Unravelling fears of genetic discrimination: an exploratory study of Dutch HCM families in an era of genetic non-discrimination acts (Q36253410)

13 August 2017

Unravelling fears of genetic discrimination: an exploratory study of Dutch HCM families in an era of genetic non-discrimination acts (English)

1 reference

13 August 2017

2

Klasien Horstman

1 reference

13 August 2017

Els Geelen

1

1 reference

13 August 2017

Carlo L M Marcelis

series ordinal

3

1 reference

13 August 2017

Pieter A Doevendans

series ordinal

4

1 reference

13 August 2017

Ine Van Hoyweghen

series ordinal

5

1 reference

13 August 2017

28 March 2012

1 reference

European Journal of Human Genetics

13 August 2017

1 reference

13 August 2017

20

1 reference

13 August 2017

10

1 reference

13 August 2017

1018-1023

1 reference

Voicing the lifeworld: Parental accounts of responsibility in genetic consultations for polycystic kidney disease.

13 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449067

Hypertrophic cardiomyopathy: from genetics to treatment

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449067

Genetic diagnostics and genetic counselling in Hypertrophic Cardiomyopathy (HCM).

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449067

Obtaining insurance after DNA diagnostics: a survey among hypertrophic cardiomyopathy mutation carriers

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449067

Diagnostic, prognostic, and therapeutic implications of genetic testing for hypertrophic cardiomyopathy

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449067

Perceptions of genetic discrimination among people at risk for Huntington's disease: a cross sectional survey

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449067

Genetic evaluation of cardiomyopathy--a Heart Failure Society of America practice guideline

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449067

Engagement with genetic discrimination: concerns and experiences in the context of Huntington disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449067

In the democracies of DNA: ontological uncertainty and political order in three states

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449067

Genetic discrimination: too few data

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449067

Getting insurance after genetic screening on familial hypercholesterolaemia; the need to educate both insurers and the public to increase adherence to national guidelines in The Netherlands

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449067

Genetic discrimination in life insurance: empirical evidence from a cross sectional survey of genetic support groups in the United Kingdom

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449067

Discrimination as a consequence of genetic testing

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449067

Investigating genetic discrimination in Australia: a large-scale survey of clinical genetics clients

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449067

Genetic discrimination: perspectives of consumers.

29 June 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.53

Genomic imprinting, small babies and assisted reproduction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.53

Verification of consumers' experiences and perceptions of genetic discrimination and its impact on utilization of genetic testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.53

Risk versus risk: decision-making dilemmas of drug regulation in the United States and Germany

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449067

What are the stakes? Genetic nondiscrimination legislation and personal genomics

21 October 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.53

Perceptions of genetic discrimination among at-risk relatives of colorectal cancer patients

21 January 2018

1 reference

12 December 2020

Architectures of genetic medicine: comparing genetic testing for breast cancer in the USA and the UK

1 reference

12 December 2020

Insurance, unfair discrimination, and genetic testing

1 reference

12 December 2020

Genetics bill cruises through Senate

1 reference

12 December 2020

Congress passes bill to ban discrimination based on individuals' genetic makeup

1 reference

12 December 2020

Making genetics not so important: family work in dealing with familial hypertrophic cardiomyopathy

1 reference

12 December 2020

Constructing "best interests": genetic testing of children in families with hypertrophic cardiomyopathy

1 reference

12 December 2020

"A slap in the face". An exploratory study of genetic discrimination in Germany.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.53

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/EJHG.2012.53

1 reference

13 August 2017

1 reference

13 August 2017

PubMed publication ID

22453290

1 reference