Phenotype wide association study links bronchopulmonary dysplasia with eosinophilia in children - Kelchtermans, Jelte; March, Michael E.; Hakonarson, Hakon; McGrath-Morrow, Sharon A. (Scientific reports, 2024)
Keywords: 631/208/248; 631/208/2489; Asthma; Asthma - genetics; Blood levels; Bronchopulmonary Dysplasia - genetics; Bronchopulmonary Dysplasia - pathology; Child; Child, Preschool; Chronic obstructive pulmonary disease; DNA Methylation; DNA probes; Dysplasia; Eosinophilia; Eosinophilia - genetics; Epidemiology; Female; Genetic Predisposition to Disease; Genome-Wide Association Study; Humanities and Social Sciences; Humans; Infant; Infant, Newborn; Inflammation; Interleukin-1 Receptor-Like 1 Protein - genetics; Leukocytes (eosinophilic); Lung diseases; Male; Methylation; multidisciplinary; Pediatrics; Phenotype; Phenotypes; Polymorphism, Single Nucleotide; Premature birth; Science; Science (multidisciplinary); Single-nucleotide polymorphism