Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young
出版年份 2020 全文链接
标题
Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young
作者
关键词
-
出版物
HERZ
Volume -, Issue -, Pages -
出版商
Springer Science and Business Media LLC
发表日期
2020-01-22
DOI
10.1007/s00059-019-04883-1
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- A compound heterozygosity of Tecrl gene confirmed in a catecholaminergic polymorphic ventricular tachycardia family
- (2019) Lijian Xie et al. European Journal of Medical Genetics
- RBM20 Mutations Induce an Arrhythmogenic Dilated Cardiomyopathy Related to Disturbed Calcium Handling
- (2018) Maarten M. G. van den Hoogenhof et al. CIRCULATION
- Exome analysis in 34 sudden unexplained death (SUD) victims mainly identified variants in channelopathy-associated genes
- (2018) Jacqueline Neubauer et al. INTERNATIONAL JOURNAL OF LEGAL MEDICINE
- Mechanical Stretching Simulates Cardiac Physiology and Pathology through Mechanosensor Piezo1
- (2018) Tzyy-Yue Wong et al. Journal of Clinical Medicine
- Post-mortem whole-exome analysis in a large sudden infant death syndrome cohort with a focus on cardiovascular and metabolic genetic diseases
- (2017) Jacqueline Neubauer et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome
- (2017) Najim Lahrouchi et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Piezo1 channels sense whole body physical activity to reset cardiovascular homeostasis and enhance performance
- (2017) Baptiste Rode et al. Nature Communications
- TECRL , a new life‐threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT
- (2016) Harsha D Devalla et al. EMBO Molecular Medicine
- Genetic investigation of 100 heart genes in sudden unexplained death victims in a forensic setting
- (2016) Sofie Lindgren Christiansen et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Postmortem genetic analysis of sudden unexplained death syndrome under 50 years of age: A next-generation sequencing study
- (2016) Yukiko Hata et al. HEART RHYTHM
- Sudden infant death syndrome caused by cardiac arrhythmias: only a matter of genes encoding ion channels?
- (2016) Georgia Sarquella-Brugada et al. INTERNATIONAL JOURNAL OF LEGAL MEDICINE
- Molecular and Functional Characterization of RareCACNA1CVariants in Sudden Unexplained Death in the Young
- (2016) Brittan S. Sutphin et al. Congenital Heart Disease
- Genetics of Sudden Cardiac Death
- (2015) C. R. Bezzina et al. CIRCULATION RESEARCH
- Use of high-throughput targeted exome-sequencing to screen for copy number variation in hypertrophic cardiomyopathy
- (2015) L.R. Lopes et al. European Journal of Medical Genetics
- Massive parallel sequencing applied to the molecular autopsy in sudden cardiac death in the young
- (2015) M. Brion et al. Forensic Science International-Genetics
- Sudden cardiac death in forensic medicine – Swiss recommendations for a multidisciplinary approach
- (2015) M Wilhelm et al. SWISS MEDICAL WEEKLY
- OBSCN Mutations Associated with Dilated Cardiomyopathy and Haploinsufficiency
- (2015) Steven Marston et al. PLoS One
- AKAP9 Is a Genetic Modifier of Congenital Long-QT Syndrome Type 1
- (2014) C. P. de Villiers et al. Circulation-Cardiovascular Genetics
- Next generation sequencing challenges in the analysis of cardiac sudden death due to arrhythmogenic disorders
- (2014) Maria Brion et al. ELECTROPHORESIS
- Arrhythmogenic cardiomyopathy and Brugada syndrome: Diseases of the connexome
- (2014) Esperanza Agullo-Pascual et al. FEBS LETTERS
- Exome analysis–based molecular autopsy in cases of sudden unexplained death in the young
- (2014) Richard D. Bagnall et al. HEART RHYTHM
- An Evaluation of Copy Number Variation Detection Tools from Whole-Exome Sequencing Data
- (2014) Renjie Tan et al. HUMAN MUTATION
- Desmosomes and the sodium channel complex: Implications for arrhythmogenic cardiomyopathy and Brugada syndrome
- (2014) Marina Cerrone et al. TRENDS IN CARDIOVASCULAR MEDICINE
- Whole Exome Sequencing Identifies a Causal RBM20 Mutation in a Large Pedigree With Familial Dilated Cardiomyopathy
- (2013) Quinn S. Wells et al. Circulation-Cardiovascular Genetics
- Genetic analysis of sudden unexplained death: A multidisciplinary approach
- (2013) Silke Kauferstein et al. FORENSIC SCIENCE INTERNATIONAL
- Postmortem genetic screening of SNPs in RyR2 gene in sudden unexplained nocturnal death syndrome in the southern Chinese Han population
- (2013) Lei Huang et al. FORENSIC SCIENCE INTERNATIONAL
- HRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia Syndromes
- (2013) Silvia G. Priori et al. HEART RHYTHM
- A robust model for read count data in exome sequencing experiments and implications for copy number variant calling
- (2012) Vincent Plagnol et al. BIOINFORMATICS
- Sarcomeric gene mutations in sudden infant death syndrome (SIDS)
- (2012) Maria Brion et al. FORENSIC SCIENCE INTERNATIONAL
- Remodeling of the cardiac sodium channel, connexin43, and plakoglobin at the intercalated disk in patients with arrhythmogenic cardiomyopathy
- (2012) Maartje Noorman et al. HEART RHYTHM
- Desmosome–Ion Channel Interactions and Their Possible Role in Arrhythmogenic Cardiomyopathy
- (2012) Mario Delmar PEDIATRIC CARDIOLOGY
- Sudden cardiac death with normal heart:
- (2010) Cristina Basso et al. CARDIOVASCULAR PATHOLOGY
- Sudden Death in the Young
- (2010) Christian van der Werf et al. Circulation-Arrhythmia and Electrophysiology
- Nationwide study of sudden cardiac death in persons aged 1–35 years
- (2010) Bo Gregers Winkel et al. EUROPEAN HEART JOURNAL
- Sudden cardiac death: epidemiology and risk factors
- (2010) A. Selcuk Adabag et al. Nature Reviews Cardiology
- Piezo1 and Piezo2 Are Essential Components of Distinct Mechanically Activated Cation Channels
- (2010) B. Coste et al. SCIENCE
- Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families
- (2008) Elijah R. Behr et al. EUROPEAN HEART JOURNAL
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now