(Q34549035)

3 August 2017

title

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

1 reference

3 August 2017

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whole genome sequencing

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Carmen Ayuso

1

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Rafael Dal-Ré Tenreiro

series ordinal

4

object named as

Rafael Dal-Ré

1 reference

3 August 2017

José M Millán

2

1 reference

3 August 2017

Marta Mancheño

series ordinal

3

1 reference

3 August 2017

publication date

16 January 2013

1 reference

European Journal of Human Genetics

3 August 2017

published in

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3 August 2017

volume

21

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3 August 2017

issue

10

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3 August 2017

page(s)

1054-1059

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https://scigraph.springernature.com/pub.10.1038/ejhg.2012.297

3 August 2017

exact match

0 references

cites work

Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778336

To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778336

A personal perspective on returning secondary results of clinical 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=3778336

Challenges 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=3778336

Exploring concordance and discordance for return of incidental findings from clinical 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=3778336

Technological advances in DNA sequence enrichment and sequencing for germline genetic diagnosis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778336

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=3778336

The role of disease characteristics in the ethical debate on personal genome testing

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778336

Next generation sequencing--implications for clinical practice

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778336

A clinical perspective on ethical issues in genetic testing

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778336

Use of whole-genome sequencing to diagnose a cryptic fusion oncogene

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778336

Personal genomes in progress: from the human genome project to the personal genome 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=3778336

Whole genome scanning: resolving clinical diagnosis and management amidst complex data

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778336

Is gene discovery research or diagnosis?

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778336

The changing landscape of genetic testing and its impact on clinical and laboratory services and research in Europe

7 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2012.297

Whole-genome sequencing and the physician.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2012.297

Downsizing genomic medicine: approaching the ethical complexity of whole-genome sequencing by starting small

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778336

New challenges for informed consent through whole genome array testing

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778336

Ensuring the safe use of genomic medicine in children

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3778336

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

27 October 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2012.297

Challenges in the clinical application of whole-genome sequencing

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23321621

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Personal genomics: information can be harmful

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23321621

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/EJHG.2012.297

1 reference

Dimensions Publication ID

3 August 2017

0 references

1 reference

3 August 2017

1 reference