about
Statins for children with familial hypercholesterolemiaStatins for children with familial hypercholesterolemiaStatins for children with familial hypercholesterolemiaIL-6 polymorphisms: a useful genetic tool for inflammation research?Effects of six APOA5 variants, identified in patients with severe hypertriglyceridemia, on in vitro lipoprotein lipase activity and receptor bindingFVII, FVIIa, and downstream markers of extrinsic pathway activation differ by EPCR Ser219Gly variant in healthy menAPOE/C1/C4/C2 gene cluster genotypes, haplotypes and lipid levels in prospective coronary heart disease risk among UK healthy menAbdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1Genetic variants in novel pathways influence blood pressure and cardiovascular disease riskBlood pressure loci identified with a gene-centric arrayReductions in all-cause, cancer, and coronary mortality in statin-treated patients with heterozygous familial hypercholesterolaemia: a prospective registry studyIntegrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease riskGene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChipImproving the cost-effectiveness equation of cascade testing for familial hypercholesterolaemiaFamilial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: consensus statement of the European Atherosclerosis SocietyGenetic loci on chromosome 5 are associated with circulating levels of interleukin-5 and eosinophil count in a European population with high risk for cardiovascular disease.Effectiveness of a self-management intervention with personalised genetic and lifestyle-related risk information on coronary heart disease and diabetes-related risk in type 2 diabetes (CoRDia): study protocol for a randomised controlled trialLarge-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetesCharacterization of DNA-binding proteins using multiplexed competitor EMSAGenome-wide association study identifies variants in casein kinase II (CSNK2A2) to be associated with leukocyte telomere length in a Punjabi Sikh diabetic cohortInflammation, insulin resistance, and diabetes--Mendelian randomization using CRP haplotypes points upstreamAssociation between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant dataCommon variants associated with plasma triglycerides and risk for coronary artery diseaseDiscovery and refinement of loci associated with lipid levels.Population genomics of cardiometabolic traits: design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) ConsortiumUse of targeted exome sequencing as a diagnostic tool for Familial HypercholesterolaemiaCholesteryl Ester Transfer Protein (CETP) polymorphisms affect mRNA splicing, HDL levels, and sex-dependent cardiovascular riskA variant in LDLR is associated with abdominal aortic aneurysmGenome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibilityA genome-wide association study identifies multiple loci for variation in human ear morphologyMendelian randomization of blood lipids for coronary heart disease.Novel and recurrent LDLR gene mutations in Pakistani hypercholesterolemia patients.Apolipoprotein E genotype, cardiovascular biomarkers and risk of stroke: systematic review and meta-analysis of 14,015 stroke cases and pooled analysis of primary biomarker data from up to 60,883 individuals.Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes lociEffect modification by population dietary folate on the association between MTHFR genotype, homocysteine, and stroke risk: a meta-analysis of genetic studies and randomised trials.The Lichfield bone study: the skeletal response to exercise in healthy young menLow-density lipoprotein receptor gene familial hypercholesterolemia variant database: update and pathological assessment.Left ventricular wall thickness and the presence of asymmetric hypertrophy in healthy young army recruits: data from the LARGE heart study.Angiotensin-converting enzyme genotype and late respiratory complications of mustard gas exposure.
P50
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P50
description
hulumtues
@sq
onderzoeker
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researcher
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հետազոտող
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name
Stephen E Humphries
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Stephen E Humphries
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Stephen E Humphries
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Stephen E Humphries
@nl
Stephen E Humphries
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type
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Stephen E Humphries
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Stephen E Humphries
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Stephen E Humphries
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Stephen E Humphries
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Stephen E Humphries
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Steve E Humphries
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Steve E Humphries
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prefLabel
Stephen E Humphries
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Stephen E Humphries
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Stephen E Humphries
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Stephen E Humphries
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Stephen E Humphries
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P106
P21
P31
P496
0000-0002-8221-6547