Evidence map›Paper›PMID 35938004›Full record

ArticleFrontiers in genetics2022

Discovery of Novel Variants on the

Xiangtao Wu, Liang Chen, Weihong Lu, Shaoru He, Xiaowen Li, Lingling Sun, Longjiang Zhang, Dejuan Wang, Ruigui Zhang, Yumei Liu and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Genes · 2024
    Article
  3. Article
  4. DigenicHeliyon · 2024
    Article
  5. 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

13 authors at 7 institutions in 1 country.

Xiangtao WuThe Second School of Clinical Medicine, Southern Medical University, Guangzhou, China.
Liang ChenDepartment of Neonatology, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Weihong LuDepartment of Pediatrics of First Affiliated Hospital of Xinxiang Medical University, Xinxiang, China.
Shaoru HeThe Second School of Clinical Medicine, Southern Medical University, Guangzhou, China.
Xiaowen LiNeonatal Diagnosis and Treatment Center, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, China International Science and Technology Cooperation Base of Child Development and Critical Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, Chongqing, China.
Lingling SunShenzhen Children's Hospital, Shenzhen, China.
Longjiang ZhangShenzhen Children's Hospital, Shenzhen, China.
Dejuan WangDepartment of Urology, The Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Ruigui ZhangDepartment of Neonatology, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Yumei LiuDepartment of Neonatology, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Yunxia SunDepartment of Neonatology, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Zhichun FengDepartment of Neonatology, Faculty of Pediatrics, Chinese PLA General Hospital, BaYi Children's Hospital, Seventh Medical Center of Chinese PLA General Hospital, Beijing, China.
Victor Wei ZhangAmCare Genomics Lab, Guangzhou, China.
Guangdong Provincial People's Hospital · CNFirst Affiliated Hospital of Xinxiang Medical University · CNShenzhen Children's Hospital · CNChinese PLA General Hospital · CNChongqing Medical University · CNGuangdong Academy of Medical Sciences · CNSixth Affiliated Hospital of Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

CHARGE syndromeinfantsmutationphenotypesrespiratory malformations

Identifiers

PMID35938004
PMCPMC9355507
OpenAlexW4286669922

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.