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Scholar Results 1 - 10 of about 24 citing Lehtinen: Association of NOS1AP genetic variants with QT interval duration in families from.... (0.08 sec) 

Gender and effects of a common genetic variant in the NOS1 regulator NOS1AP on …

- oxfordjournals.org
MD Tobin, M Kahonen, P Braund, T Nieminen, C Hajat, … - International Journal of …, 2008 - IEA
1 Department of Health Sciences, University of Leicester, UK, LE1 7RH. 2 Department of
Genetics, University of Leicester, UK, LE1 7RH. 3 Department of Clinical Physiology, Tampere
University Hospital and Medical School, University of Tampere, Finland. 4 Department of ...
Cited by 19 - Related articles - All 7 versions

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


C Newton-Cheh, M Eijgelsheim, KM Rice, PI De Bakker … - Nat Genet, 2009 - massgeneral.org
QT interval duration, reflecting myocardial repolarization on the electrocardiogram, is a heritable
risk factor for sudden cardiac death and drug-induced arrhythmias. We conducted a meta-analysis
of three genome-wide association studies in 13,685 individuals of European ancestry ...
Cited by 17 - Related articles - View as HTML - All 7 versions

Identification of a common variant at the NOS1AP locus strongly associated to QT- …

- nursing2008.com
… , ALHJ Aarnoudse, F Rivadeneira, JA Kors, J … - Human Molecular …, 2009 - Oxford Univ Press
QT-interval prolongation is an electrophysiologic phenomenon associated with sudden cardiac
death. The QT-interval in the general population is 35% heritable. In genome-wide association
studies, a common variant (rs10494366T > G) within the nitric oxide synthase 1 adaptor ...
Cited by 12 - Related articles - All 6 versions

Genetic variations in nitric oxide synthase 1 adaptor protein are associated with …

- nursing2008.com
WH Kao, DE Arking, W Post, TD Rea, N Sotoodehnia, … - Circulation, 2009 - Am Heart Assoc
From the Department of Epidemiology (WHLK, WP, JC), McKusick-Nathans Institute of Genetic
Medicine (DEA, BB, BQD, AC), Department of Medicine (WHLK, DEA, WP, GFT, JC, PMS,
AC), School of Medicine and Bloomberg School of Public Health, Johns Hopkins ...
Cited by 11 - Related articles - All 6 versions

Multiple independent genetic factors at NOS1AP modulate the QT interval in a multi …


DE Arking, A Khera, C Xing, WHL Kao, W Post, E … - PLoS ONE, 2009 - pubmedcentral.nih.gov
Extremes of electrocardiographic QT interval are associated with increased risk for sudden cardiac
death (SCD); thus, identification and characterization of genetic variants that modulate QT interval
may elucidate the underlying etiology of SCD. Previous studies have revealed an ...
Cited by 7 - Related articles - All 6 versions

Common genetic variation near the phospholamban gene is associated with …


IM Nolte, C Wallace, SJ Newhouse, D Waggott, J Fu, N … - 2009 - pubmedcentral.nih.gov
Copyright Nolte et al. This is an open-access article distributed under the terms of the Creative
Commons Attribution License, which permits unrestricted use, distribution, and reproduction
in any medium, provided the original author and source are credited.
Cited by 2 - Related articles - All 7 versions

Common variants at ten loci influence myocardial repolarization: the QTGEN …


C Newton-Cheh, M Eijgelsheim, K Rice, PIW de … - Nature …, 2009 - pubmedcentral.nih.gov
Cited by 2 - Related articles

Determinants of prolonged QT interval and their contribution to sudden death risk …


SS Chugh, K Reinier, T Singh, A Uy-Evanado, C … - Circulation, 2009 - Am Heart Assoc
Methods and Results— A case-control design was used. Cases were SCD patients with coronary
artery disease among a metropolitan area of 1 000 000 residents (2002 to 2006); controls were
area residents with coronary artery disease but no history of SCD. All cases were ...
Cited by 3 - Related articles - All 6 versions

SNP association and sequence analysis of the NOS1AP gene in SIDS


M Osawa, R Kimura, I Hasegawa, N Mukasa, F Satoh - Legal Medicine, 2009 - Elsevier
One of the speculated causes for sudden infant death syndrome (SIDS) is hereditary
disease, in which long QT in electrocardiogram has been investigated in the view of mutations
in various ion channel genes. In the present study, a novel QT interval determinant of ...
Cited by 1 - Related articles - All 6 versions

Gender and effects of a common genetic variant in the NOS1 regulator NOS1AP on …


G Epidemiology - Genetic Epidemiology, 2008 - pt.wkhealth.com
Background: A longer heart-rate corrected QT interval (QTc) is associated with increased risk
of ventricular arrhythmias. Women have longer resting QTc and are more likely than men to develop
drug-induced QT prolongation. Recent studies have shown association between resting ...
Related articles - All 2 versions


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