Emma Tonkin

1.5k total citations
41 papers, 1.1k citations indexed

About

Emma Tonkin is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Emma Tonkin has authored 41 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 9 papers in Pediatrics, Perinatology and Child Health and 8 papers in Molecular Biology. Recurrent topics in Emma Tonkin's work include BRCA gene mutations in cancer (23 papers), Genomics and Rare Diseases (11 papers) and Ethics and Legal Issues in Pediatric Healthcare (5 papers). Emma Tonkin is often cited by papers focused on BRCA gene mutations in cancer (23 papers), Genomics and Rare Diseases (11 papers) and Ethics and Legal Issues in Pediatric Healthcare (5 papers). Emma Tonkin collaborates with scholars based in United Kingdom, United States and Australia. Emma Tonkin's co-authors include Maggie Kirk, Tom Strachan, Michael J. Bamshad, Steven Lisgo, Heather Skirton, Laurie Badzek, Caroline Benjamin, Anna Middleton, Deborah Lancastle and Christine Patch and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Journal of Advanced Nursing.

In The Last Decade

Emma Tonkin

40 papers receiving 1.0k citations

Peers

Emma Tonkin
Ann D. Carlson United States
Eric A. Evans United States
Belinda McClaren Australia
Vickie L. Venne United States
Nancy Feldman United States
Christopher J. Bean United States
Emily Edelman United States
Molly B. Moravek United States
G.A.J. Dunselman Netherlands
Daniel F. Gunther United States
Ann D. Carlson United States
Emma Tonkin
Citations per year, relative to Emma Tonkin Emma Tonkin (= 1×) peers Ann D. Carlson

Countries citing papers authored by Emma Tonkin

Since Specialization
Citations

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

Fields of papers citing papers by Emma Tonkin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emma Tonkin

This figure shows the co-authorship network connecting the top 25 collaborators of Emma Tonkin. A scholar is included among the top collaborators of Emma Tonkin 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 Emma Tonkin. Emma Tonkin 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.
Chiu, Patrick, et al.. (2024). Integrating genomics into Canadian oncology nursing policy: Insights from a comparative policy analysis. Journal of Advanced Nursing. 80(11). 4488–4509. 3 indexed citations
2.
Badzek, Laurie, et al.. (2024). Consumer-oriented (patient and family) outcomes from nursing in genomics: a scoping review of the literature (2012–2022). Frontiers in Genetics. 15. 1481948–1481948. 1 indexed citations
3.
Yu, Juping, G. Parsons, Deborah Lancastle, Emma Tonkin, & Siva Ganesh. (2021). “Walking in Their Shoes”: The effects of an immersive digital story intervention on empathy in nursing students. Nursing Open. 8(5). 2813–2823. 18 indexed citations
4.
Sharif, Saghira Malik, Moira Blyth, Mushtaq Ahmed, et al.. (2020). Enhancing inclusion of diverse populations in genomics: A competence framework. Journal of Genetic Counseling. 29(2). 282–292. 13 indexed citations
5.
Tonkin, Emma, Laurie Badzek, Caroline Benjamin, et al.. (2020). A Roadmap for Global Acceleration of Genomics Integration Across Nursing. Journal of Nursing Scholarship. 52(3). 329–338. 38 indexed citations
6.
Kirk, Maggie, et al.. (2018). Increasing nursing capacity in genomics: Overview of existing global genomics resources. Nurse Education Today. 69. 53–59. 35 indexed citations
7.
Tonkin, Emma, Heather Skirton, & Maggie Kirk. (2018). The first competency based framework in genetics/genomics specifically for midwifery education and practice. Nurse Education in Practice. 33. 133–140. 13 indexed citations
8.
Kirk, Maggie, et al.. (2018). The Global Landscape of Nursing and Genomics. Journal of Nursing Scholarship. 50(3). 249–256. 72 indexed citations
9.
Tonkin, Emma & Heather Skirton. (2013). The role of genetic/genomic factors in health, illness and care provision. Nursing Standard. 28(12). 39–46. 5 indexed citations
10.
Kirk, Maggie, et al.. (2011). Genetics‐Genomics Competencies and Nursing Regulation. Journal of Nursing Scholarship. 43(2). 107–116. 55 indexed citations
11.
Kirk, Maggie, et al.. (2011). Storytellers as partners in developing a genetics education resource for health professionals. Nurse Education Today. 33(5). 518–524. 15 indexed citations
12.
Kirk, Maggie & Emma Tonkin. (2009). Understanding the role of genetics and genomics in health 2: implications for practice.. PubMed. 105(46). 19–23. 5 indexed citations
13.
Tonkin, Emma & Maggie Kirk. (2007). Genetics in Practice: Views of Nurses in Non‐genetic Specialties. Nursing and Health Sciences. 9(3). 242–242. 2 indexed citations
14.
Kirk, Maggie, Emma Tonkin, & Sarah Burke. (2007). Engaging Nurses in Genetics: The Strategic Approach of the NHS National Genetics Education and Development Centre. Journal of Genetic Counseling. 17(2). 180–188. 20 indexed citations
15.
Kirk, Maggie, et al.. (2006). Genetics and paediatric nursing. Paediatric Care. 18(7). 34–34. 1 indexed citations
16.
Kirk, Maggie, et al.. (2006). Genetics in emergency care. Emergency Nurse. 14(5). 12–14. 1 indexed citations
17.
Tonkin, Emma, Melanie Smith, Pieter J.A. Eichhorn, et al.. (2004). A giant novel gene undergoing extensive alternative splicing is severed by a Cornelia de Lange-associated translocation breakpoint at 3q26.3. Human Genetics. 115(2). 139–48. 44 indexed citations
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20.
Tonkin, Emma, Moyra Smith, Pieter J.A. Eichhorn, et al.. (2001). A novel gene is disrupted by a Cornelia de Lange-associated translocation breakpoint at 3q26.3. The American Journal of Human Genetics. 2 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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