Rare Coding Variation and Risk of Intracerebral Hemorrhage. - Wikidata - awgldk - TriplyDB

Rare Coding Variation and Risk of Intracerebral Hemorrhage.

Rare Coding Variation and Risk of Intracerebral Hemorrhage.

http://www.wikidata.org/entity/Q30279111

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Genetic risk factors for spontaneous intracerebral haemorrhage.

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P2860

Rare Coding Variation and Risk of Intracerebral Hemorrhage.

http://www.wikidata.org/entity/Q30279111

description

2015 nî lūn-bûn

@nan

2015 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

name

Rare Coding Variation and Risk of Intracerebral Hemorrhage.

@ast

Rare Coding Variation and Risk of Intracerebral Hemorrhage.

@en

type

label

Rare Coding Variation and Risk of Intracerebral Hemorrhage.

@ast

Rare Coding Variation and Risk of Intracerebral Hemorrhage.

@en

prefLabel

Rare Coding Variation and Risk of Intracerebral Hemorrhage.

@ast

Rare Coding Variation and Risk of Intracerebral Hemorrhage.

@en

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STROKEAHA.115.009838

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Rare Coding Variation and Risk of Intracerebral Hemorrhage.

@en

P2093

Alison M Ayres

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

Anand Viswanathan

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

Carl D Langefeld

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

Daniel Woo

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

David L Tirschwell

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

David McWilliams

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

Farid Radmanesh

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

Guangyun Sun

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

Guido J Falcone

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

Joshua N Goldstein

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

P2860

Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage

Heritability estimates identify a substantial genetic contribution to risk and outcome of intracerebral hemorrhage

Variants at APOE influence risk of deep and lobar intracerebral hemorrhage.

Rare-variant association testing for sequencing data with the sequence kernel association test.

COL4A2 mutations impair COL4A1 and COL4A2 secretion and cause hemorrhagic stroke.

Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies.

Apolipoprotein E genotypes are associated with lipid-lowering responses to statin treatment in diabetes: a Go-DARTS study.

P304

2299-2301

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scholarly article

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10.1161/STROKEAHA.115.009838

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8

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46

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Jonathan Rosand

Christopher D Anderson

Bradford B Worrall

James F Meschia

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2015-06-25T00:00:00Z

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26111891

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4519408

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