Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population (Q37348739)

19 August 2017

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

1 reference

19 August 2017

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Cong Li

1

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19 August 2017

Fan Wang

2

1 reference

19 August 2017

Yanzong Yang

3

1 reference

19 August 2017

Fenfen Fu

4

1 reference

19 August 2017

Chengqi Xu

5

1 reference

19 August 2017

Lisong Shi

6

1 reference

19 August 2017

Sisi Li

7

1 reference

19 August 2017

Yunlong Xia

8

1 reference

19 August 2017

Gang Wu

9

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19 August 2017

Xiang Cheng

10

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19 August 2017

Hui Liu

11

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19 August 2017

Chuchu Wang

12

1 reference

19 August 2017

Pengyun Wang

13

1 reference

19 August 2017

Jianjun Hao

14

1 reference

19 August 2017

Yuhe Ke

15

1 reference

19 August 2017

Yuanyuan Zhao

16

1 reference

19 August 2017

Mugen Liu

17

1 reference

19 August 2017

Rongfeng Zhang

18

1 reference

19 August 2017

Lianjun Gao

19

1 reference

19 August 2017

Bo Yu

20

1 reference

19 August 2017

Qiutang Zeng

21

1 reference

19 August 2017

Yuhua Liao

22

1 reference

19 August 2017

Bo Yang

23

1 reference

19 August 2017

Xin Tu

24

1 reference

19 August 2017

Qing K Wang

25

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19 August 2017

25 November 2010

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19 August 2017

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19 August 2017

129

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19 August 2017

3

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19 August 2017

239-246

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

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

Common variants in KCNN3 are associated with lone atrial fibrillation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

Impact of genetic discoveries on the classification of lone atrial fibrillation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

Variants conferring risk of atrial fibrillation on chromosome 4q25.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

Sodium channel mutations and susceptibility to heart failure and atrial fibrillation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

ATBF1 enhances the suppression of STAT3 signaling by interaction with PIAS3

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

KCNQ1 gain-of-function mutation in familial atrial fibrillation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

Prevalence of diagnosed atrial fibrillation in adults: national implications for rhythm management and stroke prevention: the AnTicoagulation and Risk Factors in Atrial Fibrillation (ATRIA) Study

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

Promoter and intronic variants affect the transcriptional regulation of the human dopamine transporter gene

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

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

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

Epidemiology, risk factors for stroke, and management of atrial fibrillation in China

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

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

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5069458

ACC/AHA/ESC 2006 guidelines for the management of patients with atrial fibrillation: full text: A report of the American College of Cardiology/American Heart Association Task Force on practice guidelines and the European Society of Cardiology Committ

2 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00439-010-0912-6

Prevalence, age distribution, and gender of patients with atrial fibrillation. Analysis and implications

21 January 2018

1 reference

12 December 2020

Stroke--1989. Recommendations on stroke prevention, diagnosis, and therapy. Report of the WHO Task Force on Stroke and other Cerebrovascular Disorders

1 reference

12 December 2020

Phased-array intracardiac echocardiography monitoring during pulmonary vein isolation in patients with atrial fibrillation: impact on outcome and complications

1 reference

12 December 2020

Membrane translocation of small GTPase Rac1 and activation of STAT1 and STAT3 in pacing-induced sustained atrial fibrillation

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S00439-010-0912-6

Identifiers

DOI

1 reference

19 August 2017

1 reference

19 August 2017

PubMed publication ID

21107608

1 reference