Evidence map›Paper›PMID 28436080›Full record

ArticleThe Journal of physiology2017

Genotype-specific pathogenic effects in human dilated cardiomyopathy.

Ilse A E Bollen, Maike Schuldt, Magdalena Harakalova, Aryan Vink, Folkert W Asselbergs, Jose R Pinto, Martina Krüger, Diederik W D Kuster, Jolanda van der Velden

Open access · hybridAbstract read
In one paragraph

Article in The Journal of physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.7field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Review
  3. RNA-Based Therapies for Treating Monogenic Cardiomyopathies.The Canadian journal of cardiology · 2026
    Review
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  9. HomozygousGenes · 2023
    Review
  10. Article
  11. Case Report: Mutation inFrontiers in pediatrics · 2023
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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 at 6 institutions in 4 countries.

Ilse A E BollenDepartment of Physiology, Amsterdam Cardiovascular Sciences, VU University Medical Center, Amsterdam, the Netherlands.ORCID 0000-0002-6378-9825
Maike SchuldtDepartment of Physiology, Amsterdam Cardiovascular Sciences, VU University Medical Center, Amsterdam, the Netherlands.
Magdalena HarakalovaDepartment of Cardiology, Division of Heart and Lungs, University of Utrecht, University Medical Center Utrecht, Utrecht, the Netherlands.
Aryan VinkDepartment of Pathology, University Medical Center Utrecht, Utrecht, the Netherlands.
Folkert W AsselbergsDepartment of Cardiology, Division of Heart and Lungs, University of Utrecht, University Medical Center Utrecht, Utrecht, the Netherlands.
Jose R PintoDepartment of Biomedical Sciences, College of Medicine, Florida State University, Tallahassee, FL, USA.
Martina KrügerInstitute of Cardiovascular Physiology, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Diederik W D KusterDepartment of Physiology, Amsterdam Cardiovascular Sciences, VU University Medical Center, Amsterdam, the Netherlands.
Jolanda van der VeldenDepartment of Physiology, Amsterdam Cardiovascular Sciences, VU University Medical Center, Amsterdam, the Netherlands.
Amsterdam UMC Location Vrije Universiteit Amsterdam · NLUtrecht University · NLFlorida State University · USHeinrich Heine University Düsseldorf · DENetherlands Heart Institute · NLUniversity Medical Center Utrecht · NL

Funding

Modulators of Cardiomyopathic DiseasesR01HL128683 · NHLBI · FLORIDA STATE UNIVERSITY · PI PINTO, JOSE RENATO · 2016 to 2020
$1.8M
NHLBI NIH HHS R01 HL128683
6 · The paper itself

Abstract

key pointsMutations in genes encoding cardiac troponin I (TNNI3) and cardiac troponin T (TNNT2) caused altered troponin protein stoichiometry in patients with dilated cardiomyopathy. TNNI3 ABSTRACT: Dilated cardiomyopathy (DCM) can be caused by mutations in sarcomeric and non-sarcomeric genes. In this study we defined the pathogenic effects of three DCM-causing mutations: the sarcomeric mutations in genes encoding cardiac troponin I (TNNI3

Indexed as

AdultCardiomyopathy, DilatedConnectinFemaleGenotypeHeart VentriclesHumansLamin Type AMaleMiddle AgedMutationMyocytes, CardiacPhosphorylationTroponin IYoung AdultConnectinLamin Type ALMNA protein, humanTNNI2 protein, humanTroponin ITTN protein, humandilated cardiomyopathyheart failureprotein phosphorylationtroponin

Identifiers

PMID28436080
PMCPMC5509872
OpenAlexW2609905866

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.