Evidence map›Paper›PMID 37679021›Full record

ArticleAJNR. American journal of neuroradiology2023

Neuroimaging Findings in Axenfeld-Rieger Syndrome: A Case Series.

Samuel White, Ajay Taranath, Prasad Hanagandi, Deepa A Taranath, Minh-Son To, Emmanuelle Souzeau, Owen M Siggs, Jamie E Craig

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

Article in AJNR. American journal of neuroradiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

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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

8 authors at 5 institutions in 2 countries.

Samuel WhiteFrom the Robinson Research Institute (S.W.), Faculty of Medicine and Health Sciences, University of Adelaide, Adelaide, South Australia, Australia s.white@adelaide.edu.au.ORCID 0000-0001-9374-3492
Ajay TaranathDepartment of Radiology (A.T.), Women's and Children's Hospital, Adelaide, South Australia, Australia.ORCID 0000-0002-2910-2436
Prasad HanagandiDepartment of Neuroradiology (P.H.), King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.ORCID 0000-0003-3654-8329
Deepa A TaranathDepartment of Ophthalmology (D.A.T., M.-S.T., E.S., O.M.S., J.E.C.), Flinders University, Bedford Park, South Australia, Australia.ORCID 0000-0002-6210-744X
Minh-Son ToDepartment of Ophthalmology (D.A.T., M.-S.T., E.S., O.M.S., J.E.C.), Flinders University, Bedford Park, South Australia, Australia.ORCID 0000-0002-8060-6218
Emmanuelle SouzeauDepartment of Ophthalmology (D.A.T., M.-S.T., E.S., O.M.S., J.E.C.), Flinders University, Bedford Park, South Australia, Australia.ORCID 0000-0002-2015-6577
Owen M SiggsDepartment of Ophthalmology (D.A.T., M.-S.T., E.S., O.M.S., J.E.C.), Flinders University, Bedford Park, South Australia, Australia.ORCID 0000-0003-2840-4851
Jamie E CraigDepartment of Ophthalmology (D.A.T., M.-S.T., E.S., O.M.S., J.E.C.), Flinders University, Bedford Park, South Australia, Australia.
Flinders University · AUGarvan Institute of Medical Research · AUKing Abdulaziz Medical City · SAThe University of Adelaide · AUWomen's and Children's Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Axenfeld-Rieger syndrome is an autosomal dominant condition associated with multisystemic features including developmental anomalies of the anterior segment of the eye. Single nucleotide and copy number variants in the paired-like homeodomain transcription factor 2 (

Indexed as

Anterior Eye SegmentEye AbnormalitiesEye Diseases, HereditaryForkhead Transcription FactorsHomeobox Protein PITX2Homeodomain ProteinsAdolescentAdultChildChild, PreschoolFemaleHumansInfantMagnetic Resonance ImagingMaleMiddle AgedForkhead Transcription FactorsFOXC1 protein, humanHomeobox Protein PITX2Homeodomain ProteinsTranscription Factors

Identifiers

PMID37679021
PMCPMC10549946
OpenAlexW4386495711

What OpenQuestion holds

Textmetadata
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.