Experiences with obtaining informed consent for genomic sequencing. - Wikidata - awgldk - TriplyDB

Experiences with obtaining informed consent for genomic sequencing.

Experiences with obtaining informed consent for genomic sequencing.

http://www.wikidata.org/entity/Q54858926

about

Incidental Findings with Genomic Testing: Implications for Genetic Counseling Practice Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.A Clinician's perspective on clinical exome sequencing.A review of consent practices and perspectives for pharmacogenetic testing Precision medicine: opportunities, possibilities, and challenges for patients and providers.How do providers discuss the results of pediatric exome sequencing with families?Parents' Perspectives on Supporting Their Decision Making in Genome-Wide Sequencing.Diagnostic exome sequencing in children: A survey of parental understanding, experience and psychological impact.The who, what, and why of research participants' intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study.Enrolling Genomics Research Participants through a Clinical Setting: the Impact of Existing Clinical Relationships on Informed Consent and Expectations for Return of Research Results.Public's Views toward Return of Secondary Results in Genomic Sequencing: It's (Almost) All about the Choice.Readability of informed consent forms for whole-exome and whole-genome sequencing.Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing.A randomized controlled study of a consent intervention for participating in an NIH genome sequencing study.A Commentary on Opportunities for the Genetic Counseling Profession through Genomic Variant Interpretation: Reflections from an Ex-Lab Rat.Genetic counselling in the era of genomic medicine.Pediatric Whole Exome Sequencing: an Assessment of Parents' Perceived and Actual Understanding.Clinical providers' experiences with returning results from genomic sequencing: an interview study."Possibly positive or certainly uncertain?": participants' responses to uncertain diagnostic results from exome sequencing.Development and Validation of a Genomic Knowledge Scale to Advance Informed Decision Making Research in Genomic Sequencing.Evaluating parents' decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized controlled trial protocol.Consent to a Postmortem Tissue Procurement Study: Distinguishing Family Decision Makers' Knowledge of the Genotype-Tissue Expression Project

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Experiences with obtaining informed consent for genomic sequencing.

http://www.wikidata.org/entity/Q54858926

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年学术文章

@wuu

2015年学术文章

@zh-cn

2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

@zh-sg

2015年學術文章

@yue

2015年學術文章

@zh

2015年學術文章

@zh-hant

name

Experiences with obtaining informed consent for genomic sequencing.

@en

Experiences with obtaining informed consent for genomic sequencing.

@nl

type

label

Experiences with obtaining informed consent for genomic sequencing.

@en

Experiences with obtaining informed consent for genomic sequencing.

@nl

prefLabel

Experiences with obtaining informed consent for genomic sequencing.

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Experiences with obtaining informed consent for genomic sequencing.

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American Journal of Medical Genetics

P1476

Experiences with obtaining informed consent for genomic sequencing.

@en

P2093

Ashley N Tomlinson

http://www.w3.org/2001/XMLSchema#string

Debra Skinner

http://www.w3.org/2001/XMLSchema#string

Denise L Perry

http://www.w3.org/2001/XMLSchema#string

Myra I Roche

http://www.w3.org/2001/XMLSchema#string

Sarah R Scollon

http://www.w3.org/2001/XMLSchema#string

P2860

Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine.

Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease

Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects

Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

Personalized disclosure by information-on-demand: attending to patients' needs in the informed consent process.

Obtaining informed consent for clinical tumor and germline exome sequencing of newly diagnosed childhood cancer patients.

Participants' recall and understanding of genomic research and large-scale data sharing.

Interventions to improve patient comprehension in informed consent for medical and surgical procedures: a systematic review.

Genetics patients' perspectives on clinical genomic testing.

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2635-2646

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10.1002/AJMG.A.37256

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11

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167A

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Barbara A Bernhardt

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2015-07-21T00:00:00Z

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280328794

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26198374

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informed consent

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4980577

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