Evidence map›Paper›PMID 39826058›Full record

ArticleJournal of assisted reproduction and genetics2025

Correction: Uniparental disomy (UPD) exclusion in embryos following Preimplantation Genetic Testing for Structural Rearrangements (PGT-SR).

Marco Fabiani, Katia Margiotti, Francesco Libotte, Chiara Alì, Costanza Zangheri, Maria Antonietta Barone, Antonella Viola, Antonella Cima, Giovanna Buonomo, Danilo Cristofano and 5 more

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

Article in Journal of assisted reproduction and genetics, 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.

Marco FabianiDepartment of Human Genetic, Altamedica, Rome, Italy. marco.fabiani@artemisia.it.ORCID http://orcid.org/0000-0002-8763-0114
Katia MargiottiDepartment of Human Genetic, Altamedica, Rome, Italy.
Francesco LibotteDepartment of Human Genetic, Altamedica, Rome, Italy.
Chiara AlìDepartment of Human Genetic, Altamedica, Rome, Italy.
Costanza ZangheriDepartment of Human Genetic, Altamedica, Rome, Italy.
Maria Antonietta BaroneDepartment of Human Genetic, Altamedica, Rome, Italy.
Antonella ViolaDepartment of Human Genetic, Altamedica, Rome, Italy.
Antonella CimaDepartment of Human Genetic, Altamedica, Rome, Italy.
Giovanna BuonomoDepartment of Reproductive Medicine, Altamedica, Fetal-Maternal Medical Centre, Rome, Italy.
Danilo CristofanoDepartment of Reproductive Medicine, Altamedica, Fetal-Maternal Medical Centre, Rome, Italy.
Assunta LippaDepartment of Reproductive Medicine, Altamedica, Fetal-Maternal Medical Centre, Rome, Italy.
Chiara PasqualeDepartment of Reproductive Medicine, Altamedica, Fetal-Maternal Medical Centre, Rome, Italy.
Mario Montanino OlivaDepartment of Reproductive Medicine, Altamedica, Fetal-Maternal Medical Centre, Rome, Italy.
Alvaro MesoracaDepartment of Human Genetic, Altamedica, Rome, Italy.
Claudio GiorlandinoDepartment of Human Genetic, Altamedica, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID39826058
PMCPMC11871272

What OpenQuestion holds

Textmetadata
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.