(Q21143760)

English

Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies

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Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies (English)

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genome-wide association study

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based on heuristic

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genetic variation

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Anna Dominiczak

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Anna Dominiczak

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Anna

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Dominiczak

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PubMed publication ID

17 August 2022

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Panos

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Deloukas

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Christopher Newton-Cheh

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Christopher

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Newton-Cheh

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Serena

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Sanna

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Andrew D. Paterson

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Patricia B Munroe

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Tim D Spector

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Ilja M Nolte

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Dongling Zheng

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John Connell

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Connell

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Morris Brown

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Kenneth Rice

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Paul I W de Bakker

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Paul I W

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de Bakker

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Dan E Arking

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author given names

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Arking

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Nicholas D Carter

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Carter

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Steve Jeffery

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Jeffery

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17 August 2022

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publication date

2009

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4

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7

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e6138

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copyright license

Creative Commons Attribution 4.0 International

9 July 2009

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April 2022 Public Data File from Crossref

copyright status

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Estimation of significance thresholds for genomewide association scans

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19 March 2017

Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order Amish

1 reference

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19 March 2017

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

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

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19 March 2017

Population structure and eigenanalysis

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19 March 2017

A mutation in the human phospholamban gene, deleting arginine 14, results in lethal, hereditary cardiomyopathy.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704957

19 March 2017

Inference of population structure using multilocus genotype data

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Nitric oxide synthase in cardiac sarcoplasmic reticulum

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Phospholamban gene dosage effects in the mammalian heart

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Targeted ablation of the phospholamban gene is associated with markedly enhanced myocardial contractility and loss of beta-agonist stimulation

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A new multipoint method for genome-wide association studies by imputation of genotypes

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7 April 2017

Genomic control for association studies

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Estimation of the multiple testing burden for genomewide association studies of nearly all common variants

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7 April 2017

Common variants at ten loci modulate the QT interval duration in the QTSCD Study

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12 September 2017

Common variants at ten loci influence QT interval duration in the QTGEN Study

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704957

12 September 2017

A common NOS1AP genetic polymorphism is associated with increased cardiovascular mortality in users of dihydropyridine calcium channel blockers

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12 September 2017

Common candidate gene variants are associated with QT interval duration in the general population

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Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study.

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Association of NOS1AP genetic variants with QT interval duration in families from the Diabetes Heart Study

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DNA analysis in inherited cardiomyopathies: current status and clinical relevance

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The effect of intensive diabetes treatment on resting heart rate in type 1 diabetes: the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications study

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12 September 2017

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

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Abrogation of ventricular arrhythmias in a model of ischemia and reperfusion by targeting myocardial calcium cycling

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Drug-induced prolongation of the QT interval

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12 September 2017

Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban

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12 September 2017

Large upward bias in estimation of locus-specific effects from genomewide scans

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12 September 2017

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

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27 September 2017

Heart rate-corrected QT interval prolongation predicts risk of coronary heart disease in black and white middle-aged men and women: the ARIC study

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Heritability of QT interval: how much is explained by genes for resting heart rate?

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30 May 2018

A genotype calling algorithm for the Illumina BeadArray platform

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30 May 2018

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

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30 May 2018

Sex differences in the evolution of the electrocardiographic QT interval with age

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30 May 2018

Identification of a common variant at the NOS1AP locus strongly associated to QT-interval duration.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704957

29 November 2018

Common variation in NOS1AP and KCNH2 genes and QT interval duration in young adults. The Cardiovascular Risk in Young Finns Study

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29 November 2018

Common variation in the NOS1AP gene is associated with reduced glucose-lowering effect and with increased mortality in users of sulfonylurea

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29 November 2018

Gender and effects of a common genetic variant in the NOS1 regulator NOS1AP on cardiac repolarization in 3761 individuals from two independent populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704957

29 November 2018

Reduced phospholamban phosphorylation is associated with impaired relaxation in left ventricular myocytes from neuronal NO synthase-deficient mice.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704957

29 November 2018

Common Genetic Variation in KCNH2 Is Associated With QT Interval Duration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704957

29 November 2018

The heterogeneous spectrum of the long QT syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704957

29 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704957

29 November 2018

The effects of intracellular Ca2+ on cardiac K+ channel expression and activity: novel insights from genetically altered mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704957

29 November 2018

A comparison of commonly used QT correction formulae: the effect of heart rate on the QTc of normal ECGs.

1 reference

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29 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2704957

29 November 2018

Are twins and singletons comparable? A study of disease-related and lifestyle characteristics in adult women

1 reference

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29 November 2018

CaM kinase augments cardiac L-type Ca2+ current: a cellular mechanism for long Q-T arrhythmias

1 reference

https://pubmed.ncbi.nlm.nih.gov/19587794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

QT interval in twins

1 reference

https://pubmed.ncbi.nlm.nih.gov/19587794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Diabetes Control and Complications Trial (DCCT). Design and methodologic considerations for the feasibility phase. The DCCT Research Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/19587794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epidemiology of Diabetes Interventions and Complications (EDIC). Design, implementation, and preliminary results of a long-term follow-up of the Diabetes Control and Complications Trial cohort

1 reference

https://pubmed.ncbi.nlm.nih.gov/19587794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19587794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alterations of sarcoplasmic reticulum proteins in failing human dilated cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/19587794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiomyocyte Overexpression of Neuronal Nitric Oxide Synthase Delays Transition Toward Heart Failure in Response to Pressure Overload by Preserving Calcium Cycling

1 reference

https://pubmed.ncbi.nlm.nih.gov/19587794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gender influences on sarcoplasmic reticulum Ca2+-handling in failing human myocardium

1 reference

https://pubmed.ncbi.nlm.nih.gov/19587794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

QT interval prolongation predicts cardiovascular mortality in an apparently healthy population

1 reference

https://pubmed.ncbi.nlm.nih.gov/19587794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation of the phospholamban promoter associated with hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/19587794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19587794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sex differences in the rate of cardiac repolarization

1 reference

https://pubmed.ncbi.nlm.nih.gov/19587794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization

1 reference

https://pubmed.ncbi.nlm.nih.gov/19587794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Calmodulin kinase II inhibition shortens action potential duration by upregulation of K+ currents

1 reference

https://pubmed.ncbi.nlm.nih.gov/19587794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phospholamban R14 deletion results in late-onset, mild, hereditary dilated cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/19587794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0006138

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2009PLoSO...4.6138N

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