Evidence map›Paper›PMID 40225146›Full record

ArticleHuman mutation2023

Early-Onset Aortic Dissection: Characterization of a New Pathogenic Splicing Variation in the

Pauline Arnaud, Margaux Cadenet, Zakaria Mougin, Carine Le Goff, Sébastien Perbet, Mathilde Francois, Sophie Dupuis-Girod, Catherine Boileau, Nadine Hanna

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Human mutation, 2023. 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
–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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  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

9 authors.

Pauline ArnaudDépartement de Génétique, AP-HP, Hôpital Bichat, F-75018 Paris, France.ORCID 0000-0001-9727-1592
Margaux CadenetDépartement de Génétique, AP-HP, Hôpital Bichat, F-75018 Paris, France.
Zakaria MouginUniversité Paris Cité, Inserm, LVTS U1148, F-75018 Paris, France.
Carine Le GoffUniversité Paris Cité, Inserm, LVTS U1148, F-75018 Paris, France.
Sébastien PerbetPôle de Médecine Péri-Opératoire, CHU Clermont-Ferrand, F-63000 Clermont-Ferrand, France.
Mathilde FrancoisService de Génétique, Hospices Civils de Lyon, Hôpital Femme-Mère-Enfant, F-69500 Bron, France.
Sophie Dupuis-GirodService de Génétique, Hospices Civils de Lyon, Hôpital Femme-Mère-Enfant, F-69500 Bron, France.
Catherine BoileauDépartement de Génétique, AP-HP, Hôpital Bichat, F-75018 Paris, France.
Nadine HannaDépartement de Génétique, AP-HP, Hôpital Bichat, F-75018 Paris, France.ORCID 0000-0001-5434-3111

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rare pathogenic variants in the

Indexed as

Aortic Aneurysm, ThoracicAortic DissectionMyosin Heavy ChainsRNA SplicingAlternative SplicingExonsHumansMutationPedigreeRNA Splice SitesYoung AdultMYH11 protein, humanMyosin Heavy ChainsRNA Splice Sites

Identifiers

PMID40225146
PMCPMC11919123

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.