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, Johnathan M. Lancaster, Krystal Brown, John Kidd, Mary B. Daly and John F. Sandbach 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

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Non-Melanoma Skin Cancers and Other Cutaneous Manifestations in Bone Marrow Failure Syndromes and Rare DNA Repair Disorders 2022 ·Frontiers in Oncology ·(unknown), Amanda Gammon, Wendy Kohlmann, Joanne Jeter	3
2	Researcher Knowledge, Attitudes, and Communication Practices for Genomic Data Sharing 2020 ·Journal of Empirical Research on Human Research Ethics ·(unknown), (unknown), Amanda Gammon, Jorge L. Contreras, Kimberly A. Kaphingst	0
3	Pancreatic cancer as a sentinel for hereditary cancer predisposition 2018 ·BMC Cancer ·Erin L. Young, Bryony A. Thompson, Deborah W. Neklason, Matthew A. Firpo, Theresa L. Werner, Russell Bell, (unknown), Alison Fraser, Amanda Gammon, (unknown), Wendy Kohlmann, Leigh Neumayer, David E. Goldgar, Sean J. Mulvihill, Lisa Cannon‐Albright, Sean V. Tavtigian	41
4	Rare hereditary cause of chronic pancreatitis in a young male: SPINK1 mutation 2017 ·Pan African Medical Journal ·(unknown), (unknown), Amanda Gammon, Michael Sossenheimer, N. Jewel Samadder	4
5	Genetic basis of Cowden syndrome and its implications for clinical practice and risk management 2016 ·The Application of Clinical Genetics ·Amanda Gammon, Kory Jasperson, (unknown)	40
6	Confidentiality & the Risk of Genetic Discrimination 2015 ·Surgical Oncology Clinics of North America ·Amanda Gammon, Deborah W. Neklason	8
7	Appreciating the broad clinical features of SMAD4 mutation carriers: a multicenter chart review 2014 ·Genetics in Medicine ·Karen E. Wain, Marissa S. Ellingson, Jamie McDonald, Amanda Gammon, Maegan E. Roberts, Pavel N. Pichurin, Ingrid Winship, Douglas L. Riegert‐Johnson, Jeffrey N. Weitzel, Noralane M. Lindor	54
8	Interest and Informational Preferences Regarding Genomic Testing for Modest Increases in Colorectal Cancer Risk 2014 ·Public Health Genomics ·Amber Anderson, Kristina G. Flores, Watcharaporn Boonyasiriwat, Amanda Gammon, Wendy Kohlmann, Wendy C. Birmingham, Mark D. Schwartz, Jewel Samadder, Kenneth M. Boucher, Anita Y. Kinney	18
9	Expanding Access to BRCA1/2 Genetic Counseling with Telephone Delivery: A Cluster Randomized Trial 2014 ·JNCI Journal of the National Cancer Institute ·Anita Y. Kinney, Karina Butler, Mark D. Schwartz, Jeanne S. Mandelblatt, Kenneth M. Boucher, (unknown), Amanda Gammon, Wendy Kohlmann, Sandra L. Edwards, Antoinette M. Stroup, Saundra S. Buys, Kristina G. Flores, Rebecca Campo	87
10	Implementation of Best Practices Regarding Treatment Fidelity in the Family Colorectal Cancer Awareness and Risk Education Randomized Controlled Trial 2014 ·SAGE Open ·Rebecca G. Simmons, Scott T. Walters, Lisa M. Pappas, Kenneth M. Boucher, Watcharaporn Boonyasiriwat, Amanda Gammon, Sally W. Vernon, (unknown), Antoinette M. Stroup, Anita Y. Kinney	3
11	Role of rapid sequence whole-body MRI screening in SDH-associated hereditary paraganglioma families 2013 ·Familial Cancer ·Kory Jasperson, Wendy Kohlmann, Amanda Gammon, (unknown), Luke Buchmann, Jason P. Hunt, Anne C. Kirchhoff, H. Jack Baskin, Akram M. Shaaban, Joshua D. Schiffman	70
12	Serrated Polyposis 2013 ·Diseases of the Colon & Rectum ·Kory Jasperson, Priyanka Kanth, Anne C. Kirchhoff, (unknown), Amanda Gammon, Wendy Kohlmann, Randall W. Burt, N. Jewel Samadder	28
13	Classification of missense substitutions in the BRCA genes: A database dedicated to Ex-UVs 2011 ·Human Mutation ·Maxime Vallée, (unknown), (unknown), Davit Babikyan, Fabienne Lesueur, Amanda Gammon, David E. Goldgar, Fergus J. Couch, Sean V. Tavtigian	51
14	Patient outcomes associated with group and individual genetic counseling formats 2011 ·Familial Cancer ·Erin Rothwell, Wendy Kohlmann, Kory Jasperson, Amanda Gammon, Bob Wong, Anita Y. Kinney	20
15	Awareness and Preferences Regarding BRCA1/2 Genetic Counseling and Testing Among Latinas and Non‐Latina White Women at Increased Risk for Hereditary Breast and Ovarian Cancer 2011 ·Journal of Genetic Counseling ·Amanda Gammon, Erin Rothwell, Rebecca G. Simmons, Jan T. Lowery, (unknown), Deirdre A. Hill, Kenneth M. Boucher, Anita Y. Kinney	44
16	Exploring attitudes, beliefs, and communication preferences of Latino community members regarding BRCA1/2 mutation testing and preventive strategies 2010 ·Genetics in Medicine ·Anita Y. Kinney, Amanda Gammon, James E. Coxworth, Sara E. Simonsen, (unknown)	88
17	Hamartomatous polyposis syndromes 2009 ·Best Practice & Research Clinical Gastroenterology ·Amanda Gammon, Kory Jasperson, Wendy Kohlmann, Randall W. Burt	92
18	Can We Identify the High-Risk Patients to Be Screened? A Genetic Approach 2007 ·Digestion ·Amanda Gammon, Wendy Kohlmann, Randall W. Burt	7
19	Impaired Intestinal Absorption of Dipeptide in Tropical Sprue Patients in India 1980 ·Clinical Science ·M.D. Hellier, V. Ganapathy, Amanda Gammon, V. I. Mathan, A.N. Radhakrishnan	4
20	Intestinal absorption in normal Indian and English people. 1976 ·BMJ ·M.D. Hellier, A.N. Radhakrishnan, V. Ganapathy, Amanda Gammon, S. J. Baker	10

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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