Evidence map›Paper›PMID 33955509›Full record

ArticleMolecular medicine reports2021

Further phenotypic features and two novel

Songting Li, Yan Zhong, Yongjia Yang, Siping He, Wenjuan He

Open access · hybridAbstract readCase Reports
In one paragraph

Article in Molecular medicine reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.4field-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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. 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

5 authors at 2 institutions in 1 country.

Songting LiChildren's Healthcare Institute, Hunan Children's Hospital, University of South China, Changsha, Hunan 410007, P.R. China.
Yan ZhongChildren's Healthcare Institute, Hunan Children's Hospital, University of South China, Changsha, Hunan 410007, P.R. China.
Yongjia YangThe Laboratory of Genetics and Metabolism, Hunan Children's Research Institute, Hunan Children's Hospital, University of South China, Changsha, Hunan 410007, P.R. China.
Siping HeDepartment of Radiology, Hunan Children's Hospital, University of South China, Changsha, Hunan 410007, P.R. China.
Wenjuan HeChildren's Healthcare Institute, Hunan Children's Hospital, University of South China, Changsha, Hunan 410007, P.R. China.
Hunan Children's Hospital · CNUniversity of South China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Short stature, onychodysplasia, facial dysmorphism and hypotrichosis (SOFT) syndrome is a rare autosomal recessive disease caused by POC1 centriolar protein A (

Indexed as

Abnormalities, MultipleCell Cycle ProteinsChildCraniofacial AbnormalitiesCytoskeletal ProteinsDwarfismExome SequencingFemaleHairHumansMuscular AtrophyNails, MalformedOsteochondrodysplasiasPhenotypeCell Cycle ProteinsCytoskeletal ProteinsPOC1A protein, humanfacial dysmorphism and hypotrichosis syndromeimagingnovel variantsonychodysplasiaPOC1 centriolar protein Ashort stature

Identifiers

PMID33955509
PMCPMC8127052
OpenAlexW3159604613

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.