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Article

Exome Sequencing of Neonatal Blood Spots and the Identification of Genes Implicated in Bronchopulmonary Dysplasia.

American journal of respiratory and critical care medicine - 1 Sept 2015

Li Jingjing, Yu Kun-Hsing, Oehlert John, Jeliffe-Pawlowski Laura L, Gould Jeffrey B, Stevenson David K, Snyder Michael, Shaw Gary M, O'Brodovich Hugh M

Abstract excerpt

RATIONALE: Bronchopulmonary dysplasia (BPD), a prevalent severe lung disease of premature infants, has a strong genetic component. Large-scale genome-wide association studies for common variants have not revealed its genetic basis. OBJECTIVES: Given the historical high mortality rate of extremely preterm infants who now survive and develop BPD, we hypothesized that risk loci underlying this disease are under...

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Source

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Identifiers

PMID: 26030808
DOI: 10.1164/rccm.201501-0168OC
PMCID: PMC4595691

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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