Evidence map›Paper›PMID 36981019›Full record

ReviewGenes2023

Homozygous

Ugo Sorrentino, Ilaria Gabbiato, Chiara Canciani, Davide Calosci, Chiara Rigon, Daniela Zuccarello, Matteo Cassina

Open access · goldFull text readCase ReportsReview
In one paragraph

Review in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Fine tuning contractility: atrial sarcomere function in health and disease.American journal of physiology. Heart and circulatory physiology · 2024
    Review
  10. Article
  11. 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

7 authors at 1 institution in 1 country.

Ugo SorrentinoClinical Genetics Unit, Department of Women's and Children's Health, University of Padova, 35128 Padova, Italy.
Ilaria GabbiatoClinical Genetics Unit, Department of Women's and Children's Health, University of Padova, 35128 Padova, Italy.
Chiara CancianiClinical Genetics Unit, Department of Women's and Children's Health, University of Padova, 35128 Padova, Italy.
Davide CalosciClinical Genetics Unit, Department of Women's and Children's Health, University of Padova, 35128 Padova, Italy.
Chiara RigonClinical Genetics Unit, Department of Women's and Children's Health, University of Padova, 35128 Padova, Italy.
Daniela ZuccarelloClinical Genetics Unit, University Hospital of Padova, 35128 Padova, Italy.ORCID 0000-0001-5826-6715
Matteo CassinaClinical Genetics Unit, Department of Women's and Children's Health, University of Padova, 35128 Padova, Italy.ORCID 0000-0003-0270-1698
University of Padua · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The

Indexed as

Cardiomyopathy, DilatedHomozygoteHumansMutationMyocardiumTroponin ITroponin Iautosomal recessivecardiac failurecongenital cardiopathyloss of functionTNNI3

Identifiers

PMID36981019
PMCPMC10048074
OpenAlexW4327954642

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read8
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.