Evidence map›Paper›PMID 36704359›Full record

ArticleFrontiers in genetics2022

Simultaneous detection of

Huagui Wei, Chunfang Wang, Weiyi Huang, Liqiao He, Yaqun Liu, Huiying Huang, Wencheng Chen, Yuzhong Zheng, Guidan Xu, Liyun Lin and 5 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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
4.1field-weighted citation impact, top 7% 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

4 citing papers in PubMed, 7 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

15 authors at 2 institutions in 1 country.

Huagui WeiCenter for Clinical Laboratory Diagnosis and Research, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Chunfang WangCenter for Clinical Laboratory Diagnosis and Research, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Weiyi HuangCenter for Clinical Laboratory Diagnosis and Research, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Liqiao HeCenter for Clinical Laboratory Diagnosis and Research, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Yaqun LiuSchool of Biotechnology and Food Engineering, Hanshan Normal University, Chaozhou, China.
Huiying HuangSchool of Biotechnology and Food Engineering, Hanshan Normal University, Chaozhou, China.
Wencheng ChenCenter for Clinical Laboratory Diagnosis and Research, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Yuzhong ZhengSchool of Biotechnology and Food Engineering, Hanshan Normal University, Chaozhou, China.
Guidan XuCenter for Clinical Laboratory Diagnosis and Research, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Liyun LinSchool of Biotechnology and Food Engineering, Hanshan Normal University, Chaozhou, China.
Wujun WeiCenter for Clinical Laboratory Diagnosis and Research, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Weizhong ChenDepartment of Medical Laboratory, Chaozhou People's Hospital Affiliated to Shantou University Medical College, Chaozhou, China.
Liying ChenCenter for Clinical Laboratory Diagnosis and Research, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Junli WangSchool of Laboratory Medicine, Youjiang Medical University for Nationalities, Baise, China.
Min LinCenter for Clinical Laboratory Diagnosis and Research, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Affiliated Hospital of Youjiang Medical University for Nationalities · CNHanshan Normal 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

G6PD deficiencyG6PD genotypemutation spectrumSNPscan assaysouthwestern China

Identifiers

PMID36704359
PMCPMC9871378
OpenAlexW4315472560

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.