Jayamanna Wickramasinghe

1.5k total citations
14 papers, 648 citations indexed

About

Jayamanna Wickramasinghe is a scholar working on Oncology, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Jayamanna Wickramasinghe has authored 14 papers receiving a total of 648 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Oncology, 6 papers in Molecular Biology and 4 papers in Pathology and Forensic Medicine. Recurrent topics in Jayamanna Wickramasinghe's work include Viral-associated cancers and disorders (4 papers), Lymphoma Diagnosis and Treatment (3 papers) and RNA modifications and cancer (2 papers). Jayamanna Wickramasinghe is often cited by papers focused on Viral-associated cancers and disorders (4 papers), Lymphoma Diagnosis and Treatment (3 papers) and RNA modifications and cancer (2 papers). Jayamanna Wickramasinghe collaborates with scholars based in United States, Tanzania and Canada. Jayamanna Wickramasinghe's co-authors include Andrew V. Kossenkov, José R. Conejo-García, Louise C. Showe, David W. Speicher, Michael J. Allegrezza, Alfredo Perales‐Puchalt, Kyle K. Payne, Melanie R. Rutkowski, Nikolaos Svoronos and Paul M. Lieberman and has published in prestigious journals such as Nature Communications, Cancer Research and Scientific Reports.

In The Last Decade

Jayamanna Wickramasinghe

14 papers receiving 641 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jayamanna Wickramasinghe United States 11 391 212 148 77 76 14 648
Krista M. Goergen United States 17 206 0.5× 132 0.6× 224 1.5× 184 2.4× 86 1.1× 31 630
R Martucci Italy 10 149 0.4× 224 1.1× 263 1.8× 91 1.2× 67 0.9× 12 678
Karen Brajão de Oliveira Brazil 16 233 0.6× 296 1.4× 310 2.1× 150 1.9× 117 1.5× 63 740
Kohei Tada Japan 15 220 0.6× 242 1.1× 158 1.1× 66 0.9× 47 0.6× 33 594
Kotaro Miyake Japan 14 342 0.9× 328 1.5× 205 1.4× 125 1.6× 132 1.7× 59 864
Xiaolan Fu China 17 361 0.9× 200 0.9× 434 2.9× 156 2.0× 219 2.9× 43 947
Julie Lorent Sweden 13 240 0.6× 443 2.1× 183 1.2× 89 1.2× 99 1.3× 15 973
Angela Grassi Italy 13 400 1.0× 107 0.5× 74 0.5× 86 1.1× 293 3.9× 27 707
Toshiyuki Morisawa Japan 7 216 0.6× 147 0.7× 232 1.6× 94 1.2× 96 1.3× 18 641
Bo Young Ahn South Korea 14 257 0.7× 166 0.8× 78 0.5× 137 1.8× 129 1.7× 23 662

Countries citing papers authored by Jayamanna Wickramasinghe

Since Specialization
Citations

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

Fields of papers citing papers by Jayamanna Wickramasinghe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jayamanna Wickramasinghe

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

All Works

14 of 14 papers shown
1.
Ye, Ying, Daniel E. Schäffer, Hao Xue, et al.. (2023). A deep learning approach reveals unexplored landscape of viral expression in cancer. Nature Communications. 14(1). 785–785. 15 indexed citations
2.
Gulve, Nitish, Chenhe Su, Zhong Deng, et al.. (2022). DAXX-ATRX regulation of p53 chromatin binding and DNA damage response. Nature Communications. 13(1). 5033–5033. 27 indexed citations
3.
Lamontagne, Jason, Samantha S. Soldan, Chenhe Su, et al.. (2021). A multi-omics approach to Epstein-Barr virus immortalization of B-cells reveals EBNA1 chromatin pioneering activities targeting nucleotide metabolism. PLoS Pathogens. 17(1). e1009208–e1009208. 28 indexed citations
4.
Lang, Fengchao, Xin Li, Olga Vladimirova, et al.. (2021). Author Correction: CTCF interacts with the lytic HSV-1 genome to promote viral transcription. Scientific Reports. 11(1). 5039–5039. 1 indexed citations
5.
Lidenge, Salum J., Andrew V. Kossenkov, For Yue Tso, et al.. (2020). Comparative transcriptome analysis of endemic and epidemic Kaposi’s sarcoma (KS) lesions and the secondary role of HIV-1 in KS pathogenesis. PLoS Pathogens. 16(7). e1008681–e1008681. 17 indexed citations
6.
Tso, For Yue, Andrew V. Kossenkov, Salum J. Lidenge, et al.. (2018). RNA-Seq of Kaposi’s sarcoma reveals alterations in glucose and lipid metabolism. PLoS Pathogens. 14(1). e1006844–e1006844. 45 indexed citations
7.
Perales‐Puchalt, Alfredo, Kyle K. Payne, Nikolaos Svoronos, et al.. (2018). Frontline Science: Microbiota reconstitution restores intestinal integrity after cisplatin therapy. Journal of Leukocyte Biology. 103(5). 799–805. 70 indexed citations
8.
Sakurai, Masayuki, Yusuke Shiromoto, Andrew V. Kossenkov, et al.. (2017). ADAR1 controls apoptosis of stressed cells by inhibiting Staufen1-mediated mRNA decay. Nature Structural & Molecular Biology. 24(6). 534–543. 121 indexed citations
9.
Lang, Fengchao, Xin Li, Olga Vladimirova, et al.. (2017). CTCF interacts with the lytic HSV-1 genome to promote viral transcription. Scientific Reports. 7(1). 36 indexed citations
10.
Yokoyama, Yuhki, Hengrui Zhu, Jeong Heon Lee, et al.. (2016). BET Inhibitors Suppress ALDH Activity by Targeting ALDH1A1 Super-Enhancer in Ovarian Cancer. Cancer Research. 76(21). 6320–6330. 116 indexed citations
11.
Perales‐Puchalt, Alfredo, Nikolaos Svoronos, Melanie R. Rutkowski, et al.. (2016). Follicle-Stimulating Hormone Receptor Is Expressed by Most Ovarian Cancer Subtypes and Is a Safe and Effective Immunotherapeutic Target. Clinical Cancer Research. 23(2). 441–453. 82 indexed citations
12.
Tesone, Amelia J., Melanie R. Rutkowski, Eva Brencicova, et al.. (2016). Satb1 Overexpression Drives Tumor-Promoting Activities in Cancer-Associated Dendritic Cells. Cell Reports. 14(7). 1774–1786. 86 indexed citations
13.
Wickramasinghe, Jayamanna, Bernard A. Goodman, & R. A. Serota. (2008). Quantum jumps of saturation level rigidity and anomalous oscillations of level number variance in the semiclassical spectrum of a modified Kepler problem. Physical Review E. 77(5). 56216–56216. 2 indexed citations
14.
Wickramasinghe, Jayamanna, Bernard A. Goodman, & R. A. Serota. (2005). Persistence of strong correlations in the energy spectrum of a separable Hamiltonian system: The rectangular box. Physical Review E. 72(5). 56209–56209. 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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