(Q30557139)

English

Return of incidental findings in genomic medicine: measuring what patients value--development of an instrument to measure preferences for information from next-generation testing (IMPRINT).

scientific article

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Return of incidental findings in genomic medicine: measuring what patients value--development of an instrument to measure preferences for information from next-generation testing (IMPRINT). (English)

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

incidental finding

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Stephanie M Fullerton

3

object named as

Stephanie M Fullerton

0 references

6

object named as

Wylie Burke

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Susan B. Trinidad

2

object named as

Susan Brown Trinidad

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8

object named as

Gail P Jarvik

0 references

object named as

Dean A Regier

9

0 references

David L Veenstra

10

object named as

David L Veenstra

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Laura M Amendola

5

object named as

Laura Amendola

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

7

object named as

Fuki M Hisama

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

author name string

Caroline Savage Bennette

1

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Donald Patrick

4

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

language of work or name

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publication date

30 May 2013

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Genetics in Medicine

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

15

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

11

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

873-881

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

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=3823641

20 June 2018

Public preferences regarding the return of individual genetic research results: findings from a qualitative focus group study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823641

20 June 2018

Conjoint Analysis Applications in Health - How are Studies being Designed and Reported?: An Update on Current Practice in the Published Literature between 2005 and 2008.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823641

20 June 2018

Things are Looking up Since We Started Listening to Patients: Trends in the Application of Conjoint Analysis in Health 1982-2007.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823641

20 June 2018

Genetics researchers' and IRB professionals' attitudes toward genetic research review: a comparative analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823641

20 June 2018

IRB perspectives on the return of individual results from genomic research

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823641

20 June 2018

Conjoint analysis applications in health--a checklist: a report of the ISPOR Good Research Practices for Conjoint Analysis Task Force

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823641

20 June 2018

Public perspectives on returning genetics and genomics research results

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823641

20 June 2018

Evaluation of the validity and utility of genetic testing for rare diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823641

20 June 2018

Clinical assessment incorporating a personal genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823641

20 June 2018

Value for money? Array genomic hybridization for diagnostic testing for genetic causes of intellectual disability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823641

20 June 2018

Handling ethical, legal and social issues in birth cohort studies involving genetic research: responses from studies in six countries

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823641

20 June 2018

The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823641

20 June 2018

Valuing the benefit of diagnostic testing for genetic causes of idiopathic developmental disability: willingness to pay from families of affected children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823641

20 June 2018

Estimating the Danish populations' preferences for pharmacogenetic testing using a discrete choice experiment. The case of treating depression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823641

20 June 2018

Using conjoint analysis to elicit preferences for health care

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823641

20 June 2018

Qualitative Research: Introducing focus groups

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823641

20 June 2018

What do patients value? Willingness to pay for ultrasound in normal pregnancy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823641

20 June 2018

What is the clinical utility of genetic testing?

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.63

21 January 2018

What Do Patients Value?

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.63

21 January 2018

Evaluating the utility of personal genomic information

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.63

21 January 2018

Women and health care professionals' preferences for Down's Syndrome screening tests: a conjoint analysis study

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.63

21 January 2018

A comparison of Australian and UK obstetricians' and midwives' preferences for screening tests for Down syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.63

21 January 2018

Bayesian and classical estimation of mixed logit: An application to genetic testing

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.63

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.63

21 January 2018

Valuing pharmacogenetic testing services: A comparison of patients' and health care professionals' preferences

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.63

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/10.1038%2FGIM.2013.63

21 January 2018

Genomic classifiers in colon cancer - clinical utility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823641

26 November 2018

The emergence of an ethical duty to disclose genetic research results: international perspectives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3823641

26 November 2018

Modelling non-demanders in choice experiments

1 reference

https://pubmed.ncbi.nlm.nih.gov/23722871

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

What influences participation in genetic carrier testing?

1 reference

https://pubmed.ncbi.nlm.nih.gov/23722871

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid prenatal diagnostic testing for Down syndrome only or longer wait for full karyotype: the views of pregnant women

1 reference

https://pubmed.ncbi.nlm.nih.gov/23722871

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/GIM.2013.63

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

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