Evidence map›Paper›PMID 35784482›Full record

ArticleFrontiers in cell and developmental biology2022

Myosin Heavy Chain Converter Domain Mutations Drive Early-Stage Changes in Extracellular Matrix Dynamics in Hypertrophic Cardiomyopathy.

Jeanne Hsieh, Kelsie L Becklin, Sophie Givens, Elizabeth R Komosa, Juan E Abrahante Lloréns, Forum Kamdar, Branden S Moriarity, Beau R Webber, Bhairab N Singh, Brenda M Ogle

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
4.3field-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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Early Cytoskeletal Remodeling Drives Hypertrophic Cardiomyopathy Pathogenesis inJournal of cardiovascular development and disease · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Undetected Neuromuscular Disease in Patients after Heart Transplantation.International journal of molecular sciences · 2024
    Article
  13. Article
  14. Multiplexed Functional Assessments ofCirculation. Genomic and precision medicine · 2024
    Article
  15. Article
  16. Article
  17. Review
  18. Review
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 1 institution in 1 country.

Jeanne HsiehDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, MN, United States.
Kelsie L BecklinDepartment of Pediatrics, University of Minnesota, Minneapolis, MN, United States.
Sophie GivensDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, MN, United States.
Elizabeth R KomosaDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, MN, United States.
Juan E Abrahante LlorénsUniversity of Minnesota Informatics Institute (UMII), University of Minnesota, Minneapolis, MN, United States.
Forum KamdarDepartment of Medicine, University of Minnesota, Minneapolis, MN, United States.
Branden S MoriarityDepartment of Pediatrics, University of Minnesota, Minneapolis, MN, United States.
Beau R WebberDepartment of Pediatrics, University of Minnesota, Minneapolis, MN, United States.
Bhairab N SinghDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, MN, United States.
Brenda M OgleDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, MN, United States.
University of Minnesota · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

More than 60% of hypertrophic cardiomyopathy (HCM)-causing mutations are found in the gene loci encoding cardiac myosin-associated proteins including myosin heavy chain (MHC) and myosin binding protein C (MyBP-C). Moreover, patients with more than one independent HCM mutation may be at increased risk for more severe disease expression and adverse outcomes. However detailed mechanistic understanding, especially at early stages of disease progression, is limited. To identify early-stage HCM triggers, we generated single (

Indexed as

extracellular matrixgene editinghypertrophic cardiomyopathyintegrinsMYH6MYH7

Identifiers

PMID35784482
PMCPMC9245526
OpenAlexW4283016605

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.