Evidence map›Paper›PMID 36967720›Full record

ArticleMolecular genetics and metabolism reports2023

Association between maternally inherited deafness, epilepsy, and intellectual disability and the m.12207G > A

Sayaka Suzuki-Ajihara, Megumi Saito-Tsuruoka, Hiroko Harashima, Katsumi Arai, Hiroyoshi Koide, Yukiko Yatsuka, Atsuko Imai-Okazaki, Yasushi Okazaki, Kei Murayama, Chikahiko Numakura and 2 more

Open access · goldFull text readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Molecular genetics and metabolism reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 98% of its field
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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. A novel tRNASer(AGY) 12244G > a variant impairs mitochondrial function and presents with classical MELAS phenotype.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Article
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

12 authors at 5 institutions in 1 country.

Sayaka Suzuki-AjiharaDepartment of Pediatrics, Saitama Medical University, Saitama, Japan.
Megumi Saito-TsuruokaDepartment of Clinical Genomics, Saitama Medical University, Saitama, Japan.
Hiroko HarashimaDepartment of Pediatrics, Saitama Medical University, Saitama, Japan.
Katsumi AraiHello Clinic, Saitama, Japan.
Hiroyoshi KoideHello Clinic, Saitama, Japan.
Yukiko YatsukaDiagnosis and Therapeutics of Intractable Diseases, Intractable Disease Research Center, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Atsuko Imai-OkazakiDiagnosis and Therapeutics of Intractable Diseases, Intractable Disease Research Center, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Yasushi OkazakiDiagnosis and Therapeutics of Intractable Diseases, Intractable Disease Research Center, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Kei MurayamaDepartment of Metabolism, Chiba Children's Hospital, Chiba, Japan.
Chikahiko NumakuraDepartment of Pediatrics, Saitama Medical University, Saitama, Japan.
Yuko AkiokaDepartment of Pediatrics, Saitama Medical University, Saitama, Japan.
Akira OhtakeDepartment of Pediatrics, Saitama Medical University, Saitama, Japan.
Saitama Medical University · JPJuntendo University · JPSaitama Medical University Hospital · JPSaitama Prefecture · JPChiba Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The identification of the m.12207G > A variant in

Indexed as

DeafnessDiabetes mellitusEpilepsyM.12207G > A MT-TS2Maternal inheritance

Identifiers

PMID36967720
PMCPMC10034148
OpenAlexW4327757278

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read9
identifiers read1
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.