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(1 - 19 of 19)
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
Blood eosinophil count and airway epithelial transcriptome relationships in COPD versus asthma
Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney
Discovery of novel heart rate-associated loci using the Exome Chip
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation
The impact of low-frequency and rare variants on lipid levels
Genome-wide association analysis identifies six new loci associated with forced vital capacity
Secretory Phospholipase A(2)-IIA and Cardiovascular Disease
The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis
Identification of seven loci affecting mean telomere length and their association with disease
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure