Evidence map›Paper›PMID 35205214›Full record

ArticleGenes2022

Laura Keil, Filip Berisha, Dorit Knappe, Christian Kubisch, Moneef Shoukier, Paulus Kirchhof, Larissa Fabritz, Yorck Hellenbroich, Rixa Woitschach, Christina Magnussen

Open access · goldAbstract readCase Reports
In one paragraph

Article in Genes, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. 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

10 authors at 3 institutions in 1 country.

Laura KeilDepartment of Cardiology, University Heart and Vascular Center Hamburg, 20251 Hamburg, Germany.
Filip BerishaDepartment of Cardiology, University Heart and Vascular Center Hamburg, 20251 Hamburg, Germany.
Dorit KnappeDepartment of Cardiology, University Heart and Vascular Center Hamburg, 20251 Hamburg, Germany.
Christian KubischInstitute of Human Genetics, University Hospital Hamburg Eppendorf, 20246 Hamburg, Germany.
Moneef ShoukierPrenatal Medicine Munich, Department of Molecular Genetics, 80639 Munich, Germany.
Paulus KirchhofDepartment of Cardiology, University Heart and Vascular Center Hamburg, 20251 Hamburg, Germany.ORCID 0000-0002-1881-0197
Larissa FabritzDepartment of Cardiology, University Heart and Vascular Center Hamburg, 20251 Hamburg, Germany.
Yorck HellenbroichInstitute of Human Genetics, University of Luebeck, 23538 Luebeck, Germany.
Rixa WoitschachInstitute of Human Genetics, University Hospital Hamburg Eppendorf, 20246 Hamburg, Germany.
Christina MagnussenDepartment of Cardiology, University Heart and Vascular Center Hamburg, 20251 Hamburg, Germany.
German Centre for Cardiovascular Research · DEUniversität Hamburg · DEUniversity of Lübeck · DE

Funding

British Heart Foundation AA/18/2/34218British Heart Foundation PG/17/30/32961British Heart Foundation PG/20/22/35093
6 · The paper itself

Abstract

We report a family with heterozygous deletion of exons 3-6 of the

Indexed as

Cardiomyopathy, DilatedHeart FailureAdultAgedDeath, Sudden, CardiacFemaleHumansLamin Type AMaleMutationLamin Type ALMNA protein, humandilated cardiomyopathyheart failureLMNA

Identifiers

PMID35205214
PMCPMC8871815
OpenAlexW4205307435

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.