Evidence map›Paper›PMID 41820113›Full record

ArticleBiochimica et biophysica acta. Molecular basis of disease2026

Corrigendum to "Novel VARS1 variants define new clinical and molecular subtypes of a rare neurodevelopmental syndrome" [Biochim. Biophys. Acta Mol. Basis Dis. 1872 (2026)/168184].

Busra Aynekin, Tracy Lau, Rauan Kaiyrzhanov, Ioannis Papazoglou, Ayten Gulec, Ummu Gulsum Ozgul Gumus, Svetlana Gorokhova, Busa Tiffany, Leonardo Simão Medeiros, Ida Vanessa Doederlein Schwartz and 13 more

Abstract readPublished Erratum
PubMed Publisher
In one paragraph

Article in Biochimica et biophysica acta. Molecular basis of disease, 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

23 authors.

Busra AynekinDepartment of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK; Department of Molecular Biology and Genetics, Biruni University, 34015, Istanbul, Türkiye.
Tracy LauDepartment of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.
Rauan KaiyrzhanovDepartment of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.
Ioannis PapazoglouLaboratory for Innovative Drugs (Lab4IND), Computational Drug Design Center (HİTMER), Bahçeşehir University, 34734, İstanbul, Türkiye.
Ayten GulecDepartment of Pediatrics, Erciyes University, Faculty of Medicine, Kayseri, Turkey.
Ummu Gulsum Ozgul GumusDepartment of Pediatrics, Erciyes University, Faculty of Medicine, Kayseri, Turkey.
Svetlana GorokhovaDepartment of Medical Genetics, Timone Children's Hospital, APHM, Marseille, France.
Busa TiffanyDepartment of Medical Genetics, Timone Children's Hospital, APHM, Marseille, France.
Leonardo Simão MedeirosMedical Genetics Service-Hospital de Clinicas de Porto Alegre-Brazil, Porto Alegre, RS, Brazil.
Ida Vanessa Doederlein SchwartzMedical Genetics Service-Hospital de Clinicas de Porto Alegre-Brazil, Porto Alegre, RS, Brazil.
Mehmet Burak MutluDepartment of Medical Genetics, Detagen Genetic Diseases Evaluation Center, Kayseri, Türkiye.
Sofia OuraniClinical Genetics Department, Archbishop Makarios III Hospital, Nicosia, Cyprus.
Anke BergmanHannover Medical School, Institute of Human Genetics, Hannover, Germany.
Kelly SchochDivision of Medical Genetics, Pediatrics, Duke University School of Medicine, Durham, NC, USA.
Huseyin PerDepartment of Pediatrics, Erciyes University, Faculty of Medicine, Kayseri, Turkey.
Nurdeniz Nalbant BingolDepartment of Translational Medicine, Institute of Health Sciences, Bursa Uludag University, Bursa, Türkiye.
Sehime G TemelDepartment of Translational Medicine, Institute of Health Sciences, Bursa Uludag University, Bursa, Türkiye; Department of Medical Genetics, Faculty of Medicine, Bursa Uludag University, Bursa, Türkiye; Department of Histology and Embryology, Faculty of Medicine, Bursa Uludag University, Bursa, Türkiye.
Serdar DurdağıLaboratory for Innovative Drugs (Lab4IND), Computational Drug Design Center (HİTMER), Bahçeşehir University, 34734, İstanbul, Türkiye; Molecular Therapy Lab, Department of Pharmaceutical Chemistry, School of Pharmacy, Bahcesehir University, Istanbul, Türkiye; Systems Biology Lab, Biruni University Scientific Research Center, Biruni University, Istanbul, Türkiye. Electronic address: serdar.durdagi@bau.edu.tr.
Semra HızDepartment of Pediatric Neurology, Faculty of Medicine, Dokuz Eylül University, Izmir, 35340, Turkey.
Geneviève BernardDepartment of Neurology and Neurosurgery, McGill University, Montreal, Canada; Department of Pediatrics, McGill University, Montreal, Canada; Child Health and Human Development Program, McGill University Health Centre Research Institute, Montreal, Canada; Department Specialized Medicine, Division of Medical Genetics, McGill University Health Centre, Montreal, Canada; Department of Human Genetics, McGill University, Montreal, Canada.
Felipe Villa TobonDepartment of Neurology and Neurosurgery, McGill University, Montreal, Canada.
Henry HouldenDepartment of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK. Electronic address: h.houlden@ucl.ac.uk.
Stephanie EfthymiouDepartment of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK. Electronic address: s.efthymiou@ucl.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID41820113

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.