Evidence map›Paper›PMID 27081529›Full record

ArticleHuman genome variation2015

6q21-22 deletion syndrome with interrupted aortic arch.

Ayumi Matsumoto, Yasuyuki Nozaki, Takaomi Minami, Eriko F Jimbo, Hirohiko Shiraishi, Takanori Yamagata

Open access · goldAbstract read
In one paragraph

Article in Human genome variation, 2015. 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
0.5field-weighted citation impact, top 24% 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. Histone deacetylase 1 and 2 are essential for murine neural crest proliferation, pharyngeal arch development, and craniofacial morphogenesis.Developmental dynamics : an official publication of the American Association of Anatomists · 2017
    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

6 authors at 1 institution in 1 country.

Ayumi MatsumotoDepartment of Pediatrics, Jichi Medical University , Tochigi, Japan.
Yasuyuki NozakiDepartment of Pediatrics, Jichi Medical University , Tochigi, Japan.
Takaomi MinamiDepartment of Pediatrics, Jichi Medical University , Tochigi, Japan.
Eriko F JimboDepartment of Pediatrics, Jichi Medical University , Tochigi, Japan.
Hirohiko ShiraishiDepartment of Pediatrics, Jichi Medical University , Tochigi, Japan.
Takanori YamagataDepartment of Pediatrics, Jichi Medical University , Tochigi, Japan.
Jichi Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interstitial deletion of 6q21-22 has been previously reported in 11 individuals, who presented with intellectual disability, facial dysmorphism, cardiac abnormality, cerebellar hypoplasia and dysplasia of the corpus callosum. Here, we report the first instance of a patient with 6q21-22 deletion presenting with interrupted aortic arch in addition to the previously described clinical signs. Array analysis using Agilent Human genome CGH 180K identified a 13.3-Mb deletion at 6q21-q22.31 (nt. 109885195-123209593).

Identifiers

PMID27081529
PMCPMC4785536
OpenAlexW2485653215

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.