(Q33401777)

26 July 2017

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

1 reference

26 July 2017

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1 reference

Christopher Newton-Cheh

3

object named as

Christopher Newton-Cheh

1 reference

26 July 2017

2

Veikko Salomaa

1 reference

26 July 2017

16

Aarno Palotie

1 reference

26 July 2017

Leena Peltonen-Palotie

14

object named as

Leena Peltonen

1 reference

26 July 2017

7

Antti Jula

1 reference

26 July 2017

Annukka Marjamaa

1

1 reference

26 July 2017

Kimmo Porthan

4

1 reference

26 July 2017

Antti Reunanen

5

1 reference

26 July 2017

Hannu Karanko

6

1 reference

26 July 2017

Päivi Lahermo

8

1 reference

26 July 2017

Heikki Väänänen

9

1 reference

26 July 2017

Lauri Toivonen

10

1 reference

26 July 2017

Heikki Swan

11

1 reference

26 July 2017

Matti Viitasalo

12

1 reference

26 July 2017

Markku S Nieminen

13

1 reference

26 July 2017

Lasse Oikarinen

15

1 reference

26 July 2017

Kimmo Kontula

17

1 reference

26 July 2017

language of work or name

English

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publication date

1 January 2009

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26 July 2017

7

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published in

Annals of Medicine

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26 July 2017

41

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26 July 2017

3

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26 July 2017

234-240

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

26 July 2017

1 reference

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

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

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

1 reference

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

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

1 reference

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

1 reference

26 July 2017

1 reference

26 July 2017

1 reference