Jayashree C. Jagtap

433 total citations
12 papers, 344 citations indexed

About

Jayashree C. Jagtap is a scholar working on Molecular Biology, Oncology and Neurology. According to data from OpenAlex, Jayashree C. Jagtap has authored 12 papers receiving a total of 344 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Oncology and 3 papers in Neurology. Recurrent topics in Jayashree C. Jagtap's work include Cell death mechanisms and regulation (6 papers), Neuroblastoma Research and Treatments (3 papers) and Cytokine Signaling Pathways and Interactions (3 papers). Jayashree C. Jagtap is often cited by papers focused on Cell death mechanisms and regulation (6 papers), Neuroblastoma Research and Treatments (3 papers) and Cytokine Signaling Pathways and Interactions (3 papers). Jayashree C. Jagtap collaborates with scholars based in India and Canada. Jayashree C. Jagtap's co-authors include Padma Shastry, Anmol Chandele, Ravi Shukla, V. S. S. Prasad, Radha Pujari, Anjali Shiras, Ashish Chugh, Ganesh Vilas Shelke, Dae‐Kyum Kim and Krishna M.G. Mallela and has published in prestigious journals such as PLoS ONE, Free Radical Biology and Medicine and Molecular Cancer.

In The Last Decade

Jayashree C. Jagtap

12 papers receiving 339 citations

Peers

Jayashree C. Jagtap

ONCOL

IMMUN

GENET

Ganchimeg Ishdorj Canada

Sinem Usluer Austria

Eiichi Nakai Japan

Heinrich Baust Germany

Peace Mabeta South Africa

Fuqiang Feng China

Hongjuan Cui China

Manon Verwijs-Janssen Netherlands

Toshiaki Kogame Japan

Vincenzo Giansanti Italy

Ganchimeg Ishdorj Canada

Jayashree C. Jagtap

250 ×1.1

81 ×1.0

ONCOL

67 ×1.1

75 ×1.4

IMMUN

55 ×1.5

GENET

Citations per year, relative to Jayashree C. Jagtap Jayashree C. Jagtap (= 1×) peers Ganchimeg Ishdorj

Countries citing papers authored by Jayashree C. Jagtap

Since Specialization

Citations

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

Fields of papers citing papers by Jayashree C. Jagtap

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jayashree C. Jagtap. 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 Jayashree C. Jagtap. The network helps show where Jayashree C. Jagtap may publish in the future.

Co-authorship network of co-authors of Jayashree C. Jagtap

This figure shows the co-authorship network connecting the top 25 collaborators of Jayashree C. Jagtap. A scholar is included among the top collaborators of Jayashree C. Jagtap 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 Jayashree C. Jagtap. Jayashree C. Jagtap is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

Shelke, Ganesh Vilas, et al.. (2017). TNF-α and IFN-γ Together Up-Regulates Par-4 Expression and Induce Apoptosis in Human Neuroblastomas. Biomedicines. 6(1). 4–4. 12 indexed citations

Pujari, Radha, et al.. (2015). Oncostatin-M Differentially Regulates Mesenchymal and Proneural Signature Genes in Gliomas via STAT3 Signaling. Neoplasia. 17(2). 225–237. 47 indexed citations

Jagtap, Jayashree C., et al.. (2014). Expression and Regulation of Prostate Apoptosis Response-4 (Par-4) in Human Glioma Stem Cells in Drug-Induced Apoptosis. PLoS ONE. 9(2). e88505–e88505. 18 indexed citations

Jagtap, Jayashree C., et al.. (2014). Secretory prostate apoptosis response (Par)‐4 sensitizes multicellular spheroids (MCS) of glioblastoma multiforme cells to tamoxifen‐induced cell death. FEBS Open Bio. 5(1). 8–19. 16 indexed citations

Jagtap, Jayashree C., et al.. (2012). Sodium valproate potentiates staurosporine‐induced apoptosis in neuroblastoma cells via Akt/survivin independently of HDAC inhibition. Journal of Cellular Biochemistry. 114(4). 854–863. 19 indexed citations

Shiras, Anjali, et al.. (2007). Differential expression and role of p21cip/waf1 and p27kip1 in TNF-α-induced inhibition of proliferation in human glioma cells. Molecular Cancer. 6(1). 42–42. 18 indexed citations

Shiras, Anjali, et al.. (2007). Independent activation of Akt and NF‐kappaB pathways and their role in resistance to TNF‐α mediated cytotoxicity in gliomas. Molecular Carcinogenesis. 47(2). 126–136. 16 indexed citations

Prasad, V. S. S., et al.. (2006). ROS-triggered caspase 2 activation and feedback amplification loop in β-carotene-induced apoptosis. Free Radical Biology and Medicine. 41(3). 431–442. 49 indexed citations

Chandele, Anmol, et al.. (2004). Upregulation of Survivin in G2/M Cells and Inhibition of Caspase 9 Activity Enhances Resistance in Staurosporine-Induced Apoptosis. Neoplasia. 6(1). 29–40. 94 indexed citations

10.

Jagtap, Jayashree C., et al.. (2003). Sodium pyruvate protects against H2O2 mediated apoptosis in human neuroblastoma cell line-SK-N-MC. Journal of Chemical Neuroanatomy. 26(2). 109–118. 49 indexed citations

11.

Jagtap, Jayashree C., et al.. (2000). Lithium induces morphological and functional differentiation in neuro2a cells. Neuroscience Research Communications. 26(1). 9–16. 1 indexed citations

12.

Mohan, D., et al.. (1999). Differential responses of staurosporine on protein kinase C activity and proliferation in two murine neuroblastoma cell lines. Cancer Letters. 139(2). 137–143. 5 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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