Evidence map›Paper›PMID 33810227›Full record

ArticleGenes2021

Special Issue "Cardiovascular Genetics".

Andreas Brodehl, Hendrik Milting, Brenda Gerull

Abstract readEditorial
In one paragraph

Article in Genes, 2021. 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
–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

2 citing papers in PubMed.

  1. Article
  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

3 authors.

Andreas BrodehlErich and Hanna Klessmann Institute, Heart and Diabetes Center NRW, University Hospital of the Ruhr-University Bochum, Georgstrasse 11, 32545 Bad Oeynhausen, Germany.ORCID 0000-0001-9202-2343
Hendrik MiltingErich and Hanna Klessmann Institute, Heart and Diabetes Center NRW, University Hospital of the Ruhr-University Bochum, Georgstrasse 11, 32545 Bad Oeynhausen, Germany.
Brenda GerullComprehensive Heart Failure Center (CHFC), Department of Internal Medicine I, University Hospital Würzburg, 97080 Würzburg, Germany.ORCID 0000-0002-1363-8826

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since the beginnings of cardiovascular genetics, it became evident in thousands of clinical cases that many cardiomyopathies, channelopathies, aortopathies as well as complex multifactorial diseases such as coronary artery disease, atherosclerosis or atrial fibrillation (AF) have a genetic etiology [...].

Indexed as

Genetic VariationCardiovascular DiseasesGenetic Association StudiesGenetic Predisposition to DiseaseHumansMutationPeriodicals as TopicPolymorphism, Single Nucleotide

Identifiers

PMID33810227
PMCPMC8065827

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.