(Q36164685)

12 August 2017

Preconception care and genetic risk: ethical issues (English)

1 reference

12 August 2017

0 references

3

Bartha M Knoppers

1 reference

12 August 2017

Guido M. W R. De Wert

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A22205578

21 December 2024

Wybo J. Dondorp

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A22205578

21 December 2024

Bartha M. Knoppers

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A22205578

21 December 2024

language of work or name

1 reference

29 December 2011

1 reference

PMC publication ID

3419287

full work available at URL

12 August 2017

https://link.springer.com/content/pdf/10.1007%2Fs12687-011-0074-9.pdf

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A22205578

https://europepmc.org/articles/PMC3419287

21 December 2024

file format

HyperText Markup Language

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A22205578

https://europepmc.org/articles/PMC3419287?pdf=render

21 December 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A22205578

http://link.springer.com/content/pdf/10.1007/s12687-011-0074-9.pdf

21 December 2024

1 reference

https://api.crossref.org/works/10.1007/S12687-011-0074-9

http://link.springer.com/article/10.1007/s12687-011-0074-9/fulltext.html

21 December 2024

file format

HyperText Markup Language

1 reference

https://api.crossref.org/works/10.1007/S12687-011-0074-9

http://link.springer.com/content/pdf/10.1007/s12687-011-0074-9

21 December 2024

1 reference

https://api.crossref.org/works/10.1007/S12687-011-0074-9

Journal of Community Genetics

21 December 2024

published in

1 reference

12 August 2017

3

1 reference

12 August 2017

3

1 reference

12 August 2017

221-228

1 reference

Creative Commons Attribution-NonCommercial 2.0 Generic

12 August 2017

start time

29 December 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Committee Opinion No. 486: Update on Carrier Screening for Cystic Fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Intrafamilial medically assisted reproduction

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Carrier testing for severe childhood recessive diseases by next-generation sequencing

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Ethical considerations in choosing a model for population‐based cystic fibrosis carrier screening

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Experience with carrier screening and prenatal diagnosis for 16 Ashkenazi Jewish genetic diseases

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Active cascade screening in primary inherited arrhythmia syndromes: does it lead to prophylactic treatment?

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Prenatal carrier testing for fragile X: counseling issues and challenges

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Benchmarks for cystic fibrosis carrier screening: a European consensus document

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Non-invasive prenatal testing: ethical issues explored

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Assessing the potential success of cystic fibrosis carrier screening: lessons learned from Tay-Sachs disease and beta-thalassemia

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Genetic diagnosis of embryos: clear explanation, not rhetoric, is needed

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

The clinical content of preconception care: genetics and genomics.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Preconception care: a 2008 update

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Disability and genetics in the era of genomic medicine

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Should physicians warn patients' relatives of genetic risks?

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Carrier screening for Gaucher disease: lessons for low-penetrance, treatable diseases

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

ESHRE Task Force on Ethics and Law 13: the welfare of the child in medically assisted reproduction

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Preimplantation genetic diagnosis: an overview of socio-ethical and legal considerations

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Cascade screening: whose information is it anyway?

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Cascade testing in familial hypercholesterolaemia: how should family members be contacted?

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Evaluation of cystic fibrosis carrier screening programs according to genetic screening criteria

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Serious genetic disorders: can or should they be defined?

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

A measure of informed choice.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Should families own genetic information? Yes.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Genetic counselling for personalised medicine

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Preconception health promotion: analysis of means and constraints.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

The human embryo: ethical and legal aspects.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Three-month follow-up of Western and non-Western participants in a study on preconceptional ancestry-based carrier couple screening for cystic fibrosis and hemoglobinopathies in the Netherlands

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Carrier matching and collective socialization in community genetics: Dor Yeshorim and the reinforcement of stigma

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Should families own genetic information? No.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

A genetic screening programme for Tay-Sachs disease and cystic fibrosis for Australian Jewish high school students.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Genetic information and the family: are we our brother's keeper?

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Medicalization as a moral problem for preventative medicine

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

Is cascade testing a sensible method of population screening?

23 September 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12687-011-0074-9

[Screening for carriers of the fragile X syndrome; ethical exploration]

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3419287

The "duty to warn" a patient's family members about hereditary disease risks

5 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22205578

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The cystic fibrosis gene: medical and social implications for heterozygote detection

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22205578

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Comparison of single-entry and double-entry two-step couple screening for cystic fibrosis carriers

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22205578

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Nederlands Tijdschrift voor Geneeskunde

11

146

611

A Jong

2002

1 reference

https://api.crossref.org/works/10.1007/S12687-011-0074-9

21 December 2024

Identifiers

1 reference

12 August 2017

1 reference

PMC publication ID

3419287

12 August 2017

1 reference

PMC publication ID

3419287