Evidence map›Paper›PMID 32174975›Full record

ArticleFrontiers in genetics2020

Chao Wang, Longlong Lin, Yan Xue, Yilin Wang, Zhao Liu, Zicheng Ou, Shengnan Wu, Xiaoping Lan, Yuanfeng Zhang, Fang Yuan and 5 more

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

Article in Frontiers in genetics, 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 31% 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, 13 citations in OpenAlex.

  1. Article
  2. Macrocephaly and Finger Changes: A Narrative Review.International journal of molecular sciences · 2024
    Review
  3. Article
  4. Article
  5. A novel nonsense variant inClinical case reports · 2021
    Article
  6. De novo loss-of-function variants in X-linked MED12 are associated with Hardikar syndrome in females.Genetics in medicine : official journal of the American College of Medical Genetics · 2021
    Article
  7. De novo variants in MED12 cause X-linked syndromic neurodevelopmental disorders in 18 females.Genetics in medicine : official journal of the American College of Medical Genetics · 2021
    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

15 authors at 3 institutions in 2 countries.

Chao WangDepartment of Neurology, Shanghai Children's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Longlong LinDepartment of Neurology, Shanghai Children's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Yan XueInstitute of Medical Science, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Yilin WangDepartment of Neurology, Shanghai Children's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Zhao LiuDivision of Pediatric Neurology, Department of Pediatrics, University of Illinois and Children's Hospital of Illinois, Peoria, IL, United States.
Zicheng OuDepartment of Pediatrics, JianNing General Hospital, Fujian, China.
Shengnan WuDepartment of Neurology, Shanghai Children's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Xiaoping LanDepartment of Neurology, Shanghai Children's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Yuanfeng ZhangDepartment of Neurology, Shanghai Children's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Fang YuanDepartment of Neurology, Shanghai Children's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Xiaona LuoDepartment of Neurology, Shanghai Children's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Chunmei WangDepartment of Neurology, Shanghai Children's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Jiaming XiDepartment of Neurology, Shanghai Children's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Xiaomin SunDepartment of Neurology, Shanghai Children's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Yucai ChenDepartment of Neurology, Shanghai Children's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Shanghai Jiao Tong University · CNShanghai Children's Hospital · CNChildren's Hospital of Illinois · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The RNA polymerase II transcription subunit 12 homolog (

Indexed as

craniofacial morphologyintellectual disabilityMED12mutationSHH signaling pathwayX-chromosome inactivation

Identifiers

PMID32174975
PMCPMC7056888
OpenAlexW3007120348

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.