(Q37146274)

18 August 2017

0 references

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

1 reference

18 August 2017

0 references

0 references

25

1 reference

18 August 2017

André G Uitterlinden

0 references

Emelia J. Benjamin

29

Emelia J Benjamin

0 references

Christopher Newton-Cheh

6

Christopher Newton-Cheh

1 reference

18 August 2017

Dawood Darbar

2

0 references

Kathryn L. Lunetta

Kathryn L Lunetta

16

0 references

Josée Dupuis

Josée Dupuis

4

0 references

Martin G Larson

Martin G Larson

17

0 references

Albert Schömig

22

Albert Schömig

1 reference

PMCID

2663727

18 August 2017

Jacqueline C M Witteman

27

Jacqueline C M Witteman

1 reference

18 August 2017

23

H-Erich Wichmann

1 reference

18 August 2017

7

Renate Schnabel

1 reference

18 August 2017

30

Patrick T Ellinor

1 reference

18 August 2017

28

Dan M Roden

1 reference

18 August 2017

9

Moritz F Sinner

1 reference

18 August 2017

5

Arne Pfeufer

1 reference

18 August 2017

3

Charlotte van Noord

1 reference

18 August 2017

11

Britt M Beckmann

1 reference

18 August 2017

15

Siegfried Perz

1 reference

18 August 2017

1

Stefan Kääb

1 reference

18 August 2017

14

Jan Heeringa

1 reference

18 August 2017

24

Gerhard Steinbeck

1 reference

18 August 2017

19

Calum A MacRae

1 reference

18 August 2017

8

Seiko Makino

1 reference

18 August 2017

10

Prince J Kannankeril

1 reference

18 August 2017

13

Brian S Donahue

1 reference

18 August 2017

20

Jeremy N Ruskin

1 reference

PMCID

2663727

18 August 2017

Annette Wacker-Gussmann

21

Annette Wacker

1 reference

18 August 2017

18

Daniel Levy

1 reference

18 August 2017

Subbarao Choudry

12

1 reference

18 August 2017

13 January 2009

1 reference

18 August 2017

European Heart Journal

1 reference

18 August 2017

30

1 reference

18 August 2017

813-819

1 reference

18 August 2017

7

1 reference

Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

Ion channel mutations in AF: signal or noise?

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

Genetics of 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=2663727

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

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=2663727

Polymorphism modulates symptomatic response to antiarrhythmic drug therapy in patients 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=2663727

A common allele on chromosome 9 associated with coronary heart disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

Molecular pathway for the localized formation of the sinoatrial node

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

HTRA1 promoter polymorphism in wet age-related macular degeneration

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

Somatic mutations in the connexin 40 gene (GJA5) in 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=2663727

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=2663727

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

KORA-gen--resource for population genetics, controls and a broad spectrum of disease phenotypes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

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=2663727

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

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=2663727

New ideas about atrial fibrillation 50 years on.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

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=2663727

Mouse Pitx2 deficiency leads to anomalies of the ventral body wall, heart, extra- and periocular mesoderm and right pulmonary isomerism

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

Dosage requirement of Pitx2 for development of multiple organs

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

Spontaneous initiation of atrial fibrillation by ectopic beats originating in the pulmonary veins

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

The transcription factor Pitx2 mediates situs-specific morphogenesis in response to left-right asymmetric signals

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

Independent risk factors for atrial fibrillation in a population-based cohort. The Framingham Heart 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=2663727

Meta-analysis in clinical trials

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

Atrial fibrillation as an independent risk factor for stroke: the Framingham 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=2663727

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

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

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

Identification of a genetic locus for familial atrial fibrillation

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

Familial aggregation of atrial fibrillation in Iceland

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

The Diagnostic Performance of Computer Programs for the Interpretation of Electrocardiograms

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

Cardiac sodium channel mutation in atrial fibrillation.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

Refinement of single-nucleotide polymorphism genotyping methods on human genomic DNA: amplifluor allele-specific polymerase chain reaction versus ligation detection reaction-TaqMan.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

A population-based study of the long-term risks associated with atrial fibrillation: 20-year follow-up of the Renfrew/Paisley study.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

Atrial fibrillation and dementia in a population-based study. The Rotterdam Study.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663727

Temporal Relations of Atrial Fibrillation and Congestive Heart Failure and Their Joint Influence on Mortality

3 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHN578

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)

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHN578

Common Variants in Myocardial Ion Channel Genes Modify the QT Interval in the General Population

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHN578

Stable microreentrant sources as a mechanism of atrial fibrillation in the isolated sheep heart

21 January 2018

1 reference

12 December 2020

Locus for atrial fibrillation maps to chromosome 6q14-16

1 reference

12 December 2020

An investigation of coronary heart disease in families. The Framingham offspring study

1 reference

12 December 2020

Familial aggregation in lone atrial fibrillation

1 reference

12 December 2020

Prevalence, incidence and lifetime risk of atrial fibrillation: the Rotterdam study

1 reference

12 December 2020

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

1 reference

12 December 2020

Left right asymmetry, the pulmonary vein, and a-fib

1 reference

12 December 2020

Identifiers

DOI

10.1093/EURHEARTJ/EHN578

1 reference

18 August 2017

1 reference

18 August 2017

1 reference

PMCID

2663727