Eliciting preferences on secondary findings: the Preferences Instrument for Genomic Secondary Results. - Wikidata - wikimedia - TriplyDB

Eliciting preferences on secondary findings: the Preferences Instrument for Genomic Secondary Results.

Eliciting preferences on secondary findings: the Preferences Instrument for Genomic Secondary Results.

http://www.wikidata.org/entity/Q30839925

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PUGS: A novel scale to assess perceptions of uncertainties in genome sequencing Preferences for the Return of Individual Results From Research on Pediatric Biobank Samples.Shaping an Effective Health Information Website on Rare Diseases Using a Group Decision-Making Tool: Inclusion of the Perspectives of Patients, Their Family Members, and Physicians.Connecting Gaucher and Parkinson Disease: Considerations for Clinical and Research Genetic Counseling Settings.When Personal Feels Invasive: Foreseeing Challenges in Precision Medicine Communication.Genetic counselling in the era of genomic medicine.Genomic sequencing identifies secondary findings in a cohort of parent study participants

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Eliciting preferences on secondary findings: the Preferences Instrument for Genomic Secondary Results.

http://www.wikidata.org/entity/Q30839925

description

2016 nî lūn-bûn

@nan

2016 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2016 թվականի օգոստոսին հրատարակված գիտական հոդված

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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Genetics in Medicine

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Eliciting preferences on secon ...... for Genomic Secondary Results

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Carla A Rich

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Richard M Myers

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Whitley V Kelley

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P2860

Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network

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

ResearchMatch: a national registry to recruit volunteers for clinical research.

Self-guided management of exome and whole-genome sequencing results: changing the results return model.

Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium.

An informatics approach to analyzing the incidentalome.

How could disclosing incidental information from whole-genome sequencing affect patient behavior?

Operational implementation of prospective genotyping for personalized medicine: the design of the Vanderbilt PREDICT project.

The development of a preference-setting model for the return of individual genomic research results.

Practices and policies of clinical exome sequencing providers: analysis and implications.

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337-344

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scholarly article

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10.1038/GIM.2016.110

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3

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Ellen Wright Clayton

M Frances Wright

Matthew J Westbrook

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Shirley Simmons

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2016-08-25T00:00:00Z

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