Evidence map›Paper›PMID 36571587›Full record

ArticleJournal of nephrology2023

Polycystic kidney disease associated with intracranial hypertension revealing a mutation of the OFD1 gene.

Céline Schultz, Jean Chiesa, Van Kien Philippe Khau, Audrézet Marie-Pierre, Olivier Moranne

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of nephrology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 37% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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 4 institutions in 1 country.

Céline SchultzService de Néphrologie Dialyse Aphérèse, Nîmes Hôpital Universitaire, Nîmes, France.
Jean ChiesaDépartement de Cytogénétique et Génétique Médicale, Hôpital Carémeau, CHU Nîmes, Nîmes University Hospital, Nîmes, France.
Van Kien Philippe KhauDépartement de Cytogénétique et Génétique Médicale, Hôpital Carémeau, CHU Nîmes, Nîmes University Hospital, Nîmes, France.
Audrézet Marie-PierreService de Génétique Médicale et Biologie de la Reproduction, CHRU, Brest, France.
Olivier MoranneService de Néphrologie Dialyse Aphérèse, Nîmes Hôpital Universitaire, Nîmes, France. olivier.moranne@chu-nimes.fr.ORCID http://orcid.org/0000-0002-3127-1415
Centre National de la Recherche Scientifique · FRCentre Hospitalier Régional Universitaire de Brest · FRCentre Hospitalier Universitaire de Nîmes · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Intracranial HypertensionPolycystic Kidney DiseasesHumansMutationProteinsOFD1 protein, humanProteinsCKDGeneticIntracranial hypertensionPolycystic kidney

Identifiers

PMID36571587
OpenAlexW4312194902

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.