Simon Patton

1.6k total citations
47 papers, 673 citations indexed

About

Simon Patton is a scholar working on Cancer Research, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Simon Patton has authored 47 papers receiving a total of 673 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Cancer Research, 11 papers in Molecular Biology and 11 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Simon Patton's work include Cancer Genomics and Diagnostics (22 papers), Lung Cancer Treatments and Mutations (9 papers) and Genetic factors in colorectal cancer (7 papers). Simon Patton is often cited by papers focused on Cancer Genomics and Diagnostics (22 papers), Lung Cancer Treatments and Mutations (9 papers) and Genetic factors in colorectal cancer (7 papers). Simon Patton collaborates with scholars based in United Kingdom, Italy and Netherlands. Simon Patton's co-authors include Zandra C. Deans, Nicola Normanno, Elisabeth Dequeker, Rob Elles, Peter W. H. Holland, Andrew J. Wallace, Michael A. Morris, Ed Schuuring, Cleo Keppens and Jennifer A. Fairley and has published in prestigious journals such as British Journal of Cancer, International Journal of Radiation Oncology*Biology*Physics and Annals of Oncology.

In The Last Decade

Simon Patton

45 papers receiving 657 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Simon Patton United Kingdom 16 326 201 178 139 109 47 673
Peter Sabatini Canada 11 393 1.2× 408 2.0× 231 1.3× 255 1.8× 112 1.0× 31 961
‪Saeid Ghorbian Iran 14 349 1.1× 373 1.9× 58 0.3× 68 0.5× 57 0.5× 64 662
Sonya Parpart-Li United States 5 501 1.5× 306 1.5× 147 0.8× 227 1.6× 120 1.1× 13 661
Christopher Schroeder Germany 17 153 0.5× 249 1.2× 162 0.9× 308 2.2× 43 0.4× 53 740
Zandra C. Deans United Kingdom 18 461 1.4× 313 1.6× 239 1.3× 234 1.7× 220 2.0× 45 921
Anne‐Katrin Emde United States 14 389 1.2× 669 3.3× 109 0.6× 271 1.9× 155 1.4× 19 1.1k
Brunella Pilato Italy 18 302 0.9× 488 2.4× 87 0.5× 172 1.2× 180 1.7× 46 810
Lei Song United States 14 288 0.9× 466 2.3× 177 1.0× 106 0.8× 119 1.1× 41 849
Giorgio Melloni United States 15 255 0.8× 497 2.5× 94 0.5× 257 1.8× 189 1.7× 41 984
Marie Wong Australia 10 281 0.9× 479 2.4× 132 0.7× 141 1.0× 167 1.5× 19 821

Countries citing papers authored by Simon Patton

Since Specialization
Citations

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

Fields of papers citing papers by Simon Patton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simon Patton

This figure shows the co-authorship network connecting the top 25 collaborators of Simon Patton. A scholar is included among the top collaborators of Simon Patton 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 Simon Patton. Simon Patton 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.
Giacomini, Patrizio, Jennifer A. Fairley, Rodrigo A. Toledo, et al.. (2025). Reporting of molecular test results from cell-free DNA analyses: expert consensus recommendations from the 2023 European Liquid Biopsy Society ctDNA Workshop. EBioMedicine. 114. 105636–105636. 5 indexed citations
2.
Venetis, Konstantinos, Francesco Pepe, Omshree Shetty, et al.. (2025). International society of liquid biopsy (ISLB) perspective on minimal requirements for ctDNA testing in solid tumors. PubMed. 8. 100301–100301. 7 indexed citations
3.
Torlakovic, Emina, Raed Al Dieri, Tony Badrick, et al.. (2025). Indirect clinical validation for predictive biomarkers in oncology: International Quality Network for Pathology (IQN Path) Position Paper. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 487(3). 565–572. 1 indexed citations
4.
Jager, Veronique de, Patrizio Giacomini, Janet A. Fairley, et al.. (2024). 112P Reporting of molecular test results from cell-free DNA analyses: Expert consensus recommendations from the 2023 European Liquid Biopsy Society ctDNA workshop. Annals of Oncology. 35. S259–S259.
5.
Penault‐Llorca, Frédérique, Keith M. Kerr, Pilar Garrido, et al.. (2022). Expert opinion on NSCLC small specimen biomarker testing — Part 1: Tissue collection and management. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 481(3). 335–350. 29 indexed citations
6.
Patton, Simon, Farrah Khawaja, Fiona Morgan, et al.. (2022). Variability in Fetal Fraction Estimation: Comparing Fetal Fractions Reported by Noninvasive Prenatal Testing Providers Globally. Clinical Chemistry. 69(2). 160–167. 10 indexed citations
7.
Radke, Teja Falk, et al.. (2020). Evaluation of current genetic testing reports in German-speaking countries with regard to secondary use and future electronic implementation. European Journal of Human Genetics. 28(5). 558–566. 1 indexed citations
8.
Keppens, Cleo, Ed Schuuring, Zandra C. Deans, et al.. (2020). External Quality Assessment Schemes for Biomarker Testing in Oncology. Journal of Molecular Diagnostics. 22(6). 736–747. 8 indexed citations
9.
Liddicoat, John, Kathleen Liddell, Stuart Hogarth, et al.. (2019). Continental drift? Do European clinical genetic testing laboratories have a patent problem?. European Journal of Human Genetics. 27(7). 997–1007. 6 indexed citations
10.
Deans, Zandra C., Christophe Roos, Farrah Khawaja, et al.. (2019). One byte at a time: evidencing the quality of clinical service next-generation sequencing for germline and somatic variants. European Journal of Human Genetics. 28(2). 202–212. 13 indexed citations
11.
Rowczenio, Dorota, Yael Shinar, Isabella Ceccherini, et al.. (2019). Current practices for the genetic diagnosis of autoinflammatory diseases: results of a European Molecular Genetics Quality Network Survey. European Journal of Human Genetics. 27(10). 1502–1508. 7 indexed citations
12.
Wyman, Allison M., et al.. (2017). Levator Ani Muscle Defects in Patients With Surgical Failure. Female Pelvic Medicine & Reconstructive Surgery. 23(2). 114–117. 2 indexed citations
13.
Ellison, Gillian, Andrew J. Wallace, Alexander Kohlmann, & Simon Patton. (2017). A comparative study of germline BRCA1 and BRCA2 mutation screening methods in use in 20 European clinical diagnostic laboratories. British Journal of Cancer. 117(5). 710–716. 7 indexed citations
14.
Venkatakrishnan, Singanallur, K. Aditya Mohan, K. Beattie, et al.. (2016). Making Advanced Scientific Algorithms and Big Scientific Data Management More Accessible. Electronic Imaging. 28(19). 1–7. 7 indexed citations
15.
Patton, Simon, et al.. (2015). Spade: Decentralized orchestration of data movement and warehousing for physics experiments. 1014–1019. 3 indexed citations
16.
Griffiths, Mike, et al.. (2014). Conversion, Correction, and International Scale Standardization: Results From a Multicenter External Quality Assessment Study for BCR-ABL1 Testing. Archives of Pathology & Laboratory Medicine. 139(4). 522–529. 2 indexed citations
17.
Losekoot, Monique, et al.. (2009). Ten Year’s Experience in External Quality Assessment for Genetic Testing of Huntington Disease in Europe: Still Room for Improvement. Clinical Genetics. 76. 104–105. 1 indexed citations
18.
Ramsden, Simon, Zandra C. Deans, David Robinson, et al.. (2006). Monitoring Standards for Molecular Genetic Testing in the United Kingdom, The Netherlands, and Ireland. Genetic Testing. 10(3). 147–156. 27 indexed citations
19.
Patton, Simon, David Barton, & Rob Elles. (2000). Retaining the Confidence of the Public in Molecular Genetic Testing – Quality Assurance. Public Health Genomics. 3(4). 164–169. 8 indexed citations
20.
Patton, Simon, et al.. (1998). Complex History of a Chromosomal Paralogy Region: Insights from Amphioxus Aromatic Amino Acid Hydroxylase Genes and Insulin -Related Genes. Molecular Biology and Evolution. 15(11). 1373–1380. 44 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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