(Q38494600)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25994868%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

review article

1 reference

title

Genetics of atrial fibrillation: from families to genomes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25994868%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

1 reference

21 May 2015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25994868%20AND%20SRC:MED&resulttype=core&format=json

Journal of Human Genetics

8 March 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25994868%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

volume

61

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25994868%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25994868%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

page(s)

61-70

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25994868%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/jhg.2015.44

8 March 2020

exact match

0 references

cites work

Prevalence and spectrum of GATA6 mutations associated with familial atrial fibrillation.

1 reference

12 December 2020

Functional Nav1.8 channels in intracardiac neurons: the link between SCN10A and cardiac electrophysiology

1 reference

12 December 2020

Promotion of atrial fibrillation by heart failure in dogs: atrial remodeling of a different sort

1 reference

12 December 2020

A novel GATA5 loss-of-function mutation underlies lone atrial fibrillation

1 reference

12 December 2020

GATA6 loss-of-function mutation in atrial fibrillation

1 reference

12 December 2020

S4153R is a gain-of-function mutation in the cardiac Ca(2+) release channel ryanodine receptor associated with catecholaminergic polymorphic ventricular tachycardia and paroxysmal atrial fibrillation.

1 reference

12 December 2020

Familial atrial fibrillation is a genetically heterogeneous disorder.

1 reference

12 December 2020

Symptomatic response to antiarrhythmic drug therapy is modulated by a common single nucleotide polymorphism in atrial fibrillation.

1 reference

12 December 2020

Pitx2c and Nkx2-5 are required for the formation and identity of the pulmonary myocardium

1 reference

12 December 2020

Novel KCNA5 mutation implicates tyrosine kinase signaling in human atrial fibrillation

1 reference

12 December 2020

Reduced Penetrance and Variable Expression of SCN5A Mutations and the Importance of Co-inherited Genetic Variants: Case Report and Review of the Literature.

1 reference

12 December 2020

Pitx2, an atrial fibrillation predisposition gene, directly regulates ion transport and intercalated disc genes

1 reference

12 December 2020

A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation

1 reference

12 December 2020

Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation

1 reference

12 December 2020

R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation

1 reference

12 December 2020

Familial aggregation of atrial fibrillation: a study in Danish twins

1 reference

12 December 2020

2014 AHA/ACC/HRS guideline for the management of patients with atrial fibrillation: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines and the Heart Rhythm Society

1 reference

12 December 2020

A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation

1 reference

12 December 2020

Mutational spectrum of the GATA5 gene associated with familial atrial fibrillation

1 reference

12 December 2020

Mutations in the cardiac transcription factor GATA4 in patients with lone atrial fibrillation.

1 reference

12 December 2020

KATP channel mutation confers risk for vein of Marshall adrenergic atrial fibrillation

1 reference

12 December 2020

Common variants in KCNN3 are associated with lone atrial fibrillation

1 reference

12 December 2020

Familial Aggregation of Lone Atrial Fibrillation in Young Persons

1 reference

12 December 2020

Stretch-sensitive KCNQ1 mutation A link between genetic and environmental factors in the pathogenesis of atrial fibrillation?

1 reference

12 December 2020

Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke.

1 reference

12 December 2020

A genome-wide association study to identify genomic modulators of rate control therapy in patients with atrial fibrillation

1 reference

12 December 2020

Twelve-single nucleotide polymorphism genetic risk score identifies individuals at increased risk for future atrial fibrillation and stroke

1 reference

12 December 2020

PITX2c Is Expressed in the Adult Left Atrium, and Reducing Pitx2c Expression Promotes Atrial Fibrillation Inducibility and Complex Changes in Gene Expression

1 reference

12 December 2020

Assessment of association of rs2200733 on chromosome 4q25 with atrial fibrillation and ischemic stroke in a Chinese Han population.

1 reference

12 December 2020

Parental atrial fibrillation as a risk factor for atrial fibrillation in offspring

1 reference

12 December 2020

High prevalence of genetic variants previously associated with Brugada syndrome in new exome data.

1 reference

12 December 2020

An atrial-fibrillation-linked connexin40 mutant is retained in the endoplasmic reticulum and impairs the function of atrial gap-junction channels

1 reference

12 December 2020

Association of the human minK gene 38G allele with atrial fibrillation: evidence of possible genetic control on the pathogenesis of atrial fibrillation

1 reference

12 December 2020

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

1 reference

12 December 2020

Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation

1 reference

12 December 2020

Localisation of SCN10A gene product Na(v)1.8 and novel pain-related ion channels in human heart

1 reference

12 December 2020

Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation

1 reference

12 December 2020

Pitx2 prevents susceptibility to atrial arrhythmias by inhibiting left-sided pacemaker specification

1 reference

12 December 2020

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

1 reference

12 December 2020

Novel KCNA5 loss-of-function mutations responsible for atrial fibrillation

1 reference

12 December 2020

A common polymorphism in SCN5A is associated with lone atrial fibrillation

1 reference

12 December 2020

A novel trafficking-defective HCN4 mutation is associated with early-onset atrial fibrillation

1 reference

12 December 2020

Sodium channel mutations and susceptibility to heart failure and atrial fibrillation

1 reference

12 December 2020

Novel GATA5 loss-of-function mutations underlie familial atrial fibrillation

1 reference

12 December 2020

Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation

1 reference

12 December 2020

A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillation

1 reference

12 December 2020

Paradigm of genetic mosaicism and lone atrial fibrillation: physiological characterization of a connexin 43-deletion mutant identified from atrial tissue

1 reference

12 December 2020

Brugada syndrome risk loci seem protective against atrial fibrillation

1 reference

12 December 2020

A KCNQ1 mutation causes age-dependant bradycardia and persistent atrial fibrillation

1 reference

12 December 2020

Familial sinus bradycardia associated with a mutation in the cardiac pacemaker channel

1 reference

12 December 2020

A novel PITX2c loss‑of‑function mutation underlies lone atrial fibrillation

1 reference

12 December 2020

Altered HCN4 channel C-linker interaction is associated with familial tachycardia-bradycardia syndrome and atrial fibrillation

1 reference

12 December 2020

Blocking Scn10a channels in heart reduces late sodium current and is antiarrhythmic

1 reference

12 December 2020

Loss-of-function mutations in APOC3, triglycerides, and coronary disease

1 reference

12 December 2020

Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry

1 reference

12 December 2020

Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation.

1 reference

12 December 2020

Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation

1 reference

12 December 2020

Mutation in nuclear pore component NUP155 leads to atrial fibrillation and early sudden cardiac death

1 reference

12 December 2020

Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation.

1 reference

12 December 2020

Cardiac sodium channel mutation in atrial fibrillation.

1 reference

12 December 2020

Variation in the 4q25 chromosomal locus predicts atrial fibrillation after coronary artery bypass graft surgery

1 reference

12 December 2020

Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation

1 reference

12 December 2020

Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese

1 reference

12 December 2020

Cloning and characterization of a mouse sensory neuron tetrodotoxin-resistant voltage-gated sodium channel gene, Scn10a

1 reference

12 December 2020

A KCNJ8 mutation associated with early repolarization and atrial fibrillation

1 reference

12 December 2020

A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channels.

1 reference

12 December 2020

Striking In vivo phenotype of a disease-associated human SCN5A mutation producing minimal changes in vitro

1 reference

12 December 2020

Gain-of-function mutation of Nav1.5 in atrial fibrillation enhances cellular excitability and lowers the threshold for action potential firing

1 reference

12 December 2020

Comprehensive mutation scanning of LMNA in 268 patients with lone atrial fibrillation

1 reference

12 December 2020

A common genetic variant within SCN10A modulates cardiac SCN5A expression

1 reference

12 December 2020

Novel genetic markers improve measures of atrial fibrillation risk prediction

1 reference

12 December 2020

Transgenic insights linking pitx2 and atrial arrhythmias

1 reference

12 December 2020

Severity of obstructive sleep apnea influences the effect of genotype on response to anti-arrhythmic drug therapy for atrial fibrillation

1 reference

12 December 2020

A tetrodotoxin-resistant voltage-gated sodium channel from human dorsal root ganglia, hPN3/SCN10A

1 reference

12 December 2020

Genetic variation in SCN10A influences cardiac conduction

1 reference

12 December 2020

KCNE3 mutation V17M identified in a patient with lone atrial fibrillation

1 reference

12 December 2020

PITX2 insufficiency leads to atrial electrical and structural remodeling linked to arrhythmogenesis

1 reference

12 December 2020

Chromosome 4q25 variants and atrial fibrillation recurrence after catheter ablation.

1 reference

12 December 2020

Calcium-handling abnormalities underlying atrial arrhythmogenesis and contractile dysfunction in dogs with congestive heart failure

1 reference

12 December 2020

Association of rs2200733 at 4q25 with atrial flutter/fibrillation diseases in an Italian population

1 reference

12 December 2020

A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation

1 reference

12 December 2020

Targeted deep sequencing reveals no definitive evidence for somatic mosaicism in atrial fibrillation.

1 reference

12 December 2020

Familial aggregation of atrial fibrillation in Iceland

1 reference

12 December 2020

Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation

1 reference

12 December 2020

A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation.

1 reference

12 December 2020

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)

1 reference

12 December 2020

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

1 reference

12 December 2020

Impact of atrial fibrillation on the risk of death: the Framingham Heart Study

1 reference

12 December 2020

Facilitatory and inhibitory effects of SCN5A mutations on atrial fibrillation in Brugada syndrome

1 reference

12 December 2020

Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

1 reference

12 December 2020

NKX2-6 mutation predisposes to familial atrial fibrillation

1 reference

12 December 2020

Evidence for reentry as a mechanism of cardiac arrhythmias

1 reference

12 December 2020

Rare variants in GJA5 are associated with early-onset lone atrial fibrillation

1 reference

12 December 2020

Characterizations of a loss-of-function mutation in the Kir3.4 channel subunit.

1 reference

12 December 2020

Novel GATA4 mutations in lone atrial fibrillation

1 reference

12 December 2020

Association between familial atrial fibrillation and risk of new-onset atrial fibrillation

1 reference

12 December 2020

Locus for atrial fibrillation maps to chromosome 6q14-16

1 reference

12 December 2020

Short QT syndrome and atrial fibrillation caused by mutation in KCNH2.

1 reference

12 December 2020

Estimation of total incremental health care costs in patients with atrial fibrillation in the United States.

1 reference

12 December 2020

Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation

1 reference

12 December 2020

Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population

1 reference

12 December 2020

Genetic Loci on Chromosomes 4q25, 7p31, and 12p12 Are Associated With Onset of Lone Atrial Fibrillation Before the Age of 40 Years

1 reference

12 December 2020

Connexin40 nonsense mutation in familial atrial fibrillation

1 reference

12 December 2020

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

1 reference

12 December 2020

Usefulness of single nucleotide polymorphism in chromosome 4q25 to predict in-hospital and long-term development of atrial fibrillation and survival in patients undergoing coronary artery bypass grafting

1 reference

12 December 2020

Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation

1 reference

12 December 2020

Independent susceptibility markers for atrial fibrillation on chromosome 4q25.

1 reference

12 December 2020

Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation

1 reference

12 December 2020

Identification of NPPA variants associated with atrial fibrillation in a Chinese GeneID population

1 reference

12 December 2020

Targeted sequencing in candidate genes for atrial fibrillation: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing Study

1 reference

12 December 2020

Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes

1 reference

12 December 2020

Genome-wide linkage scan identifies a novel genetic locus on chromosome 5p13 for neonatal atrial fibrillation associated with sudden death and variable cardiomyopathy

1 reference

12 December 2020

Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation

1 reference

12 December 2020

Mutation spectrum of the GATA4 gene in patients with idiopathic atrial fibrillation

1 reference

12 December 2020

Mutation E169K in junctophilin-2 causes atrial fibrillation due to impaired RyR2 stabilization.

1 reference

12 December 2020

GATA4 loss-of-function mutations in familial atrial fibrillation

1 reference

12 December 2020

New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants

1 reference

12 December 2020

Mechanisms by which atrial fibrillation-associated mutations in the S1 domain of KCNQ1 slow deactivation of IKs channels.

1 reference

12 December 2020

Prevalence and spectrum of GJA5 mutations associated with lone atrial fibrillation

1 reference

12 December 2020

Genetic and clinical risk prediction model for postoperative atrial fibrillation.

1 reference

12 December 2020

Uncovering an intermediate phenotype associated with rs2200733 at 4q25 in lone atrial fibrillation

1 reference

12 December 2020

Familial aggregation of lone atrial fibrillation in the Chinese population

1 reference

12 December 2020

Common genetic polymorphism at 4q25 locus predicts atrial fibrillation recurrence after successful cardioversion

1 reference

12 December 2020

Characterization of genome-wide association-identified variants for atrial fibrillation in African Americans

1 reference

12 December 2020

Epistatic effects of potassium channel variation on cardiac repolarization and atrial fibrillation risk

1 reference

12 December 2020

Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation

1 reference

12 December 2020

Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation

1 reference

12 December 2020

Worldwide epidemiology of atrial fibrillation: a Global Burden of Disease 2010 Study

1 reference

12 December 2020

De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero.

1 reference

12 December 2020

Mutations of the SCN4B-encoded sodium channel β4 subunit in familial atrial fibrillation.

1 reference

12 December 2020

J-shaped association between QTc interval duration and the risk of atrial fibrillation: results from the Copenhagen ECG study

1 reference

12 December 2020

Functional modeling in zebrafish demonstrates that the atrial-fibrillation-associated gene GREM2 regulates cardiac laterality, cardiomyocyte differentiation and atrial rhythm

1 reference

12 December 2020

Novel GATA6 loss-of-function mutation responsible for familial atrial fibrillation

1 reference

12 December 2020

KCNJ2 mutation in short QT syndrome 3 results in atrial fibrillation and ventricular proarrhythmia

1 reference

12 December 2020

1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data

1 reference

12 December 2020

A genome-wide association study of a coronary artery disease risk variant

1 reference

12 December 2020

A familial mutation renders atrial natriuretic Peptide resistant to proteolytic degradation

1 reference

12 December 2020

A common variant on chromosome 4q25 is associated with prolonged PR interval in subjects with and without atrial fibrillation.

1 reference

12 December 2020

Common and rare variants in SCN10A modulate the risk of atrial fibrillation

1 reference

12 December 2020

Familial aggregation in lone atrial fibrillation

1 reference

12 December 2020

Pacemaker channel dysfunction in a patient with sinus node disease

1 reference

12 December 2020

Variants of the lamin A/C (LMNA) gene in non-valvular atrial fibrillation patients: a possible pathogenic role of the Thr528Met mutation

1 reference

12 December 2020

Relation of 97T polymorphism in KCNE5 to risk of atrial fibrillation

1 reference

12 December 2020

Variants conferring risk of atrial fibrillation on chromosome 4q25.

1 reference

12 December 2020

Common genetic variants and response to atrial fibrillation ablation

1 reference

12 December 2020

Novel connexin40 missense mutations in patients with familial atrial fibrillation

1 reference

12 December 2020

Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation

1 reference

12 December 2020

High prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillation

1 reference

12 December 2020

KCNQ1 gain-of-function mutation in familial atrial fibrillation

1 reference

12 December 2020

Identification of a genetic locus for familial atrial fibrillation

1 reference

12 December 2020

KCNQ1 mutation Q147R is associated with atrial fibrillation and prolonged QT interval.

1 reference

12 December 2020

Novel germline GJA5/connexin40 mutations associated with lone atrial fibrillation impair gap junctional intercellular communication

1 reference

12 December 2020

Functional characterization of a trafficking-defective HCN4 mutation, D553N, associated with cardiac arrhythmia

1 reference

12 December 2020

Augmented potassium current is a shared phenotype for two genetic defects associated with familial atrial fibrillation

1 reference

12 December 2020

Mapping a novel locus for familial atrial fibrillation on chromosome 10p11-q21

1 reference

12 December 2020

Molecular pathway for the localized formation of the sinoatrial node

1 reference

12 December 2020

SCN1Bb R214Q found in 3 patients: 1 with Brugada syndrome and 2 with lone atrial fibrillation

1 reference

12 December 2020

SCN5A mutation associated with cardiac conduction defect and atrial arrhythmias.

1 reference

12 December 2020

A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation

1 reference

12 December 2020

SCN10A/Nav1.8 modulation of peak and late sodium currents in patients with early onset atrial fibrillation

1 reference

12 December 2020

Common and Rare Variants in SCN10A Modulate the Risk of Atrial Fibrillation

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FJHG.2015.44

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/JHG.2015.44

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25994868%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

1 reference