Evidence map›Paper›PMID 31263565›Full record

ArticleHuman genome variation2019

A girl with CLOVES syndrome with a recurrent

Hiroaki Hanafusa, Naoya Morisada, Tadashi Nomura, Daisuke Kobayashi, Yoshinobu Akasaka, Ming Juan Ye, Kandai Nozu, Noriyuki Nishimura, Kazumoto Iijima, Hideto Nakao

Open access · goldAbstract read
In one paragraph

Article in Human genome variation, 2019. 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
0.7field-weighted citation impact, top 29% 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. Review
  2. Article
  3. A Review on Cutaneous and Musculoskeletal Manifestations of CLOVES Syndrome.Clinical, cosmetic and investigational dermatology · 2022
    Review
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.

Hiroaki HanafusaDepartment of Clinical Genetics, Hyogo Prefectural Children's Hospital, Kobe, Japan.
Naoya MorisadaDepartment of Clinical Genetics, Hyogo Prefectural Children's Hospital, Kobe, Japan.
Tadashi Nomura3Department of Plastic Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.
Daisuke KobayashiDepartment of Orthopaedic Surgery, Hyogo Prefectural Children's Hospital, Kobe, Japan.
Yoshinobu AkasakaDepartment of Radiology, Hyogo Prefectural Children's Hospital, Kobe, Japan.
Ming Juan Ye2Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Kandai Nozu2Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Noriyuki Nishimura2Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Kazumoto Iijima2Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Hideto NakaoDepartment of Neonatology, Hyogo Prefectural Children's Hospital, Kobe, Japan.
Kobe University · JPKobe Children's Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CLOVES syndrome is characterized by congenital lipomatous overgrowth, vascular malformation, epidermal nevi, and scoliosis/spinal malformation. It is caused by somatic mosaicism of gain-of-function variants of

Indexed as

Disease geneticsPre-diabetes

Identifiers

PMID31263565
PMCPMC6591404
OpenAlexW2951036399

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.