Integrated genomic analyses in bronchopulmonary dysplasia.

doi:10.1016/j.jpeds.2014.09.052

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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....

Topics

Animals
Bronchopulmonary Dysplasia
DNA
Genetic Predisposition to Disease
Genome-Wide Association Study
Genotype
Gestational Age
Humans
Incidence
Infant

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Infant, Extremely Low Birth Weight

Infant, Newborn

Infant, Premature

Mice

Polymorphism, Single Nucleotide

Survival Rate

United States

Source

Open in PubMed Open full text

Identifiers

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

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