Evidence map›Paper›PMID 40149474›Full record

ArticleGenes2025

Long-Term Phenotypic Evolution in GRIN2A-Related Disorders: Electroclinical and Genetic Insights from Two Families with Extended Follow-Up.

Ester Di Muro, Pietro Palumbo, Massimo Carella, Mario Benvenuto, Maria Rachele Bianchi, Umberto Costantino, Giovanni Di Maggio, Marco Castori, Giuseppe d'Orsi, Orazio Palumbo

Abstract readCase Reports
In one paragraph

Article in Genes, 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

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

10 authors.

Ester Di MuroUOC Genetica Medica, Fondazione IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo, FG, Italy.ORCID 0000-0002-2588-9841
Pietro PalumboUOC Genetica Medica, Fondazione IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo, FG, Italy.ORCID 0000-0001-9498-9902
Massimo CarellaUOC Genetica Medica, Fondazione IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo, FG, Italy.ORCID 0000-0002-6830-6829
Mario BenvenutoUOC Genetica Medica, Fondazione IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo, FG, Italy.
Maria Rachele BianchiEpilepsy Center-Neurological Unit, Fondazione IRCCS Casa Sollievo della Sofferenza, Viale Cappuccini, 71013 San Giovanni Rotondo, FG, Italy.
Umberto CostantinoEpilepsy Center-Neurological Unit, Fondazione IRCCS Casa Sollievo della Sofferenza, Viale Cappuccini, 71013 San Giovanni Rotondo, FG, Italy.ORCID 0000-0003-2325-4137
Giovanni Di MaggioEpilepsy Center-Neurological Unit, Fondazione IRCCS Casa Sollievo della Sofferenza, Viale Cappuccini, 71013 San Giovanni Rotondo, FG, Italy.
Marco CastoriUOC Genetica Medica, Fondazione IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo, FG, Italy.
Giuseppe d'OrsiEpilepsy Center-Neurological Unit, Fondazione IRCCS Casa Sollievo della Sofferenza, Viale Cappuccini, 71013 San Giovanni Rotondo, FG, Italy.
Orazio PalumboUOC Genetica Medica, Fondazione IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo, FG, Italy.ORCID 0000-0001-6583-3482

Funding

European Union PNRR-MR1-2023-12377843
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

EpilepsyNeurodevelopmental DisordersReceptors, N-Methyl-D-AspartateAdultElectroencephalographyFollow-Up StudiesGenetic Association StudiesHumansMalePedigreePhenotypeYoung AdultReceptors, N-Methyl-D-Aspartatebehavioral disorderscognitive impairmentelectroencephalographyepilepsyGRIN2Along-term follow-upneurodevelopmental disorderstargeted resequencing

Identifiers

PMID40149474
PMCPMC11941913

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.