Reports. 32(5). 107979–107979. 73 indexed citations
6.
Czarnewski, Paulo, Sara Martina Parigi, Chiara Sorini, et al.. (2019). Conserved transcriptomic profile between mouse and human colitis allows unsupervised patient stratification. Nature Communications. 10(1). 2892–2892. 74 indexed citations
7.
Parigi, Sara Martina, Paulo Czarnewski, Srustidhar Das, et al.. (2018). Flt3 ligand expands bona fide innate lymphoid cell precursors in vivo. Scientific Reports. 8(1). 154–154. 9 indexed citations
8.
Jahan, Rahat, Muzafar A. Macha, Satyanarayana Rachagani, et al.. (2018). Axed MUC4 (MUC4/X) aggravates pancreatic malignant phenotype by activating integrin-β1/FAK/ERK pathway. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1864(8). 2538–2549. 25 indexed citations
9.
Schiering, Chris, et al.. (2018). Cytochrome P4501-inhibiting chemicals amplify aryl hydrocarbon receptor activation and IL-22 production in T helper 17 cells. Biochemical Pharmacology. 151. 47–58. 40 indexed citations
10.
Lakshmanan, Imayavaramban, Parthasarathy Seshacharyulu, Satyanarayana Rachagani, et al.. (2017). MUC16 Regulates TSPYL5 for Lung Cancer Cell Growth and Chemoresistance by Suppressing p53. Clinical Cancer Research. 23(14). 3906–3917. 71 indexed citations
11.
Das, Srustidhar, Surinder K. Batra, & Satyanarayana Rachagani. (2017). Mouse Model of Dextran Sodium Sulfate (DSS)-induced Colitis. BIO-PROTOCOL. 7(16). e2515–e2515. 15 indexed citations
12.
Jijon, Humberto, Lucía Suárez-López, Oscar E. Diaz, et al.. (2017). Intestinal epithelial cell-specific RARα depletion results in aberrant epithelial cell homeostasis and underdeveloped immune system. Mucosal Immunology. 11(3). 703–715. 43 indexed citations
13.
Das, Srustidhar, Satyanarayana Rachagani, Yuri Sheinin, et al.. (2015). Mice deficient in Muc4 are resistant to experimental colitis and colitis-associated colorectal cancer. Oncogene. 35(20). 2645–2654. 62 indexed citations
14.
Das, Srustidhar & Surinder K. Batra. (2015). Pancreatic Cancer Metastasis: Are we being Pre-EMTed?. Current Pharmaceutical Design. 21(10). 1249–1255. 47 indexed citations
15.
Kumar, Sushil, Srustidhar Das, Satyanarayana Rachagani, et al.. (2014). NCOA3-mediated upregulation of mucin expression via transcriptional and post-translational changes during the development of pancreatic cancer. Oncogene. 34(37). 4879–4889. 36 indexed citations
16.
Das, Srustidhar, et al.. (2013). An Escherichia coli strain for expression of the connexin45 carboxyl terminus attached to the 4th transmembrane domain. Frontiers in Pharmacology. 4. 106–106. 9 indexed citations
17.
Haridas, Dhanya, Subhankar Chakraborty, Moorthy P. Ponnusamy, et al.. (2011). Pathobiological Implications of MUC16 Expression in Pancreatic Cancer. PLoS ONE. 6(10). e26839–e26839. 107 indexed citations
18.
Torres, María P., Moorthy P. Ponnusamy, Subhankar Chakraborty, et al.. (2010). Effects of Thymoquinone in the Expression of Mucin 4 in Pancreatic Cancer Cells: Implications for the Development of Novel Cancer Therapies. Molecular Cancer Therapeutics. 9(5). 1419–1431. 113 indexed citations
19.
Luu, Ying, Wade M. Junker, Satyanarayana Rachagani, et al.. (2010). Human intestinal MUC17 mucin augments intestinal cell restitution and enhances healing of experimental colitis. The International Journal of Biochemistry & Cell Biology. 42(6). 996–1006. 29 indexed citations
20.
Ponnusamy, Moorthy P., Imayavaramban Lakshmanan, Maneesh Jain, et al.. (2010). MUC4 mucin-induced epithelial to mesenchymal transition: a novel mechanism for metastasis of human ovarian cancer cells. Oncogene. 29(42). 5741–5754. 119 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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