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Folliculin mutations are not associated with severe COPD.
Variants in FAM13A are associated with chronic obstructive pulmonary disease.
MMP12, lung function, and COPD in high-risk populations.
A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13.
Analysis of exonic elastin variants in severe, early-onset chronic obstructive pulmonary disease.
Dissecting direct and indirect genetic effects on chronic obstructive pulmonary disease (COPD) susceptibility.
Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis.
Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis.
Genetic Association and Risk Scores in a Chronic Obstructive Pulmonary Disease Meta-analysis of 16,707 Subjects.
Longitudinal Modeling of Lung Function Trajectories in Smokers with and without Chronic Obstructive Pulmonary Disease.
Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations.