Multi-ethnic genome-wide association study for atrial fibrillation

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Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation Atrial Fibrillation Mechanisms and Implications for Catheter Ablation

P2860

Q58547155-D666E0ED-CF4D-490C-9DFD-388FFF3AA05A Q59136309-932DA9F6-1A2C-445F-98E0-9933330A50E1

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Multi-ethnic genome-wide association study for atrial fibrillation

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http://www.wikidata.org/entity/Q56361973

description

article

@en

im Juni 2018 veröffentlichter wissenschaftlicher Artikel

@de

wetenschappelijk artikel

@nl

наукова стаття, опублікована в червні 2018

@uk

ലേഖനം

@ml

name

Multi-ethnic genome-wide association study for atrial fibrillation

@en

Multi-ethnic genome-wide association study for atrial fibrillation

@nl

type

Item

label

Multi-ethnic genome-wide association study for atrial fibrillation

@en

Multi-ethnic genome-wide association study for atrial fibrillation

@nl

prefLabel

Multi-ethnic genome-wide association study for atrial fibrillation

@en

Multi-ethnic genome-wide association study for atrial fibrillation

@nl

P1476

Multi-ethnic genome-wide association study for atrial fibrillation

@en

P2093

Adnan Kastrati

http://www.w3.org/2001/XMLSchema#string

Agnieszka Slowik

http://www.w3.org/2001/XMLSchema#string

Alaa A Shalaby

http://www.w3.org/2001/XMLSchema#string

Albert Hofman

http://www.w3.org/2001/XMLSchema#string

Albert Sun

http://www.w3.org/2001/XMLSchema#string

Alexandre Pereira

http://www.w3.org/2001/XMLSchema#string

Alfredo J Mansur

http://www.w3.org/2001/XMLSchema#string

Anders Hamsten

http://www.w3.org/2001/XMLSchema#string

Andre G Uitterlinden

http://www.w3.org/2001/XMLSchema#string

Andrea Natale

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P2860

Fast association tests for genes with FAST

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

Congenital heart disease caused by mutations in the transcription factor NKX2-5

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

GENCODE: the reference human genome annotation for The ENCODE Project

A global reference for human genetic variation

Measuring inconsistency in meta-analyses

A method and server for predicting damaging missense mutations

Principal components analysis corrects for stratification in genome-wide association studies

A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel

P2888

s41588-018-0133-9

P304

1225-1233

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P31

scholarly article

meta-analysis

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10.1038/S41588-018-0133-9

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P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Alexander Teumer

Caroline Hayward

Emelia J. Benjamin

Martina Müller-Nurasyid

Tõnu Esko

Mika Kähönen

Sandosh Padmanabhan

Leo-Pekka Lyytikäinen

Cecilia M Lindgren

Albert V. Smith

P577

2018-06-11T00:00:00Z

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P6179

1104478460

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P698

29892015

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P921

genome-wide association study

P932

6136836

http://www.w3.org/2001/XMLSchema#string

Multi-ethnic genome-wide association study for atrial fibrillation

about

P2860

P2860

Multi-ethnic genome-wide association study for atrial fibrillation

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P407

P433

P478

P50

P577

P6179

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P407

P433

P478

P50

P577

P6179

P698

P921

P932