Kory Jasperson

4.3k total citations · 1 hit paper
39 papers, 1.8k citations indexed

About

Kory Jasperson is a scholar working on Pathology and Forensic Medicine, Oncology and Cancer Research. According to data from OpenAlex, Kory Jasperson has authored 39 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Pathology and Forensic Medicine, 20 papers in Oncology and 9 papers in Cancer Research. Recurrent topics in Kory Jasperson's work include Genetic factors in colorectal cancer (30 papers), Colorectal Cancer Screening and Detection (16 papers) and Colorectal Cancer Treatments and Studies (11 papers). Kory Jasperson is often cited by papers focused on Genetic factors in colorectal cancer (30 papers), Colorectal Cancer Screening and Detection (16 papers) and Colorectal Cancer Treatments and Studies (11 papers). Kory Jasperson collaborates with scholars based in United States, Canada and Israel. Kory Jasperson's co-authors include Randall W. Burt, Deborah W. Neklason, Thérèse M.F. Tuohy, Amanda Gammon, Wendy Kohlmann, N. Jewel Samadder, Heather Hampel, Swati Patel, Dennis J. Ahnen and Leigha Senter and has published in prestigious journals such as Gastroenterology, The Journal of Clinical Endocrinology & Metabolism and Nature Reviews Gastroenterology & Hepatology.

In The Last Decade

Kory Jasperson

38 papers receiving 1.8k citations

Hit Papers

Hereditary and Familial Colon Cancer 2010 2026 2015 2020 2010 250 500 750

Peers

Kory Jasperson
Stephen J. Lanspa United States
Thomas J. McGarrity United States
Thomas K. Weber United States
Kuk Jin Choe South Korea
Jill D. Brensinger United States
Steven T. Brower United States
James A. Knost United States
Brenda Diergaarde United States
Stephen J. Lanspa United States
Kory Jasperson
Citations per year, relative to Kory Jasperson Kory Jasperson (= 1×) peers Stephen J. Lanspa

Countries citing papers authored by Kory Jasperson

Since Specialization
Citations

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

Fields of papers citing papers by Kory Jasperson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kory Jasperson

This figure shows the co-authorship network connecting the top 25 collaborators of Kory Jasperson. A scholar is included among the top collaborators of Kory Jasperson 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 Kory Jasperson. Kory Jasperson 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.
Aronson, Melyssa, Chrystelle Colas, Andrew Y. Shuen, et al.. (2021). Diagnostic criteria for constitutional mismatch repair deficiency (CMMRD): recommendations from the international consensus working group. Journal of Medical Genetics. 59(4). 318–327. 57 indexed citations
2.
LaDuca, Holly, Mary Helen Black, Dajun Qian, et al.. (2018). Monoallelic MUTYH carrier status is not associated with increased breast cancer risk in a multigene panel cohort. Familial Cancer. 18(2). 197–201. 17 indexed citations
3.
Aronson, Melyssa, et al.. (2018). Delineating a new feature of constitutional mismatch repair deficiency (CMMRD) syndrome: breast cancer. Familial Cancer. 18(1). 105–108. 5 indexed citations
4.
Stanich, Peter P., Rachel Pearlman, Alice Hinton, et al.. (2018). Prevalence of Germline Mutations in Polyposis and Colorectal Cancer–Associated Genes in Patients With Multiple Colorectal Polyps. Clinical Gastroenterology and Hepatology. 17(10). 2008–2015.e3. 45 indexed citations
5.
Jasperson, Kory, Ignacio Garrido‐Laguna, Howard Colman, et al.. (2017). A 30-Year-Old Man with Three Primary Malignancies: A Case of Constitutional Mismatch Repair Deficiency. ACG Case Reports Journal. 4(1). e34–e34. 3 indexed citations
6.
Jasperson, Kory, N. Jewel Samadder, Wade S. Samowitz, et al.. (2017). Colon Pathology Characteristics in Li–Fraumeni Syndrome. Clinical Gastroenterology and Hepatology. 16(1). 140–141. 5 indexed citations
7.
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
8.
Jasperson, Kory & Randall W. Burt. (2015). The Genetics of Colorectal Cancer. Surgical Oncology Clinics of North America. 24(4). 683–703. 17 indexed citations
9.
Shaco‐Levy, Ruthy, Kory Jasperson, Katie R. Martin, et al.. (2015). Morphologic characterization of hamartomatous gastrointestinal polyps in Cowden syndrome, Peutz-Jeghers syndrome, and juvenile polyposis syndrome. Human Pathology. 49. 39–48. 35 indexed citations
10.
Samadder, N. Jewel, Kory Jasperson, & Randall W. Burt. (2014). Hereditary and Common Familial Colorectal Cancer: Evidence for Colorectal Screening. Digestive Diseases and Sciences. 60(3). 734–747. 40 indexed citations
11.
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
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.
Simmons, Rebecca G., Yuan-Chin Amy Lee, Antoinette M. Stroup, et al.. (2013). Examining the challenges of family recruitment to behavioral intervention trials: factors associated with participation and enrollment in a multi-state colonoscopy intervention trial. Trials. 14(1). 116–116. 21 indexed citations
14.
Dorais, Jessie, Mark Dodson, Jacob Calvert, et al.. (2011). Fertility-Sparing Management of Endometrial Adenocarcinoma. Obstetrical & Gynecological Survey. 66(7). 443–451. 17 indexed citations
15.
Seibert, Diane, et al.. (2011). Pre- and postassessment of nurse practitioners' knowledge of hereditary colorectal cancer. Journal of the American Academy of Nurse Practitioners. 23(7). 361–369. 7 indexed citations
16.
Bellcross, Cecelia, Elvan Daniels, Debra Duquette, et al.. (2011). Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: Summary of a public health/clinical collaborative meeting. Genetics in Medicine. 1–1. 1 indexed citations
17.
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
18.
Jasperson, Kory, Thérèse M.F. Tuohy, Deborah W. Neklason, & Randall W. Burt. (2010). Hereditary and Familial Colon Cancer. Gastroenterology. 138(6). 2044–2058. 840 indexed citations breakdown →
19.
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
20.
Jasperson, Kory, Thuy M. Vu, Deborah W. Neklason, et al.. (2009). Evaluating Lynch syndrome in very early onset colorectal cancer probands without apparent polyposis. Familial Cancer. 9(2). 99–107. 22 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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