(Q30368601)

English

Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation.

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scholarly article

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Europe PubMed Central

PubMed publication ID

21 June 2017

Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation. (English)

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Europe PubMed Central

PubMed publication ID

21 June 2017

atrial fibrillation

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6

object named as

Lian-Yu Lin

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Europe PubMed Central

PubMed publication ID

21 June 2017

Jyh-Ming Jimmy Juang

object named as

Jyh-Ming Jimmy Juang

5

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object named as

Chia-Ti Tsai

1

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object named as

Fu-Tien Chiang

9

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object named as

Ling-Ping Lai

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object named as

Juey-Jen Hwang

8

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10

object named as

Jiunn-Lee Lin

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Europe PubMed Central

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21 June 2017

Sheng-Nan Chang

3

object named as

Sheng-Nan Chang

1 reference

Europe PubMed Central

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21 June 2017

4

object named as

Eric Y Chuang

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Europe PubMed Central

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21 June 2017

author name string

Chia-Shan Hsieh

2

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21 June 2017

language of work or name

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publication date

12 November 2014

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Europe PubMed Central

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21 June 2017

Journal of Medical Genetics

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Europe PubMed Central

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21 June 2017

52

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21 June 2017

1

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21 June 2017

28-36

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Europe PubMed Central

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21 June 2017

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

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https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Common variants in KCNN3 are associated with lone atrial fibrillation

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Variants conferring risk of atrial fibrillation on chromosome 4q25.

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Association of RS2200733 but not RS10033464 on 4q25 with atrial fibrillation based on the recessive model in a Taiwanese population.

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Significant association of rs13376333 in KCNN3 on chromosome 1q21 with atrial fibrillation in a Taiwanese population

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Towards a complete resolution of the genetic architecture of disease

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https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Finding the missing heritability of complex diseases

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Human genetic variation and its contribution to complex traits

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https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

A HapMap harvest of insights into the genetics of common disease

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https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Targeted screening of cis-regulatory variation in human haplotypes

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https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Exome sequencing identifies the cause of a mendelian disorder

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Targeted capture and massively parallel sequencing of 12 human exomes

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Uncovering the roles of rare variants in common disease through whole-genome sequencing

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Common variants at 30 loci contribute to polygenic dyslipidemia

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

A treasure trove for lipoprotein biology

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

A functional variant in the promoter region regulates the C-reactive protein gene and is a potential candidate for increased risk of atrial fibrillation.

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Renin-angiotensin system gene polymorphisms and atrial fibrillation

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

The accessible chromatin landscape of the human genome

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

DNase I-hypersensitive exons colocalize with promoters and distal regulatory elements

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Tachycardia of atrial myocytes induces collagen expression in atrial fibroblasts through transforming growth factor β1.

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

High prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillation

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Atrial Fibrillation associated chromosome 4q25 variants are not associated with PITX2c expression in human adult left atrial appendages

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Pitx2 prevents susceptibility to atrial arrhythmias by inhibiting left-sided pacemaker specification

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

PITX2c Is Expressed in the Adult Left Atrium, and Reducing Pitx2c Expression Promotes Atrial Fibrillation Inducibility and Complex Changes in Gene Expression

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Familial Aggregation of Lone Atrial Fibrillation in Young Persons

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102618

21 January 2018

Identifiers

10.1136/JMEDGENET-2014-102618

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

ResearchGate publication ID

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