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Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.02.01.526652Source: DataRank Database

Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms is a research paper published in bioRxiv (Cold Spring Harbor Laboratory) (2023). On theSindex it has a DataRank of 0.255. It has been cited 4 times, with 3 citing works in its 1-hop citation network.

N/A

0.255DataRank · unranked

Scored on demand from live citation data

Open Access4 citations · 3 citing works in its network

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (2 grants)OA: greenTopics (37)IDs (PubMed, OpenAlex)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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DataRank Breakdown

Base Score 95%Citation Network 5%

Base Score Contribution

0.241

From this paper's citation signal

Citation Network Contribution

0.0134

From 2 citing papers with measurable signal

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Top 3 citers driving the network score

Ranked by each citer's contribution to N(p) — log1p(C_q) divided by its reference count — out of 3 citers.

A new hypothesis to explain disease dominance
Trends in Genetics20251 citations65 referencesContributes 0.011
Genetic and epigenetic control of photoreceptor development
Current topics in developmental biology/Current Topics in Developmental Biology20252 citations217 referencesContributes 0.005
Leber Congenital Amaurosis and Early-Onset Severe Inherited Retinal Degenerations
20250 citations159 referencesContributes 0.000

Authors (5)

Chi Sun ORCID,Xiaodong Zhang ORCID,Philip A. Ruzycki ORCID,Shiming Chen ORCID,Yiqiao Zheng ORCID

Live enrichment

PubMed:36778408 OpenAlex:https://openalex.org/W4319226675

National Institutes of Health

Grant: 5R01EY032136-04

Understanding and treating CRX-linked retinopathies

National Institutes of Health

Grant: 5R01EY012543-10

CRX AND ITS REGULATORY NETWORK IN RETINAL DEGENERATIONS

greenLicense: cc-by-nc-nd

repositoryhttps://www.biorxiv.org/content/biorxiv/early/2023/02/06/2023.02.01.526652.full.pdf

publisherhttps://syndication.highwire.org/content/doi/10.1101/2023.02.01.526652

repositoryhttps://doi.org/10.1101/2023.02.01.526652

repositoryhttps://pubmed.ncbi.nlm.nih.gov/36778408

Fields of Study

Retinal Development and DisordersOcular Disorders and TreatmentsOcular Oncology and Treatments0301 basic medicine03 medical and health sciences

Keywords

Missense mutationHomeoboxGeneticsBiologyMutationGeneTranscription factorinherited retinal diseasesQH301-705.5ScienceMutation, MissenseArticleRetinaMiceRetinal DiseasesMedicine and Health SciencesAnimalsHumansphotoreceptor developmentBiology (General)DNA-binding specificityHomeodomain ProteinsCRX disease mutationsQICTS (Institute of Clinical and Translational Sciences)RGenetics and GenomicshomeodomainTrans-ActivatorsMedicineMissenseTranscription Factors

Sustainable Development Goals

SDG 0: Good health and well-being