Kevin Monahan

4.9k total citations · 2 hit papers
67 papers, 1.4k citations indexed

About

Kevin Monahan is a scholar working on Pathology and Forensic Medicine, Oncology and Surgery. According to data from OpenAlex, Kevin Monahan has authored 67 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Pathology and Forensic Medicine, 44 papers in Oncology and 21 papers in Surgery. Recurrent topics in Kevin Monahan's work include Genetic factors in colorectal cancer (47 papers), Colorectal Cancer Screening and Detection (38 papers) and Cancer Genomics and Diagnostics (11 papers). Kevin Monahan is often cited by papers focused on Genetic factors in colorectal cancer (47 papers), Colorectal Cancer Screening and Detection (38 papers) and Cancer Genomics and Diagnostics (11 papers). Kevin Monahan collaborates with scholars based in United Kingdom, United States and Spain. Kevin Monahan's co-authors include Mark McPhail, Panagiotis Vlavianos, Ameet Dhar, Lucia Possamai, Shevanthi Nayagam, James E. East, Andrew Latchford, Asha Kaur, Fiona Lalloo and James Hill and has published in prestigious journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and Gastroenterology.

In The Last Decade

Kevin Monahan

63 papers receiving 1.4k citations

Hit Papers

EUS-guided FNA for diagnosis of solid pancreatic neoplasm... 2012 2026 2016 2021 2012 2019 100 200 300 400 500

Peers

Kevin Monahan
Yung Nio Netherlands
Jan–Werner Poley Netherlands
Katharina Biermann Netherlands
Kanwal Raghav United States
Mehmet Akce United States
Susan Parry New Zealand
Tina Bocker Edmonston United States
Ho‐Kyung Chun South Korea
Kevin Monahan
Citations per year, relative to Kevin Monahan Kevin Monahan (= 1×) peers Wouter H. de Vos tot Nederveen Cappel

Countries citing papers authored by Kevin Monahan

Since Specialization
Citations

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

Fields of papers citing papers by Kevin Monahan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kevin Monahan

This figure shows the co-authorship network connecting the top 25 collaborators of Kevin Monahan. A scholar is included among the top collaborators of Kevin Monahan 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 Kevin Monahan. Kevin Monahan 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.
Laskaratos, Faidon‐Marios, et al.. (2025). The Role of Video Capsule Endoscopy in Hereditary Polyposis Syndromes: A Narrative Review. Diagnostics. 15(21). 2813–2813.
2.
Fadel, Michael G, James H. Murray, Ilaria Belluomo, et al.. (2025). Non-invasive breath testing to detect colorectal cancer: protocol for a multicentre, case–control development and validation study (COBRA2 study). BMC Cancer. 25(1). 1230–1230. 1 indexed citations
3.
Møller, Pål, Aysel Ahadova, Matthias Kloor, et al.. (2025). Colorectal carcinogenesis in the Lynch syndromes and familial adenomatous polyposis: trigger events and downstream consequences. Hereditary Cancer in Clinical Practice. 23(1). 3–3. 1 indexed citations
4.
Poo, Stephanie, Jonathan D. Walton, Sarah C. Marshall, et al.. (2025). Diagnostic yield of colonoscopy surveillance in Lynch syndrome. Frontline Gastroenterology. flgastro–2025.
5.
Latchford, Andrew, et al.. (2025). Low Yield of Genetic Testing in Serrated Polyposis Syndrome. Clinical and Translational Gastroenterology. 16(11). e00923–e00923.
6.
McVeigh, Terri, Fiona Lalloo, Kevin Monahan, et al.. (2024). Carrier testing for partners of MUTYH variant carriers: UK Cancer Genetics Group recommendations. Journal of Medical Genetics. 61(8). 813–816. 1 indexed citations
7.
McVeigh, Terri, Kevin Monahan, Joseph Christopher, et al.. (2024). Extent of investigation and management of cases of ‘unexplained’ mismatch repair deficiency (u-dMMR): a UK Cancer Genetics Group consensus. Journal of Medical Genetics. 61(7). 707–715. 1 indexed citations
8.
Monje‐Garcia, Laura, Emma Kipps, Angela F. Brady, et al.. (2023). From diagnosis of colorectal cancer to diagnosis of Lynch syndrome: The RM Partners quality improvement project. Colorectal Disease. 25(9). 1844–1851. 4 indexed citations
9.
Monahan, Kevin, et al.. (2023). Biology of Precancers and Opportunities for Cancer Interception: Lesson from Colorectal Cancer Susceptibility Syndromes. Cancer Prevention Research. 16(8). 421–427. 3 indexed citations
10.
Alexander, James L., et al.. (2023). The Diagnostic Yield of Genetic Testing in Patients With Multiple Colorectal Adenomas: A Specialist Center Cohort Study. Clinical and Translational Gastroenterology. 15(1). e00645–e00645. 4 indexed citations
11.
Monahan, Kevin, Adam Shaw, Laura Monje‐Garcia, et al.. (2023). P293 Finding the missing 95%: the English national lynch syndrome transformation project. Poster presentations. A204.2–A204. 3 indexed citations
12.
Monahan, Kevin, Neil Ryan, Laura Monje‐Garcia, et al.. (2023). The English National Lynch Syndrome transformation project: an NHS Genomic Medicine Service Alliance (GMSA) programme. SHILAP Revista de lepidopterología. 2(1). e000124–e000124. 9 indexed citations
13.
Monahan, Kevin, Nicola Bradshaw, Sunil Dolwani, et al.. (2019). Guidelines for the management of hereditary colorectal cancer from the British Society of Gastroenterology (BSG)/Association of Coloproctology of Great Britain and Ireland (ACPGBI)/United Kingdom Cancer Genetics Group (UKCGG). Gut. 69(3). 411–444. 255 indexed citations breakdown →
14.
Alexander, James L., B J Johnston, Thomas J. Smith, et al.. (2019). OWE-25 Patients with multiple adenomas in bowel cancer screening program are not referred for genetic testing. A188.1–A188. 2 indexed citations
15.
Rajendran, Arun, et al.. (2014). PWE-010 The Association Of Tgfb Signalling Pathway Gene Polymorphisms With Colorectal Cancer Risk: A Meta-analysis. Gut. 63(Suppl 1). A125.2–A125. 1 indexed citations
16.
Pannick, Samuel, et al.. (2013). PTH-052 Microscopic Colitis Is Expensive To Diagnose: An Analysis Of The Utility Of Random Colonic Biopsies. Gut. 62(Suppl 1). A232.1–A232. 1 indexed citations
17.
Vadhwana, Bhamini, et al.. (2013). PWE-197 Is MRCP a useful Investigation where the Biliary Tree is normal on Previous Imaging?. Gut. 62(Suppl 1). A210.2–A211. 2 indexed citations
18.
Stevens, Stephanie, et al.. (2013). PWE-170 A Dedicated Colorectal Cancer Genetics Service Improves Adherence with Molecular Testing for Lynch Syndrome. Gut. 62(Suppl 1). A200.1–A200. 1 indexed citations
19.
Bell, Laura, A. E. Johnston, Scott M. MacKenzie, et al.. (2011). Hypertension is an independent risk factor for colorectal polyps: Table 1. Gut. 60(Suppl 1). A65.1–A65. 1 indexed citations
20.
Monahan, Kevin, et al.. (2010). Esophageal adenocarcinoma after Nissen’s fundoplication for Barrett’s esophagus: report of a case. Surgery Today. 40(12). 1173–1175. 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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