(Q39022681)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25832998%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

title

Overcoming challenges to meaningful informed consent for whole genome sequencing in pediatric cancer research (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25832998%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

main subject

informed consent

0 references

whole genome sequencing

1 reference

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25832998%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

Jennifer A Oberg

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25832998%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

Julia L Glade Bender

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25832998%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

Paul Stuart Appelbaum

7

object named as

Paul S Appelbaum

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25832998%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

6

Wendy K Chung

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25832998%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

author name string

Elizabeth G Cohn

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25832998%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

Marilyn Morris

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25832998%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

Jenny Ruiz

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25832998%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

Jennifer M Levine

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25832998%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

publication date

1 April 2015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25832998%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

published in

Pediatric Blood & Cancer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25832998%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

volume

62

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25832998%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

issue

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25832998%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

page(s)

1374-1380

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25832998%20AND%20SRC:MED&resulttype=core&format=json

The Pediatric Cancer Genome Project

4 March 2020

cites work

1 reference

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

21 January 2018

1 reference

Disclosing pathogenic genetic variants to research participants: quantifying an emerging ethical responsibility

21 January 2018

1 reference

Research ethics recommendations for whole-genome research: consensus statement

21 January 2018

1 reference

Research ethics and the challenge of whole-genome sequencing

21 January 2018

1 reference

Disclosure of incidental findings from next-generation sequencing in pediatric genomic research

21 January 2018

1 reference

Models of consent to return of incidental findings in genomic research

21 January 2018

1 reference

Informed consent for return of incidental findings in genomic research

21 January 2018

1 reference

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

21 January 2018

1 reference

Tailoring the process of informed consent in genetic and genomic research

21 January 2018

1 reference

Genomics really gets personal: how exome and whole genome sequencing challenge the ethical framework of human genetics research

21 January 2018

1 reference

Childhood and adolescent cancer statistics, 2014.

21 January 2018

1 reference

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

21 January 2018

1 reference

Qualitative content analysis in nursing research: concepts, procedures and measures to achieve trustworthiness

21 January 2018

1 reference

Effects of informed consent for individual genome sequencing on relevant knowledge

21 January 2018

1 reference

Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group study

21 January 2018

1 reference

Motivators for participation in a whole-genome sequencing study: implications for translational genomics research

21 January 2018

1 reference

Stakeholders' opinions on the implementation of pediatric whole exome sequencing: implications for informed consent

21 January 2018

1 reference

Parental attitudes, values, and beliefs toward the return of results from exome sequencing in children

21 January 2018

1 reference

Informed consent for whole genome sequencing: a qualitative analysis of participant expectations and perceptions of risks, benefits, and harms.

21 January 2018

1 reference

Attitudes about genetics in underserved, culturally diverse populations

21 January 2018

1 reference

Return of secondary genomic findings vs patient autonomy: implications for medical care

21 January 2018

1 reference

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

21 January 2018

1 reference

“I want to know what's in Pandora's box”: Comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing

21 January 2018

1 reference