Evidence map›Paper›PMID 37308473›Full record

ArticleHuman genome variation2023

Oculofaciocardiodental syndrome caused by a novel BCOR variant.

Tomoyo Yamashita, Junko Hotta, Yukiko Jogu, Eri Sakai, Chie Ono, Haruka Bamba, Hisato Suzuki, Mamiko Yamada, Toshiki Takenouchi, Kenjiro Kosaki and 3 more

Open access · goldAbstract read
In one paragraph

Article in Human genome variation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

13 authors at 4 institutions in 1 country.

Tomoyo YamashitaDepartment of Medical Genetics, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Junko HottaDepartment of Medical Genetics, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Yukiko JoguDepartment of Medical Genetics, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Eri SakaiDepartment of Medical Genetics, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Chie OnoDepartment of Medical Genetics, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Haruka BambaDepartment of Medical Genetics, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Hisato SuzukiCenter for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
Mamiko YamadaCenter for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
Toshiki TakenouchiDepartment of Pediatrics, Keio University School of Medicine, Tokyo, Japan.ORCID http://orcid.org/0000-0002-7311-4135
Kenjiro KosakiCenter for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
Tohru YorifujiDivision of Pediatric Endocrinology and Metabolism, Children's Medical Center, Osaka City General Hospital, Osaka, Japan.
Takashi HamazakiDepartment of Pediatrics, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Toshiyuki SetoDepartment of Medical Genetics, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan. setot@omu.ac.jp.
Osaka Metropolitan University · JPKeio University · JPOsaka City General Hospital · JPOsaka City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oculofaciocardiodental syndrome is caused by variants in the BCL6 corepressor (BCOR) gene. We identified a novel heterozygous frameshift variant, NM_001123385.2(BCOR):c.2326del, that arose de novo in a Japanese girl with characteristic facial features, congenital heart disease, bilateral syndactyly of toes 2 and 3, congenital cataracts, dental abnormalities, and mild intellectual disability. Reports of BCOR variants are rare, and further case accumulation is warranted.

Identifiers

PMID37308473
PMCPMC10261115
OpenAlexW4380364271

What OpenQuestion holds

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LicenceCC BY
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.