“I want to know what's in Pandora's box”: Comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing

A Clinical Perspective on Ethical Issues in Genetic Testing

(2011) R. H. Sijmons et al.   Accountability in Research-Policies and Quality Assurance

Public attitudes toward ancillary information revealed by pharmacogenetic testing under limited information conditions

(2011) Susanne B. Haga et al.   GENETICS IN MEDICINE

Downsizing genomic medicine: Approaching the ethical complexity of whole-genome sequencing by starting small

(2011) Richard R Sharp   GENETICS IN MEDICINE

Deploying whole genome sequencing in clinical practice and public health: Meeting the challenge one bin at a time

(2011) Jonathan S Berg et al.   GENETICS IN MEDICINE

Parents' Attitudes Toward Pediatric Genetic Testing for Common Disease Risk

(2011) K. P. Tercyak et al.   PEDIATRICS

PERSONAL GENOMES: NO BAD NEWS?

(2010) RUTH CHADWICK   BIOETHICS

A formal risk-benefit framework for genomic tests: Facilitating the appropriate translation of genomics into clinical practice

(2010) David L Veenstra et al.   GENETICS IN MEDICINE

Consumer perceptions of direct-to-consumer personalized genomic risk assessments

(2010) Cinnamon S Bloss et al.   GENETICS IN MEDICINE

A timely arrival for genomic medicine

(2010) Alan N Mayer et al.   GENETICS IN MEDICINE

Supporting Patient Autonomy: The Importance of Clinician-patient Relationships

(2010) Vikki A. Entwistle et al.   JOURNAL OF GENERAL INTERNAL MEDICINE

The return of individual research findings in paediatric genetic research

(2010) K. Hens et al.   JOURNAL OF MEDICAL ETHICS

Clinical assessment incorporating a personal genome

(2010) Euan A Ashley et al.   LANCET

Personalized genomic information: preparing for the future of genetic medicine

(2010) Alan E. Guttmacher et al.   NATURE REVIEWS GENETICS

Personal genome research : what should the participant be told?

(2010) Amy L. McGuire et al.   TRENDS IN GENETICS

Disclosure of individual genetic data to research participants: the debate reconsidered

(2010) Annelien L. Bredenoord et al.   TRENDS IN GENETICS

Evaluating the utility of personal genomic information

(2009) Morris W Foster et al.   GENETICS IN MEDICINE

New challenges for informed consent through whole genome array testing

(2009) C Netzer et al.   JOURNAL OF MEDICAL GENETICS

Parents' Interest in Predictive Genetic Testing for Their Children When a Disease Has No Treatment

(2009) B. A. Tarini et al.   PEDIATRICS

Public Expectations for Return of Results from Large-Cohort Genetic Research

(2008) Juli Murphy et al.   AMERICAN JOURNAL OF BIOETHICS

Should genetic testing forBRCA1/2 be permitted for minors? Opinions ofBRCA mutation carriers and their adult offspring

(2008) Angela R. Bradbury et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Understanding Incidental Findings in the Context of Genetics and Genomics

(2008) Mildred K. Cho   JOURNAL OF LAW MEDICINE & ETHICS

Genomic Research and Incidental Findings

(2008) Brian Van Ness   JOURNAL OF LAW MEDICINE & ETHICS

Managing Incidental Findings in Human Subjects Research: Analysis and Recommendations

(2008) Susan M. Wolf et al.   JOURNAL OF LAW MEDICINE & ETHICS

Autonomy and selfishness

(2008) Grant Gillett   LANCET

Research ethics and the challenge of whole-genome sequencing

(2007) Amy L. McGuire et al.   NATURE REVIEWS GENETICS