Identification of six new genetic loci associated with atrial fibrillation in the Japanese population. (Q38833485)

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18 March 2020

title

Identification of six new genetic loci associated with atrial fibrillation in the Japanese population (English)

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18 March 2020

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23

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18 March 2020

Kouichi Ozaki

4

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18 March 2020

Ingrid Christophersen

5

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18 March 2020

Patrick T Ellinor

6

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18 March 2020

Shoichiro Tsugane

14

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18 March 2020

13

Motoki Iwasaki

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18 March 2020

20

Michiaki Kubo

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18 March 2020

17

Kenji Wakai

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18 March 2020

16

Mariko Naito

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18 March 2020

12

Taiki Yamaji

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18 March 2020

15

Keitaro Tanaka

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18 March 2020

22

Yoichiro Kamatani

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18 March 2020

10

Mamoru Satoh

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18 March 2020

9

Masayuki Yamamoto

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18 March 2020

1

Siew-Kee Low

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18 March 2020

8

Soichi Ogishima

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18 March 2020

2

Atsushi Takahashi

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18 March 2020

author name string

Yusuke Ebana

3

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18 March 2020

AFGen Consortium

7

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18 March 2020

Makoto Sasaki

11

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18 March 2020

Hideo Tanaka

18

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18 March 2020

Tetsushi Furukawa

19

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18 March 2020

Kaoru Ito

21

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18 March 2020

language of work or name

English

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publication date

17 April 2017

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18 March 2020

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18 March 2020

volume

49

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18 March 2020

issue

6

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18 March 2020

page(s)

953-958

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Prevalence of atrial fibrillation in the general population of Japan: an analysis based on periodic health examination

18 March 2020

cites work

1 reference

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

21 January 2018

1 reference

Variants conferring risk of atrial fibrillation on chromosome 4q25.

21 January 2018

1 reference

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

21 January 2018

1 reference

Common variants in KCNN3 are associated with lone atrial fibrillation

21 January 2018

1 reference

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

21 January 2018

1 reference

Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation

21 January 2018

1 reference

Incident atrial fibrillation among Asians, Hispanics, blacks, and whites

21 January 2018

1 reference

Estimation of the multiple testing burden for genomewide association studies of nearly all common variants

21 January 2018

1 reference

Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseases

21 January 2018

1 reference

Guidelines for Pharmacotherapy of Atrial Fibrillation (JCS 2013).

21 January 2018

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Overcoming the winner's curse: estimating penetrance parameters from case-control data

21 January 2018

1 reference

Cardiac neural crest expression of Hand2 regulates outflow and second heart field development

21 January 2018

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LAR receptor protein tyrosine phosphatases in the development and maintenance of excitatory synapses

21 January 2018

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Regulation of ECM degradation and axon guidance by growth cone invadosomes.

21 January 2018

1 reference

Neural crest origin of cardiac ganglion cells in the chick embryo: identification and extirpation.

21 January 2018

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Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19.

21 January 2018

1 reference

Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4.3 channel function and gating in a dominant manner

21 January 2018

1 reference

The L450F [Corrected] mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together

21 January 2018

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Mutations in KCND3 cause spinocerebellar ataxia type 22.

21 January 2018

1 reference

First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsy

21 January 2018

1 reference

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

21 January 2018

1 reference

Roles of Nebulin Family Members in the Heart

21 January 2018

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Identification of Xin-repeat proteins as novel ligands of the SH3 domains of nebulin and nebulette and analysis of their interaction during myofibril formation and remodeling

21 January 2018

1 reference

Targeted disruption of nebulette protein expression alters cardiac myofibril assembly and function

21 January 2018

1 reference

Altered regional cardiac wall mechanics are associated with differential cardiomyocyte calcium handling due to nebulette mutations in preclinical inherited dilated cardiomyopathy

21 January 2018

1 reference

Nebulette mutations are associated with dilated cardiomyopathy and endocardial fibroelastosis

21 January 2018

1 reference

Independent susceptibility markers for atrial fibrillation on chromosome 4q25.

21 January 2018

1 reference

The Tohoku Medical Megabank Project: Design and Mission

21 January 2018

1 reference

Assessing the impact of population stratification on genetic association studies

21 January 2018

1 reference

Genomic inflation factors under polygenic inheritance

21 January 2018

1 reference

Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits

21 January 2018

1 reference

A GATA-dependent right ventricular enhancer controls dHAND transcription in the developing heart

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/28416822

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NG.3842

1 reference

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18 March 2020

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