Evidence map›Paper›PMID 35571021›Full record

ArticleFrontiers in genetics2022

Genetic and Phenotype Analysis of a Chinese Cohort of Infants and Children With Epilepsy.

Zhang Chuan, Cai Ruikun, Li Qian, Mei Shiyue, Hao Shengju, Yuan Yong, Li Haibo, Xiao Neng, Zhao Yong, Xue Huiqin and 7 more

Open access · goldAbstract read
PubMed Full text at PMC Publisher
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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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  5. APakistan journal of medical sciences · 2025
    Article
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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

17 authors at 8 institutions in 1 country.

Zhang ChuanNational Research Institute for Family Planning, National Human Genetic Resources Center, Beijing, China.
Cai RuikunNational Research Institute for Family Planning, National Human Genetic Resources Center, Beijing, China.
Li QianNational Research Institute for Family Planning, National Human Genetic Resources Center, Beijing, China.
Mei ShiyueDepartment of Intensive Care Unit, Henan Provincial Key Laboratory of Children's Genetics and Metabolic Diseases, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou, China.
Hao ShengjuGansu Province Medical Genetics Center, Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, China.
Yuan YongZhongshan City People's Hospital, Affiliated Zhongshan Hospital of Sun Yat-Sen University, Guangzhou, China.
Li HaiboThe Central Laboratory of Birth Defects Prevention and Control, Ningbo Women and Children's Hospital, Ningbo, China.
Xiao NengDepartment of Pediatric Neurology, Chenzhou First People's Hospital, Chenzhou, China.
Zhao YongFoshan Women and Children Hospital, Foshan, China.
Xue HuiqinChildren's Hospital of Shanxi, Women Health Center of Shanxi, Taiyuan, China.
Wang WeijiaZhongshan City People's Hospital, Affiliated Zhongshan Hospital of Sun Yat-Sen University, Guangzhou, China.
Hui LingGansu Province Medical Genetics Center, Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, China.
Zhou BingboGansu Province Medical Genetics Center, Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, China.
Qinghua ZhangGansu Province Medical Genetics Center, Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, China.
Wang YanGansu Province Medical Genetics Center, Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, China.
Cao ZongfuNational Research Institute for Family Planning, National Human Genetic Resources Center, Beijing, China.
Ma XuNational Research Institute for Family Planning, National Human Genetic Resources Center, Beijing, China.
Gansu Provincial Maternal and Child Health Hospital · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNChenzhou First People's Hospital · CNFoshan Maternity and Child Health Care Hospital · CNShanxi Provincial Children's Hospital · CNSun Yat-sen University · CNZhengzhou University · CNZhongshan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

genetics counselinginfant and children epilepsyphenotypesvariantWES

Identifiers

PMID35571021
PMCPMC9091957
OpenAlexW4224927626

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.