Kevin Sweet

3.9k total citations
48 papers, 1.6k citations indexed

About

Kevin Sweet is a scholar working on Genetics, Oncology and Molecular Biology. According to data from OpenAlex, Kevin Sweet has authored 48 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 13 papers in Oncology and 12 papers in Molecular Biology. Recurrent topics in Kevin Sweet's work include BRCA gene mutations in cancer (29 papers), Genomics and Rare Diseases (12 papers) and Genetic factors in colorectal cancer (11 papers). Kevin Sweet is often cited by papers focused on BRCA gene mutations in cancer (29 papers), Genomics and Rare Diseases (12 papers) and Genetic factors in colorectal cancer (11 papers). Kevin Sweet collaborates with scholars based in United States, Switzerland and Canada. Kevin Sweet's co-authors include Charis Eng, Rebecca Nagy, Judith A. Westman, Amanda E. Toland, Mary C. Phelan, Steven R. Shaw, Desmond P. Kelly, Heather E. McDermid, R. Curtis Rogers and Robert A. Saul and has published in prestigious journals such as JAMA, Journal of Clinical Oncology and PLoS ONE.

In The Last Decade

Kevin Sweet

47 papers receiving 1.5k citations

Peers

Kevin Sweet

GENET

ONCOL

PFM

Nancie Petrucelli United States

Cora M. Aalfs Netherlands

Audrey Ardern‐Jones United Kingdom

Daniela Turchetti Italy

Kathleen R. Blazer United States

Laura M. Amendola United States

Dorothea Gadzicki Germany

Jill E. Stopfer United States

Martin J. Larsen Denmark

Nina Ditsch Germany

Nancie Petrucelli United States

Kevin Sweet

741 ×0.8

GENET

355 ×0.7

251 ×0.6

ONCOL

203 ×0.5

PFM

224 ×1.0

Citations per year, relative to Kevin Sweet Kevin Sweet (= 1×) peers Nancie Petrucelli

Countries citing papers authored by Kevin Sweet

Since Specialization

Citations

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

Fields of papers citing papers by Kevin Sweet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kevin Sweet

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

All Works

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20 of 20 papers shown

Sweet, Kevin, Paul L. Reiter, Patrick Schnell, et al.. (2023). Genetic counseling and testing for females at elevated risk for breast cancer: Protocol for the randomized controlled trial of the Know Your Risk intervention. Contemporary Clinical Trials. 133. 107323–107323. 2 indexed citations

Katz, Mira L., Leigha Senter, Paul L. Reiter, et al.. (2022). Development of a web-based, theory-guided narrative intervention for women at elevated risk for breast cancer. Patient Education and Counseling. 106. 163–169. 1 indexed citations

Phillips, Shannon, et al.. (2022). Hospital-based ovarian cancer patient traceback program results in minimal genetic testing uptake. Gynecologic Oncology. 164(3). 615–621. 6 indexed citations

Subhawong, Ty K., Kevin Sweet, Noam Alperin, et al.. (2021). MRI Volumetrics and Image Texture Analysis in Assessing Systemic Treatment Response in Extra-Abdominal Desmoid Fibromatosis. Radiology Imaging Cancer. 3(4). e210016–e210016. 17 indexed citations

Schmidlen, Tara, Amy C. Sturm, Shelly R. Hovick, et al.. (2018). Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing. Journal of Genetic Counseling. 27(5). 1111–1129. 22 indexed citations

Sturm, Amy C., Tara Schmidlen, Laura Scheinfeldt, et al.. (2018). Early Outcome Data Assessing Utility of a Post-Test Genomic Counseling Framework for the Scalable Delivery of Precision Health. Journal of Personalized Medicine. 8(3). 25–25. 9 indexed citations

Sweet, Kevin, Amy C. Sturm, Tara Schmidlen, et al.. (2017). Outcomes of a Randomized Controlled Trial of Genomic Counseling for Patients Receiving Personalized and Actionable Complex Disease Reports. Journal of Genetic Counseling. 26(5). 980–998. 17 indexed citations

Sweet, Kevin, Dennis Shaw, & Teresa Chapman. (2017). Cerebral palsy and seizures in a child with tubulinopathy pattern dysgenesis and focal cortical dysplasia. Radiology Case Reports. 12(2). 396–400. 2 indexed citations

Sweet, Kevin, Shelly R. Hovick, Amy C. Sturm, et al.. (2016). Counselees’ Perspectives of Genomic Counseling Following Online Receipt of Multiple Actionable Complex Disease and Pharmacogenomic Results: a Qualitative Research Study. Journal of Genetic Counseling. 26(4). 738–751. 16 indexed citations

10.

Sweet, Kevin, et al.. (2014). Clinically relevant lessons from Family HealthLink: a cancer and coronary heart disease familial risk assessment tool. Genetics in Medicine. 17(6). 493–500. 9 indexed citations

11.

Crowder, Clinton D., Kevin Sweet, Amy Lehman, & Wendy L. Frankel. (2012). Serrated Polyposis Is an Underdiagnosed and Unclear Syndrome. The American Journal of Surgical Pathology. 36(8). 1178–1185. 16 indexed citations

12.

Metcalfe, Kelly, Jan Lubiński, Henry T. Lynch, et al.. (2010). Family History of Cancer and Cancer Risks in Women with BRCA1 or BRCA2 Mutations. JNCI Journal of the National Cancer Institute. 102(24). 1874–1878. 75 indexed citations

13.

Kelly, Kimberly M., Amy K. Ferketich, Amy C. Sturm, et al.. (2009). Cancer risk and risk communication in urban, lower-income neighborhoods. Preventive Medicine. 48(4). 392–396. 15 indexed citations

14.

Dworkin, Amy M., et al.. (2009). Methylation not a frequent “second hit” in tumors with germline BRCA mutations. Familial Cancer. 8(4). 339–346. 40 indexed citations

15.

Sturm, Amy C., et al.. (2008). Lessons Learned while Developing a Cancer Family History Campaign in the Columbus, Ohio Metropolitan Area. Public Health Genomics. 11(5). 304–310. 7 indexed citations

16.

Weber, Frank, K. Fukino, Takeshi Sawada, et al.. (2005). Variability in organ-specific EGFR mutational spectra in tumour epithelium and stroma may be the biological basis for differential responses to tyrosine kinase inhibitors. British Journal of Cancer. 92(10). 1922–1926. 58 indexed citations

17.

Sweet, Kevin. (2005). Molecular Classification of Patients With Unexplained Hamartomatous and Hyperplastic Polyposis. JAMA. 294(19). 2465–2465. 160 indexed citations

18.

Nagy, Rebecca, Kevin Sweet, & Charis Eng. (2004). Highly penetrant hereditary cancer syndromes. Oncogene. 23(38). 6445–6470. 237 indexed citations

19.

Sweet, Kevin, et al.. (2004). Genetic aetiology of diffuse gastric cancer: so near, yet so far. Journal of Medical Genetics. 41(7). 481–483. 1 indexed citations

20.

Phelan, Mary C., R. Curtis Rogers, Robert A. Saul, et al.. (2001). 22q13 deletion syndrome. American Journal of Medical Genetics. 101(2). 91–99. 206 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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