(Q52560326)

English

Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial.

scientific article published on 26 April 2018

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scholarly article

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial. (English)

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

1 reference

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Jada G. Hamilton

object named as

Jada G Hamilton

19

0 references

Kasmintan A Schrader

object named as

Kasmintan A Schrader

7

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20

object named as

Kenneth Offit

1 reference

Europe PubMed Central

28 June 2018

21

object named as

Mark Robson

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

22

object named as

Kevin E Thorpe

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

Andreas Laupacis

23

object named as

Andreas Laupacis

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

author name string

Salma Shickh

1

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

Marc Clausen

2

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

Chloe Mighton

3

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

Selina Casalino

4

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

Esha Joshi

5

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

Emily Glogowski

6

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

Adena Scheer

8

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

Christine Elser

9

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

Seema Panchal

10

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

Andrea Eisen

11

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

Tracy Graham

12

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

Melyssa Aronson

13

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

Kara M Semotiuk

14

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

Laura Winter-Paquette

15

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

Michael Evans

16

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

Jordan Lerner-Ellis

17

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

June C Carroll

18

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Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

Yvonne Bombard

24

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Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

publication date

26 April 2018

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Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

8

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Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

4

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Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

e021876

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

Clinical genome sequencing and population preferences for information about 'incidental' findings-From medically actionable genes (MAGs) to patient actionable genes (PAGs)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5922516

30 June 2018

Expect the unexpected: screening for secondary findings in clinical genomics research

1 reference

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A clinical utility study of exome sequencing versus conventional genetic testing in pediatric neurology

1 reference

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30 June 2018

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics

1 reference

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Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors

1 reference

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30 June 2018

Molecular findings among patients referred for clinical whole-exome sequencing

1 reference

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30 June 2018

Interactive e-counselling for genetics pre-test decisions: where are we now?

1 reference

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30 June 2018

Return of genomic results to research participants: the floor, the ceiling, and the choices in between

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5922516

30 June 2018

Testing personalized medicine: patient and physician expectations of next-generation genomic sequencing in late-stage cancer care

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30 June 2018

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=5922516

30 June 2018

Long-QT syndrome: from genetics to management

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30 June 2018

Effects of informed consent for individual genome sequencing on relevant knowledge

1 reference

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30 June 2018

Measures of anxiety: State-Trait Anxiety Inventory (STAI), Beck Anxiety Inventory (BAI), and Hospital Anxiety and Depression Scale-Anxiety (HADS-A).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5922516

30 June 2018

Decision aids for people facing health treatment or screening decisions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5922516

30 June 2018

Whole exome and whole genome sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5922516

30 June 2018

Disclosure of individual genetic data to research participants: the debate reconsidered

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5922516

30 June 2018

Personal genome research : what should the participant be told?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5922516

30 June 2018

The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5922516

30 June 2018

Sampling in qualitative research. Purposeful and theoretical sampling; merging or clear boundaries?

1 reference

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30 June 2018

Rigor or rigor mortis: the problem of rigor in qualitative research revisited

1 reference

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30 June 2018

Sample size in qualitative research.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5922516

30 June 2018

Validation of a decisional conflict scale

1 reference

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30 June 2018

The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.

1 reference

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13 August 2018

Effect of decision aid for breast cancer prevention on decisional conflict in women with a BRCA1 or BRCA2 mutation: a multisite, randomized, controlled trial.

1 reference

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13 August 2018

DECIDE: a Decision Support Tool to Facilitate Parents' Choices Regarding Genome-Wide Sequencing.

1 reference

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13 August 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5922516

13 August 2018

Validation of a preparation for decision making scale.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5922516

13 August 2018

Randomized trial of a decision aid for individuals considering genetic testing for hereditary nonpolyposis colorectal cancer risk.

1 reference

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Applying decision analysis to facilitate informed decision making about prenatal diagnosis for Down syndrome: a randomised controlled trial.

1 reference

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13 August 2018

An interactive computer program can effectively educate patients about genetic testing for breast cancer susceptibility.

1 reference

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13 August 2018

Approaches to qualitative-quantitative methodological triangulation

1 reference

https://pubmed.ncbi.nlm.nih.gov/29700101

12 December 2020

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1 reference

https://pubmed.ncbi.nlm.nih.gov/29700101

12 December 2020

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Constructing Grounded Theory: A practical guide through qualitative analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/29700101

12 December 2020

based on heuristic

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The Genomics ADvISER: development and usability testing of a decision aid for the selection of incidental sequencing results

1 reference

https://pubmed.ncbi.nlm.nih.gov/29700101

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/BMJOPEN-2018-021876

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

1 reference

Europe PubMed Central

28 June 2018

http://europepmc.org/abstract/PMC/5922516

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