(Q34289629)

1 August 2017

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

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1 August 2017

19

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31

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39

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43

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1 August 2017

Bertram Müller-Myhsok

34

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Benno Pütz

15

Benno Pütz

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David Schlessinger

37

David Schlessinger

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Laura Crisponi

26

Laura Crisponi

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Serena Sanna

2

Serena Sanna

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Eric Boerwinkle

38

Eric Boerwinkle

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Manuela Uda

40

Manuela Uda

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Anna Köttgen

10

Anna Köttgen

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Christian Fuchsberger

Christian Fuchsberger

6

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Andrew A Hicks

Andrew A Hicks

32

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Man Li

Man Li

14

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Josef Coresh

41

Josef Coresh

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1 August 2017

28

Karl-Heinz Jöckel

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1 August 2017

27

Raimund Erbel

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1 August 2017

33

Edward Lakatta

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1 August 2017

25

Stefan Möhlenkamp

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1 August 2017

36

H-Erich Wichmann

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1 August 2017

18

Moritz F Sinner

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1 August 2017

3

Dan E Arking

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1 August 2017

7

Georg B Ehret

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1 August 2017

20

Samer S Najjar

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1 August 2017

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W H Linda Kao

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1 August 2017

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Peter P Pramstaller

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1 August 2017

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Ronald J Prineas

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1 August 2017

5

Vesela Gateva

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1 August 2017

42

Stefan Kääb

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1 August 2017

1

Arne Pfeufer

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1 August 2017

11

Siegfried Perz

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1 August 2017

12

Gianluca Usala

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1 August 2017

30

Gerhard Steinbeck

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1 August 2017

Martina Müller

4

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1 August 2017

Marco Orrú

8

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1 August 2017

Cristian Pattaro

9

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1 August 2017

Maja Barbalic

13

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1 August 2017

Angelo Scuteri

16

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1 August 2017

Thomas W Mühleisen

22

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1 August 2017

Mariano Dei

23

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1 August 2017

Christine Happle

24

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1 August 2017

Silvia Naitza

29

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1 August 2017

Aravinda Chakravarti

44

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1 August 2017

language of work or name

English

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publication date

22 March 2009

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1 August 2017

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1 August 2017

41

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407-414

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4

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https://scigraph.springernature.com/pub.10.1038/ng.362

1 August 2017

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cites work

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

Multiple independent genetic factors at NOS1AP modulate the QT interval in a multi-ethnic population

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

A HapMap harvest of insights into the genetics of common disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

Ndrg4 is required for normal myocyte proliferation during early cardiac development in zebrafish

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

SLC2A9 influences uric acid concentrations with pronounced sex-specific effects

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

Common variants in the GDF5-UQCC region are associated with variation in human height

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

The genetic study of three population microisolates in South Tyrol (MICROS): study design and epidemiological perspectives

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

Multiple genes for essential-hypertension susceptibility on chromosome 1q.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

Heritability of cardiovascular and personality traits in 6,148 Sardinians

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

A haplotype map of the human genome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

KORA-gen--resource for population genetics, controls and a broad spectrum of disease phenotypes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

Genomics in sudden cardiac death

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

Assessment of clinically silent atherosclerotic disease and established and novel risk factors for predicting myocardial infarction and cardiac death in healthy middle-aged subjects: rationale and design of the Heinz Nixdorf RECALL Study. Risk Facto

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

Tbx5 associates with Nkx2-5 and synergistically promotes cardiomyocyte differentiation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

Genomic control for association studies

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

The human inward rectifier K(+) channel subunit kir5.1 (KCNJ16) maps to chromosome 17q25 and is expressed in kidney and pancreas

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

Highly specific localization of promoter regions in large genomic sequences by PromoterInspector: a novel context analysis approach

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

The Atherosclerosis Risk in Communities (ARIC) Study: design and objectives. The ARIC investigators

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

The long QT syndrome. Prospective longitudinal study of 328 families

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

Prolonged QTc interval and high B-type natriuretic peptide levels together predict mortality in patients with advanced heart failure.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

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

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

Common Genetic Variation in KCNH2 Is Associated With QT Interval Duration

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

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

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

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

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976045

A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization

28 October 2018

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

QT interval prolongation predicts cardiovascular mortality in an apparently healthy population

1 reference

12 December 2020

ESTIMATING F-STATISTICS FOR THE ANALYSIS OF POPULATION STRUCTURE.

1 reference

12 December 2020

Sudden cardiac death in heart failure. The role of abnormal repolarization

1 reference

12 December 2020

Genome-wide association study identifies eight loci associated with blood pressure

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.362

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/NG.362

1 reference

1 August 2017

1 reference

1 August 2017

1 reference