Evidence map›Paper›PMID 33777383›Full record

ArticleClinical kidney journal2021

Joubert syndrome diagnosed renally late.

Elizabeth Collard, Catherine Byrne, Michalis Georgiou, Michel Michaelides, Abhijit Dixit

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

Article in Clinical kidney journal, 2021. 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
0.7field-weighted citation impact, top 26% 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, 12 citations in OpenAlex.

  1. A Novel Pathogenic Splicing Mutation ofPharmacogenomics and personalized medicine · 2025
    Article
  2. Renal insufficiency caused byFrontiers in medicine · 2025
    Article
  3. Article
  4. 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

5 authors at 3 institutions in 1 country.

Elizabeth CollardSchool of Medical Education, Newcastle University, Newcastle upon Tyne, UK.
Catherine ByrneDepartment of Nephrology, Nottingham University Hospitals NHS Trust, Nottingham, UK.
Michalis GeorgiouUCL Institute of Ophthalmology, University College London, London and Moorfields Eye Hospital, London, UK.
Michel MichaelidesUCL Institute of Ophthalmology, University College London, London and Moorfields Eye Hospital, London, UK.
Abhijit DixitDepartment of Clinical Genetics, Nottingham University Hospitals NHS Trust, Nottingham, UK.ORCID 0000-0001-9240-0674
Moorfields Eye Hospital NHS Foundation Trust · GBNottingham University Hospitals NHS Trust · GBNewcastle University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Joubert syndrome is a genetically heterogeneous multisystem disorder typically diagnosed in childhood. Nephronophthisis is the most common renal pathology in Joubert syndrome, and renal failure usually occurs in childhood or in young adults. We report a 61-year-old female diagnosed with

Indexed as

AHI1 mutationCKDJoubert syndromemolar tooth signnephronophthisisprognosisretinal dystrophy

Identifiers

PMID33777383
PMCPMC7986455
OpenAlexW3011472276

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.