Variants conferring risk of atrial fibrillation on chromosome 4q25. (Q33289458)

25 July 2017

Variants conferring risk of atrial fibrillation on chromosome 4q25. (English)

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25 July 2017

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Daníel F. Guðbjartsson

1

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25 July 2017

Unnur Þorsteinsdóttir

39

Unnur Thorsteinsdottir

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Solveig Gretarsdottir

4

Solveig Gretarsdottir

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Adalbjorg Jonasdottir

7

Adalbjorg Jonasdottir

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Anna Helgadottir

3

Anna Helgadottir

1 reference

25 July 2017

9

Gudmar Thorleifsson

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25 July 2017

Arnar Palsson

11

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Larry Baum

Larry Baum

22

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Eric E Smith

Eric E Smith

31

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Ka Sing Wong

Ka Sing Wong

24

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Augustine Kong

Augustine Kong

38

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Patrick Sulem

13

Patrick Sulem

1 reference

25 July 2017

32

Jonathan Rosand

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25 July 2017

40

Kari Stefansson

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25 July 2017

37

Jeffrey R Gulcher

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25 July 2017

35

Patrick T Ellinor

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25 July 2017

27

Steven M Greenberg

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25 July 2017

David O Arnar

2

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25 July 2017

Hilma Holm

5

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25 July 2017

Asgeir Sigurdsson

6

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25 July 2017

Adam Baker

8

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25 July 2017

Kristleifur Kristjansson

10

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25 July 2017

Thorarinn Blondal

12

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25 July 2017

Valgerdur M Backman

14

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25 July 2017

Gudmundur A Hardarson

15

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25 July 2017

Ebba Palsdottir

16

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25 July 2017

Agnar Helgason

17

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25 July 2017

Runa Sigurjonsdottir

18

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25 July 2017

Jon T Sverrisson

19

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25 July 2017

Konstantinos Kostulas

20

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25 July 2017

Maggie C Y Ng

21

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25 July 2017

Wing Yee So

23

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25 July 2017

Juliana C N Chan

25

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25 July 2017

Karen L Furie

26

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25 July 2017

Michelle Sale

28

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25 July 2017

Peter Kelly

29

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25 July 2017

Calum A MacRae

30

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25 July 2017

Jan Hillert

33

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25 July 2017

Ronald C W Ma

34

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25 July 2017

Gudmundur Thorgeirsson

36

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25 July 2017

language of work or name

English

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publication date

1 July 2007

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25 July 2017

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25 July 2017

448

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25 July 2017

353-357

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25 July 2017

7151

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https://scigraph.springernature.com/pub.10.1038/nature06007

25 July 2017

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cites work

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

Secular trends in incidence of atrial fibrillation in Olmsted County, Minnesota, 1980 to 2000, and implications on the projections for future prevalence

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

Familial aggregation of atrial fibrillation in Iceland

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

Familial aggregation in lone atrial fibrillation

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

KCNQ1 gain-of-function mutation in familial atrial fibrillation

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

Potassium channel gene mutations rarely cause atrial fibrillation

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

The role of Pitx2 during cardiac development. Linking left-right signaling and congenital heart diseases

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

The pitx2 homeobox protein is required early for endoderm formation and nodal signaling. .

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

Molecular pathway for the localized formation of the sinoatrial node

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

A haplotype map of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

The interrelationship between atrial fibrillation and atrial flutter

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

Identification of metabolic pathways of brain angiotensin II and III using specific aminopeptidase inhibitors: predominant role of angiotensin III in the control of vasopressin release

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

The gene encoding phosphodiesterase 4D confers risk of ischemic stroke.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

Haplotype relative risks: an easy reliable way to construct a proper control sample for risk calculations

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

Development and validation of stroke risk equation for Hong Kong Chinese patients with type 2 diabetes: the Hong Kong Diabetes Registry.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

Methylenetetrahydrofolate reductase gene A222V polymorphism and risk of ischemic stroke

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06007

7 January 2021

Identifiers

DOI

10.1038/NATURE06007

1 reference

25 July 2017

1 reference