Evidence map›Paper›PMID 33199988›Full record

ArticleExperimental and therapeutic medicine2020

Genotype-phenotype analysis in Mowat-Wilson syndrome associated with two novel and two recurrent

Dongfang Zou, Lin Wang, Feiqiu Wen, Hongdou Xiao, Jing Duan, Tongda Zhang, Zhenzhen Yin, Qiwen Dong, Jian Guo, Jianxiang Liao

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

Article in Experimental and therapeutic medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

7 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Mowat-Wilson Syndrome: Case Report and Review ofInternational journal of molecular sciences · 2024
    Review
  4. Mutated Transcripts ofMolecular syndromology · 2023
    Article
  5. Clinical Characteristics and NovelPharmacogenomics and personalized medicine · 2023
    Article
  6. Three NovelFrontiers in genetics · 2022
    Article
  7. 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.

Dongfang ZouDepartment of Neurology, Shenzhen Children's Hospital, Shenzhen, Guangdong 518038, P.R. China.
Lin WangBGI-Shenzhen, Shenzhen, Guangdong 518083, P.R. China.
Feiqiu WenDepartment of Hematology and Oncology, Shenzhen Children's Hospital, Shenzhen, Guangdong 518038, P.R. China.
Hongdou XiaoBGI-Shenzhen, Shenzhen, Guangdong 518083, P.R. China.
Jing DuanDepartment of Neurology, Shenzhen Children's Hospital, Shenzhen, Guangdong 518038, P.R. China.
Tongda ZhangBGI-Shenzhen, Shenzhen, Guangdong 518083, P.R. China.
Zhenzhen YinBGI-Shenzhen, Shenzhen, Guangdong 518083, P.R. China.
Qiwen DongBGI-Shenzhen, Shenzhen, Guangdong 518083, P.R. China.
Jian GuoBGI-Shenzhen, Shenzhen, Guangdong 518083, P.R. China.
Jianxiang LiaoDepartment of Neurology, Shenzhen Children's Hospital, Shenzhen, Guangdong 518038, P.R. China.
BGI Group (China) · CNShenzhen Children's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The current study aimed to analyze the genotype-phenotype relationship in patients with variants of zinc finger E box-binding homeobox 2 (

Indexed as

frameshift mutationMowat-Wilson Syndromenonsense mutationswhole genome sequencingzinc finger E box-binding homeobox 2

Identifiers

PMID33199988
PMCPMC7664618
OpenAlexW3096783499

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.