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Rare heterozygous missense variants in VSX2 are associated with retinal detachment

PLOS Genetics(2026)10.1371/journal.pgen.1012027Source: DataRank Database

Rare heterozygous missense variants in VSX2 are associated with retinal detachment is a research paper published in PLOS Genetics (2026). On theSindex it has a DataRank of 0.

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Enrichment:Funding (9 grants)Impact (FWCI 0.00)OA: goldTopics (39)IDs (PubMed, PMC, OpenAlex)Annotations (1)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (18)

Justin S. Dhindsa,Yifan Chen ORCID,Vida Ravanmehr ORCID,Jonathan Mitchell,Fengyuan Hu

Live enrichment

PubMed:41632798 PMC:PMC12890223 OpenAlex:https://openalex.org/W7127290872

NIH Office of the Director

Grant: 5DP5OD036131

NIH National Eye Institute

Grant: R01EY036111

NIH National Eye Institute

Grant: R01EY035646

Norn Group, Hevolution Foundation, and Rosenkranz Foundation

Grant: Longevity Impetus Grant

Texas Children's Hospital

Grant: Research Vision Scholars Program

Rice University

Grant: Start-up Funds

NIH HHS

Grant: DP5 OD036131

Robert and Janice McNair Foundation

The Cullen Foundation

FWCI

0.00

Citation Percentile

0.1%

goldLicense: cc-by

journalhttps://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1012027&type=printable

publisherhttps://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1012027&type=printable

publisherhttps://dx.plos.org/10.1371/journal.pgen.1012027

journalhttps://doi.org/10.1371/journal.pgen.1012027

repositoryhttps://pubmed.ncbi.nlm.nih.gov/41632798

Fields of Study

Retinal and Macular SurgeryRetinopathy of Prematurity StudiesRetinal Development and DisordersHumansMutation, MissenseRetinal DetachmentHeterozygoteCase-Control StudiesGenetic Predisposition to DiseaseHomeodomain ProteinsFemalePolymorphism, Single NucleotideMaleEye Proteins

MeSH Terms

Whole Genome SequencingAdultAgedEye ProteinsFemaleHeterozygoteHumansMaleMiddle AgedRetinal DetachmentCase-Control StudiesHomeodomain ProteinsGenetic Predisposition to DiseaseMutation, MissensePolymorphism, Single NucleotideGenome-Wide Association Study

Keywords

Missense mutationMendelian inheritanceCompound heterozygosityOdds ratioHeterozygote advantageGenome-wide association studyGeneAnophthalmiaDisease gene identification

Sustainable Development Goals

SDG 0: Life in Land

Rare heterozygous missense variants in VSX2 are associated with retinal detachment

FAIR Checklist

Authors (18)

Funding (9 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)