Mandatory extended searches in all genome sequencing: "incidental findings," patient autonomy, and shared decision making.
about
Stakeholder engagement in policy development: challenges and opportunities for human genomicsPractical guidance on informed consent for pediatric participants in a biorepositoryClinical integration of next generation sequencing: coverage and reimbursement challenges.Pathogenic variants for Mendelian and complex traits in exomes of 6,517 European and African Americans: implications for the return of incidental resultsReturn of results in the genomic medicine projects of the eMERGE networkComprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases.Evolution of universal review and disclosure of MRI reports to research participantsCancer screening and genetics: a tale of two paradigmsClinical genome sequencing and population preferences for information about 'incidental' findings-From medically actionable genes (MAGs) to patient actionable genes (PAGs)Return of genomic results to research participants: the floor, the ceiling, and the choices in between.Translating personalized medicine using new genetic technologies in clinical practice: the ethical issuesReturn of Results from Genomic Sequencing: A Policy Discussion of Secondary Findings for Cancer Predisposition.Genetic testing of children for diseases that have onset in adulthood: the limits of family interests.The unintended implications of blurring the line between research and clinical care in a genomic age.The translational potential of research on the ethical, legal, and social implications of genomicsThe fiduciary relationship model for managing clinical genomic "incidental" findings.Molecular findings among patients referred for clinical whole-exome sequencing.Societal preferences for the return of incidental findings from clinical genomic sequencing: a discrete-choice experiment.Managing the Ethical Issues of Genomic Research using Pathology Specimens.Reporting Incidental Findings in Genomic Scale Clinical Sequencing-A Clinical Laboratory Perspective: A Report of the Association for Molecular Pathology.Identification of Medically Actionable Secondary Findings in the 1000 Genomes.A protocol for the identification and validation of novel genetic causes of kidney diseaseLooking for Trouble: Preventive Genomic Sequencing in the General Population and the Role of Patient Choice.Association of Researcher Characteristics with Views on Return of Incidental Findings from Genomic Research.Canadian Research Ethics Board Leadership Attitudes to the Return of Genetic Research Results to Individuals and Their FamiliesPatients' views on incidental findings from clinical exome sequencing.Compare and contrast: a cross-national study across UK, USA and Greek experts regarding return of incidental findings from clinical sequencingImplications of using whole genome sequencing to test unselected populations for high risk breast cancer genes: a modelling studyLegal approaches regarding health-care decisions involving minors: implications for next-generation sequencing.Managing incidental genomic findings in clinical trials: fulfillment of the principle of justice.From "Personalized" to "Precision" Medicine: The Ethical and Social Implications of Rhetorical Reform in Genomic Medicine.Managing the ethical challenges of next-generation sequencing in genomic medicine.Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders.Interest and Attitudes of Patients With Advanced Cancer With Regard to Secondary Germline Findings From Tumor Genomic Profiling.Clinical genomics: from a truly personal genome viewpoint.Myopathology in the times of modern genetics.Ethical considerations surrounding germline next-generation sequencing of children with cancer.Revealing the incidentalome when targeting the tumor genomeClinical exome performance for reporting secondary genetic findingsIncidental findings from clinical sequencing in Greece: reporting experts' attitudes.
P2860
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P2860
Mandatory extended searches in all genome sequencing: "incidental findings," patient autonomy, and shared decision making.
description
2013 nî lūn-bûn
@nan
2013 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Mandatory extended searches in ...... y, and shared decision making.
@ast
Mandatory extended searches in ...... y, and shared decision making.
@en
Mandatory extended searches in ...... y, and shared decision making.
@nl
type
label
Mandatory extended searches in ...... y, and shared decision making.
@ast
Mandatory extended searches in ...... y, and shared decision making.
@en
Mandatory extended searches in ...... y, and shared decision making.
@nl
prefLabel
Mandatory extended searches in ...... y, and shared decision making.
@ast
Mandatory extended searches in ...... y, and shared decision making.
@en
Mandatory extended searches in ...... y, and shared decision making.
@nl
P356
P1476
Mandatory extended searches in ...... y, and shared decision making.
@en
P2093
Lainie Friedman Ross
Mark A Rothstein
P304
P356
10.1001/JAMA.2013.41700
P407
P577
2013-07-01T00:00:00Z