Peter Georgeson

1.7k total citations
17 papers, 241 citations indexed

About

Peter Georgeson is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Cancer Research. According to data from OpenAlex, Peter Georgeson has authored 17 papers receiving a total of 241 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Pathology and Forensic Medicine and 6 papers in Cancer Research. Recurrent topics in Peter Georgeson's work include Genetic factors in colorectal cancer (7 papers), Cancer Genomics and Diagnostics (5 papers) and RNA and protein synthesis mechanisms (3 papers). Peter Georgeson is often cited by papers focused on Genetic factors in colorectal cancer (7 papers), Cancer Genomics and Diagnostics (5 papers) and RNA and protein synthesis mechanisms (3 papers). Peter Georgeson collaborates with scholars based in Australia, United States and United Kingdom. Peter Georgeson's co-authors include Bernard J. Pope, Khalid Mahmood, Daniel J. Park, Jessica Chung, Gayle K. Philip, Chol‐Hee Jung, Daniel D. Buchanan, Brendan R. E. Ansell, Aaron R. Jex and Shan Li and has published in prestigious journals such as Gastroenterology, International Journal of Molecular Sciences and Genome Research.

In The Last Decade

Peter Georgeson

15 papers receiving 239 citations

Peers

Peter Georgeson
Lara Bethke United States
Luis I. Terrazas Mexico
Shaoyun Cheng China
Qinyan Li China
Yaping Zhang China
Alisha Dhiman United States
Du Cheng China
Winnie W. Hui United States
Panagiota Mamareli Germany
Lara Bethke United States
Peter Georgeson
Citations per year, relative to Peter Georgeson Peter Georgeson (= 1×) peers Lara Bethke

Countries citing papers authored by Peter Georgeson

Since Specialization
Citations

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

Fields of papers citing papers by Peter Georgeson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peter Georgeson

This figure shows the co-authorship network connecting the top 25 collaborators of Peter Georgeson. A scholar is included among the top collaborators of Peter Georgeson 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 Peter Georgeson. Peter Georgeson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
2.
Joo, Jihoon E., et al.. (2025). DNA Mismatch Repair Gene Mosaicism Is Rare in People With Mismatch Repair-Deficient Cancers. Gastroenterology. 168(5). 983–986. 1 indexed citations
3.
4.
Mouradov, Dmitri, Paul Greenfield, Shan Li, et al.. (2023). Oncomicrobial Community Profiling Identifies Clinicomolecular and Prognostic Subtypes of Colorectal Cancer. Gastroenterology. 165(1). 104–120. 53 indexed citations
5.
Clendenning, Mark, Jihoon E. Joo, Khalid Mahmood, et al.. (2023). A mosaic pathogenic variant in MSH6 causes MSH6-deficient colorectal and endometrial cancer in a patient classified as suspected Lynch syndrome: a case report. Familial Cancer. 22(4). 423–428. 2 indexed citations
6.
Chan, James, Mark Clendenning, Peter Georgeson, et al.. (2023). Inherited BRCA1 and RNF43 pathogenic variants in a familial colorectal cancer type X family. Familial Cancer. 23(1). 9–21. 5 indexed citations
7.
Mangiola, Stefano, Geoff Macintyre, Ryan Hutchinson, et al.. (2021). MSH2-deficient prostate tumours have a distinct immune response and clinical outcome compared to MSH2-deficient colorectal or endometrial cancer. Prostate Cancer and Prostatic Diseases. 24(4). 1167–1180. 6 indexed citations
8.
9.
Joo, Jihoon E., Mark Clendenning, Ee Ming Wong, et al.. (2021). DNA Methylation Signatures and the Contribution of Age-Associated Methylomic Drift to Carcinogenesis in Early-Onset Colorectal Cancer. Cancers. 13(11). 2589–2589. 18 indexed citations
10.
Pope, Bernard J., Mark Clendenning, Christophe Rosty, et al.. (2020). Germline and Tumor Sequencing as a Diagnostic Tool To Resolve Suspected Lynch Syndrome. Journal of Molecular Diagnostics. 23(3). 358–371. 11 indexed citations
11.
Georgeson, Peter, Anna Syme, Clare Sloggett, et al.. (2019). Bionitio: demonstrating and facilitating best practices for bioinformatics command-line software. GigaScience. 8(9). 10 indexed citations
12.
Georgeson, Peter, Michael D. Walsh, Mark Clendenning, et al.. (2019). Tumor mutational signatures in sebaceous skin lesions from individuals with Lynch syndrome. Molecular Genetics & Genomic Medicine. 7(7). e00781–e00781. 5 indexed citations
13.
Ansell, Brendan R. E., et al.. (2018). Annotation of the Giardia proteome through structure-based homology and machine learning. GigaScience. 8(1). 17 indexed citations
14.
Jung, Chol-Hee, Daniel J. Park, Peter Georgeson, et al.. (2018). sEst: Accurate Sex-Estimation and Abnormality Detection in Methylation Microarray Data. International Journal of Molecular Sciences. 19(10). 3172–3172. 5 indexed citations
15.
Mahmood, Khalid, Chol‐Hee Jung, Gayle K. Philip, et al.. (2017). Variant effect prediction tools assessed using independent, functional assay-based datasets: implications for discovery and diagnostics. Human Genomics. 11(1). 10–10. 60 indexed citations
16.
Vissers, Lisenka E.L.M., et al.. (2017). An Emerging Female Phenotype with Loss‐of‐Function Mutations in the Aristaless‐ Related Homeodomain Transcription Factor ARX. Human Mutation. 38(5). 548–555. 8 indexed citations
17.
Park, Daniel J., Roger Li, Edmund Lau, et al.. (2016). UNDR ROVER - a fast and accurate variant caller for targeted DNA sequencing. BMC Bioinformatics. 17(1). 165–165. 4 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

Breakdown of academic impact, for papers by Lara Bethke Breakdown of academic impact, for papers by Luis I. Terrazas Breakdown of academic impact, for papers by Shaoyun Cheng Breakdown of academic impact, for papers by Qinyan Li Breakdown of academic impact, for papers by Yaping Zhang Breakdown of academic impact, for papers by Alisha Dhiman Breakdown of academic impact, for papers by Du Cheng Breakdown of academic impact, for papers by Winnie W. Hui Breakdown of academic impact, for papers by Panagiota Mamareli
Rankless by CCL
2026