Manikandan Periyasamy

1.8k total citations
19 papers, 1.2k citations indexed

About

Manikandan Periyasamy is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Manikandan Periyasamy has authored 19 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 5 papers in Oncology and 5 papers in Genetics. Recurrent topics in Manikandan Periyasamy's work include Estrogen and related hormone effects (5 papers), Genomics and Chromatin Dynamics (4 papers) and Cancer-related Molecular Pathways (3 papers). Manikandan Periyasamy is often cited by papers focused on Estrogen and related hormone effects (5 papers), Genomics and Chromatin Dynamics (4 papers) and Cancer-related Molecular Pathways (3 papers). Manikandan Periyasamy collaborates with scholars based in United Kingdom, United States and Hungary. Manikandan Periyasamy's co-authors include Simak Ali, R. Charles Coombes, Laki Buluwela, Hetal Patel, Frances V. Fuller-Pace, Alison Harrod, Leandro Castellano, Van T.M. Nguyen, Luca Magnani and Eric O. Aboagye and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Communications.

In The Last Decade

Manikandan Periyasamy

19 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Manikandan Periyasamy United Kingdom 16 767 463 344 206 191 19 1.2k
Yari Ciribilli Italy 23 983 1.3× 521 1.1× 319 0.9× 123 0.6× 131 0.7× 54 1.3k
Dhivya R. Sudhan United States 13 639 0.8× 505 1.1× 416 1.2× 341 1.7× 147 0.8× 28 1.2k
Heather E. Cunliffe United States 19 599 0.8× 497 1.1× 367 1.1× 179 0.9× 323 1.7× 28 1.2k
Jerry Usary United States 16 894 1.2× 855 1.8× 531 1.5× 365 1.8× 222 1.2× 19 1.6k
Tracey Rowlands United States 10 1.0k 1.3× 595 1.3× 203 0.6× 115 0.6× 221 1.2× 14 1.4k
Yiqun Zhang United States 17 784 1.0× 387 0.8× 547 1.6× 205 1.0× 206 1.1× 25 1.3k
Paul M. Moseley United Kingdom 22 796 1.0× 616 1.3× 314 0.9× 116 0.6× 111 0.6× 45 1.1k
Mary Ellen Urick United States 16 672 0.9× 227 0.5× 352 1.0× 182 0.9× 166 0.9× 22 1.3k
Yari Ciani Italy 18 933 1.2× 394 0.9× 482 1.4× 213 1.0× 56 0.3× 27 1.4k
Xiaodong Liao China 12 902 1.2× 442 1.0× 303 0.9× 94 0.5× 174 0.9× 22 1.2k

Countries citing papers authored by Manikandan Periyasamy

Since Specialization
Citations

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

Fields of papers citing papers by Manikandan Periyasamy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manikandan Periyasamy

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

All Works

19 of 19 papers shown
1.
Periyasamy, Manikandan, et al.. (2025). Applications of bamboo fiber and bamboo stem ash with styrene butadiene rubber in cement mortar for sustainable structural application. Scientific Reports. 15(1). 29227–29227. 1 indexed citations
2.
Periyasamy, Manikandan, et al.. (2024). Enhancing the strength properties of concrete using coconut fiber and coconut fiber ash. AIP conference proceedings. 3037. 20053–20053. 3 indexed citations
3.
Baker, Simon C., Andrew S. Mason, Andrew Macdonald, et al.. (2022). Induction of APOBEC3-mediated genomic damage in urothelium implicates BK polyomavirus (BKPyV) as a hit-and-run driver for bladder cancer. Oncogene. 41(15). 2139–2151. 26 indexed citations
4.
Periyasamy, Manikandan, Anup K. Singh, Carolina Gemma, et al.. (2020). Induction of APOBEC3B expression by chemotherapy drugs is mediated by DNA-PK-directed activation of NF-κB. Oncogene. 40(6). 1077–1090. 16 indexed citations
5.
Patel, Hetal, Manikandan Periyasamy, Georgina P. Sava, et al.. (2018). ICEC0942, an Orally Bioavailable Selective Inhibitor of CDK7 for Cancer Treatment. Molecular Cancer Therapeutics. 17(6). 1156–1166. 111 indexed citations
6.
Periyasamy, Manikandan, Anup K. Singh, Carolina Gemma, et al.. (2017). p53 controls expression of the DNA deaminase APOBEC3B to limit its potential mutagenic activity in cancer cells. Nucleic Acids Research. 45(19). 11056–11069. 60 indexed citations
7.
Harrod, Alison, J Fulton, Van T.M. Nguyen, et al.. (2016). Genomic modelling of the ESR1 Y537S mutation for evaluating function and new therapeutic approaches for metastatic breast cancer. Oncogene. 36(16). 2286–2296. 131 indexed citations
8.
Mollet, Inês G., Dilipkumar Patel, Fatima S Govani, et al.. (2016). Low Dose Iron Treatments Induce a DNA Damage Response in Human Endothelial Cells within Minutes. PLoS ONE. 11(2). e0147990–e0147990. 38 indexed citations
9.
Nguyen, Van T.M., Iros Barozzi, Monica Faronato, et al.. (2015). Differential epigenetic reprogramming in response to specific endocrine therapies promotes cholesterol biosynthesis and cellular invasion. Nature Communications. 6(1). 10044–10044. 95 indexed citations
10.
Periyasamy, Manikandan, Hetal Patel, Chun‐Fui Lai, et al.. (2015). APOBEC3B-Mediated Cytidine Deamination Is Required for Estrogen Receptor Action in Breast Cancer. Cell Reports. 13(1). 108–121. 87 indexed citations
11.
Lai, Chun‐Fui, Hetal Patel, Manikandan Periyasamy, et al.. (2015). LRH-1 drives colon cancer cell growth by repressing the expression of theCDKN1Agene in a p53-dependent manner. Nucleic Acids Research. 44(2). 582–594. 49 indexed citations
12.
Stebbing, Justin, Yang Xu, Andrew R. Green, et al.. (2014). KSR1 regulates BRCA1 degradation and inhibits breast cancer growth. Oncogene. 34(16). 2103–2114. 14 indexed citations
13.
Pellegrino, Loredana, Justin Stebbing, Vania Braga, et al.. (2013). miR-23b regulates cytoskeletal remodeling, motility and metastasis by directly targeting multiple transcripts. Nucleic Acids Research. 41(10). 5400–5412. 96 indexed citations
14.
Lombardo, Ylenia, Aleksandra Filipović, Gemma Molyneux, et al.. (2012). Nicastrin regulates breast cancer stem cell properties and tumor growth in vitro and in vivo. Proceedings of the National Academy of Sciences. 109(41). 16558–16563. 69 indexed citations
15.
Tolhurst, Robert S., Ross S. Thomas, Hetal Patel, et al.. (2010). Transient over-expression of estrogen receptor-α in breast cancer cells promotes cell survival and estrogen-independent growth. Breast Cancer Research and Treatment. 128(2). 357–368. 21 indexed citations
16.
Thiruchelvam, Paul, Chun‐Fui Lai, Hui Hua, et al.. (2010). The liver receptor homolog-1 regulates estrogen receptor expression in breast cancer cells. Breast Cancer Research and Treatment. 127(2). 385–396. 61 indexed citations
17.
Ali, Simak, Dean A. Heathcote, Sebastian H. B. Kroll, et al.. (2009). The Development of a Selective Cyclin-Dependent Kinase Inhibitor That Shows Antitumor Activity. Cancer Research. 69(15). 6208–6215. 129 indexed citations
18.
Nicol, Samantha M., Manikandan Periyasamy, Jie Jiang, et al.. (2009). The DEAD-box protein p72 regulates ERα-/oestrogen-dependent transcription and cell growth, and is associated with improved survival in ERα-positive breast cancer. Oncogene. 28(46). 4053–4064. 95 indexed citations
19.
López‐García, Jorge, Manikandan Periyasamy, Ross S. Thomas, et al.. (2006). ZNF366 is an estrogen receptor corepressor that acts through CtBP and histone deacetylases. Nucleic Acids Research. 34(21). 6126–6136. 70 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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