Shedding light on myopia by studying complete congenital stationary night blindness.

doi:10.1016/j.preteyeres.2022.101155

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

Community

Back to search

Article

Shedding light on myopia by studying complete congenital stationary night blindness.

Progress in retinal and eye research - 1 Mar 2023

Zeitz Christina, Roger Jérome E, Audo Isabelle, Michiels Christelle, Sánchez-Farías Nuria, Varin Juliette, Frederiksen Helen, Wilmet Baptiste, Callebert Jacques, Gimenez Marie-Laure, Bouzidi Nassima, Blond Frederic, Guilllonneau Xavier, Fouquet Stéphane, Léveillard Thierry, Smirnov Vasily, Vincent Ajoy, Héon Elise, Sahel José-Alain, Kloeckener-Gruissem Barbara, Sennlaub Florian, Morgans Catherine W, Duvoisin Robert M, Tkatchenko Andrei V, Picaud Serge

Abstract excerpt

Myopia is the most common eye disorder, caused by heterogeneous genetic and environmental factors. Rare progressive and stationary inherited retinal disorders are often associated with high myopia. Genes implicated in myopia encode proteins involved in a variety of biological processes including eye morphogenesis, extracellular matrix organization, visual perception, circadian rhythms, and retinal signaling....

Read the complete abstract on PubMed

Topics

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

Share to Electroretinography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Eye Diseases, Hereditary

Share to Genetic Diseases, X-Linked

Share to Genome-Wide Association Study

Share to Membrane Proteins

Share to Mice

Share to Myopia

Share to Night Blindness

Source

Open in PubMed

Identifiers

PMID: 36669906
DOI: 10.1016/j.preteyeres.2022.101155

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Shedding light on myopia by studying complete congenital stationary night blindness.PMID 36669906Read ↗

Single‐cell RNA sequencing of retina revealed novel transcriptional landscape in high myopia and underlying cell‐type‐specific mechanismsSemantic proximity Read ↗

IMI – Myopia Genetics ReportSemantic proximity Read ↗

Molecular Genetics of Human Myopia: An UpdateSemantic proximity Read ↗

Diurnal gene expression patterns in retina and choroid distinguish myopia progression from myopia onsetSemantic proximity Read ↗

Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error.Semantic proximity Read ↗

Genome-wide analysis points to roles for extracellular matrix remodeling, the visual cycle, and neuronal development in myopia.Semantic proximity Read ↗

IMI-Myopia Genetics Report.Semantic proximity Read ↗

Applications of Genomics and Transcriptomics in Precision Medicine for Myopia Control or PreventionSemantic proximity Read ↗

Diurnal retinal and choroidal gene expression patterns support a role for circadian biology in myopia pathogenesisSemantic proximity Read ↗

Establishment and comprehensive characterization of a novel dark-reared zebrafish model for myopia studiesSemantic proximity Read ↗

Integrative Transcriptome and Proteome Analyses Elucidate the Mechanism of Lens-Induced Myopia in MiceSemantic proximity Read ↗

[Pathophysiology of myopia: nature versus nurture].Semantic proximity Read ↗

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