Evaluation of the Genetic Basis of Familial Aggregation of Pacemaker Implantation by a Large Next Generation Sequencing Panel-Reference-Cited by-同舟云学术

Evaluation of the Genetic Basis of Familial Aggregation of Pacemaker Implantation by a Large Next Generation Sequencing Panel

Published:2015-12-04 Issue:12 Volume:10 Page:e0143588
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Celestino-Soper Patrícia B. S.,Doytchinova Anisiia,Steiner Hillel A.,Uradu Andrea,Lynnes Ty C.,Groh William J.,Miller John M.,Lin Hai,Gao Hongyu,Wang Zhiping,Liu Yunlong,Chen Peng-Sheng,Vatta Matteo

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference36 articles.

1. New insights into pacemaker activity: promoting understanding of sick sinus syndrome;H Dobrzynski;Circulation,2007

2. Isolated congenital complete atrioventricular block in adult life. A prospective study;M Michaëlsson;Circulation,1995

3. Mechanisms of inherited cardiac conduction disease;JP Smits;Europace,2005

4. Long-term follow up of children with congenital complete atrioventricular block and the impact of pacemaker therapy;C Balmer;Europace,2002

5. HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies;MJ Ackerman;Heart Rhythm,2011

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Common and Rare Variant Contributions to Bradyarrhythmias from Multi-Ancestry Meta-Analyses;2023-09-25

2. Indications for genetic examinations in children with bradyarrhythmias;Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics);2022-08-11

3. The Role of TRPM4 Gene Mutations in Causing Familial Progressive Cardiac Conduction Disease: A Further Contribution;Genes;2022-01-28

4. Reevaluating the Mutation Classification in Genetic Studies of Bradycardia Using ACMG/AMP Variant Classification Framework;International Journal of Genomics;2020-02-26

5. Impact of functional studies on exome sequence variant interpretation in early-onset cardiac conduction system diseases;Cardiovascular Research;2020-01-24