Evidence map›Paper›PMID 32190315›Full record

ArticleMolecular and clinical oncology2020

Infantile macrocephaly and multiple subcutaneous lipomas diagnosed with

Yuka Yotsumoto, Atsuko Harada, Jiro Tsugawa, Yoshihiro Ikura, Hidetsuna Utsunomiya, Satoko Miyatake, Naomichi Matsumoto, Yonehiro Kanemura, Tomoko Hashimoto-Tamaoki

Open access · diamondAbstract read
In one paragraph

Article in Molecular and clinical oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 47% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. PTEN hamartoma tumor syndrome: Clinical and genetic characterization in pediatric patients.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2024
    Article
  5. Review
  6. 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

9 authors at 3 institutions in 1 country.

Yuka YotsumotoDepartment of Pediatrics, Takatsuki General Hospital, Takatsuki, Osaka 569-1192, Japan.
Atsuko HaradaDepartment of Genetic Medicine, Takatsuki General Hospital, Takatsuki, Osaka 569-1192, Japan.
Jiro TsugawaDepartment of Pediatric Surgery, Takatsuki General Hospital, Takatsuki, Osaka 569-1192, Japan.
Yoshihiro IkuraDepartment of Pathology, Takatsuki General Hospital, Takatsuki, Osaka 569-1192, Japan.
Hidetsuna UtsunomiyaDepartment of Pediatric Neuroradiology, Takatsuki General Hospital, Takatsuki, Osaka 569-1192, Japan.
Satoko MiyatakeDepartment of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.
Naomichi MatsumotoDepartment of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.
Yonehiro KanemuraDepartment of Neurosurgery, National Hospital Organization Osaka National Hospital, Osaka 540-0006, Japan.
Tomoko Hashimoto-TamaokiDepartment of Genetic Medicine, Takatsuki General Hospital, Takatsuki, Osaka 569-1192, Japan.
Takatsuki General Hospital · JPYokohama City University · JPOsaka National Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A heterozygous loss-of-function mutation of the

Indexed as

autism spectrum disorderCowden syndromelipomamacrocephalyPTENPTEN hamartoma tumor syndrome

Identifiers

PMID32190315
PMCPMC7058917
OpenAlexW3004360357

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.