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Article

Integrated genomic analyses in bronchopulmonary dysplasia.

The Journal of pediatrics - 1 Mar 2015

Ambalavanan Namasivayam, Cotten C Michael, Page Grier P, Carlo Waldemar A, Murray Jeffrey C, Bhattacharya Soumyaroop, Mariani Thomas J, Cuna Alain C, Faye-Petersen Ona M, Kelly David, Higgins Rosemary D

Abstract excerpt

OBJECTIVE: To identify single-nucleotide polymorphisms (SNPs) and pathways associated with bronchopulmonary dysplasia (BPD) because O2 requirement at 36 weeks' postmenstrual age risk is strongly influenced by heritable factors. STUDY DESIGN: A genome-wide scan was conducted on 1.2 million genotyped SNPs, and an additional 7 million imputed SNPs, using a DNA repository of extremely low birth weight infants....

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Identifiers

PMID: 25449221
DOI: 10.1016/j.jpeds.2014.09.052
PMCID: PMC4344889

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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