Wayne A. Phillips

10.7k total citations · 1 hit paper
169 papers, 7.2k citations indexed

About

Wayne A. Phillips is a scholar working on Molecular Biology, Oncology and Surgery. According to data from OpenAlex, Wayne A. Phillips has authored 169 papers receiving a total of 7.2k indexed citations (citations by other indexed papers that have themselves been cited), including 90 papers in Molecular Biology, 55 papers in Oncology and 42 papers in Surgery. Recurrent topics in Wayne A. Phillips's work include PI3K/AKT/mTOR signaling in cancer (27 papers), Esophageal Cancer Research and Treatment (22 papers) and Cancer-related gene regulation (14 papers). Wayne A. Phillips is often cited by papers focused on PI3K/AKT/mTOR signaling in cancer (27 papers), Esophageal Cancer Research and Treatment (22 papers) and Cancer-related gene regulation (14 papers). Wayne A. Phillips collaborates with scholars based in Australia, United States and Netherlands. Wayne A. Phillips's co-authors include Ian Campbell, Richard B. Pearson, Karen G. Montgomery, David Y.H. Choong, Robert J. S. Thomas, Briony E. Cristiano, John A. Hamilton, Sarah E. Russell, Richard B. Johnston and Elizabeth Vincan and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Wayne A. Phillips

168 papers receiving 7.0k citations

Hit Papers

Mutation of the PIK3CA ... 2004 2026 2011 2018 2004 200 400 600

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Wayne A. Phillips 4.1k 2.3k 1.3k 1.2k 1.1k 169 7.2k
Takeshi Uchiumi 5.6k 1.4× 3.2k 1.4× 1.1k 0.9× 924 0.7× 774 0.7× 201 9.1k
Mitsuhiko Osaki 4.1k 1.0× 1.3k 0.5× 1.8k 1.4× 727 0.6× 955 0.9× 158 6.8k
Qimin Zhan 6.8k 1.7× 2.8k 1.2× 2.7k 2.1× 1.1k 0.9× 754 0.7× 249 9.6k
John M. Mariadason 5.3k 1.3× 2.8k 1.2× 1.4k 1.1× 830 0.7× 599 0.6× 139 8.3k
Mayumi Ono 7.4k 1.8× 4.0k 1.7× 2.2k 1.7× 1.9k 1.5× 730 0.7× 214 12.1k
Vivian Wai Yan Lui 3.5k 0.9× 2.5k 1.1× 1.7k 1.4× 1.1k 0.9× 568 0.5× 112 6.9k
Peter Söderkvist 2.7k 0.7× 1.0k 0.4× 1.4k 1.1× 530 0.4× 1.1k 1.0× 174 6.0k
Mary E. Gerritsen 4.1k 1.0× 1.2k 0.5× 1.6k 1.3× 566 0.5× 750 0.7× 122 8.5k
Peter C. Lucas 4.2k 1.0× 1.8k 0.8× 2.4k 1.9× 833 0.7× 1.2k 1.1× 163 8.4k
Linda S. Steelman 7.5k 1.9× 3.3k 1.4× 1.9k 1.5× 1.1k 0.8× 428 0.4× 112 11.2k

Countries citing papers authored by Wayne A. Phillips

Since Specialization
Citations

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

Fields of papers citing papers by Wayne A. Phillips

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wayne A. Phillips. 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 Wayne A. Phillips. The network helps show where Wayne A. Phillips may publish in the future.

Co-authorship network of co-authors of Wayne A. Phillips

This figure shows the co-authorship network connecting the top 25 collaborators of Wayne A. Phillips. A scholar is included among the top collaborators of Wayne A. Phillips 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 Wayne A. Phillips. Wayne A. Phillips 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
2.
Fisher, Matthew, Mateus Crespo, Bora Gürel, et al.. (2024). Targeting a STING agonist to perivascular macrophages in prostate tumors delays resistance to androgen deprivation therapy. Journal for ImmunoTherapy of Cancer. 12(7). e009368–e009368. 7 indexed citations
3.
Bai, Yuchen, Carolin Götz, Zixuan Zhao, et al.. (2023). YBX1 integration of oncogenic PI3K/mTOR signalling regulates the fitness of malignant epithelial cells. Nature Communications. 14(1). 1591–1591. 19 indexed citations
4.
Molendijk, Jeffrey, Cathryn M. Kolka, Sandra Brosda, et al.. (2022). Elevation of fatty acid desaturase 2 in esophageal adenocarcinoma increases polyunsaturated lipids and may exacerbate bile acid‐induced DNA damage. Clinical and Translational Medicine. 12(5). e810–e810. 14 indexed citations
5.
Fujihara, Kenji M., Carlos S. Cabalag, Hyun Soo Ko, et al.. (2021). SLC7A11 Is a Superior Determinant of APR-246 (Eprenetapopt) Response than TP53 Mutation Status. Molecular Cancer Therapeutics. 20(10). 1858–1867. 28 indexed citations
6.
Janmaat, Vincent T., Manon C.W. Spaander, Auke P. Verhaar, et al.. (2021). HOXA13 in etiology and oncogenic potential of Barrett’s esophagus. Nature Communications. 12(1). 3354–3354. 6 indexed citations
7.
Yip, Hon Yan Kelvin, Annabel Chee, Ching‐Seng Ang, et al.. (2020). Control of Glucocorticoid Receptor Levels by PTEN Establishes a Failsafe Mechanism for Tumor Suppression. Molecular Cell. 80(2). 279–295.e8. 17 indexed citations
8.
Mitchell, Camilla B. & Wayne A. Phillips. (2019). Mouse Models for Exploring the Biological Consequences and Clinical Significance of PIK3CA Mutations. Biomolecules. 9(4). 158–158. 14 indexed citations
9.
Shah, Alok K., Günter Härtel, Ian Brown, et al.. (2018). Evaluation of Serum Glycoprotein Biomarker Candidates for Detection of Esophageal Adenocarcinoma and Surveillance of Barrett's Esophagus. Molecular & Cellular Proteomics. 17(12). 2324–2334. 24 indexed citations
10.
Pearson, Helen, Jason Li, Valérie S. Méniel, et al.. (2018). Identification of Pik3ca Mutation as a Genetic Driver of Prostate Cancer That Cooperates with Pten Loss to Accelerate Progression and Castration-Resistant Growth. Cancer Discovery. 8(6). 764–779. 78 indexed citations
11.
Teo, Zhi L., Sathana Dushyanthen, Franco Caramia, et al.. (2017). Combined CDK4/6 and PI3Kα Inhibition Is Synergistic and Immunogenic in Triple-Negative Breast Cancer. Cancer Research. 77(22). 6340–6352. 148 indexed citations
12.
Liu, David S., Cuong Duong, Sue Haupt, et al.. (2017). Inhibiting the system xC−/glutathione axis selectively targets cancers with mutant-p53 accumulation. Nature Communications. 8(1). 14844–14844. 260 indexed citations
13.
To, Henry, Nicholas J. Clemons, Cuong Duong, Alison H. Trainer, & Wayne A. Phillips. (2016). The Genetics of Barrett’s Esophagus: A Familial and Population-Based Perspective. Digestive Diseases and Sciences. 61(7). 1826–1834. 7 indexed citations
14.
Deuker, Marian M., et al.. (2014). PI3′-Kinase Inhibition Forestalls the Onset of MEK1/2 Inhibitor Resistance in BRAF -Mutated Melanoma. Cancer Discovery. 5(2). 143–153. 43 indexed citations
15.
Trejo, Christy L., Shon Green, Victoria Marsh, et al.. (2013). Mutationally Activated PIK3CAH1047R Cooperates with BRAFV600E to Promote Lung Cancer Progression. Cancer Research. 73(21). 6448–6461. 33 indexed citations
16.
Collisson, Eric A., Christy L. Trejo, Jillian M. Silva, et al.. (2012). A Central Role for RAF→MEK→ERK Signaling in the Genesis of Pancreatic Ductal Adenocarcinoma. Cancer Discovery. 2(8). 685–693. 219 indexed citations
17.
Tikoo, Anjali, Vincent Roh, Karen G. Montgomery, et al.. (2012). Physiological Levels of Pik3caH1047R Mutation in the Mouse Mammary Gland Results in Ductal Hyperplasia and Formation of ERα-Positive Tumors. PLoS ONE. 7(5). e36924–e36924. 58 indexed citations
18.
Brettingham‐Moore, Kate H., Cuong Duong, Danielle Greenawalt, et al.. (2011). Pretreatment Transcriptional Profiling for Predicting Response to Neoadjuvant Chemoradiotherapy in Rectal Adenocarcinoma. Clinical Cancer Research. 17(9). 3039–3047. 43 indexed citations
19.
Cristiano, Briony E., Katherine M. Hannan, Ian Campbell, et al.. (2006). A Specific Role for AKT3 in the Genesis of Ovarian Cancer through Modulation of G2-M Phase Transition. Cancer Research. 66(24). 11718–11725. 84 indexed citations
20.
Lo, Ting Ling, Permeen Yusoff, Chee Wai Fong, et al.. (2004). The Ras/Mitogen-Activated Protein Kinase Pathway Inhibitor and Likely Tumor Suppressor Proteins, Sprouty 1 and Sprouty 2 Are Deregulated in Breast Cancer. Cancer Research. 64(17). 6127–6136. 143 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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