Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation
Published 2014 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation
Authors
Keywords
-
Journal
JOURNAL OF MEDICAL GENETICS
Volume 52, Issue 1, Pages 28-36
Publisher
BMJ
Online
2014-11-13
DOI
10.1136/jmedgenet-2014-102618
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Atrial Fibrillation Associated Chromosome 4q25 Variants Are Not Associated with PITX2c Expression in Human Adult Left Atrial Appendages
- (2014) Shamone R. Gore-Panter et al. PLoS One
- A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation
- (2013) Morten Salling Olesen et al. CARDIOVASCULAR RESEARCH
- DNase I–hypersensitive exons colocalize with promoters and distal regulatory elements
- (2013) Tim R Mercer et al. NATURE 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
- Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation
- (2012) Ingrid E. Christophersen et al. EUROPEAN HEART JOURNAL
- A functional variant in the promoter region regulates the C-reactive protein gene and is a potential candidate for increased risk of atrial fibrillation
- (2012) S.-N. Chang et al. JOURNAL OF INTERNAL MEDICINE
- Familial Aggregation of Lone Atrial Fibrillation in Young Persons
- (2012) Nina Øyen et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- The accessible chromatin landscape of the human genome
- (2012) Robert E. Thurman et al. NATURE
- Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated Cardiomyopathy
- (2011) Nadine Norton et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Significant Association of rs13376333 in KCNN3 on Chromosome 1q21 With Atrial Fibrillation in a Taiwanese Population
- (2011) Shu-Hsuan Chang et al. CIRCULATION JOURNAL
- PITX2c Is Expressed in the Adult Left Atrium, and Reducing Pitx2c Expression Promotes Atrial Fibrillation Inducibility and Complex Changes in Gene Expression
- (2011) Paulus Kirchhof et al. Circulation-Cardiovascular Genetics
- Association of RS2200733 but Not RS10033464 on 4q25 with Atrial Fibrillation Based on the Recessive Model in a Taiwanese Population
- (2010) Kun-Tai Lee et al. CARDIOLOGY
- Tachycardia of atrial myocytes induces collagen expression in atrial fibroblasts through transforming growth factor 1
- (2010) C.-T. Tsai et al. CARDIOVASCULAR RESEARCH
- Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation
- (2010) Morten S. Olesen et al. CARDIOVASCULAR RESEARCH
- Common variants in KCNN3 are associated with lone atrial fibrillation
- (2010) Patrick T Ellinor et al. NATURE GENETICS
- Uncovering the roles of rare variants in common disease through whole-genome sequencing
- (2010) Elizabeth T. Cirulli et al. NATURE REVIEWS GENETICS
- Pitx2 prevents susceptibility to atrial arrhythmias by inhibiting left-sided pacemaker specification
- (2010) J. Wang et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Towards a complete resolution of the genetic architecture of disease
- (2010) Andrew B. Singleton et al. TRENDS IN GENETICS
- A Genome-Wide Association Study Identifies Susceptibility Variants for Type 2 Diabetes in Han Chinese
- (2010) Fuu-Jen Tsai et al. PLoS Genetics
- Finding the missing heritability of complex diseases
- (2009) Teri A. Manolio et al. NATURE
- Targeted capture and massively parallel sequencing of 12 human exomes
- (2009) Sarah B. Ng et al. NATURE
- Exome sequencing identifies the cause of a mendelian disorder
- (2009) Sarah B Ng 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
- Human genetic variation and its contribution to complex traits
- (2009) Kelly A. Frazer et al. NATURE REVIEWS GENETICS
- Targeted screening of cis-regulatory variation in human haplotypes
- (2008) D. J. Verlaan et al. GENOME RESEARCH
- A HapMap harvest of insights into the genetics of common disease
- (2008) Teri A. Manolio et al. JOURNAL OF CLINICAL INVESTIGATION
- A treasure trove for lipoprotein biology
- (2008) Aldons J Lusis et al. NATURE GENETICS
- Common variants at 30 loci contribute to polygenic dyslipidemia
- (2008) Sekar Kathiresan et al. NATURE GENETICS
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now