(Q30391601)

16 August 2017

Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics (English)

1 reference

16 August 2017

whole genome sequencing

1 reference

based on heuristic

inferred from title

author

Hanne Meijers-Heijboer

10

Hanne Meijers-Heijboer

0 references

Anne Cambon-Thomsen

8

Anne Cambon-Thomsen

0 references

Bartha Knoppers

9

Bartha M Knoppers

1 reference

16 August 2017

3

Pascal Borry

0 references

Heidi Carmen Howard

7

Heidi C Howard

1 reference

16 August 2017

Hans Scheffer

11

0 references

Martina C. Cornel

2

Martina C Cornel

1 reference

16 August 2017

13

Wybo Dondorp

1 reference

16 August 2017

12

Lisbeth Tranebjaerg

1 reference

16 August 2017

1

Carla G van El

1 reference

16 August 2017

Ros J Hastings

4

1 reference

16 August 2017

Florence Fellmann

5

1 reference

16 August 2017

Shirley V Hodgson

6

1 reference

16 August 2017

Guido M W R de Wert

14

1 reference

16 August 2017

ESHG Public and Professional Policy Committee

15

1 reference

16 August 2017

1 June 2013

1 reference

European Journal of Human Genetics

16 August 2017

1 reference

16 August 2017

21

1 reference

16 August 2017

6

1 reference

16 August 2017

580-584

1 reference

Diagnostic interpretation of array data using public databases and internet sources

16 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

De novo mutations in human genetic disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

Developing a policy for paediatric biobanks: principles for good practice

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

Noninvasive whole-genome sequencing of a human fetus.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

Incidental medical information in whole-exome sequencing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

The predictive capacity of personal genome sequencing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

Intratumor Heterogeneity and Branched Evolution Revealed by Multiregion Sequencing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

The ethical hazards and programmatic challenges of genomic newborn screening

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

Preconceptional genetic carrier testing and the commercial offer directly-to-consumers

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

Genetic testing and common disorders in a public health framework

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

Disclosure of individual genetic data to research participants: the debate reconsidered

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

A map of human genome variation from population-scale sequencing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

Statement of the ESHG on direct-to-consumer genetic testing for health-related purposes

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

Clinical assessment incorporating a personal genome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

Personal genomes in progress: from the human genome project to the personal genome project

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

Analysis of genetic inheritance in a family quartet by whole-genome sequencing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

Non-invasive prenatal testing: ethical issues explored

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

Exome sequencing identifies the cause of a mendelian disorder

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

The complete genome of an individual by massively parallel DNA sequencing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

GENE SEQUENCING: The Race for the $1000 Genome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3658192

The changing landscape of genetic testing and its impact on clinical and laboratory services and research in Europe

20 June 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.46

A de novo paradigm for mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.46

Whole-genome sequencing and the physician

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.46

Genome-wide arrays: quality criteria and platforms to be used in routine diagnostics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.46

Screening using whole-body magnetic resonance imaging scanning: who wants an incidentaloma?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.46

The use of arrays to detect copy-number variations in clinical practice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.46

Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.46

Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.46

Communication of biobanks' research results: what do (potential) participants want?

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23676617

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Between hype and hope: whole-genome sequencing in clinical medicine

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23676617

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/EJHG.2013.46

1 reference

16 August 2017

1 reference

16 August 2017

PubMed publication ID

23676617

1 reference