Indrika Ratnayaka

1.7k total citations
23 papers, 1.0k citations indexed

About

Indrika Ratnayaka is a scholar working on Molecular Biology, Oncology and Cell Biology. According to data from OpenAlex, Indrika Ratnayaka has authored 23 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Oncology and 6 papers in Cell Biology. Recurrent topics in Indrika Ratnayaka's work include Cancer-related Molecular Pathways (7 papers), Cancer Research and Treatments (4 papers) and Congenital heart defects research (4 papers). Indrika Ratnayaka is often cited by papers focused on Cancer-related Molecular Pathways (7 papers), Cancer Research and Treatments (4 papers) and Congenital heart defects research (4 papers). Indrika Ratnayaka collaborates with scholars based in United Kingdom, United States and Germany. Indrika Ratnayaka's co-authors include Robert Goldin, Xin Lü, S. N. Wickramasinghe, Shan Zhong, I.N. Brown, Virginie Vives, Ingrid Hoffmann, Corinna Koebnick, Claus Leitzmann and Pieter C. Dagnelie and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Indrika Ratnayaka

23 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Indrika Ratnayaka United Kingdom 18 537 224 204 179 125 23 1.0k
Leah M. Helvering United States 14 599 1.1× 269 1.2× 112 0.5× 88 0.5× 114 0.9× 17 999
Yasuhisa Oida Japan 20 432 0.8× 396 1.8× 205 1.0× 159 0.9× 36 0.3× 58 1.1k
Viktor Stránecký Czechia 18 642 1.2× 226 1.0× 177 0.9× 82 0.5× 54 0.4× 66 1.3k
Meir Krupsky Israel 17 832 1.5× 199 0.9× 90 0.4× 255 1.4× 42 0.3× 32 1.2k
Hezhi Fang China 22 996 1.9× 99 0.4× 74 0.4× 303 1.7× 73 0.6× 64 1.3k
Pasquale Piccolo Italy 17 372 0.7× 141 0.6× 92 0.5× 68 0.4× 54 0.4× 39 1.1k
Ulrich Sauer Germany 17 560 1.0× 119 0.5× 106 0.5× 166 0.9× 37 0.3× 22 1.1k
Rocío Letón Spain 20 457 0.9× 262 1.2× 121 0.6× 403 2.3× 111 0.9× 25 1.3k
Shenaz Khan United States 16 536 1.0× 87 0.4× 94 0.5× 112 0.6× 32 0.3× 21 989

Countries citing papers authored by Indrika Ratnayaka

Since Specialization
Citations

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

Fields of papers citing papers by Indrika Ratnayaka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Indrika Ratnayaka

This figure shows the co-authorship network connecting the top 25 collaborators of Indrika Ratnayaka. A scholar is included among the top collaborators of Indrika Ratnayaka 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 Indrika Ratnayaka. Indrika Ratnayaka 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.
Sugimoto, Yoichiro, Xiaotong Cheng, Joanna D.C.C. Lima, et al.. (2024). Hif-2α programs oxygen chemosensitivity in chromaffin cells. Journal of Clinical Investigation. 134(18). 6 indexed citations
2.
Neal, Alice, Svanhild Nornes, Marsha D. Wallace, et al.. (2019). Venous identity requires BMP signalling through ALK3. Nature Communications. 10(1). 453–453. 58 indexed citations
3.
Gunadasa-Rohling, Mala, Alice Neal, Andia N. Redpath, et al.. (2019). Regulatory pathways governing murine coronary vessel formation are dysregulated in the injured adult heart. Nature Communications. 10(1). 3276–3276. 17 indexed citations
4.
Hodson, Emma J., Xiaotong Cheng, David Ferguson, et al.. (2018). PHD2 inactivation in Type I cells drives HIF‐2α‐dependent multilineage hyperplasia and the formation of paraganglioma‐like carotid bodies. Apollo (University of Cambridge). 33 indexed citations
5.
Becker, Philipp, Natalia Sacilotto, Svanhild Nornes, et al.. (2016). An Intronic Flk1 Enhancer Directs Arterial-Specific Expression via RBPJ-Mediated Venous Repression. Arteriosclerosis Thrombosis and Vascular Biology. 36(6). 1209–1219. 22 indexed citations
6.
Verrill, Clare, Lucia Cerundolo, Chad M. McKee, et al.. (2015). Altered expression of epithelial-to-mesenchymal transition proteins in extraprostatic prostate cancer. Oncotarget. 7(2). 1107–1119. 3 indexed citations
7.
Royer, Christophe, Xiao Qin, Jaroslav Žák, et al.. (2014). ASPP2 Links the Apical Lateral Polarity Complex to the Regulation of YAP Activity in Epithelial Cells. PLoS ONE. 9(10). e111384–e111384. 27 indexed citations
8.
Morris, Emma V., Lucia Cerundolo, Min Lü, et al.. (2014). Nuclear iASPP may facilitate prostate cancer progression. Cell Death and Disease. 5(10). e1492–e1492. 28 indexed citations
9.
Tordella, Luca, Victoria Salter, Anna Pagotto, et al.. (2013). ASPP2 suppresses squamous cell carcinoma via RelA/p65–mediated repression of p63. Proceedings of the National Academy of Sciences. 110(44). 17969–17974. 38 indexed citations
10.
Wang, Yihua, Eleonora Lapi, Alexandra Sullivan, et al.. (2012). Autophagic activity dictates the cellular response to oncogenic RAS. Proceedings of the National Academy of Sciences. 109(33). 13325–13330. 89 indexed citations
11.
Royer, Christophe, Virginie Vives, Luca Tordella, et al.. (2010). ASPP2 Binds Par-3 and Controls the Polarity and Proliferation of Neural Progenitors during CNS Development. Developmental Cell. 19(1). 126–137. 93 indexed citations
12.
Lapi, Eleonora, Alice Sullivan, Indrika Ratnayaka, et al.. (2010). SUMO-modified nuclear cyclin D1 bypasses Ras-induced senescence. Cell Death and Differentiation. 18(2). 304–314. 30 indexed citations
13.
Slee, Elizabeth A., Barbara Benassi, Robert Goldin, et al.. (2010). Phosphorylation of Ser312 contributes to tumor suppression by p53 in vivo. Proceedings of the National Academy of Sciences. 107(45). 19479–19484. 18 indexed citations
14.
Vives, Virginie, Shan Zhong, Indrika Ratnayaka, et al.. (2006). ASPP2 is a haploinsufficient tumor suppressor that cooperates with p53 to suppress tumor growth. Genes & Development. 20(10). 1262–1267. 80 indexed citations
15.
Koebnick, Corinna, Sindy Gruendel, Ingrid Hoffmann, et al.. (2004). Long-Term Ovo-Lacto Vegetarian Diet Impairs Vitamin B-12 Status in Pregnant Women. Journal of Nutrition. 134(12). 3319–3326. 82 indexed citations
16.
Koebnick, Corinna, Pieter C. Dagnelie, Sunitha N. Wickramasinghe, et al.. (2002). Longitudinal Concentrations of Vitamin B12 and Vitamin B12-binding Proteins during Uncomplicated Pregnancy. Clinical Chemistry. 48(6). 928–933. 82 indexed citations
17.
Goldin, Robert, et al.. (1996). ROLE OF MACROPHAGES IN ACETAMINOPHEN (PARACETAMOL)-INDUCED HEPATOTOXICITY. The Journal of Pathology. 179(4). 432–435. 83 indexed citations
18.
Wickramasinghe, S. N. & Indrika Ratnayaka. (1996). Limited value of serum holo-transcobalamin II measurements in the differential diagnosis of macrocytosis.. Journal of Clinical Pathology. 49(9). 755–758. 22 indexed citations
19.
Goldin, Robert, et al.. (1995). Acetaminophen and macrophage activation. International Hepatology Communications. 4(1). 16–18. 5 indexed citations
20.
Goldin, Robert, Indrika Ratnayaka, I.N. Brown, & S. N. Wickramasinghe. (1995). The effect of Kupffer cell elimination on ethanol-induced liver damage in mice.. PubMed. 76(5). 353–9. 13 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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