Prathibha Ranganathan

5.3k total citations · 1 hit paper
18 papers, 1.2k citations indexed

About

Prathibha Ranganathan is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, Prathibha Ranganathan has authored 18 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 6 papers in Oncology and 6 papers in Cancer Research. Recurrent topics in Prathibha Ranganathan's work include Epigenetics and DNA Methylation (6 papers), Cancer Genomics and Diagnostics (4 papers) and Cancer-related gene regulation (4 papers). Prathibha Ranganathan is often cited by papers focused on Epigenetics and DNA Methylation (6 papers), Cancer Genomics and Diagnostics (4 papers) and Cancer-related gene regulation (4 papers). Prathibha Ranganathan collaborates with scholars based in India, United States and Czechia. Prathibha Ranganathan's co-authors include Anthony J. Capobianco, Kelly Weaver, Anjali A. Karande, Paturu Kondaiah, Akhilesh Pandey, Aravinda K. Chavalmane, Takashi Takahashi, Raghu Bhushan, Ravi Kiran Reddy Kalathur and Animesh Agrawal and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Nature reviews. Cancer.

In The Last Decade

Prathibha Ranganathan

17 papers receiving 1.2k citations

Hit Papers

align trajectories

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.

Notch signalling in solid tumours: a little bit of everything but not all the time

2011 632 citations Prathibha Ranganathan, Kelly Weaver et al. Nature reviews. Cancer profile →

Peers

Prathibha Ranganathan

ONCOL

PRM

IMMUN

Elizaveta V. Benevolenskaya United States

Hisanobu Oda Japan

Wojciech Michowski United States

Zarir E. Karanjawala United States

Katharine H. Wrighton United States

Lin Ye China

Jin‐Sook Jeong South Korea

Fangli Ren China

Catherine H. Wilson United Kingdom

Elizaveta V. Benevolenskaya United States

Prathibha Ranganathan

1.1k ×1.2

269 ×0.8

ONCOL

211 ×0.9

107 ×1.1

PRM

90 ×1.0

IMMUN

Citations per year, relative to Prathibha Ranganathan Prathibha Ranganathan (= 1×) peers Elizaveta V. Benevolenskaya

Countries citing papers authored by Prathibha Ranganathan

Since Specialization

Citations

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

Fields of papers citing papers by Prathibha Ranganathan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Prathibha Ranganathan

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

All Works

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18 of 18 papers shown

Keshavamurthy, R., et al.. (2024). Gene expression signature of castrate resistant prostate cancer. Gene. 925. 148603–148603.

Keshavamurthy, R., et al.. (2024). Comparative transcriptome of normal and cancer-associated fibroblasts. BMC Cancer. 24(1). 1231–1231. 2 indexed citations

Ranganathan, Prathibha, et al.. (2024). microRNA profile of endometrial cancer from Indian patients-identification of potential biomarkers for prognosis. Biochemistry and Biophysics Reports. 39. 101812–101812. 2 indexed citations

Karande, Anjali A., et al.. (2023). Emerging role of gut microbiota dysbiosis in neuroinflammation and neurodegeneration. Frontiers in Neurology. 14. 1149618–1149618. 96 indexed citations

Ranganathan, Prathibha, et al.. (2023). Epigenetic Therapy for Cancer Stem Cells. Resonance. 28(5). 697–717. 1 indexed citations

Ranganathan, Prathibha, et al.. (2019). Non-canonical Estrogen Signaling in Endocrine Resistance. Frontiers in Endocrinology. 10. 708–708. 25 indexed citations

Han, Xiaoqing, Prathibha Ranganathan, Christos Tzimas, et al.. (2017). Notch Represses Transcription by PRC2 Recruitment to the Ternary Complex. Molecular Cancer Research. 15(9). 1173–1183. 12 indexed citations

Weaver, Kelly, Marie‐Clotilde Alves‐Guerra, Ke Jin, et al.. (2014). NACK Is an Integral Component of the Notch Transcriptional Activation Complex and Is Critical for Development and Tumorigenesis. Cancer Research. 74(17). 4741–4751. 27 indexed citations

Naz, Sarwat, et al.. (2013). Protumorigenic actions of S100A2 involve regulation of PI3/Akt signaling and functional interaction with Smad3. Carcinogenesis. 35(1). 14–23. 36 indexed citations

10.

Azzam, Diana J., Dekuang Zhao, Andy J. Minn, et al.. (2013). Triple negative breast cancer initiating cell subsets differ in functional and molecular characteristics and in γ‐secretase inhibitor drug responses. EMBO Molecular Medicine. 5(10). 1502–1522. 54 indexed citations

11.

Naz, Sarwat, et al.. (2012). Regulation of S100A2 expression by TGF-β-induced MEK/ERK signalling and its role in cell migration/invasion. Biochemical Journal. 447(1). 81–91. 36 indexed citations

12.

Ranganathan, Prathibha, Kelly Weaver, & Anthony J. Capobianco. (2011). Notch signalling in solid tumours: a little bit of everything but not all the time. Nature reviews. Cancer. 11(5). 338–351. 632 indexed citations breakdown →

13.

Ranganathan, Prathibha, Rodrigo Vasquez‐Del Carpio, Fred M. Kaplan, et al.. (2011). Hierarchical Phosphorylation within the Ankyrin Repeat Domain Defines a Phosphoregulatory Loop That Regulates Notch Transcriptional Activity. Journal of Biological Chemistry. 286(33). 28844–28857. 32 indexed citations

14.

Kashyap, Manoj Kumar, Arivusudar Marimuthu, Harrys K.C. Jacob, et al.. (2009). Genomewide mRNA profiling of esophageal squamous cell carcinoma for identification of cancer biomarkers. Cancer Biology & Therapy. 8(1). 36–46. 94 indexed citations

15.

Ranganathan, Prathibha, Harsha Gowda, & Akhilesh Pandey. (2009). Molecular alterations in exocrine neoplasms of the pancreas.. Archives of Pathology & Laboratory Medicine. 133(3). 405–12. 9 indexed citations

16.

Ranganathan, Prathibha, Harsha Gowda, & Akhilesh Pandey. (2009). Molecular Alterations in Exocrine Neoplasms of the Pancreas. Archives of Pathology & Laboratory Medicine. 133(3). 405–412. 9 indexed citations

17.

Kandasamy, Kumaran, Shivakumar Keerthikumar, Renu Goel, et al.. (2008). Human Proteinpedia: a unified discovery resource for proteomics research. Nucleic Acids Research. 37(suppl_1). D773–D781. 65 indexed citations

18.

Ranganathan, Prathibha, Animesh Agrawal, Raghu Bhushan, et al.. (2007). Expression profiling of genes regulated by TGF-beta: Differential regulation in normal and tumour cells. BMC Genomics. 8(1). 98–98. 105 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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