Assessment of association of rs2200733 on chromosome 4q25 with atrial fibrillation and ischemic stroke in a Chinese Han population (Q48475735)

11 February 2018

title

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

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11 February 2018

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Lisong Shi

1

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11 February 2018

Cong Li

2

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11 February 2018

Chuchu Wang

3

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11 February 2018

Yunlong Xia

4

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11 February 2018

Gang Wu

5

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11 February 2018

Fan Wang

6

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11 February 2018

Chengqi Xu

7

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11 February 2018

Pengyun Wang

8

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11 February 2018

Xiuchun Li

9

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11 February 2018

Dan Wang

10

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11 February 2018

Xin Xiong

11

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11 February 2018

Ying Bai

12

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11 February 2018

Mugen Liu

13

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11 February 2018

Jingyu Liu

14

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11 February 2018

Xiang Ren

15

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11 February 2018

Lianjun Gao

16

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11 February 2018

Binbin Wang

17

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11 February 2018

Qiutang Zeng

18

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11 February 2018

Bo Yang

19

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11 February 2018

Xu Ma

20

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11 February 2018

Yanzong Yang

21

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11 February 2018

Xin Tu

22

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11 February 2018

Qing Kenneth Wang

23

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11 February 2018

publication date

1 December 2009

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11 February 2018

published in

Human Genetics

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11 February 2018

volume

126

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11 February 2018

issue

6

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11 February 2018

page(s)

843-849

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11 February 2018

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

cites work

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Characterization of different subsets of atrial fibrillation in general practice in France: the ALFA study. The College of French Cardiologists.

21 January 2018

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Atrial fibrillation as an independent risk factor for stroke: the Framingham Study

21 January 2018

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Prevalence, incidence, prognosis, and predisposing conditions for atrial fibrillation: population-based estimates

21 January 2018

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12 December 2020

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

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12 December 2020

Characteristics and prognosis of lone atrial fibrillation. 30-year follow-up in the Framingham Study

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12 December 2020

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

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

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Sodium channel mutations and susceptibility to heart failure and atrial fibrillation

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

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12 December 2020

Molecular genetic studies in atrial fibrillation.

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Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation.

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12 December 2020

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

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12 December 2020

Familial aggregation of atrial fibrillation in Iceland

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Molecular genetics of atrial fibrillation

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12 December 2020

ACC/AHA/ESC 2006 Guidelines for the Management of Patients With Atrial Fibrillation

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An epidemiological study on the prevalence of atrial fibrillation in the Chinese population of mainland China

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Familial aggregation in lone atrial fibrillation

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

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Variants conferring risk of atrial fibrillation on chromosome 4q25.

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12 December 2020

KCNQ1 gain-of-function mutation in familial atrial fibrillation

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

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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

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10.1007/S00439-009-0737-3

Identifiers

DOI

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11 February 2018

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11 February 2018