Evidence map›Paper›PMID 34025713›Full record

ArticleFrontiers in genetics2021

Overdosage of

Feifan Xiao, Xiuyun Liu, Yulan Lu, Bingbing Wu, Renchao Liu, Bo Liu, Kai Yan, Huiyao Chen, Guoqiang Cheng, Laishuan Wang and 8 more

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

Article in Frontiers in genetics, 2021. 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
1.3field-weighted citation impact, top 21% 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, 8 citations in OpenAlex.

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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

18 authors at 1 institution in 1 country.

Feifan XiaoCenter for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Xiuyun LiuCenter for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Yulan LuCenter for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Bingbing WuCenter for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Renchao LiuCenter for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Bo LiuCenter for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Kai YanDivision of Neonatology, Key Laboratory of Neonatal Diseases, Ministry of Health, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Huiyao ChenCenter for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Guoqiang ChengDivision of Neonatology, Key Laboratory of Neonatal Diseases, Ministry of Health, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Laishuan WangDivision of Neonatology, Key Laboratory of Neonatal Diseases, Ministry of Health, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Qi NiCenter for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Gang LiCenter for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Ping ZhangCenter for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Xiaomin PengCenter for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Yun CaoDivision of Neonatology, Key Laboratory of Neonatal Diseases, Ministry of Health, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Chun ShenDepartment of Pediatric Surgery, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Huijun WangCenter for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Wenhao ZhouCenter for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Children's Hospital of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The annular pancreas (AP) is a congenital anomaly of the pancreas that can cause acute abdominal pain and vomiting after birth. However, the genetic cause of AP is still unknown, and no study has reported AP in patients with 17q12 duplication. This study retrospectively analyzed the next-generation sequencing (NGS) data of individuals from January 2016 to June 2020 for 17q12 duplication. To identify the function of the key gene of

Indexed as

17q12 duplicationannular pancreasCNVHNF1Bzebrafish

Identifiers

PMID34025713
PMCPMC8138176
OpenAlexW3163380185

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.