Genomic information and a person’s right not to know: A closer look at variations in hypothetical informational preferences in a German sample
出版年份 2018 全文链接
标题
Genomic information and a person’s right not to know: A closer look at variations in hypothetical informational preferences in a German sample
作者
关键词
Genetic testing, Human genetics, Physicians, Clinical genetics, Genetics of disease, Educational attainment, Human learning, Learning
出版物
PLoS One
Volume 13, Issue 6, Pages e0198249
出版商
Public Library of Science (PLoS)
发表日期
2018-06-21
DOI
10.1371/journal.pone.0198249
参考文献
相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。- Cassandra’s regret: The psychology of not wanting to know.
- (2017) Gerd Gigerenzer et al. PSYCHOLOGICAL REVIEW
- Unsolved challenges of clinical whole-exome sequencing: a systematic literature review of end-users’ views
- (2016) Gabrielle Bertier et al. BMC Medical Genomics
- Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics
- (2016) Sarah S. Kalia et al. GENETICS IN MEDICINE
- Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research
- (2015) Anna Middleton et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project
- (2015) Saskia C Sanderson et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Stakeholders’ perspectives on biobank-based genomic research: systematic review of the literature
- (2015) Alma Husedzinovic et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- A New Approach to Assessing Affect and the Emotional Implications of Personal Genomic Testing for Common Disease Risk
- (2015) Suzanne C. O''Neill et al. Public Health Genomics
- The “Right Not to Know” in the Genomic Era: Time to Break From Tradition?
- (2014) Benjamin E. Berkman et al. AMERICAN JOURNAL OF BIOETHICS
- Do Participants in Genome Sequencing Studies of Psychiatric Disorders Wish to Be Informed of Their Results? A Survey Study
- (2014) Elise T. Bui et al. PLoS One
- Genetics professionals' perspectives on reporting incidental findings from clinical genome-wide sequencing
- (2013) Zoe Lohn et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Experiences and attitudes of genome investigators regarding return of individual genetic test results
- (2013) Rachel B. Ramoni et al. GENETICS IN MEDICINE
- ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
- (2013) Robert C. Green et al. GENETICS IN MEDICINE
- Incidental Findings from Clinical Genome-Wide Sequencing: A Review
- (2013) Z. Lohn et al. Journal of Genetic Counseling
- How could disclosing incidental information from whole-genome sequencing affect patient behavior?
- (2013) Kurt D Christensen et al. Personalized Medicine
- “I want to know what's in Pandora's box”: Comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing
- (2012) Anne Townsend et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Perspectives of clinical genetics professionals toward genome sequencing and incidental findings: a survey study
- (2012) AA Lemke et al. CLINICAL GENETICS
- To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts
- (2012) Gabrielle M Christenhusz et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Public attitudes towards genetic testing revisited: comparing opinions between 2002 and 2010
- (2012) Lidewij Henneman et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study
- (2012) Flavia M Facio et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Public preferences regarding the return of individual genetic research results: findings from a qualitative focus group study
- (2012) Juli Murphy Bollinger et al. GENETICS IN MEDICINE
- Return of results: not that complicated?
- (2012) James P. Evans et al. GENETICS IN MEDICINE
- Opportunities and challenges for the integration of massively parallel genomic sequencing into clinical practice: lessons from the ClinSeq project
- (2012) Leslie G. Biesecker GENETICS IN MEDICINE
- Critical social theory approach to disclosure of genomic incidental findings
- (2012) Jeffrey L Bevan et al. NURSING ETHICS
- Researchers’ opinions towards the communication of results of biobank research: a survey study
- (2011) Tineke M Meulenkamp et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Public Perspectives on Returning Genetics and Genomics Research Results
- (2011) J. O’Daniel et al. Public Health Genomics
- Public Attitudes and Beliefs About Genetics
- (2010) Celeste M. Condit Annual Review of Genomics and Human Genetics
- An epidemiologic-based survey of public attitudes towards predictive genetic testing in Russia
- (2010) Oksana A Makeeva et al. Personalized Medicine
- Construal-level theory of psychological distance.
- (2010) Yaacov Trope et al. PSYCHOLOGICAL REVIEW
- The complete genome of an individual by massively parallel DNA sequencing
- (2008) David A. Wheeler et al. NATURE
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