Evidence map›Paper›PMID 32047638›Full record

ArticleHuman genome variation2020

Novel

Nao Takizaki, Yoshinori Tsurusaki, Kaoru Katsumata, Yumi Enomoto, Hiroaki Murakami, Koji Muroya, Hiroshi Ishikawa, Noriko Aida, Gen Nishimura, Kenji Kurosawa

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

Article in Human genome variation, 2020. 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
0.4field-weighted citation impact, top 41% 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, 8 citations in OpenAlex.

  1. 3-M syndrome: evolution of the phenotype over time.Italian journal of pediatrics · 2025
    Review
  2. Article
  3. Recognition Method of Wushu Human Complex Movement Based on Bone Point Feature.Computational and mathematical methods in medicine · 2022
    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 2 institutions in 1 country.

Nao Takizaki1Division of Medical Genetics, Kanagawa Children's Medical Center, Yokohama, Japan.
Yoshinori Tsurusaki2Clinical Research Institute, Kanagawa Children's Medical Center, Yokohama, Japan.
Kaoru Katsumata3Department of Neonatology, Kanagawa Children's Medical Center, Yokohama, Japan.
Yumi Enomoto2Clinical Research Institute, Kanagawa Children's Medical Center, Yokohama, Japan.
Hiroaki Murakami1Division of Medical Genetics, Kanagawa Children's Medical Center, Yokohama, Japan.
Koji Muroya4Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center, Yokohama, Japan.
Hiroshi Ishikawa5Department of Obstetrics and Gynecology, Kanagawa Children's Medical Center, Yokohama, Japan.
Noriko Aida6Intractable Disease Center, Saitama Medical University Hospital, Saitama, Japan.
Gen Nishimura7Department of Radiology, Kanagawa Children's Medical Center, Yokohama, Japan.
Kenji Kurosawa1Division of Medical Genetics, Kanagawa Children's Medical Center, Yokohama, Japan.ORCID 0000-0002-6817-7748
Kanagawa Children's Medical Center · JPSaitama Medical University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

3M syndrome is an autosomal recessive disorder characterized by severe growth retardation, distinct facial features, and skeletal changes, including long slender tubular bones and tall vertebral bodies. We report a Japanese patient with 3M syndrome caused by the biallelic novel variants c.1705_1708del and c.1989_1999del of

Indexed as

BoneGrowth disorders

Identifiers

PMID32047638
PMCPMC7000808
OpenAlexW3004364356

What OpenQuestion holds

Textmetadata
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.