Evidence map›Paper›PMID 35754802›Full record

SynthesisFrontiers in genetics2022

Oral Phenotype of Singleton-Merten Syndrome: A Systematic Review Illustrated With a Case Report.

Margot Charlotte Riou, Muriel de La Dure-Molla, Stéphane Kerner, Sophie Rondeau, Adrien Legendre, Valerie Cormier-Daire, Benjamin P J Fournier

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

Synthesis in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. 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

7 authors at 5 institutions in 1 country.

Margot Charlotte RiouCentre de Recherche des Cordeliers, UMRS 1138, Molecular Oral Pathophysiology, Université de Paris, INSERM, Sorbonne Université, Paris, France.
Muriel de La Dure-MollaDental Department, Reference Center for Oral and Dental Rare Diseases, AP-HP, Rothschild Hospital (ORARES), Paris, France.
Stéphane KernerDental Department, Reference Center for Oral and Dental Rare Diseases, AP-HP, Rothschild Hospital (ORARES), Paris, France.
Sophie RondeauDepartment of Genetics, Necker Enfants Malades Hospital, Paris Descartes-Sorbonne Paris Cité University, Paris, France.
Adrien LegendreLaboratoire de Biologie Médicale Multisites Seqoia-FMG2025, Paris, France.
Valerie Cormier-DaireINSERM U1163 Institut Imagine, Paris, France.
Benjamin P J FournierCentre de Recherche des Cordeliers, UMRS 1138, Molecular Oral Pathophysiology, Université de Paris, INSERM, Sorbonne Université, Paris, France.
Sorbonne Université · FRAssistance Publique – Hôpitaux de Paris · FRInserm · FRInstitut des Maladies Génétiques Imagine · FRSorbonne Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

geneticsoral physiopathologyrare diseasesSingleton–Merten syndrometype 1 interferonopathy

Identifiers

PMID35754802
PMCPMC9218817
OpenAlexW4281764279

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.