Heather L. Hampel

4.0k total citations · 2 hit papers
11 papers, 2.5k citations indexed

About

Heather L. Hampel is a scholar working on Pathology and Forensic Medicine, Genetics and Cancer Research. According to data from OpenAlex, Heather L. Hampel has authored 11 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Pathology and Forensic Medicine, 6 papers in Genetics and 6 papers in Cancer Research. Recurrent topics in Heather L. Hampel's work include Genetic factors in colorectal cancer (7 papers), Cancer Genomics and Diagnostics (6 papers) and BRCA gene mutations in cancer (6 papers). Heather L. Hampel is often cited by papers focused on Genetic factors in colorectal cancer (7 papers), Cancer Genomics and Diagnostics (6 papers) and BRCA gene mutations in cancer (6 papers). Heather L. Hampel collaborates with scholars based in United States. Heather L. Hampel's co-authors include Sapna Syngal, James M. Church, Francis M. Giardiello, Randall W. Burt, Randall E. Brand, Stephanie Melillo, Glenn E. Palomaki, Monica R. McClain, Stephen N. Thibodeau and Stephen J. Salipante and has published in prestigious journals such as Journal of Clinical Investigation, Journal of Clinical Oncology and International Journal of Cancer.

In The Last Decade

Heather L. Hampel

9 papers receiving 2.4k citations

Hit Papers

ACG Clinical Guideline: Genetic Testing and Management of... 2015 2026 2018 2022 2015 2015 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Heather L. Hampel United States 8 1.7k 1.3k 875 718 452 11 2.5k
Matthew B. Yurgelun United States 24 1.4k 0.8× 1.3k 1.0× 939 1.1× 487 0.7× 457 1.0× 84 2.3k
Jennifer E. Axilbund United States 17 1.4k 0.9× 1.9k 1.5× 719 0.8× 357 0.5× 663 1.5× 27 2.5k
Brian Allen United States 17 1.4k 0.9× 1.2k 0.9× 946 1.1× 996 1.4× 206 0.5× 39 2.4k
Brandie Heald United States 24 1.0k 0.6× 753 0.6× 417 0.5× 458 0.6× 402 0.9× 97 1.8k
Leigha Senter United States 23 925 0.6× 904 0.7× 688 0.8× 971 1.4× 217 0.5× 74 2.2k
H. Lynch United States 13 3.0k 1.8× 2.4k 1.9× 1.2k 1.4× 941 1.3× 427 0.9× 16 3.7k
Peggy Conrad United States 18 1.3k 0.8× 884 0.7× 504 0.6× 416 0.6× 216 0.5× 26 1.7k
H. Mignotte France 22 800 0.5× 591 0.5× 922 1.1× 377 0.5× 417 0.9× 57 1.7k
Roger E. Moe United States 23 1.0k 0.6× 1.1k 0.8× 1.4k 1.6× 262 0.4× 611 1.4× 39 2.4k
Rachel Pearlman United States 17 873 0.5× 624 0.5× 623 0.7× 307 0.4× 174 0.4× 33 1.3k

Countries citing papers authored by Heather L. Hampel

Since Specialization
Citations

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

Fields of papers citing papers by Heather L. Hampel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Heather L. Hampel. 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 Heather L. Hampel. The network helps show where Heather L. Hampel may publish in the future.

Co-authorship network of co-authors of Heather L. Hampel

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

All Works

11 of 11 papers shown
1.
Toland, Amanda Ewart, Carolyn J. Presley, Heather L. Hampel, et al.. (2024). A video intervention to improve patient understanding of tumor genomic testing in patients with cancer. Cancer Medicine. 13(17). e70095–e70095.
2.
Syngal, Sapna, Randall E. Brand, James M. Church, et al.. (2015). ACG Clinical Guideline: Genetic Testing and Management of Hereditary Gastrointestinal Cancer Syndromes. The American Journal of Gastroenterology. 110(2). 223–262. 1007 indexed citations breakdown →
3.
Robson, Mark E., Angela R. Bradbury, Banu Arun, et al.. (2015). American Society of Clinical Oncology Policy Statement Update: Genetic and Genomic Testing for Cancer Susceptibility. Journal of Clinical Oncology. 33(31). 3660–3667. 512 indexed citations breakdown →
4.
Feero, W, Flavia M. Facio, Emily Glogowski, et al.. (2014). Preliminary validation of a consumer-oriented colorectal cancer risk assessment tool compatible with the US Surgeon General’s My Family Health Portrait. Genetics in Medicine. 17(9). 753–756. 7 indexed citations
5.
Rios, Jonathan J., Victoria Mgbemena, Heather L. Hampel, et al.. (2014). Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic. EBioMedicine. 2(1). 74–81. 36 indexed citations
6.
Salipante, Stephen J., et al.. (2014). Microsatellite Instability Detection by Next Generation Sequencing. Clinical Chemistry. 60(9). 1192–1199. 283 indexed citations
7.
Espenschied, Carin R., et al.. (2012). Reflex Immunohistochemistry and Microsatellite Instability Testing of Colorectal Tumors for Lynch Syndrome Among US Cancer Programs and Follow-Up of Abnormal Results. Journal of Clinical Oncology. 30(10). 1058–1063. 159 indexed citations
8.
Palomaki, Glenn E., Monica R. McClain, Stephanie Melillo, Heather L. Hampel, & Stephen N. Thibodeau. (2009). EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome. Genetics in Medicine. 11(1). 42–65. 357 indexed citations
9.
Chen, Huiping, Nicholas P. Taylor, Kaisa Sotamaa, et al.. (2007). Evidence for heritable predisposition to epigenetic silencing of MLH1. International Journal of Cancer. 120(8). 1684–1688. 64 indexed citations
10.
Bennett, Robin L., Heather L. Hampel, Jessica B. Mandell, & Joan H. Marks. (2003). Genetic counselors: translating genomic science into clinical practice. Journal of Clinical Investigation. 112(9). 1274–1279. 32 indexed citations
11.
Bennett, Robin L., Heather L. Hampel, Jessica B. Mandell, & Joan H. Marks. (2003). Genetic counselors: translating genomic science into clinical practice. Journal of Clinical Investigation. 112(9). 1274–1279.

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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