(Q34507484)

2 August 2017

title

Informed consent for exome sequencing in diagnostics: exploring first experiences and views of professionals and patients (English)

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2 August 2017

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T Rigter

1

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2 August 2017

C J A van Aart

2

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2 August 2017

M W Elting

3

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2 August 2017

Q Waisfisz

4

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2 August 2017

M C Cornel

5

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2 August 2017

L Henneman

6

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2 August 2017

publication date

4 November 2013

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2 August 2017

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2 August 2017

volume

85

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2 August 2017

issue

5

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2 August 2017

page(s)

417-422

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Genetics patients' perspectives on clinical genomic testing

2 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231277

Recommendations for returning genomic incidental findings? We need to talk!

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231277

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231277

Reflecting on earlier experiences with unsolicited findings: points to consider for next-generation sequencing and informed consent in diagnostics

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231277

Next-generation sequencing: does the next generation still have a right to an open future?

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231277

Point-counterpoint. Patient autonomy and incidental findings in clinical genomics

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231277

Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231277

Description and pilot results from a novel method for evaluating return of incidental findings from next-generation sequencing technologies

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231277

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231277

Perspectives of clinical genetics professionals toward genome sequencing and incidental findings: a survey study

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231277

Opportunities and challenges for the integration of massively parallel genomic sequencing into clinical practice: lessons from the ClinSeq project

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231277

The legal risks of returning results of genomics research

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231277

What can exome sequencing do for you?

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231277

Diagnostic exome sequencing in persons with severe intellectual disability

7 July 2018

1 reference

The clinical implementation of whole genome sequencing: a conversation with seven scientific experts.

21 January 2018

1 reference

Whole-genome sequencing and the physician

21 January 2018

1 reference

Working towards ethical management of genetic testing

21 January 2018

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Aims and harvest of moral case deliberation

21 January 2018

1 reference

Feedback of individual genetic results to research participants: in favor of a qualified disclosure policy

21 January 2018

1 reference

New challenges for informed consent through whole genome array testing

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231277

Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time

27 October 2018

1 reference

Incidental findings in genetic research and clinical diagnostic tests: a systematic review

21 January 2018

1 reference

Challenges in the clinical application of whole-genome sequencing

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24117109

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1111/CGE.12299

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2 August 2017

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2 August 2017

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