Evidence map›Paper›PMID 42758868›Full record

ArticleHepatology communications2026

Genetic testing and exchangeable copper can improve the accuracy of Wilson disease diagnoses.

Marina Berenguer, Mercè Torra, Carmen Espinós, Rocío Andreu Escrivá, Anna Pocurull, Ângela Carvalho-Gomes, Anna Miralpeix, Gustavo Rojas Echarry, Sarai Romero-Moreno, Clara Sanchez and 6 more

Abstract read
In one paragraph

Article in Hepatology communications, 2026. 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

16 authors.

Marina BerenguerHepatology Unit, Department of Gastroenterology, La Fe University Hospital, Valencia, Spain.ORCID 0000-0001-9246-4264
Mercè TorraBiochemistry and Molecular Genetics Unit, Hospital Clínic Barcelona, IDIBAPS, Barcelona, Spain.ORCID 0000-0002-0851-7720
Carmen EspinósCentro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.ORCID 0000-0003-4435-1809
Rocío Andreu EscriváClinical Laboratory Unit, La Fe University Hospital, Valencia, Spain.ORCID 0009-0004-1301-1793
Anna PocurullLiver Unit, Hospital Clínic, IDIBAPS, Universitat de Barcelona, Barcelona, Spain.ORCID 0000-0002-1970-1822
Ângela Carvalho-GomesHepatology Unit, Department of Gastroenterology, La Fe University Hospital, Valencia, Spain.ORCID 0000-0001-5424-3479
Anna MiralpeixLiver Unit, Hospital Clínic, IDIBAPS, Universitat de Barcelona, Barcelona, Spain.ORCID 0000-0002-1265-0380
Gustavo Rojas EcharryDepartment of Pathology, La Fe University Hospital, Valencia, Spain.ORCID 0009-0006-8775-5335
Sarai Romero-MorenoHepatology Unit, Department of Gastroenterology, La Fe University Hospital, Valencia, Spain.ORCID 0009-0004-8692-3179
Clara SanchezHepatology Unit, Department of Gastroenterology, La Fe University Hospital, Valencia, Spain.ORCID 0009-0009-0985-4807
Eva SilgoHepatology Unit, Department of Gastroenterology, La Fe University Hospital, Valencia, Spain.
Christian Palacios-MartínezLaboratory of Rare Neurodegenerative Diseases, Centro de Investigación Príncipe Felipe, Valencia, Spain.
Celia BadenasBiochemistry and Molecular Genetics Unit, Hospital Clínic Barcelona, IDIBAPS, Barcelona, Spain.
Judith Perez-RojasDepartment of Pathology, La Fe University Hospital, Valencia, Spain.ORCID 0000-0002-6091-0888
Cristina Aguado CodinaClinical Laboratory Unit, La Fe University Hospital, Valencia, Spain.
Zoe MariñoCentro de Investigacion Biomedica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.ORCID 0000-0001-6321-9534

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

ATP7Bceruloplasmincirrhosisgeneticsliver diseaseneurology

Identifiers

PMID42758868
PMCPMC13592991

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.