Paradigm shifts in the genetics of inherited arrhythmias: Using next‐generation sequencing technologies to uncover hidden etiologies

Paradigm shifts in the genetics of inherited arrhythmias: Using next‐generation sequencing technologies to uncover hidden etiologies

Bibliographic Details
Main Author:	Naomasa Makita
Format:	Article
Language:	English
Published:	Wiley 2013-12-01
Series:	Journal of Arrhythmia
Subjects:	Next‐generation sequencing Exome Calmodulin Long QT syndrome Inherited arrhythmia
Online Access:	https://doi.org/10.1016/j.joa.2013.09.001

Similar Items

Value of next-generation sequencing in inherited arrhythmia syndromes
by: Min Jae Kim, et al.
Published: (2023-07-01)

Calmodulin Mutations in Human Disease
by: John W. Hussey, et al.
Published: (2023-12-01)

Moderately Prolonged QTc in Computer-Assessed ECG, Random Variation or Significant Risk Factor? A Literature Review
by: Jan Hysing, et al.
Published: (2022-09-01)

Inherited Arrhythmias in the Pediatric Population: An Updated Overview
by: Marco Valerio Mariani, et al.
Published: (2024-01-01)

Editorial: Methods and applications in cardiac electrophysiology–application to inherited arrhythmias
by: Nathalie Neyroud, et al.
Published: (2024-03-01)

Management of Arrhythmias in COVID-19
by: Yusuf Ziya Şener, et al.
Published: (2022-03-01)

Preventing and Treating Torsades de Pointes in the Mother, Fetus and Newborn in the Highest Risk Pregnancies with Inherited Arrhythmia Syndromes
by: Annette Wacker-Gussmann, et al.
Published: (2023-05-01)

Evaluation of cardiac arrhythmia incidence in patients treated with oral moxifloxacin
by: Casit Olgun Celik, et al.
Published: (2019-01-01)

Inherited heart rhythm and conduction disorders in children with infectious diseases
by: S. N. Chuprova, et al.
Published: (2020-07-01)

COVID-19 and arrhythmia: The factors associated and the role of myocardial electrical impulse propagation. An observational study based on cardiac telemetric monitoring
by: Domenico Cozzolino, et al.
Published: (2022-09-01)

Future direction of substrate‐based catheter ablation in Brugada syndrome and other inherited primary arrhythmia syndromes: Systematic review and meta‐analysis
by: Gusti Ngurah Prana Jagannatha MD, et al.
Published: (2023-12-01)

Clinical and genetic characteristics of 18 cases with suspected congenital long QT syndrome: A retrospective cross-sectional study
by: Ying Zhang, et al.
Published: (2024-01-01)

Inherited arrhythmias: The cardiac channelopathies
by: Shashank P Behere, et al.
Published: (2015-01-01)

Effectiveness of whole-exome sequencing for the identification of causal mutations in patients with suspected inherited ocular diseases
by: Vianey Ordoñez-Labastida, et al.
Published: (2022-10-01)

Sexual Dimorphisms, Anti-Hormonal Therapy and Cardiac Arrhythmias
by: Virginie Grouthier, et al.
Published: (2021-02-01)

Drug-induced arrhythmias
by: M. V. Leonova
Published: (2021-01-01)

The mitochondrial DNA mutations associated with cardiac arrhythmia investigated in an LQTS family
by: Fatemeh Khatami, et al.
Published: (2014-09-01)

Guilt and Reproductive Decision‐Making in Patients With Inherited Cardiac Diseases
by: Emily Smith, et al.
Published: (2024-04-01)

Arrhythmia-Associated Calmodulin E105A Mutation Alters the Binding Affinity of CaM to a Ryanodine Receptor 2 CaM-Binding Pocket
by: Angelos Thanassoulas, et al.
Published: (2023-10-01)

Clinical and Genetic Re-Evaluation of Inherited Retinal Degeneration Pedigrees following Initial Negative Findings on Panel-Based Next Generation Sequencing
by: Kirk A. J. Stephenson, et al.
Published: (2022-01-01)

An analysis of the electrocardiogram QT interval
by: N.R. Koehler, et al.
Published: (2004-01-01)

Modeling Human Cardiac Arrhythmias: Insights from Zebrafish
by: Sébastien Gauvrit, et al.
Published: (2022-01-01)

Evaluation of association between asymptomatic COVID-19 and ventricular arrhythmias
by: Fatih Çölkesen, et al.
Published: (2021-03-01)

Treatment of cardiac arrhythmias in a mouse model of Rett syndrome with Na+-channel-blocking antiepileptic drugs
by: José A. Herrera, et al.
Published: (2015-04-01)

Contribution of Fetal Magnetocardiography to Diagnosis, Risk Assessment, and Treatment of Fetal Arrhythmia
by: Annette Wacker‐Gussmann, et al.
Published: (2022-08-01)

CARDIAC ARRHYTHMIAS AND ECG PARAMETERS IN PATIENTS WITH ARTERIAL HYPERTENSION AND METABOLIC SYNDROME
by: Kh. Kh. Kh.Kh, et al.
Published: (2011-02-01)

Molecular Approach of Hereditary Arrhythmias, Long QT Syndrome, and Arrhythmogenic Right Ventricular Cardiomyopathy
by: Hanife Saat, et al.
Published: (2022-06-01)

The Whole-Exome Sequencing of a Cohort of 19 Families with Adolescent Idiopathic Scoliosis (AIS): Candidate Pathways
by: Laura Marie-Hardy, et al.
Published: (2023-11-01)

Development of automated patch clamp assays to overcome the burden of variants of uncertain significance in inheritable arrhythmia syndromes
by: Joanne G. Ma, et al.
Published: (2023-11-01)

QT interval prolongation in Takotsubo syndrome: a frightening feature with no major prognostic impact
by: Ana Isabel Pinho, et al.
Published: (2023-12-01)

Precision Medicine through Next-Generation Sequencing in Inherited Eye Diseases in a Korean Cohort
by: Dabin Moon, et al.
Published: (2021-12-01)

Psychotherapeutic drug‐induced life‐threatening arrhythmias: A retrospective analysis using the Japanese adverse drug event report database
by: Saki Yokohara, et al.
Published: (2023-12-01)

Fatal arrhythmia following ingestion of hawthorn root () extract: a case report
by: Sergio Villegas-Belman, et al.
Published: (2022-12-01)

Genome Editing and Cardiac Arrhythmias
by: Oliver M. Moore, et al.
Published: (2023-05-01)

Ondansetron-induced QT prolongation among various age groups: a systematic review and meta-analysis
by: Kamaldeep Singh, et al.
Published: (2023-07-01)

Electrocardiographic changes after high-dose corticosteroid pulse therapy in pemphigus patients
by: Mehdi Pishgahi, et al.
Published: (2018-11-01)

The phenomenon of dormant inheritance in inheritance law
by: O. Ye. Kukhariev
Published: (2022-06-01)

Understanding Calmodulin Variants Affecting Calcium-Dependent Inactivation of L-Type Calcium Channels through Whole-Cell Simulation of the Cardiac Ventricular Myocyte
by: Matthew D. McCoy, et al.
Published: (2022-12-01)

Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance
by: Valerie Jacquemin, et al.
Published: (2023-03-01)

Anxiety and Depression in Cardiac Inherited Disease: Prevalence and Association With Clinical and Psychosocial Factors
by: Claire E. O’Donovan, et al.
Published: (2019-12-01)