Evidence map›Paper›PMID 42728323›Full record

ArticleEuropean journal of human genetics : EJHG2026

Correction: Hemizygous loss-of-function variants of EIF1AX are associated with a syndromic neurodevelopmental disorder.

Kazuyuki Komatsu, Atsushi Sugie, Yohei Nitta, Jiro Osaka, Ummul Halilunnisa Mansoor Hussain, Mitsuru Kubota, Nobuyuki Shimozawa, Melissa T Carter, Petra J G Zwijnenburg, Quinten Waisfisz and 4 more

Abstract readPublished Erratum
PubMed Publisher
In one paragraph

Article in European journal of human genetics : EJHG, 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

14 authors.

Kazuyuki KomatsuDepartment of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu, Japan.ORCID http://orcid.org/0000-0001-9861-8412
Atsushi SugieBrain Research Institute, Niigata University, Niigata, Japan. sugie@kit.ac.jp.ORCID http://orcid.org/0000-0002-2090-8839
Yohei NittaBrain Research Institute, Niigata University, Niigata, Japan.ORCID http://orcid.org/0000-0002-0712-428X
Jiro OsakaBrain Research Institute, Niigata University, Niigata, Japan.
Ummul Halilunnisa Mansoor HussainDepartment of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Mitsuru KubotaDepartment of General Pediatrics and Interdisciplinary Medicine, National Center for Child Health and Development, Tokyo, Japan.ORCID http://orcid.org/0000-0002-5395-8226
Nobuyuki ShimozawaDivision of Genomics Research, Life Science Research Center, Gifu University, Gifu, Japan.
Melissa T CarterDepartment of Genetics, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON, Canada.
Petra J G ZwijnenburgDepartment of Human Genetics, Emma Center for Personalized Medicine, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.
Quinten WaisfiszDepartment of Human Genetics, Emma Center for Personalized Medicine, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.
Felix BoschannInstitute of Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.ORCID http://orcid.org/0000-0001-9410-9290
Denise HornInstitute of Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
Mitsuko NakashimaDepartment of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu, Japan. sb8901@cc.saga-u.ac.jp.
Hirotomo SaitsuDepartment of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu, Japan.ORCID http://orcid.org/0000-0003-0723-0960

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID42728323

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.