Evidence map›Paper›PMID 35154713›Full record

ArticleClinical case reports2022

Family with congenital contractural arachnodactyly due to a novel multiexon deletion of the

Hiroki Yagi, Hiroshi Takiguchi, Norifumi Takeda, Ryo Inuzuka, Yuki Taniguchi, Kristine Joyce Porto, Hiroyuki Ishiura, Jun Mitsui, Hiroyuki Morita, Issei Komuro

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

Article in Clinical case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. ACase reports in genetics · 2024
    Article
  3. 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

10 authors at 1 institution in 1 country.

Hiroki YagiDepartment of Cardiovascular Medicine The University of Tokyo Hospital Tokyo Japan.
Hiroshi TakiguchiDepartment of Cardiovascular Medicine The University of Tokyo Hospital Tokyo Japan.
Norifumi TakedaDepartment of Cardiovascular Medicine The University of Tokyo Hospital Tokyo Japan.ORCID https://orcid.org/0000-0003-4818-3347
Ryo InuzukaMarfan Syndrome Center The University of Tokyo Hospital Tokyo Japan.
Yuki TaniguchiMarfan Syndrome Center The University of Tokyo Hospital Tokyo Japan.
Kristine Joyce PortoDepartment of Neurology The University of Tokyo Hospital Tokyo Japan.
Hiroyuki IshiuraDepartment of Neurology The University of Tokyo Hospital Tokyo Japan.
Jun MitsuiDepartment of Neurology The University of Tokyo Hospital Tokyo Japan.
Hiroyuki MoritaDepartment of Cardiovascular Medicine The University of Tokyo Hospital Tokyo Japan.
Issei KomuroDepartment of Cardiovascular Medicine The University of Tokyo Hospital Tokyo Japan.
University of Tokyo Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital contractural arachnodactyly (CCA) is caused by pathogenic

Indexed as

array‐CGHBeals syndromecamptodactylycopy number variationintegrative genomics viewer

Identifiers

PMID35154713
PMCPMC8826123
OpenAlexW4210869222

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.