Evidence map›Paper›PMID 35083019›Full record

ArticleCardiogenetics2022

Cardiovascular Characteristics of Patients with Genetic Variation in Desmoplakin (

Nosheen Reza, Alejandro de Feria, Jessica L Chowns, Lily Hoffman-Andrews, Laura Vann, Jessica Kim, Amy Marzolf, Anjali Tiku Owens

Open access · goldAbstract read
In one paragraph

Article in Cardiogenetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Homozygous NonsenseJournal of clinical medicine · 2026
    Article
  2. Identification of novel and known variants inFrontiers in cardiovascular medicine · 2026
    Article
  3. Review
  4. Article
  5. Heterozygous desmoplakin (BMJ case reports · 2024
    Article
  6. Article
  7. Review
  8. International journal of molecular sciences · 2023
    Article
  9. The Many Faces of Arrhythmogenic Cardiomyopathy: An Overview.The application of clinical genetics · 2023
    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

8 authors at 1 institution in 1 country.

Nosheen RezaDivision of Cardiovascular Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.
Alejandro de FeriaDivision of Cardiovascular Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.
Jessica L ChownsDivision of Cardiovascular Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.
Lily Hoffman-AndrewsDivision of Cardiovascular Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.
Laura VannDivision of Cardiovascular Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.
Jessica KimDivision of Cardiovascular Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.
Amy MarzolfDivision of Cardiovascular Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.
Anjali Tiku OwensDivision of Cardiovascular Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.
University of Pennsylvania · US

Funding

Institutional Clinical and Translational Science AwardKL2TR001879 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI MEAGHER, EMMA ANNE · 2016 to 2025
$13.7M
NRSA Training CoreTL1TR001880 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI MEAGHER, EMMA ANNE · 2016 to 2025
$10.0M
NCATS NIH HHS KL2 TR001879NCATS NIH HHS TL1 TR001880
6 · The paper itself

Abstract

backgroundVariants in the desmoplakin (

methodsWe aimed to evaluate the clinical manifestations of cardiac disease associated with variants in

resultsAmong individuals with disease-causing variants in

conclusionsOur data suggest

Indexed as

arrhythmiaarrhythmogenic cardiomyopathydesmoplakindilated cardiomyopathygeneticsgenotypeheart failurephenotype

Identifiers

PMID35083019
PMCPMC8785953
OpenAlexW4206569360

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.