Ram S. Mani

5.0k total citations · 1 hit paper
24 papers, 2.4k citations indexed

About

Ram S. Mani is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Cancer Research. According to data from OpenAlex, Ram S. Mani has authored 24 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 8 papers in Pulmonary and Respiratory Medicine and 6 papers in Cancer Research. Recurrent topics in Ram S. Mani's work include Prostate Cancer Treatment and Research (8 papers), Epigenetics and DNA Methylation (7 papers) and DNA Repair Mechanisms (3 papers). Ram S. Mani is often cited by papers focused on Prostate Cancer Treatment and Research (8 papers), Epigenetics and DNA Methylation (7 papers) and DNA Repair Mechanisms (3 papers). Ram S. Mani collaborates with scholars based in United States, India and United Kingdom. Ram S. Mani's co-authors include Sooryanarayana Varambally, Arul M. Chinnaiyan, Nallasivam Palanisamy, Qi Cao, Xuhong Cao, Scott A. Tomlins, Arul M. Chinnaiyan, Jung H. Kim, Jindan Yu and Bharathi Laxman and has published in prestigious journals such as Science, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Ram S. Mani

24 papers receiving 2.4k citations

Hit Papers

Genomic Loss of microRNA-101 Leads to Overexpression of H... 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
Ram S. Mani United States 15 1.9k 951 494 358 189 24 2.4k
Jonathan C. Zhao United States 23 1.9k 1.0× 1.1k 1.1× 807 1.6× 403 1.1× 185 1.0× 34 2.5k
Eijiro Nakamura Japan 21 1.4k 0.7× 1.3k 1.4× 524 1.1× 441 1.2× 193 1.0× 36 2.3k
Meena Augustus United States 16 1.4k 0.7× 619 0.7× 451 0.9× 236 0.7× 221 1.2× 35 1.9k
Puay Leng Lee Singapore 17 1.6k 0.9× 525 0.6× 172 0.3× 512 1.4× 248 1.3× 18 2.1k
Peter Horak Germany 20 1.2k 0.7× 590 0.6× 242 0.5× 457 1.3× 235 1.2× 68 1.9k
Jin Eun Choi South Korea 28 1.5k 0.8× 593 0.6× 569 1.2× 683 1.9× 159 0.8× 96 2.2k
Sophie Gad France 20 1.0k 0.5× 619 0.7× 394 0.8× 362 1.0× 119 0.6× 38 1.7k
Julie A. Hong United States 25 1.9k 1.0× 419 0.4× 260 0.5× 556 1.6× 522 2.8× 50 2.4k
Dongwang Yan China 27 1.8k 0.9× 1.3k 1.3× 205 0.4× 458 1.3× 176 0.9× 48 2.3k
Nilgun Tasdemir United States 15 1.1k 0.6× 349 0.4× 176 0.4× 429 1.2× 183 1.0× 26 1.6k

Countries citing papers authored by Ram S. Mani

Since Specialization
Citations

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

Fields of papers citing papers by Ram S. Mani

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ram S. Mani. 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 Ram S. Mani. The network helps show where Ram S. Mani may publish in the future.

Co-authorship network of co-authors of Ram S. Mani

This figure shows the co-authorship network connecting the top 25 collaborators of Ram S. Mani. A scholar is included among the top collaborators of Ram S. Mani 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 Ram S. Mani. Ram S. Mani 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.
Sahoo, Subhransu S., Susmita G. Ramanand, Ileana Cuevas, et al.. (2025). A distinct mechanism of epigenetic reprogramming silences PAX2 and initiates endometrial carcinogenesis. Journal of Clinical Investigation. 135(16). 2 indexed citations
2.
Gao, Yunpeng, et al.. (2024). ChIPr: accurate prediction of cohesin-mediated 3D genome organization from 2D chromatin features. Genome biology. 25(1). 15–15. 5 indexed citations
3.
Khan, Shahanshah, Youn-Tae Kwak, Lan Peng, et al.. (2023). NLRP12 downregulates the Wnt/β-catenin pathway via interaction with STK38 to suppress colorectal cancer. Journal of Clinical Investigation. 133(19). 19 indexed citations
4.
Neeb, Antje, Lorenzo Buroni, Denisa Bogdan, et al.. (2023). Critical role of antioxidant programs in enzalutamide-resistant prostate cancer. Oncogene. 42(30). 2347–2359. 7 indexed citations
5.
Udden, S. M. Nashir, GuemHee Baek, Kamal Pandey, et al.. (2023). Towards precision radiation oncology: endocrine therapy response as a biomarker for personalization of breast radiotherapy. npj Precision Oncology. 7(1). 11–11. 1 indexed citations
6.
Yuan, Jiapei, Kathleen E. Houlahan, Susmita G. Ramanand, et al.. (2022). Prostate Cancer Transcriptomic Regulation by the Interplay of Germline Risk Alleles, Somatic Mutations, and 3D Genomic Architecture. Cancer Discovery. 12(12). 2838–2855. 4 indexed citations
7.
Baek, GuemHee, Suzanne Carreira, Wei Yuan, et al.. (2022). Targeting radioresistance and replication fork stability in prostate cancer. JCI Insight. 7(9). 7 indexed citations
8.
Sahoo, Subhransu S., Susmita G. Ramanand, Yunpeng Gao, et al.. (2022). FOXA2 suppresses endometrial carcinogenesis and epithelial-mesenchymal transition by regulating enhancer activity. Journal of Clinical Investigation. 132(12). 15 indexed citations
9.
Bono, Johann S. de, Christina Guo, Bora Gürel, et al.. (2020). Prostate carcinogenesis: inflammatory storms. Nature reviews. Cancer. 20(8). 455–469. 137 indexed citations
10.
Ramanand, Susmita G. & Ram S. Mani. (2019). Genetic, Environmental, and Nuclear Factors Governing Genomic Rearrangements. Advances in experimental medicine and biology. 1210. 57–66. 5 indexed citations
11.
Puliyappadamba, Vineshkumar Thidil, et al.. (2018). RDNA-12. ATR INHIBITOR VE-822 IS A NOVEL RADIO- SENSITIZER FOR GLIOMA. Neuro-Oncology. 20(suppl_6). vi224–vi224. 1 indexed citations
12.
Mani, Ram S., M. Asif Amin, Xiangyi Li, et al.. (2016). Inflammation-Induced Oxidative Stress Mediates Gene Fusion Formation in Prostate Cancer. Cell Reports. 17(10). 2620–2631. 61 indexed citations
13.
Banerjee, Rajat, Nickole Russo, Min Liu, et al.. (2014). TRIP13 promotes error-prone nonhomologous end joining and induces chemoresistance in head and neck cancer. Nature Communications. 5(1). 4527–4527. 119 indexed citations
14.
Mani, Ram S.. (2014). The emerging role of speckle-type POZ protein (SPOP) in cancer development. Drug Discovery Today. 19(9). 1498–1502. 67 indexed citations
15.
Mani, Ram S., Matthew K. Iyer, Qi Cao, et al.. (2011). TMPRSS2–ERG-Mediated Feed-Forward Regulation of Wild-Type ERG in Human Prostate Cancers. Cancer Research. 71(16). 5387–5392. 35 indexed citations
16.
Banerjee, Rajat, Ram S. Mani, Nickole Russo, et al.. (2011). The tumor suppressor gene rap1GAP is silenced by miR-101-mediated EZH2 overexpression in invasive squamous cell carcinoma. Oncogene. 30(42). 4339–4349. 90 indexed citations
17.
Mani, Ram S. & Arul M. Chinnaiyan. (2010). Triggers for genomic rearrangements: insights into genomic, cellular and environmental influences. Nature Reviews Genetics. 11(12). 819–829. 103 indexed citations
18.
Varambally, Sooryanarayana, Qi Cao, Ram S. Mani, et al.. (2008). Genomic Loss of microRNA-101 Leads to Overexpression of Histone Methyltransferase EZH2 in Cancer. Science. 322(5908). 1695–1699. 833 indexed citations breakdown →
19.
Cao, Qi, Jiali Yu, Saravana M. Dhanasekaran, et al.. (2008). Repression of E-cadherin by the polycomb group protein EZH2 in cancer. Oncogene. 27(58). 7274–7284. 452 indexed citations
20.
Mani, Ram S., C. R. Srikumari Srisailapathy, Vikas Malhotra, et al.. (2008). Functional consequences of novel connexin 26 mutations associated with hereditary hearing loss. European Journal of Human Genetics. 17(4). 502–509. 63 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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