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1. A Polygenic Risk Score for Idiopathic Pulmonary Fibrosis and Interstitial Lung Abnormalities

6. Among Individuals At-Risk, Pre-Clinical Pulmonary Fibrosis Occurs Commonly and Is Progressive

7. Integration of DNA Methylation, Gene Expression, and Proteomics of Idiopathic Pulmonary Fibrosis Lung Tissue Reveals Molecular Signatures of Disease

8. Functional Validation of MUC5B and DSP Genetic Variants in Idiopathic Pulmonary Fibrosis (IPF) by Expression Quantitative Trait Locus (EQTL) and Co-Localization Analyses

10. Circulating Plasma Proteins Differentially Detected in Idiopathic Pulmonary Fibrosis and in Subjects with Pre-Clinical Pulmonary Fibrosis

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