(Q34519498)

2 August 2017

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

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2 August 2017

13

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Thomas Illig

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Christopher Newton-Cheh

5

object named as

Christopher Newton-Cheh

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2 August 2017

Martin G Larson

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Heinz Erich Wichmann

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object named as

H Erich Wichmann

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2 August 2017

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Joel N Hirschhorn

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2 August 2017

Christopher J O'Donnell

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object named as

Christopher J O'Donnell

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2 August 2017

1

Dan E Arking

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2 August 2017

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W H Linda Kao

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2 August 2017

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Aravinda Chakravarti

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2 August 2017

2

Arne Pfeufer

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2 August 2017

10

Siegfried Perz

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2 August 2017

20

Stefan Kääb

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2 August 2017

9

Mahmut Akyol

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2 August 2017

11

Shapour Jalilzadeh

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2 August 2017

17

Eduardo Marbán

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2 August 2017

3

Wendy Post

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2 August 2017

Morna Ikeda

6

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2 August 2017

Kristen West

7

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2 August 2017

Carl Kashuk

8

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2 August 2017

Chao-Yu Guo

14

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2 August 2017

Peter M Spooner

21

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2 August 2017

language of work or name

English

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publication date

30 April 2006

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2 August 2017

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2 August 2017

38

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2 August 2017

644-651

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2 August 2017

6

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https://scigraph.springernature.com/pub.10.1038/ng1790

2 August 2017

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cites work

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

1 reference

The prognostic value of the QT interval and QT interval dispersion in all-cause and cardiac mortality and morbidity in a population of Danish citizens

21 January 2018

1 reference

Prolonged QTc interval, impaired pulmonary function, and a very lean body mass jointly predict all-cause mortality in elderly men.

21 January 2018

1 reference

Prolonged QT interval predicts cardiac and all-cause mortality in the elderly. The Rotterdam Study

21 January 2018

1 reference

Assessment of QT interval and QT dispersion for prediction of all-cause and cardiovascular mortality in American Indians: The Strong Heart Study

21 January 2018

1 reference

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

21 January 2018

1 reference

Genetics of cardiac arrhythmias and sudden cardiac death

21 January 2018

1 reference

Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes

21 January 2018

1 reference

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

21 January 2018

1 reference

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

21 January 2018

1 reference

Complement factor H polymorphism in age-related macular degeneration

21 January 2018

1 reference

Complement factor H variant increases the risk of age-related macular degeneration

21 January 2018

1 reference

Complement factor H polymorphism and age-related macular degeneration

21 January 2018

1 reference

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

21 January 2018

1 reference

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

21 January 2018

1 reference

A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization

21 January 2018

1 reference

Two-stage designs for gene-disease association studies with sample size constraints.

21 January 2018

1 reference

The use of measured genotype information in the analysis of quantitative phenotypes in man. I. Models and analytical methods.

21 January 2018

1 reference

Comparison of linkage-disequilibrium methods for localization of genes influencing quantitative traits in humans

21 January 2018

1 reference

Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies

21 January 2018

1 reference

CAPON: a protein associated with neuronal nitric oxide synthase that regulates its interactions with PSD95

21 January 2018

1 reference

Calcium channel alpha2delta subunits: differential expression, function, and drug binding

21 January 2018

1 reference

Prediction of complete gene structures in human genomic DNA

21 January 2018

1 reference

Dexras1: a G protein specifically coupled to neuronal nitric oxide synthase via CAPON

21 January 2018

1 reference

Regulation of the mammalian heart function by nitric oxide.

21 January 2018

1 reference

Neuronal nitric oxide synthase negatively regulates xanthine oxidoreductase inhibition of cardiac excitation-contraction coupling

21 January 2018

1 reference

Differential K+ channel clustering activity of PSD-95 and SAP97, two related membrane-associated putative guanylate kinases

21 January 2018

1 reference

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

21 January 2018

1 reference

Recommendations for standardization and specifications in automated electrocardiography: bandwidth and digital signal processing. A report for health professionals by an ad hoc writing group of the Committee on Electrocardiography and Cardiac Electr

21 January 2018

1 reference

Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays.

21 January 2018

1 reference

Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes

21 January 2018

1 reference

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

21 January 2018

1 reference

7 January 2021

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7 January 2021

QT interval prolongation predicts cardiovascular mortality in an apparently healthy population

1 reference

7 January 2021

Association between QT interval and coronary heart disease in middle-aged and elderly men. The Zutphen Study

1 reference

7 January 2021

TWIK-1, a ubiquitous human weakly inward rectifying K+ channel with a novel structure

1 reference

7 January 2021

SAP97 interacts with Kv1.5 in heterologous expression systems.

1 reference

7 January 2021

A haplotype map of the human genome

1 reference

7 January 2021

Source consistency filtering. Application to resting ECGs

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG1790

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Dimensions Publication ID

2 August 2017

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