Amanda Gammon

1.9k total citations
34 papers, 1.1k citations indexed

About

Amanda Gammon is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Amanda Gammon has authored 34 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 7 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Amanda Gammon's work include BRCA gene mutations in cancer (19 papers), Genetic factors in colorectal cancer (5 papers) and Ethics in Clinical Research (5 papers). Amanda Gammon is often cited by papers focused on BRCA gene mutations in cancer (19 papers), Genetic factors in colorectal cancer (5 papers) and Ethics in Clinical Research (5 papers). Amanda Gammon collaborates with scholars based in United States, United Kingdom and Australia. Amanda Gammon's co-authors include Kory Jasperson, Wendy Kohlmann, Anita Y. Kinney, Saundra S. Buys, Randall W. Burt, John F. Sandbach, Mary B. Daly, Krystal Brown, John Kidd and Jennifer Saam and has published in prestigious journals such as Journal of Clinical Oncology, JNCI Journal of the National Cancer Institute and Cancer.

In The Last Decade

Amanda Gammon

32 papers receiving 1.1k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Amanda Gammon 678 317 282 261 251 34 1.1k
Daniela Turchetti 589 0.9× 250 0.8× 219 0.8× 397 1.5× 293 1.2× 94 1.2k
Kristen M. Shannon 771 1.1× 419 1.3× 570 2.0× 342 1.3× 312 1.2× 43 1.5k
Leon C. Verhoog 860 1.3× 337 1.1× 251 0.9× 209 0.8× 411 1.6× 9 1.1k
Mercedes Castiel 825 1.2× 311 1.0× 249 0.9× 194 0.7× 220 0.9× 16 1.4k
Carina C. M. Bartels 962 1.4× 358 1.1× 221 0.8× 186 0.7× 401 1.6× 11 1.2k
Lisa R. Susswein 575 0.8× 192 0.6× 331 1.2× 236 0.9× 249 1.0× 25 913
Susan Randall Armel 963 1.4× 536 1.7× 251 0.9× 331 1.3× 352 1.4× 51 1.5k
Charité Ricker 871 1.3× 258 0.8× 213 0.8× 297 1.1× 262 1.0× 60 1.1k
Amy Finch 1.1k 1.6× 333 1.1× 256 0.9× 198 0.8× 205 0.8× 29 1.6k
Jessica N. Everett 316 0.5× 312 1.0× 306 1.1× 149 0.6× 397 1.6× 30 985

Countries citing papers authored by Amanda Gammon

Since Specialization
Citations

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

Fields of papers citing papers by Amanda Gammon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amanda Gammon

This figure shows the co-authorship network connecting the top 25 collaborators of Amanda Gammon. A scholar is included among the top collaborators of Amanda Gammon 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 Amanda Gammon. Amanda Gammon 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.
Gammon, Amanda, et al.. (2022). Non-Melanoma Skin Cancers and Other Cutaneous Manifestations in Bone Marrow Failure Syndromes and Rare DNA Repair Disorders. Frontiers in Oncology. 12. 837059–837059. 3 indexed citations
2.
Birmingham, Wendy C., et al.. (2019). Female family members lack understanding of indeterminate negative BRCA1/2 test results shared by probands. Journal of Genetic Counseling. 28(5). 950–961. 3 indexed citations
3.
Young, Erin L., Bryony A. Thompson, Deborah W. Neklason, et al.. (2018). Pancreatic cancer as a sentinel for hereditary cancer predisposition. BMC Cancer. 18(1). 697–697. 41 indexed citations
4.
Gammon, Amanda, et al.. (2017). Rare hereditary cause of chronic pancreatitis in a young male: SPINK1 mutation. Pan African Medical Journal. 28. 110–110. 4 indexed citations
5.
Steffen, Laurie E., Ruofei Du, Amanda Gammon, et al.. (2017). Genetic Testing in a Population-Based Sample of Breast and Ovarian Cancer Survivors from the REACH Randomized Trial: Cost Barriers and Moderators of Counseling Mode. Cancer Epidemiology Biomarkers & Prevention. 26(12). 1772–1780. 22 indexed citations
6.
Gammon, Amanda, et al.. (2016). Genetic basis of Cowden syndrome and its implications for clinical practice and risk management. The Application of Clinical Genetics. Volume 9. 83–92. 40 indexed citations
7.
Gammon, Amanda & Deborah W. Neklason. (2015). Confidentiality & the Risk of Genetic Discrimination. Surgical Oncology Clinics of North America. 24(4). 667–681. 8 indexed citations
8.
Kinney, Anita Y., Karina Butler, Mark D. Schwartz, et al.. (2014). Expanding Access to BRCA1/2 Genetic Counseling with Telephone Delivery: A Cluster Randomized Trial. JNCI Journal of the National Cancer Institute. 106(12). dju328–dju328. 87 indexed citations
9.
Wain, Karen E., Marissa S. Ellingson, Jamie McDonald, et al.. (2014). Appreciating the broad clinical features of SMAD4 mutation carriers: a multicenter chart review. Genetics in Medicine. 16(8). 588–593. 54 indexed citations
10.
Anderson, Amber, Kristina G. Flores, Watcharaporn Boonyasiriwat, et al.. (2014). Interest and Informational Preferences Regarding Genomic Testing for Modest Increases in Colorectal Cancer Risk. Public Health Genomics. 17(1). 48–60. 18 indexed citations
11.
Simmons, Rebecca G., Scott T. Walters, Lisa M. Pappas, et al.. (2014). Implementation of Best Practices Regarding Treatment Fidelity in the Family Colorectal Cancer Awareness and Risk Education Randomized Controlled Trial. SAGE Open. 4(4). 3 indexed citations
12.
Jasperson, Kory, Priyanka Kanth, Anne C. Kirchhoff, et al.. (2013). Serrated Polyposis. Diseases of the Colon & Rectum. 56(11). 1211–1216. 28 indexed citations
13.
Jasperson, Kory, Wendy Kohlmann, Amanda Gammon, et al.. (2013). Role of rapid sequence whole-body MRI screening in SDH-associated hereditary paraganglioma families. Familial Cancer. 13(2). 257–265. 70 indexed citations
14.
Vallée, Maxime, Davit Babikyan, Fabienne Lesueur, et al.. (2011). Classification of missense substitutions in the BRCA genes: A database dedicated to Ex-UVs. Human Mutation. 33(1). 22–28. 51 indexed citations
15.
Rothwell, Erin, Wendy Kohlmann, Kory Jasperson, et al.. (2011). Patient outcomes associated with group and individual genetic counseling formats. Familial Cancer. 11(1). 97–106. 20 indexed citations
16.
17.
Gammon, Amanda, Kory Jasperson, Wendy Kohlmann, & Randall W. Burt. (2009). Hamartomatous polyposis syndromes. Best Practice & Research Clinical Gastroenterology. 23(2). 219–231. 92 indexed citations
18.
Gammon, Amanda, Wendy Kohlmann, & Randall W. Burt. (2007). Can We Identify the High-Risk Patients to Be Screened? A Genetic Approach. Digestion. 76(1). 7–19. 7 indexed citations
19.
Hellier, M.D., V. Ganapathy, Amanda Gammon, V. I. Mathan, & A.N. Radhakrishnan. (1980). Impaired Intestinal Absorption of Dipeptide in Tropical Sprue Patients in India. Clinical Science. 58(5). 431–433. 4 indexed citations
20.
Hellier, M.D., A.N. Radhakrishnan, V. Ganapathy, Amanda Gammon, & S. J. Baker. (1976). Intestinal absorption in normal Indian and English people.. BMJ. 1(6003). 186–188. 10 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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