Obtaining insurance after DNA diagnostics: a survey among hypertrophic cardiomyopathy mutation carriers (Q34328510)

1 August 2017

title

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

1 reference

hypertrophic cardiomyopathy

1 August 2017

main subject

1 reference

6

Arthur A M Wilde

1 reference

1 August 2017

Imke Christiaans

1

1 reference

1 August 2017

Tjitske M Kok

2

1 reference

1 August 2017

Irene M van Langen

3

1 reference

1 August 2017

Erwin Birnie

4

1 reference

1 August 2017

Gouke J Bonsel

5

1 reference

1 August 2017

Ellen M A Smets

7

1 reference

1 August 2017

publication date

12 August 2009

1 reference

European Journal of Human Genetics

1 August 2017

published in

1 reference

1 August 2017

volume

18

1 reference

1 August 2017

issue

2

1 reference

1 August 2017

page(s)

251-253

1 reference

Single-gene mutations and increased left ventricular wall thickness in the community: the Framingham Heart Study

1 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987186

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987186

Historical trends in reported survival rates in patients with hypertrophic cardiomyopathy

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987186

Genetic information and testing in insurance and employment: technical, social and ethical issues

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987186

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987186

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987186

Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987186

Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases.

6 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2009.145

Quality of life and psychological distress in hypertrophic cardiomyopathy mutation carriers: a cross-sectional cohort study.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2009.145

Disclosure of genetic tests for health insurance: is it ethical not to?

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987186

European practices of genetic information and insurance: lessons for the Genetic Information Nondiscrimination Act

27 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19672285

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/EJHG.2009.145

1 reference

1 August 2017

1 reference

1 August 2017

1 reference