Andrew Latchford

5.3k total citations · 1 hit paper
81 papers, 2.0k citations indexed

About

Andrew Latchford is a scholar working on Pathology and Forensic Medicine, Oncology and Surgery. According to data from OpenAlex, Andrew Latchford has authored 81 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Pathology and Forensic Medicine, 34 papers in Oncology and 25 papers in Surgery. Recurrent topics in Andrew Latchford's work include Genetic factors in colorectal cancer (61 papers), Colorectal Cancer Screening and Detection (21 papers) and Gastric Cancer Management and Outcomes (16 papers). Andrew Latchford is often cited by papers focused on Genetic factors in colorectal cancer (61 papers), Colorectal Cancer Screening and Detection (21 papers) and Gastric Cancer Management and Outcomes (16 papers). Andrew Latchford collaborates with scholars based in United Kingdom, United States and Netherlands. Andrew Latchford's co-authors include Susan K. Clark, Kay Neale, Robin Phillips, R K S Phillips, Evelien Dekker, Ian Tomlinson, Monique E. van Leerdam, Pauline Rogers, James E. East and Warren Hyer and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and Nature Biotechnology.

In The Last Decade

Andrew Latchford

72 papers receiving 2.0k citations

Hit Papers

Guidelines for the management of hereditary colorectal ca... 2019 2026 2021 2023 2019 50 100 150 200 250

Peers

Andrew Latchford
Gerrit Griffioen Netherlands
Stephen J. Lanspa United States
L Herrera United States
H. Aste Italy
J P Sheffield United Kingdom
Bhavana Konda United States
Andrew Latchford
Citations per year, relative to Andrew Latchford Andrew Latchford (= 1×) peers Steffen Bülow

Countries citing papers authored by Andrew Latchford

Since Specialization
Citations

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

Fields of papers citing papers by Andrew Latchford

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrew Latchford

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew Latchford. A scholar is included among the top collaborators of Andrew Latchford 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 Andrew Latchford. Andrew Latchford 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.
Latchford, Andrew, et al.. (2025). One hundred years of the St Mark’s hospital polyposis registry. Familial Cancer. 24(2). 37–37.
3.
Poo, Stephanie, Jonathan D. Walton, Sarah C. Marshall, et al.. (2025). Diagnostic yield of colonoscopy surveillance in Lynch syndrome. Frontline Gastroenterology. flgastro–2025.
4.
Latchford, Andrew, et al.. (2025). Low Yield of Genetic Testing in Serrated Polyposis Syndrome. Clinical and Translational Gastroenterology. 16(11). e00923–e00923.
5.
Pellisé, María, Barbara A.J. Bastiaansen, Monique E. van Leerdam, et al.. (2024). Risk of Cancer and Reoperation After Ileorectal Anastomosis and Ileal Pouch-Anal Anastomosis in Familial Adenomatous Polyposis. The American Journal of Gastroenterology. 120(9). 2132–2138. 2 indexed citations
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.
Butler, Andrew J., Susan K. Clark, Andrew Latchford, et al.. (2024). Treatment of Complex Desmoid Tumors in Familial Adenomatous Polyposis Syndrome by Intestinal Transplantation. Transplantation Direct. 10(2). e1571–e1571. 4 indexed citations
8.
Plazzer, John‐Paul, et al.. (2024). Phenotype Correlations With Pathogenic DNA Variants in the MUTYH Gene: A Review of Over 2000 Cases. Human Mutation. 2024(1). 8520275–8520275. 2 indexed citations
9.
Aelvoet, Arthur S., Duncan Spalding, Olivier R. Busch, et al.. (2024). Outcomes following duodenectomy in patients with familial adenomatous polyposis. SHILAP Revista de lepidopterología. 12(5). E659–E665. 1 indexed citations
10.
Aelvoet, Arthur S., John Gásdal Karstensen, Barbara A.J. Bastiaansen, et al.. (2023). Cold snare polypectomy for duodenal adenomas in familial adenomatous polyposis: a prospective international cohort study. SHILAP Revista de lepidopterología. 11(11). E1056–E1062. 3 indexed citations
11.
Sherwood, Kitty, Lynn Martin, Archie Campbell, et al.. (2023). Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair. Nature Communications. 14(1). 3636–3636. 7 indexed citations
12.
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
13.
Patel, Roshani, Kit Curtius, Ripple Man, et al.. (2023). Long-term outcomes of pouch surveillance and risk of neoplasia in familial adenomatous polyposis. Endoscopy. 55(9). 836–846. 2 indexed citations
14.
Valle, Laura, Lior H. Katz, Andrew Latchford, et al.. (2023). Position statement of the International Society for Gastrointestinal Hereditary Tumours (InSiGHT) on APC I1307K and cancer risk. Journal of Medical Genetics. 60(11). 1035–1043. 12 indexed citations
15.
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
16.
Noble, Alistair, Lydia Durant, Ripple Man, et al.. (2022). Altered Mucosal Immune-Microbiota Interactions in Familial Adenomatous Polyposis. Clinical and Translational Gastroenterology. 13(7). e00428–e00428. 9 indexed citations
17.
Schenck, Ryan O., Daniel J. Weisenberger, Christopher Kimberley, et al.. (2022). Fluctuating methylation clocks for cell lineage tracing at high temporal resolution in human tissues. Nature Biotechnology. 40(5). 720–730. 27 indexed citations
18.
Latchford, Andrew & Susan K. Clark. (2022). Gastrointestinal aspects of Peutz-Jeghers syndrome. Best Practice & Research Clinical Gastroenterology. 58-59. 101789–101789. 13 indexed citations
19.
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 →
20.
Latchford, Andrew, et al.. (2001). The continuing tale of cytokeratins in Barrett's mucosa: As you like it. Gut. 49(6). 746–747. 9 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026