about
Genetic variants in novel pathways influence blood pressure and cardiovascular disease riskBlood pressure loci identified with a gene-centric arrayGene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChipThe association of the PON1 Q192R polymorphism with coronary heart disease: findings from the British Women's Heart and Health cohort study and a meta-analysisImportance of Genetic Studies in Consanguineous Populations for the Characterization of Novel Human Gene FunctionsMosaic structural variation in children with developmental disordersAssociation between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant dataPopulation genomics of cardiometabolic traits: design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) ConsortiumDoes milk intake promote prostate cancer initiation or progression via effects on insulin-like growth factors (IGFs)? A systematic review and meta-analysisCausal Associations of Adiposity and Body Fat Distribution with Coronary Heart Disease, Stroke Subtypes and Type 2 Diabetes: A Mendelian Randomization Analysis.Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study.Whole-genome sequence-based analysis of thyroid function.Mendelian randomization of blood lipids for coronary heart disease.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 lociA pathway-based data integration framework for prediction of disease progressionManual 768 or 384 well microplate gel 'dry' electrophoresis for PCR checking and SNP genotyping.Data Resource Profile: Accessible Resource for Integrated Epigenomic Studies (ARIES).LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis.MIDAS: software for analysis and visualisation of interallelic disequilibrium between multiallelic markersCubic exact solutions for the estimation of pairwise haplotype frequencies: implications for linkage disequilibrium analyses and a web tool 'CubeX'The association of C-reactive protein and CRP genotype with coronary heart disease: findings from five studies with 4,610 cases amongst 18,637 participantsA study of relationships between single nucleotide polymorphisms from the growth hormone-insulin-like growth factor axis and bone mass: the Hertfordshire cohort study.An expectation-maximization program for determining allelic spectrum from CNV data (CoNVEM): insights into population allelic architecture and its mutational history.Functional Analysis of the Coronary Heart Disease Risk Locus on Chromosome 21q22.Genome-wide data-mining of candidate human splice translational efficiency polymorphisms (STEPs) and an online database.Identifying low density lipoprotein cholesterol associated variants in the Annexin A2 (ANXA2) gene.Gene-centric association signals for haemostasis and thrombosis traits identified with the HumanCVD BeadChip.A multi-cohort study of polymorphisms in the GH/IGF axis and physical capability: the HALCyon programme.Predicting the functional consequences of cancer-associated amino acid substitutions.Canonical correlation analysis for gene-based pleiotropy discoveryRanking non-synonymous single nucleotide polymorphisms based on disease conceptsNonsense mutation in coiled-coil domain containing 151 gene (CCDC151) causes primary ciliary dyskinesia.Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with HeightGenotype of galectin 2 (LGALS2) is associated with insulin-glucose profile in the British Women's Heart and Health Study.Sequential sentinel SNP Regional Association Plots (SSS-RAP): an approach for testing independence of SNP association signals using meta-analysis data.Influence of adiposity-related genetic markers in a population of saudi arabians where other variables influencing obesity may be reduced.Mendelian randomization studies do not support a role for raised circulating triglyceride levels influencing type 2 diabetes, glucose levels, or insulin resistance.Haptoglobin duplicon, hemoglobin, and vitamin C: analyses in the british women's heart and health study and Caerphilly prospective study.
P50
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P50
description
hulumtues
@sq
onderzoeker
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հետազոտող
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name
Tom R Gaunt
@nl
Tom R Gaunt
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Tom R. Gaunt
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Tom R. Gaunt
@es
type
label
Tom R Gaunt
@nl
Tom R Gaunt
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Tom R. Gaunt
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Tom R. Gaunt
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T R Gaunt
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Tom Gaunt
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Tom R Gaunt
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Tom R Gaunt
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Tom R Gaunt
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Tom R. Gaunt
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Tom R. Gaunt
@es
P1053
O-3918-2014
P106
P21
P2456
P31
P3829
P4012
P496
0000-0003-0924-3247