(Q35863638)

English

Utility and limitations of exome sequencing as a genetic diagnostic tool for conditions associated with pediatric sudden cardiac arrest/sudden cardiac death.

scientific article published on 19 July 2015

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scholarly article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26187847%20AND%20SRC:MED&resulttype=core&format=json

19 February 2020

Utility and limitations of exome sequencing as a genetic diagnostic tool for conditions associated with pediatric sudden cardiac arrest/sudden cardiac death (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26187847%20AND%20SRC:MED&resulttype=core&format=json

19 February 2020

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Ramakrishnan Rajagopalan

9

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19 February 2020

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Mindy H Li

1

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19 February 2020

Jenica L Abrudan

2

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19 February 2020

Matthew C Dulik

3

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19 February 2020

Ariella Sasson

4

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19 February 2020

Joshua Brunton

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19 February 2020

Vijayakumar Jayaraman

6

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19 February 2020

Noreen Dugan

7

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19 February 2020

Danielle Haley

8

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19 February 2020

Sawona Biswas

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19 February 2020

Mahdi Sarmady

11

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19 February 2020

Elizabeth T DeChene

12

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19 February 2020

Matthew A Deardorff

13

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19 February 2020

Alisha Wilkens

14

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19 February 2020

Sarah E Noon

15

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19 February 2020

Maria I Scarano

16

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19 February 2020

Avni B Santani

17

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19 February 2020

Peter S White

18

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19 February 2020

Jeffrey Pennington

19

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19 February 2020

Laura K Conlin

20

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19 February 2020

Nancy B Spinner

21

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19 February 2020

Ian D Krantz

22

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19 February 2020

Victoria L Vetter

23

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19 February 2020

publication date

19 July 2015

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19 February 2020

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19 February 2020

9

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19 February 2020

15

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19 February 2020

Genetic testing in cardiovascular diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4506570

11 July 2018

Sequencing depth and coverage: key considerations in genomic analyses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4506570

11 July 2018

Clinical whole-exome sequencing for the diagnosis of mendelian disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4506570

11 July 2018

The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4506570

11 July 2018

The role and challenges of exome sequencing in studies of human diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4506570

11 July 2018

Yield of molecular and clinical testing for arrhythmia syndromes: report of 15 years' experience.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4506570

11 July 2018

Genetic testing for inherited cardiac disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4506570

11 July 2018

Interpreting secondary cardiac disease variants in an exome cohort

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4506570

11 July 2018

Clinical application of exome sequencing in undiagnosed genetic conditions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4506570

11 July 2018

Pediatric sudden cardiac arrest

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4506570

11 July 2018

Exome sequencing as a tool for Mendelian disease gene discovery

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4506570

11 July 2018

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).

1 reference

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11 July 2018

Strategies for exome and genome sequence data analysis in disease-gene discovery projects

1 reference

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11 July 2018

Targeted capture and massively parallel sequencing of 12 human exomes

1 reference

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11 July 2018

Initial sequencing and analysis of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4506570

11 July 2018

Clinical whole-exome sequencing: are we there yet?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4506570

24 September 2018

Familial cardiological and targeted genetic evaluation: low yield in sudden unexplained death and high yield in unexplained cardiac arrest syndromes

1 reference

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24 September 2018

Genetic analysis of sudden unexplained death: a multidisciplinary approach.

1 reference

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24 September 2018

Practices and policies of clinical exome sequencing providers: analysis and implications.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4506570

24 September 2018

Contribution of inherited heart disease to sudden cardiac death in childhood.

1 reference

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24 September 2018

Postmortem long QT syndrome genetic testing for sudden unexplained death in the young

1 reference

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Riverine export of aged terrestrial organic matter to the North Atlantic Ocean

1 reference

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21 January 2018

Identifiers

10.1186/S40246-015-0038-Y

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Europe PubMed Central

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19 February 2020

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19 February 2020

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19 February 2020

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