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(1 - 18 of 18)
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
The genomics of heart failure
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
Rare and low-frequency coding variants alter human adult height
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension