Peggy Conrad

3.0k total citations · 1 hit paper
26 papers, 1.7k citations indexed

About

Peggy Conrad is a scholar working on Pathology and Forensic Medicine, Oncology and Cancer Research. According to data from OpenAlex, Peggy Conrad has authored 26 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Pathology and Forensic Medicine, 18 papers in Oncology and 6 papers in Cancer Research. Recurrent topics in Peggy Conrad's work include Genetic factors in colorectal cancer (24 papers), Colorectal Cancer Screening and Detection (13 papers) and Colorectal Cancer Treatments and Studies (9 papers). Peggy Conrad is often cited by papers focused on Genetic factors in colorectal cancer (24 papers), Colorectal Cancer Screening and Detection (13 papers) and Colorectal Cancer Treatments and Studies (9 papers). Peggy Conrad collaborates with scholars based in United States, Canada and Spain. Peggy Conrad's co-authors include Jonathan P. Terdiman, Molly S. Daniels, Henry T. Lynch, Karen H. Lu, Mark F. Munsell, Kristin G. White, David M. Gershenson, Charlotte C. Sun, Russell R. Broaddus and Marvin H. Sleisenger and has published in prestigious journals such as New England Journal of Medicine, Journal of Clinical Oncology and Gastroenterology.

In The Last Decade

Peggy Conrad

25 papers receiving 1.6k citations

Hit Papers

Prophylactic Surgery to Reduce the Risk of Gynecologic Ca... 2006 2026 2012 2019 2006 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peggy Conrad United States 18 1.3k 884 504 416 264 26 1.7k
Neil Ryan United Kingdom 22 602 0.5× 509 0.6× 483 1.0× 227 0.5× 383 1.5× 58 1.4k
Valérie Bonadona France 6 592 0.4× 414 0.5× 292 0.6× 322 0.8× 146 0.6× 11 947
Laura Renkonen‐Sinisalo Finland 22 858 0.7× 643 0.7× 346 0.7× 219 0.5× 99 0.4× 48 1.3k
Rachel Pearlman United States 17 873 0.7× 624 0.7× 623 1.2× 307 0.7× 68 0.3× 33 1.3k
Christopher Arnell United States 7 866 0.7× 659 0.7× 530 1.1× 528 1.3× 105 0.4× 14 1.4k
Furio Maggiorotto Italy 20 322 0.2× 516 0.6× 534 1.1× 200 0.5× 151 0.6× 44 1.3k
H. T. Lynch United States 9 911 0.7× 885 1.0× 572 1.1× 545 1.3× 142 0.5× 11 1.5k
Astrid Stormorken Norway 12 643 0.5× 428 0.5× 326 0.6× 234 0.6× 65 0.2× 24 811
Annette Bröcker‐Vriends Netherlands 13 538 0.4× 399 0.5× 365 0.7× 207 0.5× 28 0.1× 14 1.2k
Jai Min Ryu South Korea 18 257 0.2× 365 0.4× 584 1.2× 149 0.4× 66 0.3× 114 1.0k

Countries citing papers authored by Peggy Conrad

Since Specialization
Citations

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

Fields of papers citing papers by Peggy Conrad

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peggy Conrad

This figure shows the co-authorship network connecting the top 25 collaborators of Peggy Conrad. A scholar is included among the top collaborators of Peggy Conrad 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 Peggy Conrad. Peggy Conrad 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.
Kidambi, Trilokesh D., Rita J. Jeremy, Peggy Conrad, et al.. (2016). Differences in neuropsychological and behavioral parameters and brain structure in patients with familial adenomatous polyposis: a sibling-paired study. Hereditary Cancer in Clinical Practice. 14(1). 20–20. 6 indexed citations
2.
Lu, Karen H., David S. Loose, Melinda S. Yates, et al.. (2013). Prospective Multicenter Randomized Intermediate Biomarker Study of Oral Contraceptive versus Depo-Provera for Prevention of Endometrial Cancer in Women with Lynch Syndrome. Cancer Prevention Research. 6(8). 774–781. 69 indexed citations
3.
Yurgelun, Matthew B., Rowena Mercado, Margery Rosenblatt, et al.. (2012). Impact of genetic testing on endometrial cancer risk-reducing practices in women at risk for Lynch syndrome. Gynecologic Oncology. 127(3). 544–551. 20 indexed citations
4.
Kuppermann, Miriam, Grace Wang, Shirley Wong, et al.. (2012). Preferences for outcomes associated with decisions to undergo or forgo genetic testing for Lynch syndrome. Cancer. 119(1). 215–225. 17 indexed citations
5.
Khan, Omar, Amie Blanco, Peggy Conrad, et al.. (2011). Performance of Lynch Syndrome Predictive Models in a Multi-Center US Referral Population. The American Journal of Gastroenterology. 106(10). 1822–1827. 23 indexed citations
6.
Stoffel, Elena M., Rowena Mercado, Wendy Kohlmann, et al.. (2010). Prevalence and Predictors of Appropriate Colorectal Cancer Surveillance in Lynch Syndrome. The American Journal of Gastroenterology. 105(8). 1851–1860. 51 indexed citations
7.
Yeung, Anthony T., Xinming Li, Steven H. Seeholzer, et al.. (2008). One-Hit Effects in Cancer: Altered Proteome of Morphologically Normal Colon Crypts in Familial Adenomatous Polyposis. Cancer Research. 68(18). 7579–7586. 34 indexed citations
8.
Truta, Brindusa, Yunn-Yi Chen, Amie Blanco, et al.. (2008). Tumor histology helps to identify Lynch syndrome among colorectal cancer patients. Familial Cancer. 7(3). 267–274. 10 indexed citations
9.
Stoffel, Elena M., Beth Ford, Rowena Mercado, et al.. (2008). Sharing Genetic Test Results in Lynch Syndrome: Communication With Close and Distant Relatives. Clinical Gastroenterology and Hepatology. 6(3). 333–338. 92 indexed citations
10.
Schmeler, Kathleen M., Henry T. Lynch, Lee-may Chen, et al.. (2006). Prophylactic Surgery to Reduce the Risk of Gynecologic Cancers in the Lynch Syndrome. New England Journal of Medicine. 354(3). 261–269. 516 indexed citations breakdown →
11.
Schmeler, Kathleen M., Henry T. Lynch, Lee-may Chen, et al.. (2006). Prophylactic Surgery to Reduce the Risk of Gynecologic Cancers in the Lynch Syndrome. Obstetrical & Gynecological Survey. 61(5). 319–321. 2 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.
Broaddus, Russell R., Henry T. Lynch, Molly S. Daniels, et al.. (2005). Pathologic features of endometrial carcinoma associated with HNPCC. Cancer. 106(1). 87–94. 214 indexed citations
16.
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
17.
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
18.
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
19.
Terdiman, Jonathan P., James R. Gum, Peggy Conrad, et al.. (2001). Efficient detection of hereditary nonpolyposis colorectal cancer gene carriers by screening for tumor microsatellite instability before germline genetic testing. Gastroenterology. 120(1). 21–30. 126 indexed citations
20.
Terdiman, Jonathan P., Peggy Conrad, & Marvin H. Sleisenger. (1999). Genetic Testing in Hereditary Colorectal Cancer: Indications and Procedures. The American Journal of Gastroenterology. 94(9). 2344–2356. 42 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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