Common variants for atrial fibrillation: results from genome-wide association studies (Q37898563)

25 August 2017

1 reference

title

Common variants for atrial fibrillation: results from genome-wide association studies (English)

1 reference

genome-wide association study

25 August 2017

main subject

0 references

Atrial Fibrillation

0 references

author name string

Xinyuan Liu

1

1 reference

25 August 2017

Fei Wang

2

1 reference

25 August 2017

Ashley C Knight

3

1 reference

25 August 2017

Jiangmin Zhao

4

1 reference

25 August 2017

Junjie Xiao

5

1 reference

25 August 2017

publication date

7 July 2011

1 reference

25 August 2017

1 reference

25 August 2017

volume

131

1 reference

25 August 2017

issue

1

1 reference

25 August 2017

page(s)

33-39

1 reference

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

25 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic features

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

Sudden death associated with short-QT syndrome linked to mutations in HERG.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

KCNQ1 gain-of-function mutation in familial atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

Cardiac sodium channel mutation in atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

Common variants in KCNN3 are associated with lone atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

Variants conferring risk of atrial fibrillation on chromosome 4q25.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

Association of RS2200733 but not RS10033464 on 4q25 with atrial fibrillation based on the recessive model in a Taiwanese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

The association of the 4q25 susceptibility variant for atrial fibrillation with stroke is limited to stroke of cardioembolic etiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

Independent susceptibility markers for atrial fibrillation on chromosome 4q25.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

Sodium channel mutations and susceptibility to heart failure and atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

Effects of potassium channel blockers on changes in refractoriness of atrial cardiomyocytes induced by stretch.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

Truncation of PITX2 differentially affects its activity on physiological targets.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

Genome-wide association studies of atrial fibrillation: past, present, and future

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

2-Aminoethoxydiphenyl borate, a inositol 1,4,5-triphosphate receptor inhibitor, prevents atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1052-3

Stabilizing ryanodine receptor type 2: a novel strategy for the treatment of atrial fibrillation

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

[KCNE3 R53H substitution in familial atrial fibrillation]

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

A gain-of-function TBX5 mutation is associated with atypical Holt-Oram syndrome and paroxysmal atrial fibrillation

1 reference

12 December 2020

MicroRNA expression signature in atrial fibrillation with mitral stenosis

1 reference

12 December 2020

Taxol, a microtubule stabilizer, prevents atrial fibrillation in in vitro atrial fibrillation models using rabbit hearts

1 reference

12 December 2020

10.1007/S00439-011-1052-3

Identifiers

DOI

1 reference

25 August 2017

1 reference