Epigenome-wide association study (EWAS) on lipids: the Rotterdam Study. - Wikidata - awgldk - TriplyDB

Epigenome-wide association study (EWAS) on lipids: the Rotterdam Study.

Epigenome-wide association study (EWAS) on lipids: the Rotterdam Study.

http://www.wikidata.org/entity/Q37631057

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The State of Cardiovascular Genomics: Abundant Data, Limited Information.The Epigenomic Analysis of Human Obesity.Blood triglyceride levels are associated with DNA methylation at the serine metabolism gene PHGDH.Critical Role of the Human ATP-Binding Cassette G1 Transporter in Cardiometabolic Diseases.The Rotterdam Study: 2018 update on objectives, design and main results.Cell-type deconvolution from DNA methylation: a review of recent applications.DNA methylation in human lipid metabolism and related diseases.Direct and indirect genetic effects on triglycerides through omics and correlated phenotypes Epigenetic prediction of complex traits and death Application of novel and existing methods to identify genes with evidence of epigenetic association: results from GAW20

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Epigenome-wide association study (EWAS) on lipids: the Rotterdam Study.

http://www.wikidata.org/entity/Q37631057

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

@pt

bilimsel makale

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scientific article published on 07 February 2017

@en

vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

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vědecký článek

@cs

name

Epigenome-wide association study (EWAS) on lipids: the Rotterdam Study.

@en

Epigenome-wide association study

@nl

type

label

Epigenome-wide association study (EWAS) on lipids: the Rotterdam Study.

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Epigenome-wide association study

@nl

prefLabel

Epigenome-wide association study (EWAS) on lipids: the Rotterdam Study.

@en

Epigenome-wide association study

@nl

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S13148-016-0304-4

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Clinical epigenetics

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Epigenome-wide association study (EWAS) on lipids: the Rotterdam Study.

@en

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Andre G Uitterlinden

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BIOS consortium

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Joyce B J van Meurs

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Kim V E Braun

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Klodian Dhana

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Paul S de Vries

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Mutations in the 3beta-hydroxysterol Delta24-reductase gene cause desmosterolosis, an autosomal recessive disorder of cholesterol biosynthesis

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Discovery and refinement of loci associated with lipid levels.

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s13148-016-0304-4

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15

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scholarly article

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10.1186/S13148-016-0304-4

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9

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2017-02-07T00:00:00Z

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28194238

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5297218

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