Genetic variants in CETP increase risk of intracerebral hemorrhage. - Wikidata - awgldk - TriplyDB

Genetic variants in CETP increase risk of intracerebral hemorrhage.

Genetic variants in CETP increase risk of intracerebral hemorrhage.

http://www.wikidata.org/entity/Q30275688

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CD36 Gene Polymorphisms Are Associated with Intracerebral Hemorrhage Susceptibility in a Han Chinese Population.Genetic variants influencing elevated myeloperoxidase levels increase risk of stroke.Advancing stroke genomic research in the age of Trans-Omics big data science: Emerging priorities and opportunities.Association of CETP Gene Variants With Risk for Vascular and Nonvascular Diseases Among Chinese Adults.Trials and Tribulations of CETP Inhibitors.Genetics of Spontaneous Intracerebral Hemorrhage.Influences Hematoma Volume and Outcome in Spontaneous Intracerebral Hemorrhage Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease

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P2860

Genetic variants in CETP increase risk of intracerebral hemorrhage.

http://www.wikidata.org/entity/Q30275688

description

2016 nî lūn-bûn

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2016 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2016 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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Genetic variants in CETP increase risk of intracerebral hemorrhage.

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Genetic variants in CETP increase risk of intracerebral hemorrhage.

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Genetic variants in CETP increase risk of intracerebral hemorrhage.

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Genetic variants in CETP increase risk of intracerebral hemorrhage.

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Genetic variants in CETP increase risk of intracerebral hemorrhage.

@ast

Genetic variants in CETP increase risk of intracerebral hemorrhage.

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Annals of Neurology

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Genetic variants in CETP increase risk of intracerebral hemorrhage.

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Agnieszka Slowik

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Alessandro Biffi

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Alessandro Pezzini

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Alexander Pichler

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Alison M Ayres

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Anand Viswanathan

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Andrea Morotti

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Andrzej Urbanik

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Arne Lindgren

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Bo Norrving

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P2860

Common variants at 30 loci contribute to polygenic dyslipidemia

Genotype imputation with thousands of genomes

Effects of statins on high-density lipoproteins: a potential contribution to cardiovascular benefit

PLINK: a tool set for whole-genome association and population-based linkage analyses

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

Common genetic variation near MC4R is associated with waist circumference and insulin resistance

Discovery and refinement of loci associated with lipid levels.

A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium

Fast model-based estimation of ancestry in unrelated individuals

Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study

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730-740

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scholarly article

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10.1002/ANA.24780

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5

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80

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Christopher D Anderson

Rustam Al-Shahi Salman

Koen M van Nieuwenhuizen

Elisa Cuadrado-Godia

Björn M Hansen

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2016-09-22T00:00:00Z

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27717122

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