Satrajit Sinha

7.3k total citations
112 papers, 5.3k citations indexed

About

Satrajit Sinha is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, Satrajit Sinha has authored 112 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 85 papers in Molecular Biology, 42 papers in Oncology and 24 papers in Cancer Research. Recurrent topics in Satrajit Sinha's work include Cancer-related Molecular Pathways (32 papers), Genomics and Chromatin Dynamics (27 papers) and Cancer-related gene regulation (12 papers). Satrajit Sinha is often cited by papers focused on Cancer-related Molecular Pathways (32 papers), Genomics and Chromatin Dynamics (27 papers) and Cancer-related gene regulation (12 papers). Satrajit Sinha collaborates with scholars based in United States, Italy and China. Satrajit Sinha's co-authors include Rose‐Anne Romano, Kirsten Smalley, Sankar N. Maity, Benoît De Crombrugghe, Barbara Birkaya, In‐San Kim, Rumela Chakrabarti, S. Raghavan, Elaine Fuchs and Rose-Anne Romano and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Satrajit Sinha

108 papers receiving 5.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Satrajit Sinha United States 39 3.5k 1.9k 754 619 533 112 5.3k
Cristina Montagna United States 36 3.0k 0.8× 1.4k 0.7× 756 1.0× 811 1.3× 505 0.9× 124 4.8k
Shiaw‐Yih Lin United States 36 4.8k 1.3× 2.4k 1.3× 1.1k 1.4× 589 1.0× 545 1.0× 78 6.3k
David Wotton United States 33 5.5k 1.6× 1.2k 0.6× 681 0.9× 907 1.5× 668 1.3× 72 6.7k
Elsa R. Flores United States 35 3.9k 1.1× 2.8k 1.5× 1.1k 1.5× 416 0.7× 582 1.1× 86 5.5k
Jenő Gyuris United States 23 4.0k 1.1× 1.7k 0.9× 473 0.6× 540 0.9× 462 0.9× 56 5.5k
David Cobrinik United States 34 3.0k 0.9× 2.5k 1.3× 590 0.8× 510 0.8× 336 0.6× 74 4.8k
Vimla Band United States 31 2.8k 0.8× 1.4k 0.7× 568 0.8× 430 0.7× 430 0.8× 70 4.2k
Anne‐Catherine Prats France 43 4.4k 1.2× 838 0.4× 834 1.1× 551 0.9× 422 0.8× 88 5.6k
Stefan K. Bohlander Germany 52 5.4k 1.5× 1.6k 0.9× 1.7k 2.2× 976 1.6× 934 1.8× 184 9.2k
Ralph Meuwissen Netherlands 19 2.6k 0.7× 1.4k 0.8× 1.0k 1.4× 428 0.7× 348 0.7× 25 4.1k

Countries citing papers authored by Satrajit Sinha

Since Specialization
Citations

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

Fields of papers citing papers by Satrajit Sinha

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Satrajit Sinha

This figure shows the co-authorship network connecting the top 25 collaborators of Satrajit Sinha. A scholar is included among the top collaborators of Satrajit Sinha 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 Satrajit Sinha. Satrajit Sinha 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.
Min, Sangwon, et al.. (2024). ΔNp63 regulates Sfrp1 expression to direct salivary gland branching morphogenesis. PLoS ONE. 19(5). e0301082–e0301082.
2.
Luo, Wei, Richard M Jin, Lloyd Miller, et al.. (2023). Ets1 and IL17RA cooperate to regulate autoimmune responses and skin immunity to Staphylococcus aureus. Frontiers in Immunology. 14.
3.
Bard, Jonathan, et al.. (2021). Transcriptomic and Single-Cell Analysis Reveals Regulatory Networks and Cellular Heterogeneity in Mouse Primary Sjögren’s Syndrome Salivary Glands. Frontiers in Immunology. 12. 729040–729040. 20 indexed citations
4.
Min, Sangwon, Christian Gluck, Jonathan Bard, et al.. (2020). p63 and Its Target Follistatin Maintain Salivary Gland Stem/Progenitor Cell Function through TGF-β/Activin Signaling. iScience. 23(9). 101524–101524. 22 indexed citations
5.
Gluck, Christian, Maria Tsompana, Norma J. Nowak, et al.. (2019). Molecular dissection of the oncogenic role of ETS1 in the mesenchymal subtypes of head and neck squamous cell carcinoma. PLoS Genetics. 15(7). e1008250–e1008250. 27 indexed citations
6.
Osterburg, Christian, Dario Antonini, Raffaele Ambrosio, et al.. (2018). Protein aggregation of the p63 transcription factor underlies severe skin fragility in AEC syndrome. Proceedings of the National Academy of Sciences. 115(5). E906–E915. 36 indexed citations
7.
Sethi, Isha, Christian Gluck, Huiqing Zhou, Michael Buck, & Satrajit Sinha. (2017). Evolutionary re-wiring of p63 and the epigenomic regulatory landscape in keratinocytes and its potential implications on species-specific gene expression and phenotypes. Nucleic Acids Research. 45(14). 8208–8224. 33 indexed citations
8.
Sethi, Isha, Satrajit Sinha, & Michael Buck. (2014). Role of chromatin and transcriptional co-regulators in mediating p63-genome interactions in keratinocytes. BMC Genomics. 15(1). 1042–1042. 31 indexed citations
9.
Chakrabarti, Rumela, Julie Hwang, Andrés Blanco, et al.. (2012). Elf5 inhibits the epithelial–mesenchymal transition in mammary gland development and breast cancer metastasis by transcriptionally repressing Snail2. Nature Cell Biology. 14(11). 1212–1222. 224 indexed citations
10.
Yang, Xinping, Hai Lü, Bin Yan, et al.. (2011). ΔNp63 Versatilely Regulates a Broad NF-κB Gene Program and Promotes Squamous Epithelial Proliferation, Migration, and Inflammation. Cancer Research. 71(10). 3688–3700. 101 indexed citations
11.
Lü, Hai, Xinping Yang, Praveen Duggal, et al.. (2011). TNF-α Promotes c-REL/ΔNp63α Interaction and TAp73 Dissociation from Key Genes That Mediate Growth Arrest and Apoptosis in Head and Neck Cancer. Cancer Research. 71(21). 6867–6877. 64 indexed citations
12.
Escamilla, Rosalba, Rumela Chakrabarti, Rose-Anne Romano, et al.. (2010). Genome-wide search identifies Ccnd2 as a direct transcriptional target of Elf5 in mouse mammary gland. BMC Molecular Biology. 11(1). 68–68. 15 indexed citations
13.
Huang, Yiping, Alice Chuang, Nanette J. Liégeois, et al.. (2010). Phospho-ΔNp63α/NF-Y protein complex transcriptionally regulates DDIT3 expression in squamous cell carcinoma cells upon cisplatin exposure. Cell Cycle. 9(2). 328–338. 27 indexed citations
14.
Sinha, Satrajit, et al.. (2009). Antisense RNA-mediated inhibition of GMFAD2-1 encoding omega-6-desaturase.. Indian Journal of Plant Physiology. 14(4). 336–343. 1 indexed citations
15.
Su, Xiaohua, Maryline Paris, Young Jin Gi, et al.. (2009). TAp63 Prevents Premature Aging by Promoting Adult Stem Cell Maintenance. Cell stem cell. 5(1). 64–75. 192 indexed citations
16.
Romano, Rose‐Anne, Satrajit Sinha, & Priyadharsini Nagarajan. (2008). Transcriptional Control of the Differentiation Program of Interfollicular Epidermal Keratinocytes. Critical Reviews in Eukaryotic Gene Expression. 18(1). 57–79. 20 indexed citations
17.
Romano, Rose‐Anne, Barbara Birkaya, & Satrajit Sinha. (2006). A Functional Enhancer of Keratin14 Is a Direct Transcriptional Target of ΔNp63. Journal of Investigative Dermatology. 127(5). 1175–1186. 87 indexed citations
18.
Romano, Rose‐Anne, Barbara Birkaya, & Satrajit Sinha. (2006). Defining the Regulatory Elements in the Proximal Promoter of ΔNp63 in Keratinocytes: Potential Roles for Sp1/Sp3, NF-Y, and p63. Journal of Investigative Dermatology. 126(7). 1469–1479. 46 indexed citations
19.
Tummala, Ramakumar & Satrajit Sinha. (2005). Differentiation‐specific transcriptional regulation of the ESE‐2 gene by a novel keratinocyte‐restricted factor. Journal of Cellular Biochemistry. 97(4). 766–781. 16 indexed citations
20.
Sinha, Satrajit. (2004). Regulation of Intermediate Filament Gene Expression. Methods in cell biology. 78. 267–296. 2 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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