Genetic determinants of circulating sphingolipid concentrations in European populations. - Wikidata - awgldk - TriplyDB

Genetic determinants of circulating sphingolipid concentrations in European populations.

Genetic determinants of circulating sphingolipid concentrations in European populations.

http://www.wikidata.org/entity/Q37350436

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Discovery of sexual dimorphisms in metabolic and genetic biomarkers Common variants in SLC17A3 gene affect intra-personal variation in serum uric acid levels in longitudinal time series Predictive value of 8 genetic loci for serum uric acid concentration Genetics of human metabolism: an update Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels Alterations in hepatic one-carbon metabolism and related pathways following a high-fat dietary intervention The Cooperative Health Research in South Tyrol (CHRIS) study: rationale, objectives, and preliminary results A genome-wide association study of brain lesion distribution in multiple sclerosis Genomics of post-prandial lipidomic phenotypes in the Genetics of Lipid lowering Drugs and Diet Network (GOLDN) study.Lipidomic analyses in epidemiology.Meta-analysis of genome-wide association studies identifies three novel loci for saturated fatty acids in East Asians.Genetic loci associated with circulating levels of very long-chain saturated fatty acids.Integration of Genome-Wide SNP Data and Gene-Expression Profiles Reveals Six Novel Loci and Regulatory Mechanisms for Amino Acids and Acylcarnitines in Whole Blood.Interactions between genetic variants in glucose transporter type 9 (SLC2A9) and dietary habits in serum uric acid regulation.Interrogating causal pathways linking genetic variants, small molecule metabolites, and circulating lipids Identification and validation of genes affecting aortic lesions in mice Evaluating the discriminative power of multi-trait genetic risk scores for type 2 diabetes in a northern Swedish population.Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.A genome-wide association study of metabolic traits in human urine.Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study.Localising loci underlying complex trait variation using Regional Genomic Relationship Mapping.Genetic determinants of plasma triglycerides Novel genetic associations with serum level metabolites identified by phenotype set enrichment analyses.Admixture analysis of spontaneous hepatitis C virus clearance in individuals of African descent.High-Performance Mixed Models Based Genome-Wide Association Analysis with omicABEL software Analytical methods in untargeted metabolomics: state of the art in 2015.Linkage and association of phospholipid transfer protein activity to LASS4 Integrated metabolomics and genomics: systems approaches to biomarkers and mechanisms of cardiovascular disease.The polypyrimidine tract binding protein regulates desaturase alternative splicing and PUFA composition.Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traits.Genome-Wide Association Study with Targeted and Non-targeted NMR Metabolomics Identifies 15 Novel Loci of Urinary Human Metabolic Individuality.Nonadditive Effects of Genes in Human Metabolomics.Sphingomyelin is associated with kidney disease in type 1 diabetes (The FinnDiane Study).Phospholipid flippases: building asymmetric membranes and transport vesicles.Dietary long-chain polyunsaturated fatty acids upregulate expression of FADS3 transcripts.Genetic predictors of susceptibility to cutaneous fungal infections: a pilot genome wide association study to refine a candidate gene search.Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placenta.Developing biobanks in developing countries.Lipidomic and metabolic changes in the P4-type ATPase ATP10D deficient C57BL/6J wild type mice upon rescue of ATP10D function.Discovering and validating between-subject variations in plasma lipids in healthy subjects

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Genetic determinants of circulating sphingolipid concentrations in European populations.

http://www.wikidata.org/entity/Q37350436

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on 02 October 2009

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Genetic determinants of circulating sphingolipid concentrations in European populations.

@en

Genetic determinants of circulating sphingolipid concentrations in European populations.

@nl

type

label

Genetic determinants of circulating sphingolipid concentrations in European populations.

@en

Genetic determinants of circulating sphingolipid concentrations in European populations.

@nl

prefLabel

Genetic determinants of circulating sphingolipid concentrations in European populations.

@en

Genetic determinants of circulating sphingolipid concentrations in European populations.

@nl

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JOURNAL.PGEN.1000672

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Genetic determinants of circulating sphingolipid concentrations in European populations.

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A Cecilej W Janssens

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Aaron Isaacs

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Alan Wright

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Anatoly V Kirichenko

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Asa Johansson

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Ben A Oostra

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Carsten Gnewuch

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Christian Hengstenberg

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Christine Schwienbacher

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Christopher S Franklin

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

P2860

Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum

Estimation of significance thresholds for genomewide association scans

Characterization of a putative type IV aminophospholipid transporter P-type ATPase

Common variants at 30 loci contribute to polygenic dyslipidemia

Genomewide association analysis of coronary artery disease

Moderation of breastfeeding effects on the IQ by genetic variation in fatty acid metabolism

Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I

Association studies of 23 positional/functional candidate genes on chromosome 10 in late-onset Alzheimer's disease

Genomic control for association studies

GenABEL: an R library for genome-wide association analysis

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e1000672

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scholarly article

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10.1371/JOURNAL.PGEN.1000672

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10

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5

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Thomas Meitinger

Heribert Schunkert

Jeanette Erdmann

Veronique Vitart

Cornelia M. van Duijn

Caroline Hayward

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2009-10-02T00:00:00Z

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26864813

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19798445

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