Genome-Wide Linkage Scan Identifies a Novel Genetic Locus on Chromosome 5p13 for Neonatal Atrial Fibrillation Associated With Sudden Death and Variable Cardiomyopathy

No abstract is available for this paper.

• Publication year

  2004

• Venue

  Circulation

• Publication date

  2004-12-21

• Fields of study

  Medicine

• Identifiers
  DOI 10.1161/01.CIR.0000150333.87176.C7PMID 15596564PMCID PMC1618875
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Mega2: data-handling for facilitating genetic linkage and association analyses

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• Locus for Atrial Fibrillation Maps to Chromosome 6q14‐16

  2003cited by this paper
• Ventricular Fibrillation Resulting from Acute Right Ventricular Infarction from Isolated Occlusion of a Right Ventricular Branch Artery

  2003cited by this paper
• LQT4 gene: the "missing" ankyrin.

  2003cited by this paper
• Mutation of MEF2A in an Inherited Disorder with Features of Coronary Artery Disease

  2003cited by this paper
• KCNQ1 gain-of-function mutation in familial atrial fibrillation.

  2003cited by this paper
• KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death

  2003cited by this paper
• Atrial Fibrillation in Patients with Congestive Heart Failure

  2003cited by this paper
• Atrial Electrophysiology and Mechanisms of Atrial Fibrillation

  2003cited by this paper
• Atrial fibrillation: strategies to control, combat, and cure

  2002cited by this paper
• Molecular mechanisms of remodeling in human atrial fibrillation.

  2002cited by this paper
• ACC/AHA/ESC Guidelines for the Management of Patients With Atrial Fibrillation: Executive Summary A Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines and the European Society of Cardiology Committee for Practice Guidelines and Policy Conference

  2001cited by this paper
• Structural remodelling during chronic atrial fibrillation: act of programmed cell survival.

  2001cited by this paper
• The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.

  1998cited by this paper
• Spontaneous initiation of atrial fibrillation by ectopic beats originating in the pulmonary veins.

  1998cited by this paper
• The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.

  1998cited by this paper
• Prevalence, incidence, prognosis, and predisposing conditions for atrial fibrillation: population-based estimates.

  1998cited by this paper
• Identification of a genetic locus for familial atrial fibrillation.

  1997cited by this paper
• Tachycardia-induced cardiomyopathy: a review of animal models and clinical studies.

  1997cited by this paper
• Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics.

  1996cited by this paper
• Secular trends in the prevalence of atrial fibrillation: The Framingham Study.

  1996cited by this paper
• Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

  1996cited by this paper
• Prevalence, age distribution, and gender of patients with atrial fibrillation. Analysis and implications.

  1995cited by this paper
• SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome.

  1995cited by this paper
• Faster sequential genetic linkage computations.

  1993cited by this paper
• Prolonged Atrial Conduction: A Major Predisposing Factor for the Development of Atrial Flutter

  1978cited by this paper

• Genetics and Pharmacogenetics of Atrial Fibrillation

  2024cites this paper
• From the sideline: Tissue‐specific nucleoporin function in health and disease, an update

  2023cites this paper
• The Role of Nucleoporins in Cardiac Tissue Development and Disease.

  2023cites this paper
• Mouse models of spontaneous atrial fibrillation

  2022cites this paper
• Structure and Function of the Nuclear Pore Complex.

  2022cites this paper
• A novel PRRX1 loss-of-function variation contributing to familial atrial fibrillation and congenital patent ductus arteriosus

  2022cites this paper
• Cytoskeletal Protein Variants Driving Atrial Fibrillation: Potential Mechanisms of Action

  2022cites this paper
• 5p13 microduplication in a malformed fetus and his unaffected father

  2022cites this paper
• The history and geographic distribution of a KCNQ1 atrial fibrillation risk allele

  2021cites this paper
• Atrial Fibrillation Genomics: Discovery and Translation

  2021cites this paper
• The Genetic Puzzle of Familial Atrial Fibrillation

  2020cites this paper
• Clinical and genetic relationships between the QTc interval and risk of a stroke among atrial fibrillation patients undergoing catheter ablation

  2020cites this paper
• Association Between Atrial Fibrillation and Sudden Cardiac Death

  2020cites this paper
• The molecular genetic basis of atrial fibrillation

  2020cites this paper
• Genetic and Molecular Basis of Cardiac Arrhythmias

  2020cites this paper
• Atrial fibrillation—a complex polygenetic disease

  2020cites this paper
• Nucleoporins in cardiovascular disease.

  2020cites this paper
• [The sudden death among the young persons under effect of the different forms of physical loads].

  2019cites this paper
• Chapter 15. Inherited Conduction Disease and Atrial Fibrillation

  2019cites this paper
• Inherited Conduction Disease and Atrial Fibrillation

  2018cites this paper
• Personalizing therapy for atrial fibrillation: the role of stem cell and in silico disease models

  2018cites this paper
• 49 – Genetics of Atrial Fibrillation

  2018cites this paper
• Genetics of Atrial Fibrillation

  2018cites this paper
• The Role of Pharmacogenetics in Atrial Fibrillation Therapeutics: Is Personalized Therapy in Sight?

  2016cites this paper
• Genomics of Atrial Fibrillation

  2016cites this paper
• Rs7193343 polymorphism in zinc finger homeobox 3 (ZFHX3) gene and atrial fibrillation: an updated meta-analysis of 10 case-control comparisons

  2015cites this paper
• Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation

  2015cites this paper
• Common and Rare Variants in SCN10A Modulate the Risk of Atrial Fibrillation

  2015cites this paper
• Genetics of atrial fibrillation: from families to genomes

  2015cites this paper
• Common and Rare Variants in SCN 10 A Modulate the Risk of Atrial Fibrillation

  2014cites this paper
• NKX2-6 mutation predisposes to familial atrial fibrillation.

  2014cites this paper
• Genetic aspects of lone atrial fibrillation: what do we know?

  2014cites this paper
• Pathophysiology of idiopathic atrial fibrillation - prognostic and treatment implications.

  2014cites this paper
• 49 – Genetics of Atrial Fibrillation

  2014cites this paper
• Genetic Discoveries in Atrial Fibrillation and Implications for Clinical Practice.

  2014cites this paper
• Pharmacogenomics of Antiarrhythmic Drug Therapy for Atrial Fibrillation

  2014cites this paper
• Improved understanding of the pathophysiology of atrial fibrillation through the lens of discrete pathological pathways

  2014cites this paper
• New mechanisms underlying the variable phenotypes caused by N- and C-terminal mutations in the cardiac sodium channel.

  2014cites this paper
• Understanding the genetic basis of atrial fibrillation : next steps after genome-wide association studies

  2014cites this paper
• A novel PITX 2 c loss ‐ of ‐ function mutation underlies lone atrial fibrillation

  2013cites this paper
• A novel PITX2c loss‑of‑function mutation underlies lone atrial fibrillation.

  2013cites this paper
• Prevalence and spectrum of GJA5 mutations associated with lone atrial fibrillation.

  2013cites this paper
• Mutations of the SCN4B-encoded sodium channel β4 subunit in familial atrial fibrillation.

  2013cites this paper
• A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation.

  2013cites this paper
• Genetic mechanisms of atrial fibrillation: impact on response to treatment

  2013cites this paper
• Molecular approaches to tissue transplantation and transfusion medicine in Maori and Polynesians in New Zealand

  2013cites this paper
• Relación entre la morfología de la válvula y la raíz aórtica con la recurrencia de la fibrilación auricular no valvular

  2013cites this paper
• Genetics of Atrial Fibrillation and Standstill

  2013cites this paper
• The Genetics of Cardiac Electrophysiology in Humans

  2013cites this paper
• A novel GATA5 loss-of-function mutation underlies lone atrial fibrillation.

  2013cites this paper
• Atrial fibrillation : insights concerning the arrhythmogenic substrate

  2012cites this paper
• 2012 HRS/EHRA/ECAS expert consensus statement on catheter and surgical ablation of atrial fibrillation: recommendations for patient selection, procedural techniques, patient management and follow-up, definitions, endpoints, and research trial design

  2012cites this paper
• Personalized medicine and atrial fibrillation: will it ever happen?

  2012cites this paper
• Novel GATA6 loss-of-function mutation responsible for familial atrial fibrillation.

  2012cites this paper
• Population-based prediction of atrial fibrillation

  2012cites this paper
• Gain-of-function mutations in SCN5A gene lead to type-3 long QT syndrome

  2012cites this paper
• 2012 HRS/EHRA/ECAS Expert Consensus Statement on Catheter and Surgical Ablation of Atrial Fibrillation: recommendations for patient selection, procedural techniques, patient management and follow-up, definitions, endpoints, and research trial design.

  2012cites this paper
• Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population

  2011cites this paper
• Monogenic atrial fibrillation as pathophysiological paradigms.

  2011cites this paper
• The genetics of atrial fibrillation: from the bench to the bedside.

  2011cites this paper
• Terapia anticoagulante en fibrilación auricular

  2011cites this paper
• Novel GATA4 mutations in lone atrial fibrillation.

  2011cites this paper
• Lone atrial fibrillation: what is known and what is to come

  2011cites this paper
• The "missing" link in atrial fibrillation heritability.

  2011cites this paper
• GATA4 loss-of-function mutations in familial atrial fibrillation.

  2011cites this paper
• Novel GATA 4 mutations in lone atrial fibrillation

  2011cites this paper
• Monogenic atrial fibrillation as pathophysiological paradigms

  2011cites this paper
• [Anticoagulation and atrial fibrillation].

  2011cites this paper
• Pathophysiology of atrial fibrillation

  2011cites this paper
• Genetic and Molecular Basis of Arrhythmias

  2011cites this paper
• Atrial fibrillation in congestive heart failure.

  2010cites this paper
• Familial aggregation of lone atrial fibrillation in the Chinese population.

  2010cites this paper
• Novel connexin40 missense mutations in patients with familial atrial fibrillation.

  2010cites this paper
• Genetics and Genomics of Arrhythmias

  2010cites this paper
• Lone AF - Etiologic Factors and Genetic Insights into Pathophysiolgy.

  2010cites this paper
• Genetics of atrial fibrillation.

  2010cites this paper
• Connexin40 nonsense mutation in familial atrial fibrillation.

  2010cites this paper
• The genetics of atrial fibrillation

  2010cites this paper
• Lone AF - etiologic factors and genetic insights into pathophysiolgy.

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• Contemporary Reviews in Cardiovascular Medicine

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• Genetics of Atrial Fibrillation: Implications for Future Research Directions and Personalized Medicine

  2010cites this paper
• CHAPTER 62 – Genetics and Genomics of Arrhythmias

  2009cites this paper
• Molecular genetics of atrial fibrillation

  2009cites this paper
• Arrhythmia pharmacogenomics: methodological considerations.

  2009cites this paper
• Genetics of atrial fibrillation.

  2009cites this paper
• Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation.

  2009cites this paper
• Angiotensin II receptor blockers in the prevention of atrial fibrillation

  2009cites this paper
• Mutation in nuclear pore component NUP155 leads to atrial fibrillation and early sudden cardiac death.

  2008influential citation
• Atrial Fibrillation Genetic Considerations: The Basic Scientist's Perspective

  2008cites this paper
• Familial Atrial Fibrillation and Standstill

  2008cites this paper
• Prolonged signal-averaged P-wave duration as an intermediate phenotype for familial atrial fibrillation.

  2008cites this paper
• Genetics of Atrial Fibrillation

  2008cites this paper
• Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation.

  2008cites this paper
• New risk factors for atrial fibrillation: causes of 'not-so-lone atrial fibrillation'.

  2008cites this paper
• The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG).

  2008cites this paper
• Cardiac sodium channel mutation in atrial fibrillation.

  2008cites this paper
• Genetics of atrial fibrillation.

  2008cites this paper
• Genetics of Atrial Fibrillation: The Clinician's Perspective

  2008cites this paper
• Confronting the genetic complexity of atrial fibrillation: this too shall pass.

  2007cites this paper
• Genetic factors for lone atrial fibrillation.

  2007cites this paper