Publications for Ulrica Swartling
Co-author map based on ISI articles 2007-
Publications mentioned in social media 2 times*
Journal Articles
Ulrica Swartling, Mats Hansson, Johnny Ludvigsson and Anders Nordgren
"My parents decide if I can. I decide if I want to." Children’s views on participation in medical research
Journal of Empirical Research on Human Research Ethics, 2011, 6(4), 68-74.
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G. Helgesson, M.G. Hansson, Johnny Ludvigsson and Ulrica Swartling
Practical matters, rather than lack of trust, motivate non-participation in a long-term cohort trial
Pediatric Diabetes, 2009, 10(6), 408-412.
Web of Science® Times Cited: 5 |
Ulrica Swartling, G. Helgesson, M G Hansson and Johnny Ludvigsson
Split views among parents regarding childrens right to decide about participation in research: a questionnaire survey
Journal of Medical Ethics, 2009, 35(7), 450-455.
Web of Science® Times Cited: 2 |
Ulrica Swartling, Gert Helgesson, Mats G Hansson and Johnny Ludvigsson
Parental authority, research interests and children's right to decide in medical research - an uneasy tension?
Clinical ethics, 2008, 3, 69-74.
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Ulrica Swartling and G Helgesson
Self-assessed understanding as a tool for evaluating consent: Reflections on a longitudinal study
Journal of Medical Ethics, 2008, 34(7), 557-562.
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Gert Helgesson and Ulrica Swartling
Views on data use, confidentiality and consent in a predictive screening involving children
Journal of Medical Ethics, 2008, 34(3), 206-209.
Web of Science® Times Cited: 4 |
Ulrica Swartling, S Eriksson, Johnny Ludvigsson and Gert Helgesson
Concern, pressure and lack of knowledge affect choice of not wanting to know high-risk status
European Journal of Human Genetics, 2007, 15(5), 556-562.
Web of Science® Times Cited: 5 |
Ulrica Swartling, Gert Helgesson and Stefan Eriksson
Limited relevance of the right not to know - reflections on a screening study
Accountability in Research, 2007, 14, 197-209.
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Gert Helgesson, Johnny Ludvigsson and Ulrica Swartling
How to handle informed consent in longitudinal studies when participants have a limited understanding of the study
Journal of Medical Ethics, 2005, 31(11), 670-673.
Web of Science® Times Cited: 10 |
Ulrica Gustafsson Stolt, Gert Helgesson, Per-Erik Liss, Tommy Svensson and Johnny Ludvigsson
Information and informed consent in a longitudinal screening involving children: a questionnaire survey
European Journal of Human Genetics, 2005, 13(3), 376-383.
Web of Science® Times Cited: 13 |
Ulrica Gustafsson Stolt, Per-Erik Liss and Johnny Ludvigsson
Nurses’ views of longitudinal genetic screening of and research on children
British Journal of Nursing, 2005, 14(2), 71-77.
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Ulrica Gustafsson Stolt, Johnny Ludvigsson, Per Erik Liss and Tommy Svensson
Bioethical theory and practice in genetic screening for type 1 diabetes
Medicine, Health care and Philosophy, 2003, 6(1), 45-50.
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Ulrica Gustafsson Stolt, Per-Erik Liss and Johnny Ludvigsson
Parents want to know if their child is at high risk of getting diabetes
Annals of the New York Academy of Sciences, 2003, 1005, 395-399.
Web of Science® Times Cited: 3 |
Ulrica Gustafsson Stolt, Per-Erik Liss, Tommy Svensson and Johnny Ludvigsson
Attitudes to bioethical issues: a case study of a screening project
Social Science and Medicine, 2002, 54(9), 1333-1344.
Web of Science® Times Cited: 11 |
Johnny Ludvigsson, Ulrica Gustafsson Stolt, Per-Erik Liss and Tommy Svensson
Mothers of children in ABIS, a population-based screening for prediabetes, experience few ethical conflicts and have a positive attitude
Annals of the New York Academy of Sciences, 2002, 958, 376-381.
Web of Science® Times Cited: 4 |
Ph.D. Theses
* Social media data based on publications from 2011 to present and with a DOI; data delivered by Altmetric.com.
Ph.D., Lic. Theses
