(Q24651891)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17534376%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

title

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

1 reference

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31 December 2019

1

1 reference

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31 December 2019

Pascale Guicheney

9

1 reference

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31 December 2019

author name string

Nicaud V

2

1 reference

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31 December 2019

Chaouch S

3

1 reference

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31 December 2019

Berthet M

4

1 reference

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31 December 2019

Forhan A

5

1 reference

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31 December 2019

Tichet J

6

1 reference

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31 December 2019

Tiret L

7

1 reference

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31 December 2019

Balkau B

8

1 reference

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31 December 2019

language of work or name

English

0 references

publication date

30 May 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17534376%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Human Genetics

31 December 2019

published in

1 reference

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31 December 2019

volume

15

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31 December 2019

issue

9

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31 December 2019

page(s)

974-979

1 reference

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A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene

31 December 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234597

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234597

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234597

Further insights into the effect of quinidine in short QT syndrome caused by a mutation in HERG

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234597

Testing for association between disease and linked marker loci: a log-linear-model analysis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234597

Sotalol testing unmasks altered repolarization in patients with suspected acquired long-QT-syndrome--a case-control pilot study using i.v. sotalol

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234597

QT interval change with age in an overtly healthy older population.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234597

The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA study

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234597

Common Variants in Myocardial Ion Channel Genes Modify the QT Interval in the General Population

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234597

Single nucleotide polymorphism map of five long-QT genes.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234597

Mutation in the KCNQ1 gene leading to the short QT-interval syndrome.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234597

A new algorithm for haplotype-based association analysis: the Stochastic-EM algorithm.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234597

Association between HERG K897T polymorphism and QT interval in middle-aged Finnish women

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234597

Sex differences in the rate of cardiac repolarization

28 November 2018

1 reference

12 December 2020

Heritability of ECG measurements in adult male twins

1 reference

12 December 2020

QT interval is linked to 2 long-QT syndrome loci in normal subjects

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

Possible association of the human KCNE1 (minK) gene and QT interval in healthy subjects: evidence from association and linkage analyses in Israeli families

1 reference

12 December 2020

Genetic and environmental sources of QT interval variability in Israeli families: the kibbutz settlements family study

1 reference

12 December 2020

1 reference

12 December 2020

A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization

1 reference

12 December 2020

Identifiers

DOI

10.1038/SJ.EJHG.5201866

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17534376%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

31 December 2019

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17534376%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17534376%20AND%20SRC:MED&resulttype=core&format=json