Evidence map›Paper›PMID 36421840›Full record

ReviewGenes2022

Minh-Tuan Huynh, Alexis Proust, Jérôme Bouligand, Elena Popescu

Open access · goldAbstract readReviewCase Reports
In one paragraph

Review in Genes, 2022. 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
0.7field-weighted citation impact, top 32% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. A Novel Variant inMolecular syndromology · 2024
    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

4 authors at 2 institutions in 1 country.

Minh-Tuan HuynhCentre Hospitalier du Havre, Unité de Génétique Clinique, 29 Avenue Pierre Mendès-France, 76290 Montivilliers, France.ORCID 0000-0002-9183-7345
Alexis ProustLaboratoire de Génétique Moléculaire, Pharmacogénétique et Hormonologie, Hôpital Bicêtre, APHP Université Paris Saclay, 94270 Le Kremlin-Bicêtre, France; Inserm UMR_S 1185, Faculté de Médecine Paris Saclay, Université Paris Saclay, 94270 Le Kremlin-Bicêtre, France.
Jérôme BouligandLaboratoire de Génétique Moléculaire, Pharmacogénétique et Hormonologie, Hôpital Bicêtre, APHP Université Paris Saclay, 94270 Le Kremlin-Bicêtre, France; Inserm UMR_S 1185, Faculté de Médecine Paris Saclay, Université Paris Saclay, 94270 Le Kremlin-Bicêtre, France.
Elena PopescuCentre Hospitalier du Havre, Service de Cardiologie, 29 Avenue Pierre Mendès-France, 76290 Montivilliers, France.
Inserm · FRGroupe Hospitalier du Havre · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disease-associated pathogenic variants in the A-Kinase Anchor Protein 9 (

Indexed as

Brugada SyndromeChannelopathiesA Kinase Anchor ProteinsArrhythmias, CardiacCytoskeletal ProteinsDeath, Sudden, CardiacHumansMaleMiddle AgedAKAP9 protein, humanA Kinase Anchor ProteinsCytoskeletal ProteinsAKAP9 haploinsufficiencylong QT syndrome 11novel frameshiftsudden cardiac arrestvariant

Identifiers

PMID36421840
PMCPMC9690169
OpenAlexW4309787127

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.