Kate Dunlop

669 total citations
34 papers, 369 citations indexed

About

Kate Dunlop is a scholar working on Genetics, Public Health, Environmental and Occupational Health and Oncology. According to data from OpenAlex, Kate Dunlop has authored 34 papers receiving a total of 369 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 11 papers in Public Health, Environmental and Occupational Health and 9 papers in Oncology. Recurrent topics in Kate Dunlop's work include BRCA gene mutations in cancer (16 papers), Genomics and Rare Diseases (7 papers) and Ethics in Clinical Research (7 papers). Kate Dunlop is often cited by papers focused on BRCA gene mutations in cancer (16 papers), Genomics and Rare Diseases (7 papers) and Ethics in Clinical Research (7 papers). Kate Dunlop collaborates with scholars based in Australia, United Kingdom and United States. Kate Dunlop's co-authors include Anne Ε. Cust, Amelia K. Smit, Ainsley J. Newson, Judy Kirk, Phyllis Butow, Louise Keogh, Kristine Barlow‐Stewart, Nicole Rankin, Sylvia A. Metcalfe and Amy Nisselle and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and BMC Public Health.

In The Last Decade

Kate Dunlop

31 papers receiving 361 citations

Peers

Kate Dunlop
Amelia K. Smit Australia
Madeleine Freeman United Kingdom
Tatiane Yanes Australia
Aliya Collier United States
Patti Vegella United States
Margaret M. McGovern United States
Carol A. Christianson United States
Sherry Grumet United States
Dominique Fetzer United States
Sandra Suther United States
Amelia K. Smit Australia
Kate Dunlop
Citations per year, relative to Kate Dunlop Kate Dunlop (= 1×) peers Amelia K. Smit

Countries citing papers authored by Kate Dunlop

Since Specialization
Citations

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

Fields of papers citing papers by Kate Dunlop

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kate Dunlop

This figure shows the co-authorship network connecting the top 25 collaborators of Kate Dunlop. A scholar is included among the top collaborators of Kate Dunlop 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 Dunlop. Kate Dunlop 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.
Goldsbury, David, Yoon‐Jung Kang, Catherine Tang, et al.. (2025). Sociodemographic and health factors associated with genetic testing in Australia: insights from a cohort-based study of 45,061 participants. European Journal of Human Genetics. 33(6). 819–824.
2.
Dunlop, Kate, Amelia K. Smit, April Morrow, et al.. (2025). Building capacity for genomics in primary care: a scoping review of practitioner attitudes, education needs, and enablers. Frontiers in Medicine. 12. 1577958–1577958.
3.
Dunlop, Kate, et al.. (2024). A review of skin cancer primary prevention activities in primary care settings. Public Health Research & Practice. 34(2). 4 indexed citations
4.
Nisselle, Amy, Bronwyn Terrill, Belinda McClaren, et al.. (2023). Investigating genomic medicine practice and perceptions amongst Australian non-genetics physicians to inform education and implementation. npj Genomic Medicine. 8(1). 13–13. 12 indexed citations
5.
Dunlop, Kate, Amelia K. Smit, Louise Keogh, et al.. (2023). Acceptability of risk-tailored cancer screening among Australian GPs: a qualitative study. British Journal of General Practice. 74(740). e156–e164. 3 indexed citations
6.
Dunlop, Kate, Henry Marshall, Emily Stone, et al.. (2022). Motivation is not enough: A qualitative study of lung cancer screening uptake in Australia to inform future implementation. PLoS ONE. 17(9). e0275361–e0275361. 12 indexed citations
7.
Smit, Amelia K., David Espinoza, Mary‐Anne Young, et al.. (2021). Knowledge, views and expectations for cancer polygenic risk testing in clinical practice: A cross‐sectional survey of health professionals. Clinical Genetics. 100(4). 430–439. 24 indexed citations
8.
Hickerton, Chriselle, Amy Nisselle, Belinda McClaren, et al.. (2021). General practitioners’ views on genomics, practice and education: A qualitative interview study. Australian Journal of General Practice. 50(10). 747–752. 13 indexed citations
9.
Smit, Amelia K., et al.. (2020). Implementation considerations for offering personal genomic risk information to the public: a qualitative study. BMC Public Health. 20(1). 1028–1028. 12 indexed citations
10.
Barlow‐Stewart, Kristine, et al.. (2020). Disclosure to genetic relatives without consent – Australian genetic professionals’ awareness of the health privacy law. BMC Medical Ethics. 21(1). 13–13. 13 indexed citations
11.
Dunlop, Kate, et al.. (2019). Scoping the Scene: What Do Nurses, Midwives, and Allied Health Professionals Need and Want to Know About Genomics?. Frontiers in Genetics. 10. 1066–1066. 15 indexed citations
12.
Smit, Amelia K., Ainsley J. Newson, Louise Keogh, et al.. (2019). GP attitudes to and expectations for providing personal genomic risk information to the public: a qualitative study. BJGP Open. 3(1). bjgpopen18X101633–bjgpopen18X101633. 20 indexed citations
13.
Smit, Amelia K., Ainsley J. Newson, Megan Best, et al.. (2018). Distress, uncertainty, and positive experiences associated with receiving information on personal genomic risk of melanoma. European Journal of Human Genetics. 26(8). 1094–1100. 16 indexed citations
14.
Dunlop, Kate, et al.. (2018). The Democratic Party of Japan in power : challenges and failures. Routledge eBooks. 4 indexed citations
15.
Smit, Amelia K., Louise Keogh, Ainsley J. Newson, et al.. (2017). Does personalized melanoma genomic risk information trigger conversations about skin cancer prevention and skin examination with family, friends and health professionals?. British Journal of Dermatology. 177(3). 779–790. 13 indexed citations
16.
Smit, Amelia K., David Espinoza, Ainsley J. Newson, et al.. (2016). A Pilot Randomized Controlled Trial of the Feasibility, Acceptability, and Impact of Giving Information on Personalized Genomic Risk of Melanoma to the Public. Cancer Epidemiology Biomarkers & Prevention. 26(2). 212–221. 34 indexed citations
17.
Meiser, Bettina, Michelle Peate, Philip B. Mitchell, et al.. (2016). A Psycho‐Educational Intervention for People with a Family History of Depression: Pilot Results. Journal of Genetic Counseling. 26(2). 312–321. 5 indexed citations
18.
Dunlop, Kate, Kristine Barlow‐Stewart, Phyllis Butow, & Paul Heinrich. (2011). A Model of Professional Development for Practicing Genetic Counselors: Adaptation of Communication Skills Training in Oncology. Journal of Genetic Counseling. 20(3). 217–230. 11 indexed citations
19.
Dunlop, Kate & Kristine Barlow‐Stewart. (2009). ‘Start the Conversation’: The New South Wales (Australia) Family Health History Campaign. Public Health Genomics. 13(5). 301–309. 9 indexed citations
20.
Dunlop, Kate, et al.. (2006). Successful treatment of recalcitrant necrotizing eosinophilic folliculitis using indomethacin and cephalexin. Australasian Journal of Dermatology. 47(4). 281–285. 1 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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