(Q36391360)

13 August 2017

The Achilles' heel of cardiovascular genetic testing: distinguishing pathogenic mutations from background genetic noise (English)

1 reference

13 August 2017

A P Landstrom

1

1 reference

13 August 2017

M J Ackerman

series ordinal

2

1 reference

13 August 2017

language of work or name

English

0 references

publication date

1 October 2011

1 reference

Clinical Pharmacology & Therapeutics

13 August 2017

1 reference

13 August 2017

90

1 reference

13 August 2017

4

1 reference

13 August 2017

496-499

1 reference

https://scigraph.springernature.com/pub.10.1038/clpt.2011.192

13 August 2017

0 references

cites work

Mutation type is not clinically useful in predicting prognosis in hypertrophic cardiomyopathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3495562

Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3495562

Arrhythmogenic right ventricular cardiomyopathy/dysplasia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3495562

Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3495562

The role of molecular autopsy in unexplained sudden cardiac death

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3495562

Yield of genetic testing in hypertrophic cardiomyopathy

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3495562

Effect of clinical phenotype on yield of long QT syndrome genetic testing

21 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21934721

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noise.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21934721

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21934721

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/CLPT.2011.192

1 reference

Dimensions Publication ID

13 August 2017

0 references

1 reference

13 August 2017

PubMed publication ID

21934721

1 reference