Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Severe retinopathy of prematurity associated with FZD4 mutations.

Ophthalmic genetics - 1 Mar 2010

Ells Anna, Guernsey Duane L, Wallace Karin, Zheng Binyou, Vincer Michael, Allen Alexander, Ingram April, DaSilva Orlando, Siebert Lee, Sheidow Thomas, Beis Jill, Robitaille Johane M

Abstract excerpt

PURPOSE: To determine whether mutations in the FZD4 gene are a risk factor for developing severe ROP. METHODS: Three Canadian tertiary care centers recruited premature infants prospectively and retrospectively, and assigned affectation status based on the maximum degree of severity of ROP recorde...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Birth Weight
Share to Frizzled Receptors
Share to Gestational Age

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant, Newborn

Share to Receptors, G-Protein-Coupled

Share to Retinopathy of Prematurity

Share to Risk Factors

Share to Sequence Homology, Amino Acid

Source

Identifiers

PMID: 20141357
DOI: 10.3109/13816810903479834

Genes

FZD4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-20141357-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Severe retinopathy of prematurity associated with FZD4 mutations.PMID 20141357Read ↗

Ocular phenotype and genetical analysis in patients with retinopathy of prematurity.Semantic proximity Read ↗

Clinical presentation and genetic correlation of patients with mutations affecting the FZD4 gene.Semantic proximity Read ↗

Frizzled-4 Variations Associated with Retinopathy and Intrauterine Growth Retardation: A Potential Marker for Prematurity and Retinopathy.Semantic proximity Read ↗

Genetic variants of FZD4 and LRP5 genes in patients with advanced retinopathy of prematurity.Semantic proximity Read ↗

A novel variant in the FZD4 gene leading to familial exudative vitreoretinopathy: A case report and literature review.Semantic proximity Read ↗

Mutation spectrum of NDP, FZD4 and TSPAN12 genes in Indian patients with retinopathy of prematurity.Semantic proximity Read ↗

Severe Familial Exudative Vitreoretinopathy, Congenital Hearing Loss, and Developmental Delay in a Child With Biallelic Variants in FZD4.Semantic proximity Read ↗

Identification of novel FZD4 mutations in Indian patients with familial exudative vitreoretinopathy.Semantic proximity Read ↗

FZD4 in a Large Chinese Population With Familial Exudative Vitreoretinopathy: Molecular Characteristics and Clinical Manifestations.Semantic proximity Read ↗

Novel frizzled-4 gene mutations in chinese patients with familial exudative vitreoretinopathy.Semantic proximity Read ↗

Familial exudative vitreoretinopathy (FEVR) in a child with novel microarray-defined deletion of 11q14 previously diagnosed as retinopathy of prematurity (ROP).Semantic proximity Read ↗

Identification of Novel FZD4 Mutations in Familial Exudative Vitreoretinopathy and Investigating the Pathogenic Mechanisms of FZD4 Mutations.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.