Phenotype wide association study links bronchopulmonary dysplasia with eosinophilia in children
Author:
Funder
Parker B Francis Foundation
National Institute of Environmental Health Sciences
Publisher
Springer Science and Business Media LLC
Link
https://www.nature.com/articles/s41598-024-72348-5.pdf
Reference75 articles.
1. Siffel, C., Kistler, K. D., Lewis, J. F. M. & Sarda, S. P. Global incidence of bronchopulmonary dysplasia among extremely preterm infants: A systematic literature review. J. Matern. Fetal Neonatal Med. 34, 1721–1731. https://doi.org/10.1080/14767058.2019.1646240 (2021).
2. Thébaud, B. et al. Bronchopulmonary dysplasia. Nat. Rev. Dis. Primers 5, 78. https://doi.org/10.1038/s41572-019-0127-7 (2019).
3. Yu, K.-H., Li, J., Snyder, M., Shaw, G. M. & O’Brodovich, H. M. The genetic predisposition to bronchopulmonary dysplasia. Curr. Opin. Pediatr. 28, 318–323. https://doi.org/10.1097/mop.0000000000000344 (2016).
4. Parad, R. B. et al. Role of genetic susceptibility in the development of bronchopulmonary dysplasia. J. Pediatr. 203, 234–241. https://doi.org/10.1016/j.jpeds.2018.07.099 (2018).
5. Hadchouel, A. et al. Identification of SPOCK2 as a susceptibility gene for bronchopulmonary dysplasia. Am. J. Respir. Crit. Care Med. 184, 1164–1170. https://doi.org/10.1164/rccm.201103-0548OC (2011).
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