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Article

Genetic variants associated with severe retinopathy of prematurity in extremely low birth weight infants.

Investigative ophthalmology & visual science - 12 Aug 2014

Hartnett M Elizabeth, Morrison Margaux A, Smith Silvia, Yanovitch Tammy L, Young Terri L, Colaizy Tarah, Momany Allison, Dagle John, Carlo Waldemar A, Clark Erin A S, Page Grier, Murray Jeff, DeAngelis Margaret M, Cotten C Michael

Abstract excerpt

PURPOSE: To determine genetic variants associated with severe retinopathy of prematurity (ROP) in a candidate gene cohort study of US preterm infants. METHODS: Preterm infants in the discovery cohort were enrolled through the Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network, and those in the replication cohort were from the University of Iowa. All infants...

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Source

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Identifiers

PMID: 25118269
DOI: 10.1167/iovs.14-14841
PMCID: PMC4188045

Genes

BDNF

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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