about
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variantsGenetic variants regulating ORMDL3 expression contribute to the risk of childhood asthmaLoss-of-function mutations in APOC3, triglycerides, and coronary diseaseAssociation of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacksPhenotypic consequences of variation across the aldosterone synthase and 11-beta hydroxylase locus in a hypertensive cohort: data from the MRC BRIGHT Study.Identifying systematic heterogeneity patterns in genetic association meta-analysis studies.A rare variant of the leptin gene has large effects on blood pressure and carotid intima-medial thickness: a study of 1428 individuals in 248 families.Gearing up for genome-wide gene-association studies.Vitamin D levels and susceptibility to asthma, elevated immunoglobulin E levels, and atopic dermatitis: A Mendelian randomization study.Genetic susceptibility to coronary artery disease: from promise to progress.Using eQTL weights to improve power for genome-wide association studies: a genetic study of childhood asthma.Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.Polymorphisms in genes involved in folate metabolism as risk factors for oedematous severe childhood malnutrition: a hypothesis-generating study.Glutathione S-transferase polymorphisms may be associated with risk of oedematous severe childhood malnutrition.Impact of lipoprotein(a) levels and apolipoprotein(a) isoform size on risk of coronary heart disease.Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis.A mouse-to-man candidate gene study identifies association of chronic otitis media with the loci TGIF1 and FBXO11Cardiovascular twist to the rapidly evolving apolipoprotein L1 story.Reports of the death of the epistasis model are greatly exaggerated.Novel genetic variants linked to coronary artery disease by genome-wide association are not associated with carotid artery intima-media thickness or intermediate risk phenotypes.Genetic variation at the locus encompassing 11-beta hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretion.Ambulatory blood pressure is associated with polymorphic variation in P2X receptor genes.Association between common polymorphisms of the proopiomelanocortin gene and body fat distribution: a family study.Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks.Genotype at the -174G/C polymorphism of the interleukin-6 gene is associated with common carotid artery intimal-medial thickness: family study and meta-analysis.A common LPA null allele associates with lower lipoprotein(a) levels and coronary artery disease risk.Measured haplotype analysis of the aldosterone synthase gene and heart size.Lack of genetic support for shared aetiology of Coronary Artery Disease and Late-onset Alzheimer's disease.Increased Support for Linkage of a Novel Locus on Chromosome 5q13 for Essential Hypertension in the British Genetics of Hypertension StudyGenetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traitsAssociation between Aldosterone Production and Variation in the 11β-Hydroxylase (CYP11B1) GeneElectrocardiographic measures of left ventricular hypertrophy show greater heritability than echocardiographic left ventricular massEpistasis Between Type 2 Diabetes Susceptibility Loci on Chromosomes 1q21-25 and 10q23-26 in Northern EuropeansQuantitative Trait Genetic Linkage Analysis of Body Mass Index in Familial Coronary Artery DiseaseAssociation between Angiotensin-Converting Enzyme Gene Polymorphisms and Diabetic Nephropathy: Case-Control, Haplotype, and Family-Based Study in Three European PopulationsAnalysis of 14 Candidate Genes for Diabetic Nephropathy on Chromosome 3q in European Populations: Strongest Evidence for Association With a Variant in the Promoter Region of the Adiponectin GeneDifferential Gene Expression in Macrophages From Human Atherosclerotic Plaques Shows Convergence on Pathways Implicated by Genome-Wide Association Study Risk VariantsTrans-ethnic association study of blood pressure determinants in over 750,000 individualsAnalysis of 51 proposed hypertrophic cardiomyopathy genes from genome sequencing data in sarcomere negative cases has negligible diagnostic yield
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P50
description
researcher ORCID ID=0000-0003-4564-2165
@en
name
Martin Farrall
@en
Martin Farrall
@nl
type
label
Martin Farrall
@en
Martin Farrall
@nl
prefLabel
Martin Farrall
@en
Martin Farrall
@nl
P106
P31
P496
0000-0003-4564-2165