Ancestry and genetic associations with bronchopulmonary dysplasia in preterm infants

Bronchopulmonary dysplasia in premature infants is a common and often severe lung disease with long-term sequelae. A genetic component is suspected but not fully defined. We performed an ancestry and genome-wide association study to identify variants, genes, and pathways associated with survival wit...

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Pubblicato in:Am J Physiol Lung Cell Mol Physiol
Autori principali: Torgerson, Dara G., Ballard, Philip L., Keller, Roberta L., Oh, Sam S., Huntsman, Scott, Hu, Donglei, Eng, Celeste, Burchard, Esteban G., Ballard, Roberta A.
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Physiological Society 2018
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6295513/
https://ncbi.nlm.nih.gov/pubmed/30113228
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajplung.00073.2018
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