“Not pathogenic until proven otherwise”: perspectives of UK clinical genomics professionals toward secondary findings in context of a Genomic Medicine Multidisciplinary Team and the 100,000 Genomes Project

Insights from early experience of a Rare Disease Genomic Medicine Multidisciplinary Team: a qualitative study

(2017) Elizabeth Ormondroyd et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium

(2016) Laura M. Amendola et al.   AMERICAN JOURNAL OF HUMAN GENETICS

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

A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories

(2016) Julianne M. O’Daniel et al.   GENETICS IN MEDICINE

Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies

(2016) Michael P. Mackley et al.   GENETICS IN MEDICINE

Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records

(2016) Sara L. Van Driest et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Genetic identification of familial hypercholesterolemia within a single U.S. health care system

(2016) Noura S. Abul-Husn et al.   SCIENCE

Freedom of Choice About Incidental Findings Can Frustrate Participants' True Preferences

(2015) Jennifer Viberg et al.   BIOETHICS

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

The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists

(2015) Kym Boycott et al.   JOURNAL OF MEDICAL GENETICS

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders

(2015) Jenny C Taylor et al.   NATURE GENETICS

Attitudes of Genetics Professionals Toward the Return of Incidental Results from Exome and Whole-Genome Sequencing

(2014) Joon-Ho Yu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between

(2014) Gail P. Jarvik et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Return of results: Ethical and legal distinctions between research and clinical care

(2014) Wylie Burke et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

The hidden harm behind the return of results from personal genome services: a need for rigorous and responsible evaluation

(2014) A. Cecile J.W. Janssens   GENETICS IN MEDICINE

The unintended implications of blurring the line between research and clinical care in a genomic age

(2014) Benjamin E Berkman et al.   Personalized Medicine

Do Researchers Have an Obligation to Actively Look for Genetic Incidental Findings?

(2013) Catherine Gliwa et al.   AMERICAN JOURNAL OF BIOETHICS

Genetics professionals' perspectives on reporting incidental findings from clinical genome-wide sequencing

(2013) Zoe Lohn et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Whole-genome sequencing in health care

(2013) Carla G van El et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Informed consent for whole-genome sequencing studies in the clinical setting. Proposed recommendations on essential content and process

(2013) Carmen Ayuso et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Processes and factors involved in decisions regarding return of incidental genomic findings in research

(2013) Robert Klitzman et al.   GENETICS IN MEDICINE

Attitudes of Canadian researchers toward the return to participants of incidental and targeted genomic findings obtained in a pediatric research setting

(2013) Conrad V. Fernandez 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

The Indispensable Role of Professional Judgment in Genomic Medicine

(2013) Amy L. McGuire et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

A Closer Look at the Recommended Criteria for Disclosing Genetic Results: Perspectives of Medical Genetic Specialists, Genomic Researchers, and Institutional Review Board Chairs

(2013) Debra S. Brandt et al.   Journal of Genetic Counseling

Views of Genetics Health Professionals on the Return of Genomic Results

(2013) Megan E. Grove et al.   Journal of Genetic Counseling

Patient Autonomy and Incidental Findings in Clinical Genomics

(2013) S. M. Wolf et al.   SCIENCE

“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

Exploring concordance and discordance for return of incidental findings from clinical sequencing

(2012) Robert C. Green et al.   GENETICS IN MEDICINE

Genetics specialists’ perspectives on disclosure of genomic incidental findings in the clinical setting

(2012) Nancy R. Downing et al.   PATIENT EDUCATION AND COUNSELING

Genomics really gets personal: How exome and whole genome sequencing challenge the ethical framework of human genetics research

(2011) Holly K. Tabor et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A