about
Rapid molecular genetic diagnosis of hypertrophic cardiomyopathy by semiconductor sequencing.Association analysis of polymorphisms in ROCK2 with cardiovascular disease in a Chinese population.Large scale meta-analyses of fasting plasma glucose raising variants in GCK, GCKR, MTNR1B and G6PC2 and their impacts on type 2 diabetes mellitus risk.Association between telomere length and type 2 diabetes mellitus: a meta-analysis.Polymorphism of tumor necrosis factor alpha (TNF-alpha) gene promoter, circulating TNF-alpha level, and cardiovascular risk factor for ischemic stroke.Rs2200733 and rs10033464 on chromosome 4q25 confer risk of cardioembolic stroke: an updated meta-analysis.Functional analysis LRP6 novel mutations in patients with coronary artery disease.C-reactive protein polymorphisms and genetic susceptibility to ischemic stroke and hemorrhagic stroke in the Chinese Han population.Value of SOFA, APACHE IV and SAPS II scoring systems in predicting short-term mortality in patients with acute myocarditisCommon variants in KCNQ1 confer increased risk of type 2 diabetes and contribute to the diabetic epidemic in East Asians: a replication and meta-analysis.A novel loss-of-function DDAH1 promoter polymorphism is associated with increased susceptibility to thrombosis stroke and coronary heart disease.Functional consequences of a novel point mutation in the CYP21A2 gene identified in a Chinese Han patient with nonclassic 21-hydroxylase deficiency.Applications of the method of high resolution melting analysis for diagnosis of Leber's disease and the three primary mutation spectrum of LHON in the Han Chinese population.Novel URAT1 mutations caused acute renal failure after exercise in two Chinese families with renal hypouricemia.Prevalence of common mutations in the CYP17A1 gene in Chinese Han population.Confirmation of genomewide association signals in Chinese Han population reveals risk loci for ischemic stroke.Telomere length and risk of stroke in Chinese.Association of chromosome 9p21 genetic variants with risk of coronary heart disease in the East Asian population: a meta-analysis.9p21 is a shared susceptibility locus strongly for coronary artery disease and weakly for ischemic stroke in Chinese Han populationAssociation between polymorphisms of CYP2J2 and EPHX2 genes and risk of coronary artery diseaseAssociation of putative functional variants in the PLAU gene and the PLAUR gene with myocardial infarctionPlasma tissue kallikrein level is negatively associated with incident and recurrent stroke: a multicenter case-control study in China[Development of the high resolution melting method for genotyping CYP2C9*3 (1075A/C, rs1057910) and VKORC1 (-1639A/G, rs9923231)]Comparison of high-resolution melting analysis, TaqMan Allelic discrimination assay, and sanger sequencing for Clopidogrel efficacy genotyping in routine molecular diagnosticsA functional variant in APOA5/A4/C3/A1 gene cluster contributes to elevated triglycerides and severity of CAD by interfering with microRNA 3201 binding efficiencyAssociation between variants of EXT2 and type 2 diabetes: a replication and meta-analysisJoint Effects of GWAS SNPs in Coagulation System Confer Risk to Hypertensive Intracerebral HemorrhagePrognostic value of elevated cardiac troponin I in patients with intracerebral hemorrhage
P50
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P50
description
investigador
@es
researcher
@en
name
Hu Ding
@en
type
label
Hu Ding
@en
prefLabel
Hu Ding
@en
P31
P496
0000-0002-1814-1552