Alison McEwen

598 total citations
52 papers, 314 citations indexed

About

Alison McEwen is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and General Health Professions. According to data from OpenAlex, Alison McEwen has authored 52 papers receiving a total of 314 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 16 papers in Pediatrics, Perinatology and Child Health and 11 papers in General Health Professions. Recurrent topics in Alison McEwen's work include BRCA gene mutations in cancer (20 papers), Genomics and Rare Diseases (13 papers) and Childhood Cancer Survivors' Quality of Life (6 papers). Alison McEwen is often cited by papers focused on BRCA gene mutations in cancer (20 papers), Genomics and Rare Diseases (13 papers) and Childhood Cancer Survivors' Quality of Life (6 papers). Alison McEwen collaborates with scholars based in Australia, New Zealand and United Kingdom. Alison McEwen's co-authors include Chris Jacobs, Ashley Crook, Toby Newton‐John, Samantha Wake, Ebony Richardson, Clara Gaff, Mary‐Anne Young, David J. Amor, Adrienne Sexton and Melissa Martyn and has published in prestigious journals such as SHILAP Revista de lepidopterología, Developmental Medicine & Child Neurology and Gynecologic Oncology.

In The Last Decade

Alison McEwen

45 papers receiving 310 citations

Peers

Alison McEwen
Andrea Shugar Canada
Erica Ramos United States
Karen Forrest Keenan United Kingdom
Alice Bonuccelli Italy
Charlotte von der Lippe Norway
Sandra Blum Belgium
Sara Dishon Israel
Kabir Matharu United States
Joanna H. Fanos United States
Nikkola Carmichael United States
Andrea Shugar Canada
Alison McEwen
Citations per year, relative to Alison McEwen Alison McEwen (= 1×) peers Andrea Shugar

Countries citing papers authored by Alison McEwen

Since Specialization
Citations

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

Fields of papers citing papers by Alison McEwen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alison McEwen

This figure shows the co-authorship network connecting the top 25 collaborators of Alison McEwen. A scholar is included among the top collaborators of Alison McEwen 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 Alison McEwen. Alison McEwen 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.
Dive, Lisa, et al.. (2025). Generative AI and the profession of genetic counseling. Journal of Genetic Counseling. 34(2). e2009–e2009. 1 indexed citations
2.
3.
Dive, Lisa, et al.. (2025). A scoping review of the development of genetic counseling practices in Asia. Journal of Genetic Counseling. 34(3). e70036–e70036.
4.
McEwen, Alison, et al.. (2025). Developing global consensus about core knowledge and skills for genetic counselor education. Journal of Genetic Counseling. 34(5). e70116–e70116.
5.
Mackley, Michael P., Pankaj B. Agrawal, Sara Ali, et al.. (2025). Genomic sequencing technologies for rare disease in mainstream healthcare: the current state of implementation. European Journal of Human Genetics. 33(11). 1402–1413. 1 indexed citations
6.
7.
McEwen, Alison, et al.. (2024). Parents’ perspectives on conversations about prognosis and an assessment of prognostic information available online: A mixed-methods study. Disability and health journal. 18(2). 101718–101718. 1 indexed citations
8.
Macintosh, Rebecca, Joanna Sweeting, Jodie Ingles, et al.. (2024). A mixed-methods assessment of the Australasian Society of Genetic Counselors (ASGC) Mentor Program. SHILAP Revista de lepidopterología. 2(Suppl 2). 101865–101865.
9.
Arpone, Marta, Erin Turbitt, & Alison McEwen. (2024). Race, ethnicity, and ancestry reporting in genetic counseling research: A focused mapping review and synthesis. Journal of Genetic Counseling. 34(1). e1884–e1884. 2 indexed citations
10.
Turbitt, Erin, et al.. (2023). Parents' preferences for receiving and discussing prognostic genetic information regarding their children's neurodevelopmental condition: A qualitative study. Developmental Medicine & Child Neurology. 66(7). 872–881. 5 indexed citations
11.
Pate, James W., et al.. (2023). Free Online Decision Tools to Support Parents Making Decisions About Their Children's Chronic Health Condition: An Environmental Scan. Academic Pediatrics. 23(5). 874–883. 1 indexed citations
12.
Turbitt, Erin, Kris Rogers, Kathy Tucker, et al.. (2023). A survey of genetic and palliative care health professionals’ views of integrating genetics into palliative care. European Journal of Human Genetics. 32(1). 109–116.
13.
Richardson, Ebony, Alison McEwen, Toby Newton‐John, & Chris Jacobs. (2023). Defining core outcomes of reproductive genetic carrier screening: A Delphi survey of Australian and New Zealand stakeholders. Prenatal Diagnosis. 43(9). 1150–1165.
14.
Yeates, Laura, et al.. (2022). Using codesign focus groups to develop an online COmmunity suPporting familiEs after Sudden Cardiac Death (COPE-SCD) in the young. BMJ Open. 12(8). e053785–e053785. 5 indexed citations
15.
O’Brian, Sue, Kris Rogers, Mark Onslow, et al.. (2022). Stuttering, family history and counselling: A contemporary database. Journal of Fluency Disorders. 73. 105925–105925. 2 indexed citations
16.
Willis, Amanda, et al.. (2021). My Research Results: a program to facilitate return of clinically actionable genomic research findings. European Journal of Human Genetics. 30(3). 363–366. 7 indexed citations
17.
Crook, Ashley, Chris Jacobs, Toby Newton‐John, Rosie O’Shea, & Alison McEwen. (2021). Genetic counseling and testing practices for late-onset neurodegenerative disease: a systematic review. Journal of Neurology. 269(2). 676–692. 11 indexed citations
18.
19.
Amor, David J., et al.. (2018). Attitudes of sperm, egg and embryo donors and recipients towards genetic information and screening of donors. Reproductive Health. 15(1). 26–26. 17 indexed citations
20.
Wiltshire, Esko, Guido Davidzon, Salvatore DiMauro, et al.. (2008). Juvenile Alpers Disease. Archives of Neurology. 65(1). 121–4. 30 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Andrea Shugar Breakdown of academic impact, for papers by Erica Ramos Breakdown of academic impact, for papers by Karen Forrest Keenan Breakdown of academic impact, for papers by Alice Bonuccelli Breakdown of academic impact, for papers by Charlotte von der Lippe Breakdown of academic impact, for papers by Sandra Blum Breakdown of academic impact, for papers by Sara Dishon Breakdown of academic impact, for papers by Kabir Matharu Breakdown of academic impact, for papers by Joanna H. Fanos Breakdown of academic impact, for papers by Nikkola Carmichael
Rankless by CCL
2026