Evidence map›Paper›PMID 35054374›Full record

ArticleDiagnostics (Basel, Switzerland)2022

Identification of the First Single

Luke Mansard, Christel Vaché, Julie Bianchi, Corinne Baudoin, Isabelle Perthus, Bertrand Isidor, Catherine Blanchet, David Baux, Michel Koenig, Vasiliki Kalatzis and 1 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. The gasdermin family: emerging therapeutic targets in diseases.Signal transduction and targeted therapy · 2024
    Review
  3. Article
  4. [Splicing mutations ofLin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2024
    Article
  5. Alternative splicing in shaping the molecular landscape of the cochlea.Frontiers in cell and developmental biology · 2023
    Review
  6. Genetic Testing for Rare Diseases.Diagnostics (Basel, Switzerland) · 2022
    Article
  7. Article
  8. A novel non-sense variant inFrontiers in neurology
    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

11 authors at 3 institutions in 1 country.

Luke MansardMolecular Genetics Laboratory, Univ Montpellier, CHU Montpellier, 34000 Montpellier, France.ORCID 0000-0003-0449-0994
Christel VachéMolecular Genetics Laboratory, Univ Montpellier, CHU Montpellier, 34000 Montpellier, France.ORCID 0000-0001-7076-9139
Julie BianchiMolecular Genetics Laboratory, Univ Montpellier, CHU Montpellier, 34000 Montpellier, France.
Corinne BaudoinMolecular Genetics Laboratory, Univ Montpellier, CHU Montpellier, 34000 Montpellier, France.
Isabelle PerthusDepartment of Clinical Genetics, Reference Center for Rare Diseases, University Hospital of Clermont-Ferrand, 63000 Clermont-Ferrand, France.ORCID 0000-0002-3845-6180
Bertrand IsidorDepartment of Medical Genetics, CHU Nantes, 44000 Nantes, France.
Catherine BlanchetNational Reference Centre for Inherited Sensory Diseases, Otolaryngology Department, Univ Montpellier, CHU Montpellier, 34000 Montpellier, France.
David BauxMolecular Genetics Laboratory, Univ Montpellier, CHU Montpellier, 34000 Montpellier, France.ORCID 0000-0003-3423-1221
Michel KoenigMolecular Genetics Laboratory, Univ Montpellier, CHU Montpellier, 34000 Montpellier, France.
Vasiliki KalatzisInstitute for Neurosciences of Montpellier (INM), Univ Montpellier, Inserm, 34000 Montpellier, France.ORCID 0000-0002-9626-8807
Anne-Françoise RouxMolecular Genetics Laboratory, Univ Montpellier, CHU Montpellier, 34000 Montpellier, France.ORCID 0000-0001-5914-2335
Université de Montpellier · FRInserm · FRCentre Hospitalier Universitaire de Nantes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

DFNA5GSDMEhearing losssingle-exon CNV

Identifiers

PMID35054374
PMCPMC8774889
OpenAlexW4205624297

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.