Downsizing genomic medicine: approaching the ethical complexity of whole-genome sequencing by starting small
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Incidental Findings with Genomic Testing: Implications for Genetic Counseling PracticeWe screen newborns, don't we?: realizing the promise of public health genomicsGenomic intensive care: should we perform genome testing in critically ill newborns?Patient feedback and early outcome data with a novel tiered-binned model for multiplex breast cancer susceptibility testing.Self-guided management of exome and whole-genome sequencing results: changing the results return model.Genetics patients' perspectives on clinical genomic testing.Prenatal whole genome sequencing: just because we can, should we?Genetic testing integration panels (GTIPs): a novel approach for considering integration of direct-to-consumer and other new genetic tests into patient care.The ethical hazards and programmatic challenges of genomic newborn screening.Patient-controlled encrypted genomic data: an approach to advance clinical genomics.The challenge of consent in clinical genome-wide testing.Informed consent for whole-genome sequencing studies in the clinical setting. Proposed recommendations on essential content and processThe challenge of informed consent and return of results in translational genomics: empirical analysis and recommendations.Exome sequencing and the genetics of intellectual disability.Multiplex genetic testing: reconsidering utility and informed consent in the era of next-generation sequencingWhole-genome sequencing in newborn screening? A statement on the continued importance of targeted approaches in newborn screening programmesInformed consent and genomic incidental findings: IRB chair perspectives.Development of a tiered and binned genetic counseling model for informed consent in the era of multiplex testing for cancer susceptibilityClinical and ethical considerations of massively parallel sequencing in transplantation science.Perspectives of clinical genetics professionals toward genome sequencing and incidental findings: a survey study.Integrating genomics into clinical oncology: ethical and social challenges from proponents of personalized medicine.Genomic counseling: next generation counseling.Information Topics of Greatest Interest for Return of Genome Sequencing Results among Women Diagnosed with Breast Cancer at a Young Age.Exome sequencing: dual role as a discovery and diagnostic tool.Technological advances in DNA sequence enrichment and sequencing for germline genetic diagnosis.Incidental findings from clinical genome-wide sequencing: a review.Next-generation sequencing applied to rare diseases genomics.Managing the ethical challenges of next-generation sequencing in genomic medicine.Is there a duty to recontact in light of new genetic technologies? A systematic review of the literature.Immune biomarkers: the promises and pitfalls of personalized medicine.A Framework for Unrestricted Prenatal Whole-Genome Sequencing: Respecting and Enhancing the Autonomy of Prospective Parents.Genetics professionals' opinions of whole-genome sequencing in the newborn period.Ethical considerations associated with clinical use of next-generation sequencing in children.Ethical challenges of the use of whole exome sequencing in the clinic.Practices and policies of clinical exome sequencing providers: analysis and implications.[Personalised medicine. Aims and challenges].Informed consent for whole genome sequencing: a qualitative analysis of participant expectations and perceptions of risks, benefits, and harms.Genetics professionals' perspectives on reporting incidental findings from clinical genome-wide sequencing“I want to know what's in Pandora's box”: Comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing
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Downsizing genomic medicine: approaching the ethical complexity of whole-genome sequencing by starting small
description
wetenschappelijk artikel
@nl
наукова стаття, опублікована в березні 2011
@uk
name
Downsizing genomic medicine: a ...... e sequencing by starting small
@en
Downsizing genomic medicine: a ...... e sequencing by starting small
@nl
type
label
Downsizing genomic medicine: a ...... e sequencing by starting small
@en
Downsizing genomic medicine: a ...... e sequencing by starting small
@nl
prefLabel
Downsizing genomic medicine: a ...... e sequencing by starting small
@en
Downsizing genomic medicine: a ...... e sequencing by starting small
@nl
P2860
P1433
P1476
Downsizing genomic medicine: a ...... e sequencing by starting small
@en
P2860
P2888
P356
10.1097/GIM.0B013E31820F603F
P407
P577
2011-03-01T00:00:00Z
P6179
1043423374