Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrationsGenome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distributionCommon genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studiesGenetic studies of body mass index yield new insights for obesity biologyMeta-analysis and imputation refines the association of 15q25 with smoking quantityKLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephronGenome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controlsGenome-wide association study of genetic determinants of LDL-c response to atorvastatin therapy: importance of Lp(a)Genome-wide association analyses identify 18 new loci associated with serum urate concentrationsBiological, clinical and population relevance of 95 loci for blood lipidsGenome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controlsGenetic variants in novel pathways influence blood pressure and cardiovascular disease riskBlood pressure loci identified with a gene-centric arrayHundreds of variants clustered in genomic loci and biological pathways affect human heightCommon variants near MC4R are associated with fat mass, weight and risk of obesityGenome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemiaSix new loci associated with body mass index highlight a neuronal influence on body weight regulationAssociation scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variantsGene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChipControversies Surrounding Renal Denervation: Lessons Learned From Real-World Experience in Two United Kingdom CentersRenal artery sympathetic denervation: observations from the UK experience.Genetic risk, coronary heart disease events, and the clinical benefit of statin therapy: an analysis of primary and secondary prevention trialsCommon variants in genes underlying monogenic hypertension and hypotension and blood pressure in the general populationMedical training in the UK: sleepwalking to disasterSLC2A9 is a high-capacity urate transporter in humansTesting the role of predicted gene knockouts in human anthropometric trait variationDirectional dominance on stature and cognition in diverse human populationsGenetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarizationPopulation genomics of cardiometabolic traits: design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) ConsortiumGenome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibilityGenome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension.Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility lociCausal Associations of Adiposity and Body Fat Distribution with Coronary Heart Disease, Stroke Subtypes and Type 2 Diabetes: A Mendelian Randomization Analysis.Meta-analysis of genome-wide association studies of HDL cholesterol response to statins.Genome-wide analysis of blood pressure variability and ischemic stroke.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 lociPhenotypic consequences of variation across the aldosterone synthase and 11-beta hydroxylase locus in a hypertensive cohort: data from the MRC BRIGHT Study.Predicting deleterious nsSNPs: an analysis of sequence and structural attributes.Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies.
P50
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P50
description
British genomic medicine researcher
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Brits onderzoeker
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հետազոտող
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name
Mark Caulfield
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Mark Caulfield
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Mark Caulfield
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Mark Caulfield
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Mark Caulfield
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type
label
Mark Caulfield
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Mark Caulfield
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Mark Caulfield
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Mark Caulfield
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Mark Caulfield
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altLabel
Mark J Caulfield
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Mark Jonathan Caulfield
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Mark Seielstad
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Sir Mark Caulfield
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Sir Mark Jonathan Caulfield
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prefLabel
Mark Caulfield
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Mark Caulfield
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Mark Caulfield
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Mark Caulfield
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Mark Caulfield
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P166
P106
P1153
7102853527
P166
P21
P31
P3885
mark-caulfield
P4789
P496
0000-0001-9295-3594
P569
1960-01-01T00:00:00Z