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Genetic studies of body mass index yield new insights for obesity biologyCilostazol versus aspirin for secondary prevention of vascular events after strokeGenetic variants in novel pathways influence blood pressure and cardiovascular disease riskGenome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetesAnalysis of protein-coding genetic variation in 60,706 humansA comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery diseaseLarge-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetesTriglyceride-mediated pathways and coronary disease: collaborative analysis of 101 studiesLipid-related markers and cardiovascular disease prediction.Common variants associated with plasma triglycerides and risk for coronary artery diseaseMultiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular diseaseDiscovery and refinement of loci associated with lipid levels.Homocysteine and coronary heart disease: meta-analysis of MTHFR case-control studies, avoiding publication biasAssociation between C reactive protein and coronary heart disease: mendelian randomisation analysis based on individual participant dataRare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart diseaseCholesterol ester transfer protein inhibition by TA-8995 in patients with mild dyslipidaemia (TULIP): a randomised, double-blind, placebo-controlled phase 2 trialGenome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from IndiaGenome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibilityGenetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility lociThe genetic architecture of type 2 diabetesRare and low-frequency coding variants alter human adult heightGenetic variation at 16q24.2 is associated with small vessel stroke.Genetic association of long-chain acyl-CoA synthetase 1 variants with fasting glucose, diabetes, and subclinical atherosclerosisExome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption.Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration.Are myocardial infarction--associated single-nucleotide polymorphisms associated with ischemic stroke?Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes lociFactors associated with adherence to anti-hypertensive treatment in Pakistan.Molecular analysis of the XLRS1 gene in 4 females affected with X-linked juvenile retinoschisis.The Karachi intracranial stenosis study (KISS) Protocol: an urban multicenter case-control investigation reporting the clinical, radiologic and biochemical associations of intracranial stenosis in PakistanThe burden of stroke and transient ischemic attack in Pakistan: a community-based prevalence study.Common coding variant in SERPINA1 increases the risk for large artery stroke.Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe HypercholesterolemiaGenetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles.Apolipoprotein(a) isoform size, lipoprotein(a) concentration, and coronary artery disease: a mendelian randomisation analysisCausal Assessment of Serum Urate Levels in Cardiometabolic Diseases Through a Mendelian Randomization Study.A novel MMP12 locus is associated with large artery atherosclerotic stroke using a genome-wide age-at-onset informed approachBRCA2 variants and cardiovascular disease in a multi-ethnic study.
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Danish Saleheen
@ast
Danish Saleheen
@en
Danish Saleheen
@es
Danish Saleheen
@nl
Danish Saleheen
@sl
type
label
Danish Saleheen
@ast
Danish Saleheen
@en
Danish Saleheen
@es
Danish Saleheen
@nl
Danish Saleheen
@sl
prefLabel
Danish Saleheen
@ast
Danish Saleheen
@en
Danish Saleheen
@es
Danish Saleheen
@nl
Danish Saleheen
@sl
P106
P21
P31
P569
2000-01-01T00:00:00Z