Candidate gene approach to identifying rare genetic variants associated with lone atrial fibrillation (Q37626338)

21 August 2017

Candidate gene approach to identifying rare genetic variants associated with lone atrial fibrillation (English)

1 reference

21 August 2017

0 references

Dawood Darbar

9

0 references

Dan Roden

series ordinal

8

object named as

Dan M Roden

1 reference

21 August 2017

1

Peter Weeke

1 reference

21 August 2017

3

Marcia Blair

1 reference

21 August 2017

6

Gayle Kucera

1 reference

21 August 2017

2

Babar Parvez

1 reference

21 August 2017

7

Tanya Stubblefield

1 reference

PMC publication ID

3947369

21 August 2017

Laura Finlayson-Short

series ordinal

4

object named as

Laura Short

1 reference

21 August 2017

Christie Ingram

5

1 reference

21 August 2017

10 October 2013

1 reference

21 August 2017

1 reference

21 August 2017

11

1 reference

21 August 2017

1

1 reference

21 August 2017

46-52

1 reference

Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation

21 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

Epistatic effects of potassium channel variation on cardiac repolarization and atrial fibrillation risk

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

A map of human genome variation from population-scale sequencing

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

Impact of genetic discoveries on the classification of lone atrial fibrillation

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

Augmented potassium current is a shared phenotype for two genetic defects associated with familial atrial fibrillation

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

New roles of calsequestrin and triadin in cardiac muscle.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

Calcium handling abnormalities in atrial fibrillation as a target for innovative therapeutics.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

Genetics of atrial fibrillation: rare mutations, common polymorphisms, and clinical relevance

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

Variants conferring risk of atrial fibrillation on chromosome 4q25.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

Potassium channel gene mutations rarely cause atrial fibrillation

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

KCNQ1 gain-of-function mutation in familial atrial fibrillation

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

Identification of a genetic locus for familial atrial fibrillation

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

Familial aggregation of atrial fibrillation in Iceland

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

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

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

Impact of atrial fibrillation on the risk of death: the Framingham Heart Study

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

Genetic Loci on Chromosomes 4q25, 7p31, and 12p12 Are Associated With Onset of Lone Atrial Fibrillation Before the Age of 40 Years

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype?

3 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947369

Locus for atrial fibrillation maps to chromosome 6q14-16

3 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24120998

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24120998

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.HRTHM.2013.10.025

1 reference

21 August 2017

1 reference

PMC publication ID

3947369

21 August 2017

PubMed publication ID

24120998

1 reference

PMC publication ID

3947369