Jeffery P. Struewing

27.3k citations
81 papers · 7.7k indexed · 3 hit papers · h-index 37
Topics
BRCA gene mutations in cancer (43 papers)Cancer Genomics and Diagnostics (22 papers)DNA Repair Mechanisms (16 papers)

In The Last Decade

Jeffery P. Struewing

81 papers receiving 7.5k citations

Hit Papers

The Risk of Cancer Associated with Specific Mutations ofB...199420262004201519971994199550010001.5k

Peers

Jeffery P. Struewing
Comparison fields: 5 of 136
  • Genetics 4.4k
  • Molecular Biology 2.8k
  • Oncology 2.4k
  • Cancer Research 1.9k
  • Pathology and Forensic Medicine 1.4k
Replace Deborah Ford with:
Deborah Ford United Kingdom
Nathan A. Ellis United States
Mark H. Greene United States
Gilbert Lenoir France
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Frederick P. Li United States
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Jeffery P. Struewing relative to Deborah Ford United Kingdom Deborah Ford's profile →
Citations per field
00.5×1.5×1.9×
Deborah Ford · 1×
Citations per year

Countries citing papers authored by Jeffery P. Struewing

Since Specialization
Citations

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

Fields of papers citing papers by Jeffery P. Struewing

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jeffery P. Struewing. 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 Jeffery P. Struewing. The network helps show where Jeffery P. Struewing may publish in the future.

Co-authorship network of co-authors of Jeffery P. Struewing

This figure shows the co-authorship network connecting the top 25 collaborators of Jeffery P. Struewing. A scholar is included among the top collaborators of Jeffery P. Struewing 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 Jeffery P. Struewing. Jeffery P. Struewing 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
#WorkIndexed citations
1 8
2 18
3 6
4 129
5
DNA damage in breast cancer plus another primary cancer, early onset breast cancer, thyroid cancer and cancer-free individuals
1
6 52
7 3
8
A Natural History of Melanomas and Dysplastic Nevi: An Atlas of Lesions in Melanoma-Prone Families
6
9 23
10 17
11 39
12 129
13 13
14
The Risk of Cancer Associated with Specific Mutations ofBRCA1andBRCA2among Ashkenazi Jewsbreakdown →
1677
15 298
16
The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individualsbreakdown →
512
17 85
18 10
19 15
20 22

About Jeffery P. Struewing

Jeffery P. Struewing is a scholar working on Genetics, Cancer Research and Reproductive Medicine, having authored 81 papers that have together received 7.7k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (43 papers), Cancer Genomics and Diagnostics (22 papers) and DNA Repair Mechanisms (16 papers). The work is most often cited by research in Genetics (4.4k citations), Reproductive Medicine (1.1k citations) and Cancer Research (1.9k citations). Jeffery P. Struewing has collaborated with scholars based in United States, Israel and Canada. Frequent co-authors include Lawrence C. Brody, Margaret A. Tucker, Sholom Wacholder, Patricia Hartge, Mary McAdams, Nicholas C. Dracopoli, Christopher J. Hussussian, M. A. Tucker, Delphine S. Ally and Paul Higgins. Their work appears in journals such as New England Journal of Medicine, The Lancet and Nature Genetics.

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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