Evidence map›Paper›PMID 39587357›Full record

ArticleEuropean journal of human genetics : EJHG2025

Correction: Slowly progressive autosomal dominant Alport Syndrome due to COL4A3 splicing variant.

Sergio Daga, Lorenzo Loberti, Giulia Rollo, Loredaria Adamo, Olga Lorenza Colavecchio, Giulia Brunelli, Kristina Zguro, Sergio Antonio Tripodi, Andrea Guarnieri, Guido Garosi and 5 more

Abstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in European journal of human genetics : EJHG, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Sergio Daga *Medical Genetics, University of Siena, Siena, Italy.ORCID http://orcid.org/0000-0002-6419-9456
Lorenzo Loberti *Medical Genetics, University of Siena, Siena, Italy.ORCID http://orcid.org/0000-0001-5020-8393
Giulia RolloMedical Genetics, University of Siena, Siena, Italy.
Loredaria AdamoMedical Genetics, University of Siena, Siena, Italy.
Olga Lorenza ColavecchioGenetica Medica, Azienda Ospedaliero-Universitaria Senese, Siena, Italy.
Giulia BrunelliMedical Genetics, University of Siena, Siena, Italy.
Kristina ZguroMedical Genetics, University of Siena, Siena, Italy.
Sergio Antonio TripodiDepartment of Pathology, AOUS, Siena, Italy.
Andrea GuarnieriDepartment of Medical Sciences, Nephrology, Dialysis and Transplantation Unit, University Hospital of Siena, Siena, Italy.
Guido GarosiDepartment of Medical Sciences, Nephrology, Dialysis and Transplantation Unit, University Hospital of Siena, Siena, Italy.
Romina D'AurizioInstitute of Informatics and Telematics, CNR, Pisa, Italy.ORCID http://orcid.org/0000-0002-1728-6397
Francesca ArianiMedical Genetics, University of Siena, Siena, Italy.
Rossella TitaGenetica Medica, Azienda Ospedaliero-Universitaria Senese, Siena, Italy.
Alessandra RenieriMedical Genetics, University of Siena, Siena, Italy. alessandra.renieri@unisi.it.ORCID http://orcid.org/0000-0002-0846-9220
Anna Maria PintoGenetica Medica, Azienda Ospedaliero-Universitaria Senese, Siena, Italy. annamaria.pinto@dbm.unisi.it.ORCID http://orcid.org/0000-0001-6259-6901

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID39587357
PMCPMC11985972

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.