Robert C.G. Martin

27.4k total citations · 1 hit paper
491 papers, 15.4k citations indexed

About

Robert C.G. Martin is a scholar working on Oncology, Surgery and Hepatology. According to data from OpenAlex, Robert C.G. Martin has authored 491 papers receiving a total of 15.4k indexed citations (citations by other indexed papers that have themselves been cited), including 230 papers in Oncology, 207 papers in Surgery and 132 papers in Hepatology. Recurrent topics in Robert C.G. Martin's work include Hepatocellular Carcinoma Treatment and Prognosis (127 papers), Pancreatic and Hepatic Oncology Research (112 papers) and Cholangiocarcinoma and Gallbladder Cancer Studies (86 papers). Robert C.G. Martin is often cited by papers focused on Hepatocellular Carcinoma Treatment and Prognosis (127 papers), Pancreatic and Hepatic Oncology Research (112 papers) and Cholangiocarcinoma and Gallbladder Cancer Studies (86 papers). Robert C.G. Martin collaborates with scholars based in United States, China and Italy. Robert C.G. Martin's co-authors include Charles R. Scoggins, Kelly M. McMasters, Murray F. Brennan, David P. Jaques, Prejesh Philips, Susan Ellis, Matthew Bower, Vic Velanovich, Arnold J. Stromberg and R. Dirk Noyes and has published in prestigious journals such as Nature Communications, Journal of Clinical Oncology and The EMBO Journal.

In The Last Decade

Robert C.G. Martin

475 papers receiving 15.1k citations

Hit Papers

Quality of Complication Reporting in the Surgical Literature 2002 2026 2010 2018 2002 100 200 300 400 500
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Quality of Complication Reporting in the Surgical Literature
    2002 501 citations Robert C.G. Martin et al. profile →

Peers

Robert C.G. Martin
Thierry de Baère France
Jürgen Weitz Germany
Peter J. Allen United States
T. Peter Kingham United States
Akimasa Nakao Japan
Ramesh K. Ramanathan United States
Valérie Boige France
Andrea Tannapfel Germany
Sheung Tat Fan Hong Kong
Kiyoshi Hasegawa Japan
Thierry de Baère France
Robert C.G. Martin
Citations per year, relative to Robert C.G. Martin Robert C.G. Martin (= 1×) peers Thierry de Baère

Countries citing papers authored by Robert C.G. Martin

Since Specialization
Citations

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

Fields of papers citing papers by Robert C.G. Martin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert C.G. Martin. 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 Robert C.G. Martin. The network helps show where Robert C.G. Martin may publish in the future.

Co-authorship network of co-authors of Robert C.G. Martin

This figure shows the co-authorship network connecting the top 25 collaborators of Robert C.G. Martin. A scholar is included among the top collaborators of Robert C.G. Martin 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 Robert C.G. Martin. Robert C.G. Martin 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.
Scoggins, Charles R., et al.. (2024). Optimization of Exocrine Pancreatic Insufficiency in Pancreatic Adenocarcinoma Patients. Nutrients. 16(20). 3499–3499.
2.
Shi, Xiaoju, Qianqian Zheng, Xingtong Wang, et al.. (2024). Compromised macrophages contribute to progression of MASH to hepatocellular carcinoma in FGF21KO mice. Science Advances. 10(43). eado9311–eado9311. 5 indexed citations
3.
Martin, Robert C.G., Rebekah R. White, Malcolm M. Bilimoria, et al.. (2024). Effectiveness and Safety of Irreversible Electroporation When Used for the Ablation of Stage 3 Pancreatic Adenocarcinoma: Initial Results from the DIRECT Registry Study. Cancers. 16(23). 3894–3894. 4 indexed citations
4.
Philips, Prejesh, et al.. (2024). Preoperative liquid biopsy for optimal patient selection in metastatic colorectal cancer. Surgery. 179. 108810–108810. 1 indexed citations
5.
6.
Woeste, Matthew R., Rejeena Shrestha, Anne E. Geller, et al.. (2023). Irreversible electroporation augments β-glucan induced trained innate immunity for the treatment of pancreatic ductal adenocarcinoma. Journal for ImmunoTherapy of Cancer. 11(4). e006221–e006221. 16 indexed citations
7.
Wadhwa, S., Prejesh Philips, Robert C.G. Martin, et al.. (2023). Interval Sentinel Lymph Nodes With the Use of Routine Lymphoscintigraphy in Extremity Melanoma. Journal of Surgical Research. 293. 613–617. 1 indexed citations
8.
Tan, Min, Santiago Vázquez, Jingwen Zhang, et al.. (2023). Abstract 638: EPB-53 prevents NASH-HCC transition via regulation of SPHK1-S1P-HIPPO signaling and immune modulation in a murine model. Cancer Research. 83(7_Supplement). 638–638. 1 indexed citations
9.
Geller, Anne E., Rejeena Shrestha, Matthew R. Woeste, et al.. (2022). The induction of peripheral trained immunity in the pancreas incites anti-tumor activity to control pancreatic cancer progression. Nature Communications. 13(1). 759–759. 64 indexed citations
10.
11.
Li, Yan, Young Ki Hong, Xingtong Wang, et al.. (2022). Epigenetic modulation enhances immunotherapy for pancreatic ductal adenocarcinoma. Clinical & Translational Immunology. 11(12). e1430–e1430. 8 indexed citations
12.
Martin, Robert C.G., et al.. (2022). Impact of margin accentuation with intraoperative irreversible electroporation on local recurrence in resected pancreatic cancer. Surgery. 173(3). 581–589. 5 indexed citations
13.
Woeste, Matthew R., Michael E. Egger, Prejesh Philips, et al.. (2021). Hepatopancreatobiliary readmission score out performs administrative LACE+ index as a predictive tool of readmission. The American Journal of Surgery. 223(5). 933–938. 1 indexed citations
14.
Martin, Robert C.G., et al.. (2020). Enhanced recovery after surgery is safe for cytoreductive surgery with hyperthermic intraperitoneal chemotherapy. The American Journal of Surgery. 220(6). 1428–1432. 10 indexed citations
15.
Beitel-White, Natalie, Robert C.G. Martin, Yan Li, et al.. (2019). Real-time prediction of patient immune cell modulation during irreversible electroporation therapy. Scientific Reports. 9(1). 17739–17739. 29 indexed citations
16.
Pandit, Harshul, et al.. (2018). Enrichment of cancer stem cells via β-catenin contributing to the tumorigenesis of hepatocellular carcinoma. BMC Cancer. 18(1). 783–783. 46 indexed citations
17.
Brown, Russell E., Merrick I. Ross, Michael J. Edwards, et al.. (2010). The Prognostic Significance of Nonsentinel Lymph Node Metastasis in Melanoma. Annals of Surgical Oncology. 17(12). 3330–3335. 26 indexed citations
18.
Martin, Robert C.G., David F. Barker, Mark A. Doll, et al.. (2008). Manganese Superoxide Dismutase Gene Coding Region Polymorphisms Lack Clinical Incidence in General Population. DNA and Cell Biology. 27(6). 321–323. 3 indexed citations
19.
20.
Li, Yan, John M. Wo, Susan Ellis, et al.. (2006). Morphological Transformation in Esophageal Submucosa by Bone Marrow Cells: Esophageal Implantation under External Esophageal Perfusion. Stem Cells and Development. 15(5). 697–705. 6 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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