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

Insight from OPN1LW Gene Haplotypes into the Cause and Prevention of Myopia

25 May 2022

Abstract excerpt

Nearsightedness (myopia) is a global health problem of staggering proportions that has driven the hunt for environmental and genetic risk factors in hopes of gaining insight into the underlying mechanism and providing new avenues of intervention. Myopia is the dominant risk factor for leading causes of blindness, including myopic maculopathy and retinal detachment. The fundamental defect in myopia—an excessively...

Read the complete abstract on PubMed

Topics

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

Share to Corneal surgery and disorders
Share to Ophthalmology and Visual Impairment Studies
Share to Retinal Diseases and Treatments

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 35741704
DOI: 10.3390/genes13060942

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Insight from OPN1LW Gene Haplotypes into the Cause and Prevention of MyopiaPMID 35741704Read ↗

Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic Mechanism.Semantic proximity Read ↗

IMI – Myopia Genetics ReportSemantic proximity Read ↗

Intermixing the OPN1LW and OPN1MW Genes Disrupts the Exonic Splicing Code Causing an Array of Vision DisordersSemantic proximity Read ↗

Update on the epidemiology and genetics of myopic refractive errorSemantic proximity Read ↗

Myopia and Late-Onset Progressive Cone Dystrophy Associate to LVAVA/MVAVA Exon 3 Interchange Haplotypes of Opsin Genes on Chromosome X.Semantic proximity Read ↗

Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia.Semantic proximity Read ↗

Nature and nurture: the complex genetics of myopia and refractive error.Semantic proximity Read ↗

Molecular Genetics of Human Myopia: An UpdateSemantic proximity Read ↗

CPSF1 mutations are associated with early-onset high myopia and involved in retinal ganglion cell axon projectionSemantic proximity Read ↗

Myopia Genetics and HereditySemantic proximity Read ↗

Associations between RetNet gene polymorphisms and efficacy of orthokeratology for myopia control : sample from a clinical retrospective studySemantic proximity Read ↗

IMI-Myopia Genetics Report.Semantic proximity Read ↗

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