Carla van El

3.4k total citations
58 papers, 1.7k citations indexed

About

Carla van El is a scholar working on Genetics, Public Health, Environmental and Occupational Health and Molecular Biology. According to data from OpenAlex, Carla van El has authored 58 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 17 papers in Public Health, Environmental and Occupational Health and 13 papers in Molecular Biology. Recurrent topics in Carla van El's work include BRCA gene mutations in cancer (18 papers), Ethics in Clinical Research (14 papers) and Genomics and Rare Diseases (12 papers). Carla van El is often cited by papers focused on BRCA gene mutations in cancer (18 papers), Ethics in Clinical Research (14 papers) and Genomics and Rare Diseases (12 papers). Carla van El collaborates with scholars based in Netherlands, United Kingdom and France. Carla van El's co-authors include Martina C. Cornel, Heidi Howard, Pascal Borry, Wybo Dondorp, Lidewij Henneman, Ros Hastings, Florence Fellmann, Shirley V. Hodgson, Anne Cambon‐Thomsen and Hans Scheffer and has published in prestigious journals such as PLoS ONE, Human Reproduction and BMC Health Services Research.

In The Last Decade

Carla van El

50 papers receiving 1.7k citations

Peers

Carla van El
Wendy R. Uhlmann United States
Sharon Hensley Alford United States
Christine Patch United Kingdom
Stephen C. Groft United States
Julianne O’Daniel United States
June A. Peters United States
Aaron J. Goldenberg United States
Carla van El
Citations per year, relative to Carla van El Carla van El (= 1×) peers Robin Z. Hayeems

Countries citing papers authored by Carla van El

Since Specialization
Citations

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

Fields of papers citing papers by Carla van El

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Carla van El. 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 Carla van El. The network helps show where Carla van El may publish in the future.

Co-authorship network of co-authors of Carla van El

This figure shows the co-authorship network connecting the top 25 collaborators of Carla van El. A scholar is included among the top collaborators of Carla van El 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 Carla van El. Carla van El 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.
Wert, Guido de, Carla van El, Angus Clarke, et al.. (2025). Cascade counselling and testing. Recommendations of the European Society of Human Genetics. European Journal of Human Genetics. 34(2). 171–184.
2.
Causio, Francesco Andrea, Flavia Beccia, Antonio Cristiano, et al.. (2025). Public perceptions and engagement in mHealth: a European survey on attitudes toward health apps use and data sharing. European Journal of Public Health. 35(3). 401–406.
3.
Cornel, Martina C., Karuna R. M. van der Meij, Carla van El, Tessel Rigter, & Lidewij Henneman. (2024). Genetic Screening—Emerging Issues. Genes. 15(5). 581–581. 2 indexed citations
4.
Capalbo, Antonio, G. de Wert, Lidewij Henneman, et al.. (2024). An ESHG–ESHRE survey on the current practice of expanded carrier screening in medically assisted reproduction. Human Reproduction. 39(8). 1844–1855. 2 indexed citations
5.
Causio, Francesco Andrea, Flavia Beccia, Giovanna Elisa Calabrò, et al.. (2024). European survey: citizens' attitudes on personalized medicine, genetic testing and health data sharing – design and delivery. Personalized Medicine. 21(3). 163–166. 2 indexed citations
6.
Helmrich, Isabel R. A. Retel, Sophie van Baalen, B.C. van Beers, et al.. (2024). The need to set explicit goals for human germline gene editing public dialogues. Journal of Community Genetics. 15(3). 259–265. 4 indexed citations
7.
Henneman, Lidewij, et al.. (2024). Engagement of patients and the public in personalised prevention in Europe using genomic information: a scoping review. Frontiers in Public Health. 12. 1456853–1456853.
8.
El, Carla van, et al.. (2023). Between desire and fear: a qualitative interview study exploring the perspectives of carriers of a genetic condition on human genome editing. Humanities and Social Sciences Communications. 10(1). 3 indexed citations
9.
El, Carla van, Phillis Lakeman, Mariëtte Goddijn, et al.. (2022). Dynamics of reproductive genetic technologies: Perspectives of professional stakeholders. PLoS ONE. 17(6). e0269719–e0269719. 4 indexed citations
10.
Jansen, Marleen E., et al.. (2019). Parental perspectives on retention and secondary use of neonatal dried bloodspots: a Dutch mixed methods study. BMC Pediatrics. 19(1). 230–230. 5 indexed citations
11.
Boccia, Stefania, Roberta Pastorino, Walter Ricciardi, et al.. (2019). How to Integrate Personalized Medicine into Prevention? Recommendations from the Personalized Prevention of Chronic Diseases (PRECeDI) Consortium. Public Health Genomics. 22(5-6). 208–214. 19 indexed citations
12.
El, Carla van, Valentina Baccolini, Péter Pikó, & Martina C. Cornel. (2018). Stakeholder Views on Active Cascade Screening for Familial Hypercholesterolemia. Healthcare. 6(3). 108–108. 15 indexed citations
13.
Wert, Guido de, Björn Heindryckx, Guido Pennings, et al.. (2018). Responsible innovation in human germline gene editing: Background document to the recommendations of ESHG and ESHRE. European Journal of Human Genetics. 26(4). 450–470. 32 indexed citations
14.
Wert, Guido de, Guido Pennings, Angus Clarke, et al.. (2018). Human germline gene editing: Recommendations of ESHG and ESHRE. European Journal of Human Genetics. 26(4). 445–449. 33 indexed citations
15.
Cornel, Martina C. & Carla van El. (2017). Barriers and Facilitating Factors for Implementation of Genetic Services: A Public Health Perspective. Frontiers in Public Health. 5. 195–195. 15 indexed citations
16.
El, Carla van, Maaike Kempes, J.I.M. Egger, et al.. (2014). Neuroimaging in the Courtroom: Normative Frameworks and Consensual Practices. AJOB Neuroscience. 5(2). 37–39. 1 indexed citations
17.
El, Carla van, Martina C. Cornel, Pascal Borry, et al.. (2013). Whole-genome sequencing in health care. European Journal of Human Genetics. 21(6). 580–584. 256 indexed citations
18.
Hastings, Ros, Guido de Wert, Brian Fowler, et al.. (2012). The changing landscape of genetic testing and its impact on clinical and laboratory services and research in Europe. European Journal of Human Genetics. 20(9). 911–916. 28 indexed citations
19.
El, Carla van, et al.. (2012). Governing biological material at the intersection of care and research: the use of dried blood spots for biobanking. Croatian Medical Journal. 53(4). 390–397. 12 indexed citations
20.
El, Carla van. (2006). Marian van der Klein, Ziek, zwak of zwanger. Vrouwen en arbeidsongeschiktheid in Nederlandse sociale verzekeringen, 1890-1940. TSEG/ Low Countries Journal of Social and Economic History. 3(4). 155–155.

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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