Evidence map›Paper›PMID 41718420›Full record

ArticleInternational journal of neonatal screening2026

Neonatal Genetic Screening Results for Spinal Muscular Atrophy in Romania: Insights from a 3-Years Pilot Program.

Madalina Cristina Leanca, Gelu Onose, Georgiana Nicolae, Elena Neagu, Daniela Vasile, Ecaterina Bercu, Oana Mirabela Balanescu, Andrei Capitanescu, Constantin Munteanu, Cristina Popescu and 1 more

Abstract read
In one paragraph

Article in International journal of neonatal screening, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Madalina Cristina LeancaFaculty of Medicine, University of Medicine and Pharmacy "Carol Davila", 37 Dionisie Lupu Street, 020021 Bucharest, Romania.
Gelu OnoseFaculty of Medicine, University of Medicine and Pharmacy "Carol Davila", 37 Dionisie Lupu Street, 020021 Bucharest, Romania.ORCID 0000-0002-6346-8941
Georgiana NicolaeFaculty of Medicine, University of Medicine and Pharmacy "Carol Davila", 37 Dionisie Lupu Street, 020021 Bucharest, Romania.ORCID 0000-0001-6028-2407
Elena NeaguGenetics Laboratory, National University Center for Children Neurorehabilitation "Robanescu-Padure", 44 Dumitru Minca Street, 041408 Bucharest, Romania.ORCID 0009-0008-7300-528X
Daniela VasileGenetics Laboratory, National University Center for Children Neurorehabilitation "Robanescu-Padure", 44 Dumitru Minca Street, 041408 Bucharest, Romania.
Ecaterina BercuGenetics Laboratory, National University Center for Children Neurorehabilitation "Robanescu-Padure", 44 Dumitru Minca Street, 041408 Bucharest, Romania.
Oana Mirabela BalanescuGenetics Laboratory, National University Center for Children Neurorehabilitation "Robanescu-Padure", 44 Dumitru Minca Street, 041408 Bucharest, Romania.
Andrei CapitanescuChildren's Emergency Clinical Hospital "Maria Sklodowska Curie", 20 Constantin Brancoveanu, 075534 Bucharest, Romania.ORCID 0000-0003-2183-0727
Constantin MunteanuTeaching Emergency Hospital "Bagdasar-Arseni", 12 Berceni Avenue, 041915 Bucharest, Romania.ORCID 0000-0002-1084-7710
Cristina PopescuFaculty of Medicine, University of Medicine and Pharmacy "Carol Davila", 37 Dionisie Lupu Street, 020021 Bucharest, Romania.
Andrada MireaFaculty of Medicine, University of Medicine and Pharmacy "Carol Davila", 37 Dionisie Lupu Street, 020021 Bucharest, Romania.ORCID 0009-0008-0532-2021

Funding

"Publication of this paper was supported by the University of Medicine and Pharmacy "Carol Davila" through the institutional program Publish not Perish" not applicable
6 · The paper itself

Abstract

Spinal muscular atrophy (SMA) is a severe genetic neuromuscular disorder caused by bi-allelic deletions or pathogenic

Indexed as

early diagnosisgenetic testingneonatal screeningRomanian pilot programspinal muscular atrophy

Identifiers

PMID41718420
PMCPMC12957999

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.