Single nucleotide polymorphisms in arrhythmia genes modify the risk of cardiac events and sudden death in long QT syndrome-Reference-Cited by-同舟云学术

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Single nucleotide polymorphisms in arrhythmia genes modify the risk of cardiac events and sudden death in long QT syndrome

Published:2014-01 Issue:1 Volume:11 Page:76-82
ISSN:1547-5271
Container-title:Heart Rhythm
language:en
Short-container-title:Heart Rhythm

Author:

Earle Nikki,Yeo Han Dug,Pilbrow Anna,Crawford Jackie,Smith Warren,Shelling Andrew N.,Cameron Vicky,Love Donald R.,Skinner Jonathan R.

Publisher

Elsevier BV

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference36 articles.

1. 25th Anniversary of the International Long-QT Syndrome Registry: an ongoing quest to uncover the secrets of long-QT syndrome;Moss;Circulation,2005

2. Sudden cardiac death and genetic ion channelopathies: long QT, Brugada, short QT, catecholaminergic polymorphic ventricular tachycardia, and iiopathic ventricular fibrillation;Napolitano;Circulation,2012

3. Common genetic variation modulating cardiac ECG parameters and susceptibility to sudden cardiac death;Kolder;J Mol Cell Cardiol,2012

4. Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in us white community-based populations;Kao;Circulation,2009

5. Variants in the 3′ untranslated region of the KCNQ1-encoded K v7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner;Amin;Eur Heart J,2012

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1. From genes to clinical management: A comprehensive review of long QT syndrome pathogenesis and treatment;Heart Rhythm O2;2024-08

2. The role of the neural NO synthase adapter protein in the pathogenesis of metabolic syndrome and type 2 diabetes mellitus;Сибирский научный медицинский журнал;2023-10-27

3. Genetic Predictors of Ibrutinib-related Cardiovascular Side Effects in Patients with Chronic Lymphocytic Leukemia;Clinical Cancer Research;2023-09-22

4. VEGF-A related SNPs: a cardiovascular context;Frontiers in Cardiovascular Medicine;2023-05-23

5. To Modify or Not to Modify: Allele‐Specific Effects of 3'UTR‐ KCNQ1 Single Nucleotide Polymorphisms on Clinical Phenotype in a Long QT 1 Founder Population Segregating a Dominant‐Negative Mutation;Journal of the American Heart Association;2022-09-20

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