Rony E. Duncan

1.3k total citations
34 papers, 931 citations indexed

About

Rony E. Duncan is a scholar working on Pediatrics, Perinatology and Child Health, General Health Professions and Genetics. According to data from OpenAlex, Rony E. Duncan has authored 34 papers receiving a total of 931 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Pediatrics, Perinatology and Child Health, 10 papers in General Health Professions and 10 papers in Genetics. Recurrent topics in Rony E. Duncan's work include BRCA gene mutations in cancer (9 papers), Ethics and Legal Issues in Pediatric Healthcare (8 papers) and Adolescent and Pediatric Healthcare (6 papers). Rony E. Duncan is often cited by papers focused on BRCA gene mutations in cancer (9 papers), Ethics and Legal Issues in Pediatric Healthcare (8 papers) and Adolescent and Pediatric Healthcare (6 papers). Rony E. Duncan collaborates with scholars based in Australia, United Kingdom and United States. Rony E. Duncan's co-authors include Susan M. Sawyer, Sarah Drew, Martin B. Delatycki, Lynn Gillam, Robert Williamson, Julian Savulescu, John Rogers, Jan Hodgson, Moya Vandeleur and Rosalie Aroni and has published in prestigious journals such as Nature, Cochrane Database of Systematic Reviews and Social Science & Medicine.

In The Last Decade

Rony E. Duncan

34 papers receiving 887 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rony E. Duncan Australia 17 315 256 216 198 136 34 931
William H. McKellin Canada 14 146 0.5× 132 0.5× 131 0.6× 170 0.9× 53 0.4× 34 871
Joanna H. Fanos United States 18 257 0.8× 125 0.5× 301 1.4× 52 0.3× 29 0.2× 30 762
Katherine K. Rogers United States 12 265 0.8× 71 0.3× 81 0.4× 72 0.4× 296 2.2× 13 641
Murrey Olmsted United States 16 88 0.3× 104 0.4× 476 2.2× 158 0.8× 32 0.2× 46 1.1k
Merle Spriggs Australia 17 265 0.8× 144 0.6× 71 0.3× 187 0.9× 19 0.1× 49 739
Benjamin E. Berkman United States 19 363 1.2× 72 0.3× 598 2.8× 134 0.7× 16 0.1× 64 1.4k
Norman P. Spack United States 15 120 0.4× 161 0.6× 100 0.5× 67 0.3× 103 0.8× 21 1.9k
Marian McLaughlin United Kingdom 14 170 0.5× 172 0.7× 38 0.2× 109 0.6× 40 0.3× 42 860
Anne M. Lovell United States 21 76 0.2× 218 0.9× 112 0.5× 396 2.0× 24 0.2× 66 1.5k
Lieve Denayer Belgium 18 285 0.9× 244 1.0× 592 2.7× 55 0.3× 14 0.1× 25 923

Countries citing papers authored by Rony E. Duncan

Since Specialization
Citations

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

Fields of papers citing papers by Rony E. Duncan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rony E. Duncan. 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 Rony E. Duncan. The network helps show where Rony E. Duncan may publish in the future.

Co-authorship network of co-authors of Rony E. Duncan

This figure shows the co-authorship network connecting the top 25 collaborators of Rony E. Duncan. A scholar is included among the top collaborators of Rony E. Duncan 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 Rony E. Duncan. Rony E. Duncan 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
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Gillam, Lynn, et al.. (2015). “I’m scared of being like mum”: The Experience of Adolescents Living in Families with Huntington Disease. Journal of Huntington s Disease. 4(3). 209–217. 20 indexed citations
3.
4.
Metcalfe, Sylvia A., et al.. (2014). Measuring informed choice in population-based reproductive genetic screening: a systematic review. European Journal of Human Genetics. 23(1). 8–21. 37 indexed citations
5.
Duncan, Rony E., et al.. (2014). Balancing Parental Involvement With Adolescent Friendly Health Care in Teenagers With Diabetes: Are We Getting It Right?. Journal of Adolescent Health. 55(1). 59–64. 18 indexed citations
6.
Gillam, Lynn, et al.. (2013). “It was the missing piece”: adolescent experiences of predictive genetic testing for adult-onset conditions. Genetics in Medicine. 15(8). 643–649. 34 indexed citations
7.
Aroni, Rosalie, et al.. (2013). Confidential Consultations With Adolescents: An Exploration of Australian Parents’ Perspectives. Journal of Adolescent Health. 52(6). 786–791. 23 indexed citations
8.
Gillam, Lynn, et al.. (2012). Predictive genetic testing in minors for late-onset conditions: a chronological and analytical review of the ethical arguments: Figure 1. Journal of Medical Ethics. 38(9). 519–524. 46 indexed citations
9.
Jaques, Alice M., Obioha C. Ukoumunne, Alison D. Archibald, et al.. (2012). Development of a fragile X syndrome (FXS) knowledge scale: towards a modified multidimensional measure of informed choice for FXS population carrier screening. Health Expectations. 18(1). 69–80. 10 indexed citations
10.
Delatycki, Martin B., et al.. (2012). Ethical dilemmas associated with genetic testing: which are most commonly seen and how are they managed?. Genetics in Medicine. 15(5). 345–353. 8 indexed citations
11.
Rahman, Belinda, et al.. (2011). Adolescents with Implantable Cardioverter Defibrillators: A Patient and Parent Perspective. Pacing and Clinical Electrophysiology. 35(1). 62–72. 38 indexed citations
12.
Duncan, Rony E., et al.. (2011). Breaching Confidentiality with Adolescent Clients: A Survey of Australian Psychologists about the Considerations that Influence Their Decisions. Psychiatry Psychology and Law. 19(2). 209–220. 11 indexed citations
13.
Duncan, Rony E., et al.. (2011). Confidentiality With Adolescents in the Medical Setting: What Do Parents Think?. Journal of Adolescent Health. 49(4). 428–430. 48 indexed citations
14.
Duncan, Rony E., Lynn Gillam, Julian Savulescu, et al.. (2009). The challenge of developmentally appropriate care: predictive genetic testing in young people for familial adenomatous polyposis. Familial Cancer. 9(1). 27–35. 26 indexed citations
15.
Duncan, Rony E., Lynn Gillam, Julian Savulescu, et al.. (2008). “You're one of us now”: Young people describe their experiences of predictive genetic testing for Huntington disease (HD) and familial adenomatous polyposis (FAP). American Journal of Medical Genetics Part C Seminars in Medical Genetics. 148C(1). 47–55. 76 indexed citations
16.
Drew, Sarah, et al.. (2007). Qualitative Epidemiology: Moving Beyond an Oxymoron. Victoria University Research Repository (Victoria University). 2 indexed citations
17.
Duncan, Rony E., Lynn Gillam, Julian Savulescu, et al.. (2007). “Holding your breath”: Interviews with young people who have undergone predictive genetic testing for Huntington disease. American Journal of Medical Genetics Part A. 143A(17). 1984–1989. 44 indexed citations
18.
Duncan, Rony E., Bennett Foddy, & Martin B. Delatycki. (2006). Refusing to provide a prenatal test: can it ever be ethical?. BMJ. 333(7577). 1066–1068. 13 indexed citations
19.
Duncan, Rony E., Martin B. Delatycki, Steven Collins, et al.. (2005). Ethical considerations in presymptomatic testing for variant CJD. Journal of Medical Ethics. 31(11). 625–630. 10 indexed citations
20.
Williamson, Robert & Rony E. Duncan. (2002). DNA testing for all. Nature. 418(6898). 585–586. 11 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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