Kate Shane-Carson

865 total citations
14 papers, 104 citations indexed

About

Kate Shane-Carson is a scholar working on Genetics, Sociology and Political Science and Oncology. According to data from OpenAlex, Kate Shane-Carson has authored 14 papers receiving a total of 104 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 4 papers in Sociology and Political Science and 4 papers in Oncology. Recurrent topics in Kate Shane-Carson's work include BRCA gene mutations in cancer (9 papers), Global Cancer Incidence and Screening (3 papers) and Cancer Genomics and Diagnostics (3 papers). Kate Shane-Carson is often cited by papers focused on BRCA gene mutations in cancer (9 papers), Global Cancer Incidence and Screening (3 papers) and Cancer Genomics and Diagnostics (3 papers). Kate Shane-Carson collaborates with scholars based in United States. Kate Shane-Carson's co-authors include Susan Steelman, Lola Cook, Rachel Nusbaum, Jennifer Malinowski, Rachel J. Meadows, Tasleem J. Padamsee, Kai He, Annemarie Sommer, Leigha Senter and Caroline Astbury and has published in prestigious journals such as Journal of Clinical Oncology, Breast Cancer Research and Patient Education and Counseling.

In The Last Decade

Kate Shane-Carson

11 papers receiving 102 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kate Shane-Carson United States 6 62 29 22 22 20 14 104
Muhammad Danyal Ahsan United States 6 107 1.7× 39 1.3× 15 0.7× 28 1.3× 20 1.0× 32 154
T. Tillmanns United States 4 100 1.6× 23 0.8× 17 0.8× 18 0.8× 22 1.1× 10 168
Meagan Farmer United States 8 107 1.7× 12 0.4× 22 1.0× 22 1.0× 30 1.5× 12 161
Giovanna Traficante Italy 5 44 0.7× 19 0.7× 14 0.6× 11 0.5× 24 1.2× 11 106
Stacy J. Hines‐Dowell United States 7 109 1.8× 13 0.4× 22 1.0× 26 1.2× 39 1.9× 10 156
Jessica Profato United States 7 91 1.5× 50 1.7× 16 0.7× 50 2.3× 35 1.8× 10 135
Sabrina Talukdar United Kingdom 3 141 2.3× 65 2.2× 19 0.9× 36 1.6× 40 2.0× 6 169
Jacqueline A. Odgis United States 6 89 1.4× 10 0.3× 12 0.5× 21 1.0× 32 1.6× 8 124
Maira Kentwell Australia 6 131 2.1× 40 1.4× 24 1.1× 33 1.5× 28 1.4× 12 158
Meera Warby Australia 9 102 1.6× 18 0.6× 33 1.5× 18 0.8× 25 1.3× 11 183

Countries citing papers authored by Kate Shane-Carson

Since Specialization
Citations

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

Fields of papers citing papers by Kate Shane-Carson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kate Shane-Carson. 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 Kate Shane-Carson. The network helps show where Kate Shane-Carson may publish in the future.

Co-authorship network of co-authors of Kate Shane-Carson

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

All Works

14 of 14 papers shown
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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
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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
6.
Meadows, Rachel J., Wilson S. Figueroa, Kate Shane-Carson, & Tasleem J. Padamsee. (2022). Predicting breast cancer risk in a racially diverse, community‐based sample of potentially high‐risk women. Cancer Medicine. 11(21). 4043–4052. 5 indexed citations
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Byrne, Lindsey, Kate Shane-Carson, Alexandra J. Spencer, et al.. (2022). Genetic Counseling Referrals Among Cancer Registry Patients Who Meet NCCN Guidelines: An Ohio Study. Oncology Issues. 37(4). 42–52.
8.
Meadows, Rachel J., Kate Shane-Carson, Celia E. Wills, et al.. (2022). EPR22-113: Awareness, Utilization, and NCCN Guideline-Adherence to Breast Cancer Risk Management Behavior Among a Community-Based Sample of High-Risk Women. Journal of the National Comprehensive Cancer Network. 20(3.5). EPR22–113.
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Cook, Lola, et al.. (2021). Telehealth for genetic counseling: A systematic evidence review. Journal of Genetic Counseling. 30(5). 1361–1378. 46 indexed citations
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Peshkin, Beth N., Leigha Senter, Shari Baldinger, et al.. (2018). Predictors of risk-reducing surgery intentions following genetic counseling for hereditary breast and ovarian cancer. Translational Behavioral Medicine. 10(2). 337–346. 10 indexed citations
11.
Shukuya, Takehito, Sandipkumar Patel, Kate Shane-Carson, et al.. (2017). Lung Cancer Patients with Germline Mutations Detected by Next-Generation Sequencing and/or Liquid Biopsy. Journal of Thoracic Oncology. 13(2). e17–e19. 10 indexed citations
12.
Oxnard, Geoffrey R., et al.. (2017). OA 06.02 Final Report of the INHERIT EGFR Study - 33 Unrelated Kindreds Carrying Germline EGFR Mutations. Journal of Thoracic Oncology. 12(11). S1758–S1758. 8 indexed citations
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Oxnard, Geoffrey R., Jennifer Heng, Irene Rainville, et al.. (2015). Initial results of a prospective, multicenter trial to study inherited lung cancer risk associated with germline EGFR T790M: INHERIT EGFR.. Journal of Clinical Oncology. 33(15_suppl). 1505–1505. 2 indexed citations
14.
Pyatt, Robert E., Aimee McKinney, Caroline Astbury, et al.. (2012). 12q14 microdeletion associated with HMGA2 gene disruption and growth restriction. American Journal of Medical Genetics Part A. 158A(11). 2925–2930. 16 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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2026