(Q30591763)

19 October 2017

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

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19 October 2017

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12

Amy L McGuire

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19 October 2017

Laurence B. McCullough

11

object named as

Laurence B McCullough

1 reference

19 October 2017

8

Christine M Eng

1 reference

19 October 2017

1

Sarah Scollon

1 reference

19 October 2017

2

Katie Bergstrom

1 reference

19 October 2017

3

Robin A Kerstein

1 reference

19 October 2017

9

Murali M Chintagumpala

1 reference

19 October 2017

10

Stacey L Berg

1 reference

19 October 2017

13

Sharon E Plon

1 reference

19 October 2017

7

Richard A Gibbs

1 reference

19 October 2017

Tao Wang

4

1 reference

19 October 2017

Susan G Hilsenbeck

5

1 reference

19 October 2017

Uma Ramamurthy

6

1 reference

19 October 2017

D Williams Parsons

14

1 reference

19 October 2017

17 September 2014

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19 October 2017

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19 October 2017

6

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19 October 2017

9

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19 October 2017

69

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Creative Commons Attribution 4.0 International

19 October 2017

start time

17 September 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

exact match

https://scigraph.springernature.com/pub.10.1186/s13073-014-0069-3

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cites work

Patient involvement in informed consent for pediatric phase I cancer research.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4195891

Participants' recall and understanding of genomic research and large-scale data sharing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4195891

Clinical whole-exome sequencing for the diagnosis of mendelian disorders

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4195891

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4195891

Attitudes of patients with cancer about personalized medicine and somatic genetic testing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4195891

Next-generation sequencing in the clinic: are we ready?

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4195891

Effects of informed consent for individual genome sequencing on relevant knowledge

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4195891

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4195891

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4195891

To share or not to share: a randomized trial of consent for data sharing in genome research

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4195891

Communicating genetic and genomic information: health literacy and numeracy considerations

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4195891

Exploring the public understanding of basic genetic concepts

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4195891

Quality of informed consent in cancer clinical trials: a cross-sectional survey

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4195891

Diagnosis, disclosure, and informed consent: learning from parents of children with cancer

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4195891

Trends in cancer incidence among children in the U.S.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4195891

Informed consent for treatment of childhood cancer: factors affecting parents' decision making

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4195891

Suggestions from adolescents, young adults, and parents for improving informed consent in phase 1 pediatric oncology trials.

20 June 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13073-014-0069-3

General public's knowledge, interest and information needs related to genetic cancer: an exploratory study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13073-014-0069-3

Australian study on public knowledge of human genetics and health.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13073-014-0069-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13073-014-0069-3

Outcomes of informed consent among parents of children in cancer clinical trials

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13073-014-0069-3

Comparison of the informed consent process for randomized clinical trials in pediatric and adult oncology

21 January 2018

1 reference

12 December 2020

Participation in cancer clinical trials: race-, sex-, and age-based disparities

1 reference

12 December 2020

Two models of implementing informed consent

1 reference

12 December 2020

Attitudes of 47 mothers of pediatric oncology patients toward genetic testing for cancer predisposition

1 reference

12 December 2020

Willingness to participate in biomedical research. African-americans vs whites

1 reference

12 December 2020

10.1186/S13073-014-0069-3

Identifiers

DOI

1 reference

Dimensions Publication ID

19 October 2017

0 references

1 reference

19 October 2017

PubMed publication ID

25317207

1 reference