Characterization of the severe asthma phenotype by the National Heart, Lung, and Blood Institute's Severe Asthma Research ProgramWendy C. Moore, Sally E. Wenzel, Eugene R. Bleecker et al.|Journal of Allergy and Clinical Immunology|2007Cited by 933
Inherited causes of clonal haematopoiesis in 97,691 whole genomesAlexander G. Bick, Stephanie M. Gogarten, Joshua S. Weinstock et al.|Nature|2020Cited by 740
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease riskNick Shrine, Eugene R. Bleecker, Abril G. Izquierdo et al.|Nature Genetics|2023Cited by 183
Chronic obstructive pulmonary disease and related phenotypes: polygenic risk scores in population-based and case-control cohortsMatthew Moll, Rajesh Rawal, Phuwanat Sakornsakolpat et al.|The Lancet Respiratory Medicine|2020Cited by 125
Overlap of Genetic Risk between Interstitial Lung Abnormalities and Idiopathic Pulmonary FibrosisBrian D. Hobbs, Gary M. Hunninghake, Victor E. Ortega et al.|American Journal of Respiratory and Critical Care Medicine|2019Cited by 115