Caron Molster

1.6k total citations
28 papers, 910 citations indexed

About

Caron Molster is a scholar working on Genetics, Pulmonary and Respiratory Medicine and General Health Professions. According to data from OpenAlex, Caron Molster has authored 28 papers receiving a total of 910 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 6 papers in Pulmonary and Respiratory Medicine and 5 papers in General Health Professions. Recurrent topics in Caron Molster's work include Genomics and Rare Diseases (7 papers), Cystic Fibrosis Research Advances (5 papers) and Health Systems, Economic Evaluations, Quality of Life (4 papers). Caron Molster is often cited by papers focused on Genomics and Rare Diseases (7 papers), Cystic Fibrosis Research Advances (5 papers) and Health Systems, Economic Evaluations, Quality of Life (4 papers). Caron Molster collaborates with scholars based in Australia, United States and United Kingdom. Caron Molster's co-authors include Peter O’Leary, Hugh Dawkins, Margaret McNeil, Geoffrey N. Soutar, Susannah Maxwell, Debra Urwin, Colleen Fisher, Simon Woods, Hanns Lochmüller and Leanne Youngs and has published in prestigious journals such as Journal of Business Ethics, Journal of Medical Genetics and Advances in experimental medicine and biology.

In The Last Decade

Caron Molster

28 papers receiving 864 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Caron Molster Australia 17 389 209 126 109 98 28 910
Michelle L. McGowan United States 22 380 1.0× 518 2.5× 62 0.5× 28 0.3× 175 1.8× 63 1.3k
Béatrice Godard Canada 20 632 1.6× 522 2.5× 47 0.4× 12 0.1× 195 2.0× 75 1.3k
James E. Weber United States 21 122 0.3× 340 1.6× 31 0.2× 46 0.4× 188 1.9× 43 1.4k
Mary A. Majumder United States 14 146 0.4× 222 1.1× 14 0.1× 24 0.2× 113 1.2× 65 609
Vardit Ravitsky Canada 22 292 0.8× 625 3.0× 115 0.9× 10 0.1× 155 1.6× 111 1.6k
Ine Van Hoyweghen Belgium 19 237 0.6× 181 0.9× 10 0.1× 17 0.2× 94 1.0× 80 938
Rachel Iredale United Kingdom 18 727 1.9× 357 1.7× 20 0.2× 12 0.1× 249 2.5× 45 1.2k
Stephen J. Miller United States 16 145 0.4× 62 0.3× 25 0.2× 32 0.3× 93 0.9× 48 1.0k
Karen Kaiser United States 17 101 0.3× 226 1.1× 115 0.9× 9 0.1× 226 2.3× 54 1.3k
Paul Gibson Canada 16 111 0.3× 112 0.5× 78 0.6× 14 0.1× 93 0.9× 50 1.6k

Countries citing papers authored by Caron Molster

Since Specialization
Citations

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

Fields of papers citing papers by Caron Molster

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Caron Molster

This figure shows the co-authorship network connecting the top 25 collaborators of Caron Molster. A scholar is included among the top collaborators of Caron Molster 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 Caron Molster. Caron Molster 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.
Molster, Caron, et al.. (2022). The diagnostic odyssey: insights from parents of children living with an undiagnosed condition. Orphanet Journal of Rare Diseases. 17(1). 233–233. 59 indexed citations
2.
Molster, Caron, et al.. (2019). Identifying Perceptions and Preferences of the General Public Concerning Universal Screening of Children for Familial Hypercholesterolaemia. Public Health Genomics. 22(1-2). 25–35. 14 indexed citations
3.
Baynam, Gareth, et al.. (2018). Changes to the Employers' Use of Genetic Information and Non-discrimination for Health Insurance in the USA: Implications for Australians. Frontiers in Public Health. 6. 183–183. 2 indexed citations
4.
Molster, Caron, et al.. (2018). The Evolution of Public Health Genomics: Exploring Its Past, Present, and Future. Frontiers in Public Health. 6. 247–247. 42 indexed citations
5.
Baynam, Gareth, Nicholas Pachter, Lyn Schofield, et al.. (2017). 3-Dimensional Facial Analysis—Facing Precision Public Health. Frontiers in Public Health. 5. 31–31. 9 indexed citations
6.
McCormack, Pauline, Anna Kole, Sabina Gainotti, et al.. (2016). ‘You should at least ask’. The expectations, hopes and fears of rare disease patients on large-scale data and biomaterial sharing for genomics research. European Journal of Human Genetics. 24(10). 1403–1408. 65 indexed citations
7.
Hansson, Mats, Hanns Lochmüller, Olaf Rieß, et al.. (2016). The risk of re-identification versus the need to identify individuals in rare disease research. European Journal of Human Genetics. 24(11). 1553–1558. 42 indexed citations
8.
Molster, Caron, et al.. (2016). Survey of healthcare experiences of Australian adults living with rare diseases. Orphanet Journal of Rare Diseases. 11(1). 30–30. 107 indexed citations
9.
Walker, C. E., Geoff Davis, Laura Miller, et al.. (2016). The collective impact of rare diseases in Western Australia: an estimate using a population-based cohort. Genetics in Medicine. 19(5). 546–552. 77 indexed citations
10.
Molster, Caron, Beverley McNamara, Leanne Youngs, et al.. (2013). Informing Public Health Policy Through Deliberative Public Engagement: Perceived Impact on Participants and Citizen–Government Relations. Genetic Testing and Molecular Biomarkers. 17(9). 713–718. 12 indexed citations
11.
Molster, Caron, et al.. (2012). Key outcomes from stakeholder workshops at a symposium to inform the development of an Australian national plan for rare diseases. Orphanet Journal of Rare Diseases. 7(1). 50–50. 14 indexed citations
12.
Molster, Caron, et al.. (2011). Blueprint for a deliberative public forum on biobanking policy: were theoretical principles achievable in practice?. Health Expectations. 16(2). 211–224. 31 indexed citations
13.
Molster, Caron, et al.. (2011). An Australian Approach to the Policy Translation of Deliberated Citizen Perspectives on Biobanking. Public Health Genomics. 15(2). 82–91. 23 indexed citations
14.
Molster, Caron, et al.. (2011). Motivating intentions to adopt risk-reducing behaviours for chronic diseases: Impact of a public health tool for collecting family health histories. Health Promotion Journal of Australia. 22(1). 57–62. 8 indexed citations
15.
Maxwell, Susannah, et al.. (2011). Perceptions of Population Cystic Fibrosis Prenatal and Preconception Carrier Screening Among Individuals with Cystic Fibrosis and Their Family Members. Genetic Testing and Molecular Biomarkers. 15(3). 159–164. 22 indexed citations
16.
Maxwell, Susannah, et al.. (2009). Communicating Familial Hypercholesterolemia Genetic Information Within Families. Genetic Testing and Molecular Biomarkers. 13(3). 301–306. 19 indexed citations
17.
Molster, Caron, et al.. (2009). A survey of folate knowledge and consumer behaviours in Western Australia prior to the introduction of mandatory food fortification. Australian and New Zealand Journal of Public Health. 33(6). 577–582. 10 indexed citations
18.
Molster, Caron, et al.. (2008). Australian Study on Public Knowledge of Human Genetics and Health. Public Health Genomics. 12(2). 84–91. 107 indexed citations
19.
Molster, Caron, Carol Bower, & Peter O’Leary. (2007). Australian survey on community knowledge and attitudes regarding the fortification of food with folic acid. Birth Defects Research Part A Clinical and Molecular Teratology. 79(9). 664–670. 3 indexed citations
20.
Molster, Caron, Carol Bower, & Peter O’Leary. (2007). Community attitudes to the collection and use of identifiable data for health research – is it an invasion of privacy?. Australian and New Zealand Journal of Public Health. 31(4). 313–317. 9 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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