Evidence map›Paper›PMID 39493792›Full record

ArticleClinical case reports2024

Xiaoli Du, Cara L Barnett, Kimberly M Widmeyer, Xinjian Wang, Diana S Brightman, Carolee W Noonan, Kathryn N Weaver, Robert J Hopkin, Yaning Wu

Abstract read
In one paragraph

Article in Clinical case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Genetic landscape of phospholamban cardiomyopathies.Frontiers in cell and developmental biology · 2025
    Review
  4. Clinical case reports · 2024
    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.

Xiaoli DuDivision of Human Genetics Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA.
Cara L BarnettDivision of Human Genetics Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA.
Kimberly M WidmeyerDivision of Human Genetics Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA.
Xinjian WangDivision of Human Genetics Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA.
Diana S BrightmanDivision of Human Genetics Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA.
Carolee W NoonanDivision of Human Genetics Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA.
Kathryn N WeaverDivision of Human Genetics, Department of Pediatrics, Cincinnati Children's Hospital Medical Center University of Cincinnati College of Medicine Cincinnati Ohio USA.ORCID https://orcid.org/0000-0002-3991-135X
Robert J HopkinDivision of Human Genetics, Department of Pediatrics, Cincinnati Children's Hospital Medical Center University of Cincinnati College of Medicine Cincinnati Ohio USA.
Yaning WuDivision of Human Genetics, Department of Pediatrics, Cincinnati Children's Hospital Medical Center University of Cincinnati College of Medicine Cincinnati Ohio USA.ORCID https://orcid.org/0000-0002-5591-9335

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have established an association between

Indexed as

dual diagnosishearing lossovarian insufficiencyPerrault syndromePLN (phospholamban)RMND1 (required for meiotic nuclear division 1 homolog)

Identifiers

PMID39493792
PMCPMC11527736

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.