(Q27023696)

English

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

scientific article

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scholarly article

1 reference

4 references

22 July 2019

19 September 2019

19 November 2020

6 April 2021

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

0 references

informed consent

1 reference

6 April 2021

preventive health services

1 reference

22 July 2019

biomedical investigative technique

1 reference

19 September 2019

genetic testing

1 reference

19 November 2020

Quinten Waisfisz

8

object named as

Quinten Waisfisz

0 references

6

object named as

Pascal Borry

0 references

Lidewij Henneman

2

object named as

Lidewij Henneman

0 references

Martina C. Cornel

11

object named as

Martina C. Cornel

1 reference

Helger G Yntema

5

object named as

Helger G. Yntema

1 reference

author name string

Tessel Rigter

1

1 reference

Ulf Kristoffersson

3

1 reference

Alison Hall

4

1 reference

Holger Tönnies

7

1 reference

Mariet W. Elting

9

1 reference

Wybo J. Dondorp

10

1 reference

language of work or name

1 reference

publication date

October 2013

1 reference

1 October 2013

4 references

22 July 2019

19 September 2019

19 November 2020

6 April 2021

5 references

22 July 2019

19 September 2019

19 November 2020

6 April 2021

34

1 reference

10

1 reference

1322-8

1 reference

copyright license

Creative Commons Attribution 3.0 Unported

4 references

Europe PubMed Central

22 July 2019

Europe PubMed Central

19 September 2019

Europe PubMed Central

19 November 2020

Europe PubMed Central

6 April 2021

copyright status

0 references

Disease gene identification strategies for exome sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

21 March 2017

Research ethics and the challenge of whole-genome sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

21 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

28 September 2017

Population studies: return of research results and incidental findings Policy Statement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

28 September 2017

Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

28 September 2017

Effects of informed consent for individual genome sequencing on relevant knowledge

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

28 September 2017

Next-generation sequencing demands next-generation phenotyping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

28 September 2017

One thing leads to another: the cascade of obligations when researchers report genetic research results to study participants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

28 September 2017

Taxonomizing, sizing, and overcoming the incidentalome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

28 September 2017

Health-care providers' views on pursuing reproductive benefit through newborn screening: the case of sickle cell disorders.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

28 September 2017

What can exome sequencing do for you?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

28 September 2017

Managing incidental findings on abdominal CT: white paper of the ACR incidental findings committee

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

28 September 2017

Genotype to phenotype-discovery and characterization of novel genomic disorders in a "genotype-first" era.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

28 September 2017

Predictive diagnosis of the cancer prone Li-Fraumeni syndrome by accident: new challenges through whole genome array testing.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

28 September 2017

Managing incidental findings in human subjects research: analysis and recommendations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

28 September 2017

Revisiting Wilson and Jungner in the genomic age: a review of screening criteria over the past 40 years

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

28 September 2017

A proposal for a model of informed consent for the collection, storage and use of biological materials for research purposes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

28 September 2017

Genomic microarrays in human genetic disease and cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

28 September 2017

Benign anatomical mistakes: incidentaloma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

28 September 2017

Ethical considerations associated with clinical use of next-generation sequencing in children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

31 May 2018

Newborn screening for sickle cell disease: whose reproductive benefit?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4285964

31 May 2018

Reply to Ross' commentary: Reproductive benefit through newborn screening: preferences, policy and ethics

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22370

21 January 2018

The expansion of newborn screening: is reproductive benefit an appropriate pursuit?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22370

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22370

21 January 2018

Diagnostic exome sequencing in persons with severe intellectual disability

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22370

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22370

21 January 2018

Genetics professionals' perspectives on reporting incidental findings from clinical genome-wide sequencing

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22370

21 January 2018

Unexpected findings in cancer predisposition genes detected by array comparative genomic hybridisation: what are the issues?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22370

21 January 2018

Whole-genome sequencing and the physician

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22370

21 January 2018

Genome-wide arrays: quality criteria and platforms to be used in routine diagnostics.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22370

21 January 2018

New challenges for informed consent through whole genome array testing

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22370

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22370

21 January 2018

Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22370

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22370

21 January 2018

Clinical obligations and public health programmes: healthcare provider reasoning about managing the incidental results of newborn screening

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22370

21 January 2018

Challenges in the clinical application of whole-genome sequencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/23784691

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Changing the game with whole exome sequencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/23784691

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/HUMU.22370

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

0 references

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