(Q34724819)

4 August 2017

title

The 'thousand-dollar genome': an ethical exploration (English)

1 reference

4 August 2017

0 references

Wybo J Dondorp

1

1 reference

4 August 2017

Guido M W R de Wert

series ordinal

2

1 reference

4 August 2017

publication date

1 June 2013

1 reference

European Journal of Human Genetics

4 August 2017

published in

1 reference

4 August 2017

volume

21 Suppl 1

1 reference

4 August 2017

page(s)

S6-26

1 reference

A map of human genome variation from population-scale sequencing

4 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=3660958

Blurring lines. The research activities of direct-to-consumer genetic testing companies raise questions about consumers as research subjects

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

A novel custom resequencing array for dilated cardiomyopathy

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Clinical assessment incorporating a personal genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

The personal genome--the future of personalised medicine?

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

What next for preimplantation genetic screening (PGS)? A position statement from the ESHRE PGD Consortium Steering Committee

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Ethical challenges in providing noninvasive prenatal diagnosis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Increased nuchal translucency in euploid fetuses--what should we be telling the parents?

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Non-invasive prenatal testing: ethical issues explored

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Genomic and personalized medicine: foundations and applications

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Public health genomics and genetic test evaluation: the challenge of conducting behavioural research on the utility of lifestyle-genetic tests

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

What next for preimplantation genetic screening? High mitotic chromosome instability rate provides the biological basis for the low success rate

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Array analysis and karyotyping: workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Genetic testing in asymptomatic minors: Recommendations of the European Society of Human Genetics

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Predictive diagnosis of the cancer prone Li-Fraumeni syndrome by accident: new challenges through whole genome array testing.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

THE MORAL OBLIGATION TO CREATE CHILDREN WITH THE BEST CHANCE OF THE BEST LIFE

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Generations of sequencing technologies

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Genetic mapping in human disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

The use of cell-free fetal nucleic acids in maternal blood for non-invasive prenatal diagnosis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Genome-based prediction of common diseases: advances and prospects

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Comparing whole genomes using DNA microarrays

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Next-generation sequencing: the race is on.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Genomic medicine in prenatal diagnosis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Letting the genome out of the bottle--will we get our wish?

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

What will whole genome searches for susceptibility genes for common complex disease offer to clinical practice?

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Copy-number variation and association studies of human disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Deciphering the role of heterozygous mutations in genes associated with parkinsonism

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

A vision of the future of newborn screening

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Newborn screening technology: proceed with caution

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Comparative genomic hybridization and prenatal diagnosis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

GENE SEQUENCING: The Race for the $1000 Genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Genomic medicine: genetic variation and its impact on the future of health care

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Neonatal screening by DNA microarray: spots and chips

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

The $1000 genome: ethical and legal issues in whole genome sequencing of individuals

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

A vision for the future of genomics research

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Global gene expression profiling of end-stage dilated cardiomyopathy using a human cardiovascular-based cDNA microarray

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Ethical, legal, and practical concerns about recontacting patients to inform them of new information: the case in medical genetics

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Is there a case in favour of predictive genetic testing in young children?

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

The duty to recontact: attitudes of genetics service providers.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Generic Consent for Genetic Screening

7 July 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.73

Genetic profiling of newborns: ethical and social issues.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.73

Research ethics. Children and population biobanks

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.73

Screening for conditions that do not meet the Wilson and Jungner criteria: the case of Duchenne muscular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.73

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.73

Coming soon to your clinic: patient-friendly ART.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.73

Genetic research on stored tissue samples from minors: a systematic review of the ethical literature

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

New challenges for informed consent through whole genome array testing

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Predictive genetic testing for conditions that present in childhood.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization

26 October 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.73

How Attitudes Research Contributes to Overoptimistic Expectations of Personal Genome Testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.73

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.73

[The scope of prenatal diagnostic testing for chromosomal aberrations: broad or narrow? Ethical considerations on the choice of tests]

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

[Neonatal screening: dynamics and ethics]

9 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660958

Neonatal screening: old dogma or sound principle?

9 December 2018

1 reference

12 December 2020

Microarray genetic screening: a prenatal roadblock for life?

1 reference

12 December 2020

ACOG Practice Bulletin No. 88, December 2007. Invasive prenatal testing for aneuploidy

1 reference

12 December 2020

Successful pregnancies after application of array-comparative genomic hybridization in PGS-aneuploidy screening

1 reference

12 December 2020

Current controversies in prenatal diagnosis 3: For prenatal diagnosis, should we offer less or more than metaphase karyotyping?

1 reference

12 December 2020

Comparison of multiplex ligation-dependent probe amplification and karyotyping in prenatal diagnosis

1 reference

12 December 2020

Why Realistic Test Scenarios in Translational Genomics Research Remain Hypothetical

1 reference

12 December 2020

Chasing a disease to the vanishing point

1 reference

12 December 2020

Challenges in the clinical application of whole-genome sequencing

1 reference

12 December 2020

Parents' interest in predictive genetic testing for their children when a disease has no treatment

1 reference

12 December 2020

Heredity: science and society on the possibilities and limits of genetic testing and gene therapy. Report issued by a Committee of the Health Council of The Netherlands

1 reference

12 December 2020

Informed Consent and the Bio-banking of Material from Children.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.73

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/EJHG.2013.73

1 reference

4 August 2017

1 reference

4 August 2017

1 reference