Brian Allen

4.3k total citations · 2 hit papers
39 papers, 2.4k citations indexed

About

Brian Allen is a scholar working on Pathology and Forensic Medicine, Cancer Research and Oncology. According to data from OpenAlex, Brian Allen has authored 39 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Pathology and Forensic Medicine, 18 papers in Cancer Research and 17 papers in Oncology. Recurrent topics in Brian Allen's work include Genetic factors in colorectal cancer (20 papers), Cancer Genomics and Diagnostics (18 papers) and BRCA gene mutations in cancer (15 papers). Brian Allen is often cited by papers focused on Genetic factors in colorectal cancer (20 papers), Cancer Genomics and Diagnostics (18 papers) and BRCA gene mutations in cancer (15 papers). Brian Allen collaborates with scholars based in United States, Canada and United Kingdom. Brian Allen's co-authors include Anne‐Renee Hartman, Richard Wenstrup, Jonathan P. Terdiman, Nanda Singh, John Kidd, Judy E. Garber, Nadine Tung, Sapna Syngal, Marvin H. Sleisenger and Brindusa Truta and has published in prestigious journals such as Journal of Clinical Oncology, Gastroenterology and Cancer.

In The Last Decade

Brian Allen

38 papers receiving 2.4k citations

Hit Papers

Frequency of Germline Mutations in 25 Cancer Susceptibili... 2016 2026 2019 2022 2016 2017 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Brian Allen United States 17 1.4k 1.2k 996 946 675 39 2.4k
Kelsey Moyes United States 8 2.0k 1.4× 1.6k 1.4× 621 0.6× 1.1k 1.2× 552 0.8× 17 2.8k
Mark Clendenning Australia 25 2.1k 1.5× 1.8k 1.5× 412 0.4× 1.1k 1.1× 614 0.9× 63 2.9k
Christopher Arnell United States 7 866 0.6× 659 0.6× 528 0.5× 530 0.6× 326 0.5× 14 1.4k
Heather L. Hampel United States 8 1.7k 1.2× 1.3k 1.1× 718 0.7× 875 0.9× 329 0.5× 11 2.5k
Rachel Pearlman United States 17 873 0.6× 624 0.5× 307 0.3× 623 0.7× 220 0.3× 33 1.3k
Michelle Landon United States 4 1.1k 0.8× 840 0.7× 238 0.2× 542 0.6× 239 0.4× 4 1.4k
Paulo Fidalgo Portugal 19 1.1k 0.7× 778 0.7× 247 0.2× 380 0.4× 422 0.6× 45 1.6k
U Chetty United Kingdom 23 1.2k 0.8× 1.4k 1.2× 378 0.4× 1.7k 1.8× 467 0.7× 50 2.7k
Susanne Taucher Austria 23 456 0.3× 1.1k 0.9× 256 0.3× 954 1.0× 316 0.5× 45 1.7k
Guido M.J.M. Roemen Netherlands 17 453 0.3× 530 0.5× 143 0.1× 326 0.3× 686 1.0× 29 1.4k

Countries citing papers authored by Brian Allen

Since Specialization
Citations

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

Fields of papers citing papers by Brian Allen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Brian Allen

This figure shows the co-authorship network connecting the top 25 collaborators of Brian Allen. A scholar is included among the top collaborators of Brian Allen 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 Brian Allen. Brian Allen 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.
Rini, Brian I., Jun Zhang, O. Hall, et al.. (2023). 1910P Evaluation of a genome-wide methylome enrichment platform for circulating tumor DNA quantification and prognostic performance in renal cell carcinoma (RCC). Annals of Oncology. 34. S1028–S1028. 1 indexed citations
2.
Liu, Geoffrey, Jun Zhang, O. Hall, et al.. (2023). 866P Prognostic performance of a genome-wide methylome enrichment platform in head and neck cancer. Annals of Oncology. 34. S561–S561. 1 indexed citations
3.
Janes, Sam M., Jennifer Dickson, Anand Devaraj, et al.. (2019). P1.11-19 Trial in Progress: Cancer Screening Study With or Without Low Dose Lung CT to Validate a Multi-Cancer Early Detection Blood Test. Journal of Thoracic Oncology. 14(10). S523–S523. 5 indexed citations
4.
Chaffee, Kari G., Ann L. Oberg, Robert R. McWilliams, et al.. (2017). Prevalence of germ-line mutations in cancer genes among pancreatic cancer patients with a positive family history. Genetics in Medicine. 20(1). 119–127. 97 indexed citations
5.
Kurian, Allison W., Elisha Hughes, Elizabeth A. Handorf, et al.. (2017). Breast and Ovarian Cancer Penetrance Estimates Derived From Germline Multiple-Gene Sequencing Results in Women. JCO Precision Oncology. 1(1). 1–12. 131 indexed citations
6.
Yurgelun, Matthew B., Matthew H. Kulke, Charles S. Fuchs, et al.. (2017). Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer. Journal of Clinical Oncology. 35(10). 1086–1095. 344 indexed citations breakdown →
7.
Shahda, Safi, Kirsten M. Timms, Julia Reid, et al.. (2017). Homologous recombination deficiency (HRD) in patients with pancreatic cancer (PC) and response to chemotherapy.. Journal of Clinical Oncology. 35(4_suppl). 317–317. 3 indexed citations
8.
Ring, Kari L., Amanda Bruegl, Brian Allen, et al.. (2016). Germline multi-gene hereditary cancer panel testing in an unselected endometrial cancer cohort. Modern Pathology. 29(11). 1381–1389. 86 indexed citations
9.
Petersen, Gloria M., Kari G. Chaffee, Robert R. McWilliams, et al.. (2016). Genetic heterogeneity and survival among pancreatic adenocarcinoma (PDAC) patients with positive family history.. Journal of Clinical Oncology. 34(15_suppl). 4108–4108. 9 indexed citations
10.
Kurian, Allison W., Elisha Hughes, Elizabeth A. Handorf, et al.. (2016). Association of ovarian cancer (OC) risk with mutations detected by multiple-gene germline sequencing in 95,561 women.. Journal of Clinical Oncology. 34(15_suppl). 5510–5510. 2 indexed citations
11.
Yurgelun, Matthew B., Brian Allen, Rajesh Kaldate, et al.. (2015). Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome. Gastroenterology. 149(3). 604–613.e20. 184 indexed citations
12.
Yang, Kathleen Y., Brian Allen, Peggy Conrad, et al.. (2006). Awareness of gynecologic surveillance in women from hereditary non-polyposis colorectal cancer families. Familial Cancer. 5(4). 405–409. 5 indexed citations
13.
Truta, Brindusa, Brian Allen, Peggy Conrad, et al.. (2005). A comparison of the phenotype and genotype in adenomatous polyposis patients with and without a family history. Familial Cancer. 4(2). 127–133. 22 indexed citations
14.
Lu, Karen H., Wendy Kohlmann, Patrice Watson, et al.. (2005). Gynecologic Cancer as a “Sentinel Cancer” for Women With Hereditary Nonpolyposis Colorectal Cancer Syndrome. Obstetrics and Gynecology. 105(3). 569–574. 251 indexed citations
15.
Velayos, Fernando, Brian Allen, Peggy Conrad, et al.. (2005). Low Rate of Microsatellite Instability in Young Patients with Adenomas: Reassessing the Bethesda Guidelines. The American Journal of Gastroenterology. 100(5). 1143–1149. 35 indexed citations
16.
Kane, Mark, John Holt, & Brian Allen. (2004). Results concerning the generalized partially linear single-index model. Journal of Statistical Computation and Simulation. 74(12). 897–912. 2 indexed citations
17.
Allen, Brian & Jonathan P. Terdiman. (2003). Hereditary polyposis syndromes and hereditary non-polyposis colorectal cancer. Best Practice & Research Clinical Gastroenterology. 17(2). 237–258. 37 indexed citations
18.
Truta, Brindusa, Brian Allen, Peggy Conrad, et al.. (2003). Genotype and phenotype of patients with both familial adenomatous polyposis and thyroid carcinoma. Familial Cancer. 2(2). 95–99. 45 indexed citations
19.
Reyes, Carolina, Brian Allen, Jonathan P. Terdiman, & Leslie Wilson. (2002). Comparison of selection strategies for genetic testing of patients with hereditary nonpolyposis colorectal carcinoma. Cancer. 95(9). 1848–1856. 62 indexed citations
20.
Terdiman, Jonathan P., Theodore R. Levin, Brian Allen, et al.. (2002). Hereditary nonpolyposis colorectal cancer in young colorectal cancer patients: High-risk clinic versus population-based registry. Gastroenterology. 122(4). 940–947. 27 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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