Evidence map›Paper›PMID 37714428›Full record

ArticleKidney international2024

Multipopulation genome-wide association meta-analysis in pediatric steroid-sensitive nephrotic syndrome.

Olivia Boyer, Guillaume Dorval

Abstract readComment
PubMed Publisher
In one paragraph

Article in Kidney international, 2024. 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
–field-weighted citation impact
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. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Olivia BoyerNéphrologie Pédiatrique, Centre de Référence du Syndrome Néphrotique Idiopathique de l'Enfant et l'Adulte, Hôpital Necker-Enfants Malades, Assistance Publique - Hôpitaux de Paris (APHP), INSERM U1163, Institut Imagine, Université Paris Cité, Paris, France. Electronic address: olivia.boyer@aphp.fr.
Guillaume DorvalService de Médecine Génomique des Maladies Rares, Centre de Référence MAladies REnales Héréditaires de l'Enfant et de l'Adulte (MARHEA), Hôpital Necker-Enfants Malades, Assistance Publique - Hôpitaux de Paris (APHP), INSERM U1163, Institut Imagine, Université Paris Cité, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Nephrotic SyndromeChildGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMeta-Analysis as Topicchildrengenome-wide association meta-analysisHLAnephrinsteroid-sensitive nephrotic syndrome

Identifiers

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.