Evidence map›Paper›PMID 42026184›Full record

ArticleNature genetics2026

Publisher Correction: Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder.

Daniel Greene, Rodrigo Mendez, Jon Lees, Mafalda Barbosa, Alessandro Bruselles, Luigi Chiriatti, Federico Ferraro, Cecilia Mancini, Rachel Schot, Frank Sleutels and 21 more

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

Article in Nature genetics, 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

5 · Who and what money

Authors and funding

31 authors.

Daniel Greene *Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Rodrigo Mendez *Department of Medicine, Stanford University, Stanford, CA, USA.
Jon LeesBristol Medical School, University of Bristol, Bristol, UK.
Mafalda BarbosaDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Alessandro BrusellesOncology and Molecular Medicine, Istituto Superiore di Sanità, Rome, Italy.ORCID http://orcid.org/0000-0002-1556-4998
Luigi ChiriattiMolecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Federico FerraroDepartment of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, the Netherlands.ORCID http://orcid.org/0000-0003-1365-2529
Cecilia ManciniMolecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Rachel SchotDepartment of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, the Netherlands.ORCID http://orcid.org/0000-0001-9578-4095
Frank SleutelsDepartment of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, the Netherlands.ORCID http://orcid.org/0000-0001-6813-5209
Enrico BertiniMuscular and Neurodegenerative Disorders, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID http://orcid.org/0000-0001-9276-4590
Devon E BonnerDepartment of Pediatrics, Stanford University, Stanford, CA, USA.
Arjan BoumanDepartment of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, the Netherlands.
Alice S BrooksDepartment of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, the Netherlands.
T Homas A CassiniVanderbilt University Medical Center, Nashville, TN, USA.
Kimberly M EzellVanderbilt University Medical Center, Nashville, TN, USA.
Natalia Gomez-OspinaDepartment of Pediatrics, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-6740-1154
Tjitske KleefstraDepartment of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, the Netherlands.
Michael O'DonoghueNeurology, Nottingham University Hospital NHS Trust, Nottingham, UK.
Lynette RivesVanderbilt University Medical Center, Nashville, TN, USA.
Vandana ShashiDuke University School of Medicine, Durham, NC, USA.
Rebecca C SpillmannDuke University School of Medicine, Durham, NC, USA.
Mohamed WafikGuy's and St Thomas' NHS Foundation Trust, London, UK.ORCID http://orcid.org/0000-0002-9622-5268
Undiagnosed Diseases Network
Kathleen FresonDepartment of Cardiovascular Sciences, Center for Molecular and Vascular Biology, KU Leuven, Leuven, Belgium.ORCID http://orcid.org/0000-0002-4381-2442
Tahsin Stefan BarakatDepartment of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, the Netherlands.ORCID http://orcid.org/0000-0003-1231-1562
Marco TartagliaMolecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID http://orcid.org/0000-0001-7736-9672
Jonathan A BernsteinDepartment of Pediatrics, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0001-5369-346X
Andrew D MumfordBristol Medical School, University of Bristol, Bristol, UK.
Matthew T WheelerDepartment of Medicine, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0001-8721-3022
Ernest TurroDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA. ernest.turro@mssm.edu.ORCID http://orcid.org/0000-0002-1820-6563

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID42026184
PMCPMC13175887

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.