High prevalence of four long QT syndrome founder mutations in the Finnish population (Q33401777)

26 July 2017

title

High prevalence of four long QT syndrome founder mutations in the Finnish population (English)

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26 July 2017

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Christopher Newton-Cheh

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object named as

Christopher Newton-Cheh

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26 July 2017

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Veikko Salomaa

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26 July 2017

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Aarno Palotie

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26 July 2017

Leena Peltonen-Palotie

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object named as

Leena Peltonen

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Antti Jula

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Annukka Marjamaa

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26 July 2017

Kimmo Porthan

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Antti Reunanen

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Hannu Karanko

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Päivi Lahermo

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Heikki Väänänen

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Lauri Toivonen

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Heikki Swan

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Matti Viitasalo

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Markku S Nieminen

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Lasse Oikarinen

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Kimmo Kontula

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language of work or name

English

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publication date

1 January 2009

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26 July 2017

number of pages

7

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published in

Annals of Medicine

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26 July 2017

volume

41

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26 July 2017

issue

3

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26 July 2017

page(s)

234-240

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Relationship of electrocardiographic repolarization measures to echocardiographic left ventricular mass in men with hypertension

26 July 2017

cites work

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704397

Common NOS1AP variants are associated with a prolonged QTc interval in the Rotterdam Study

21 June 2018

1 reference

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Confirmation of associations between ion channel gene SNPs and QTc interval duration in healthy subjects

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704397

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704397

Long QT syndrome: reduced repolarization reserve and the genetic link

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704397

The congenital long QT syndromes from genotype to phenotype: clinical implications

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704397

Genetics of cardiac arrhythmias

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704397

The long QT syndrome: therapeutic implications of a genetic diagnosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704397

QT interval is a heritable quantitative trait with evidence of linkage to chromosome 3 in a genome-wide linkage analysis: The Framingham Heart Study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704397

Drug-induced prolongation of the QT interval

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704397

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704397

Long QT syndromes and torsade de pointes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704397

21 June 2018

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The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704397

Electrocardiographic detection of left ventricular hypertrophy by the simple QRS voltage-duration product

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704397

Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland

21 June 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668530

Magnetocardiographic QT interval dispersion in postmyocardial infarction patients with sustained ventricular tachycardia: validation of automated QT measurements.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668530

Further evidence of inherited long QT syndrome gene mutations in antiarrhythmic drug-associated torsades de pointes

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668530

Common Genetic Variation in KCNH2 Is Associated With QT Interval Duration

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668530

Effect of heart rate and autonomic tone on the QT interval

21 January 2018

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12 December 2020

The normal unipolar precordial and limb lead electrocardiogram

1 reference

12 December 2020

Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population

1 reference

12 December 2020

Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patients

1 reference

12 December 2020

Association of torsades de pointes with novel and known single nucleotide polymorphisms in long QT syndrome genes

1 reference

12 December 2020

Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?

1 reference

12 December 2020

Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?

1 reference

12 December 2020

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

1 reference

12 December 2020

Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns

1 reference

12 December 2020

Survey of the coding region of the HERG gene in long QT syndrome reveals six novel mutations and an amino acid polymorphism with possible phenotypic effects

1 reference

12 December 2020

A founder mutation of the potassium channel KCNQ1 in long QT syndrome: implications for estimation of disease prevalence and molecular diagnostics

1 reference

12 December 2020

Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome

1 reference

12 December 2020

10.1080/07853890802668530

Identifiers

DOI

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26 July 2017

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26 July 2017

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