Evidence map›Paper›PMID 37510387›Full record

ArticleGenes2023

Functional Characteristics of Diverse

Itsuka Matsushita, Hiroto Izumi, Shinji Ueno, Takaaki Hayashi, Kaoru Fujinami, Kazushige Tsunoda, Takeshi Iwata, Yoshiaki Kiuchi, Hiroyuki Kondo

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. An Unusual Presentation of Novel Missense Variant inCurrent issues in molecular biology · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 1 country.

Itsuka MatsushitaDepartment of Ophthalmology, University of Occupational and Environmental Health, Kitakyushu 807-8555, Japan.
Hiroto IzumiDepartment of Occupational Pneumology, University of Occupational and Environmental Health, Kitakyushu 807-8555, Japan.ORCID 0000-0003-0327-582X
Shinji UenoDepartment of Ophthalmology, Hirosaki University Graduate School of Medicine, Hirosaki 036-8562, Japan.
Takaaki HayashiDepartment of Ophthalmology, The Jikei University School of Medicine, Tokyo 105-8461, Japan.ORCID 0000-0002-1535-0279
Kaoru FujinamiDepartment of Ophthalmology, National Hospital Organization Tokyo Medical Center, Tokyo 152-8902, Japan.
Kazushige TsunodaDepartment of Ophthalmology, National Hospital Organization Tokyo Medical Center, Tokyo 152-8902, Japan.ORCID 0009-0001-4913-1277
Takeshi IwataDivision of Molecular and Cellular Biology, National Institute of Sensory Organs, National Hospital Organization Tokyo Medical Center, Tokyo 152-8902, Japan.
Yoshiaki KiuchiDepartment of Ophthalmology and Visual Science, Graduate School of Biomedical and Health Sciences, Hiroshima 734-8551, Japan.ORCID 0000-0003-1915-1864
Hiroyuki KondoDepartment of Ophthalmology, University of Occupational and Environmental Health, Kitakyushu 807-8555, Japan.ORCID 0000-0002-3194-152X
Tokyo Medical Center · JPUniversity of Occupational and Environmental Health Japan · JPHirosaki University · JPHiroshima University · JPJikei University School of Medicine · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human fovea is a specialized pit structure in the central retina. Foveal hypoplasia is a condition where the foveal pit does not fully develop, and it is associated with poor vision. Autosomal dominant isolated foveal hypoplasia (FVH1) is a rare condition of foveal hypoplasia (FH) that lacks any other ocular manifestations. FVH1 is associated with hypomorphic mutations in the

Indexed as

Homeodomain ProteinsPAX6 Transcription FactorDNAEye Diseases, HereditaryFovea CentralisHumansMutationNystagmus, CongenitalPaired Box Transcription FactorsRepressor ProteinsDNAHomeodomain ProteinsPaired Box Transcription FactorsPAX6 protein, humanPAX6 Transcription FactorRepressor Proteinsaniridiacorneal opacityDNA bindingfoveal hypoplasiaFVH1paired domainPAX6proline-serine-threonine-rich domaintranscriptional activity

Identifiers

PMID37510387
PMCPMC10379490
OpenAlexW4385070155

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.