Carolyn Deters

700 total citations
11 papers, 386 citations indexed

About

Carolyn Deters is a scholar working on Pathology and Forensic Medicine, Cancer Research and Oncology. According to data from OpenAlex, Carolyn Deters has authored 11 papers receiving a total of 386 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pathology and Forensic Medicine, 9 papers in Cancer Research and 6 papers in Oncology. Recurrent topics in Carolyn Deters's work include Cancer Genomics and Diagnostics (9 papers), Genetic factors in colorectal cancer (9 papers) and Pancreatic and Hepatic Oncology Research (6 papers). Carolyn Deters is often cited by papers focused on Cancer Genomics and Diagnostics (9 papers), Genetic factors in colorectal cancer (9 papers) and Pancreatic and Hepatic Oncology Research (6 papers). Carolyn Deters collaborates with scholars based in United States, Canada and Spain. Carolyn Deters's co-authors include Henry T. Lynch, Jane F. Lynch, Randall E. Brand, David Hogg, Ramon M. Fusaro, Norman J. Lassam, Ling Liu, Scott E. Kern, Joseph A. Knezetic and Michael Goggins and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Cancer and Oncogene.

In The Last Decade

Carolyn Deters

11 papers receiving 375 citations

Peers

Carolyn Deters

ONCOL

CR

PFM

MB

GENET

P. Cusumano Belgium

B. Högel Germany

Zuzana Kos Canada

T Frebourg France

LFA Wessels Netherlands

Fléjou Jf France

B. Szynglarewicz Poland

Bárbara Alemar Brazil

Nathalie L.G. Sieben Netherlands

Ann Forslund United States

P. Cusumano Belgium

Carolyn Deters

179 ×0.6

ONCOL

168 ×0.9

CR

78 ×0.6

PFM

79 ×0.7

MB

27 ×0.4

GENET

Citations per year, relative to Carolyn Deters Carolyn Deters (= 1×) peers P. Cusumano

Countries citing papers authored by Carolyn Deters

Since Specialization

Citations

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

Fields of papers citing papers by Carolyn Deters

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carolyn Deters

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

All Works

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11 of 11 papers shown

1.

Tarafa, Gemma, David Tuck, Daniela P. Ladner, et al.. (2008). Mutational load distribution analysis yields metrics reflecting genetic instability during pancreatic carcinogenesis. Proceedings of the National Academy of Sciences. 105(11). 4306–4311. 11 indexed citations

2.

Lynch, Henry T., Carolyn Deters, Carrie Snyder, et al.. (2005). BRCA1 and pancreatic cancer: pedigree findings and their causal relationships. Cancer Genetics and Cytogenetics. 158(2). 119–125. 70 indexed citations

3.

Lynch, Henry T., Carolyn Deters, Jane F. Lynch, & Randall E. Brand. (2004). Familial pancreatic carcinoma in Jews. Familial Cancer. 3(3-4). 233–240. 29 indexed citations

4.

Liu, Ling, Ron Agatep, Anne Summers, et al.. (2003). Germline splicing mutations of CDKN2A predispose to melanoma. Oncogene. 22(41). 6387–6394. 24 indexed citations

5.

Lynch, Henry T., et al.. (2003). Familial sarcoma. Cancer. 98(9). 1947–1957. 28 indexed citations

6.

Lynch, Henry T., et al.. (2002). Challenging Pancreatic Cancer-Prone Pedigrees: A Nosologic Dilemma. The American Journal of Gastroenterology. 97(12). 3062–3070. 1 indexed citations

7.

Lynch, Henry T., Randall E. Brand, Carolyn Deters, Trudy G. Shaw, & Jane F. Lynch. (2001). Hereditary Pancreatic Cancer. Pancreatology. 1(5). 466–471. 39 indexed citations

8.

Lynch, Henry T., Randall E. Brand, Carolyn Deters, & Ramon M. Fusaro. (2001). Update on familial pancreatic cancer. Current Gastroenterology Reports. 3(2). 121–128. 3 indexed citations

9.

Lynch, Henry T., Randall E. Brand, David Hogg, et al.. (2001). Phenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma–pancreatic carcinoma–prone families. Cancer. 94(1). 84–96. 163 indexed citations

10.

Evans, Sue, Stephen J. Lemon, Carolyn Deters, et al.. (1997). Using data mining to characterize DNA mutations by patient clinical features.. PubMed. 253–7. 3 indexed citations

11.

Evans, Sue, Stephen J. Lemon, Carolyn Deters, Ramon M. Fusaro, & Henry T. Lynch. (1997). Automated Detection of Hereditary Syndromes Using Data Mining. Computers and Biomedical Research. 30(5). 337–348. 15 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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