Wei Zhao
occupation: researcher
Articles 35
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Genomic profiling of human vascular cells identifies TWIST1 as a causal gene for common vascular diseases
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Elevated Plasma Ceramides Are Associated With Antiretroviral Therapy Use and Progression of Carotid Artery Atherosclerosis in HIV Infection
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Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
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Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
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Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
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Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.
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Multiplexed Targeted Resequencing Identifies Coding and Regulatory Variation Underlying Phenotypic Extremes of High-Density Lipoprotein Cholesterol in Humans
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Anxiety and depression in spasmodic dysphonia patients
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Rare and low-frequency coding variants alter human adult height
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Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms
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Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity
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Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
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The genetic architecture of type 2 diabetes
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Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2
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Causal Assessment of Serum Urate Levels in Cardiometabolic Diseases Through a Mendelian Randomization Study
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Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes
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Common and Rare Genetic Variation in CCR2, CCR5, or CX3CR1 and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic Traits
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The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
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Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
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Genome-wide interrogation reveals hundreds of long intergenic noncoding RNAs that associate with cardiometabolic traits
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Systolic Blood Pressure and Risk of Type 2 Diabetes: A Mendelian Randomization Study
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Loss of Function of GALNT2 Lowers High-Density Lipoproteins in Humans, Nonhuman Primates, and Rodents.
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A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease
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Genetic association of long-chain acyl-CoA synthetase 1 variants with fasting glucose, diabetes, and subclinical atherosclerosis
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Physical activity, smoking, and genetic predisposition to obesity in people from Pakistan: the PROMIS study
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Association of HDL cholesterol efflux capacity with incident coronary heart disease events: a prospective case-control study
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Otolaryngology Needs in a Free Clinic Providing Indigent Care
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A novel interaction between the FLJ33534 locus and smoking in obesity: a genome-wide study of 14 131 Pakistani adults
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A replication study of 49 Type 2 diabetes risk variants in a Punjabi Pakistani population.
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Human knockouts in a cohort with a high rate of consanguinity
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A novel MMP12 locus is associated with large artery atherosclerotic stroke using a genome-wide age-at-onset informed approach
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Epidemiology and public health policy of tobacco use and cardiovascular disorders in low- and middle-income countries
Human - wd:Q37640082