Identification of rare variants in TNNI3 with atrial fibrillation in a Chinese GeneID population
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Title
Identification of rare variants in TNNI3 with atrial fibrillation in a Chinese GeneID population
Authors
Keywords
Atrial fibrillation (AF), Hypertrophic cardiomyopathy, Cardiac troponin I, <em class=EmphasisTypeItalic >TNNI3</em> mutations, Whole exome sequencing
Journal
MOLECULAR GENETICS AND GENOMICS
Volume 291, Issue 1, Pages 79-92
Publisher
Springer Nature
Online
2015-07-13
DOI
10.1007/s00438-015-1090-y
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Note: Only part of the references are listed.- Integrating Genetic, Transcriptional, and Functional Analyses to Identify 5 Novel Genes for Atrial Fibrillation
- (2014) Moritz F. Sinner et al. CIRCULATION
- Sequence Kernel Association Tests for the Combined Effect of Rare and Common Variants
- (2013) Iuliana Ionita-Laza et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Worldwide Epidemiology of Atrial Fibrillation
- (2013) Sumeet S. Chugh et al. CIRCULATION
- Atrial fibrillation: the role of common and rare genetic variants
- (2013) Morten S Olesen et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- High Prevalence of Long QT Syndrome–Associated SCN5A Variants in Patients With Early-Onset Lone Atrial Fibrillation
- (2012) Morten S. Olesen et al. Circulation-Cardiovascular Genetics
- 2012 focused update of the ESC Guidelines for the management of atrial fibrillation
- (2012) et al. EUROPEAN HEART JOURNAL
- wANNOVAR: annotating genetic variants for personal genomes via the web
- (2012) Xiao Chang et al. JOURNAL OF MEDICAL GENETICS
- Meta-analysis identifies six new susceptibility loci for atrial fibrillation
- (2012) Patrick T Ellinor et al. NATURE GENETICS
- Primer3—new capabilities and interfaces
- (2012) Andreas Untergasser et al. NUCLEIC ACIDS RESEARCH
- Structural Dynamics of Troponin I during Ca2+-Activation of Cardiac Thin Filaments: A Multi-Site Förster Resonance Energy Transfer Study
- (2012) Hui Wang et al. PLoS One
- Predicting the Functional Effect of Amino Acid Substitutions and Indels
- (2012) Yongwook Choi et al. PLoS One
- 2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy: Executive Summary
- (2011) Bernard J. Gersh et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han population
- (2011) Fan Wang et al. NATURE GENETICS
- Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population
- (2010) Pengyun Wang et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- Identification of NPPA variants associated with atrial fibrillation in a Chinese GeneID population
- (2010) Xiang Ren et al. CLINICA CHIMICA ACTA
- Common variants in KCNN3 are associated with lone atrial fibrillation
- (2010) Patrick T Ellinor et al. NATURE GENETICS
- Missing heritability and strategies for finding the underlying causes of complex disease
- (2010) Evan E. Eichler et al. NATURE REVIEWS GENETICS
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
- (2010) K. Wang et al. NUCLEIC ACIDS RESEARCH
- Familial Aggregation of Atrial Fibrillation
- (2009) Ingrid Elisabeth Christophersen et al. Circulation-Arrhythmia and Electrophysiology
- Atrial fibrillation in mainland China: epidemiology and current management
- (2009) S Zhang HEART
- Assessment of association of rs2200733 on chromosome 4q25 with atrial fibrillation and ischemic stroke in a Chinese Han population
- (2009) Lisong Shi et al. HUMAN GENETICS
- Finding the missing heritability of complex diseases
- (2009) Teri A. Manolio et al. NATURE
- A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke
- (2009) Daniel F Gudbjartsson et al. NATURE GENETICS
- Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
- (2009) Emelia J Benjamin et al. NATURE GENETICS
- Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
- (2009) Prateek Kumar et al. Nature Protocols
- Mutation in Nuclear Pore Component NUP155 Leads to Atrial Fibrillation and Early Sudden Cardiac Death
- (2008) Xianqin Zhang et al. CELL
- Epidemiology, Risk Factors for Stroke, and Management of Atrial Fibrillation in China
- (2008) Dayi Hu et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Atrial Natriuretic Peptide Frameshift Mutation in Familial Atrial Fibrillation
- (2008) Denice M. Hodgson-Zingman et al. NEW ENGLAND JOURNAL OF MEDICINE
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