Evidence map›Paper›PMID 36246595›Full record

ArticleFrontiers in genetics2022

Molecular prevalence of

Haiyan Luo, Ting Huang, Qing Lu, Liuyang Zhang, Yonghua Xu, Yan Yang, Zhen Guo, Huizhen Yuan, Yinqin Shen, Shuhui Huang 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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 20% 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.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. 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

13 authors at 1 institution in 1 country.

Haiyan LuoDepartment of Medical Genetics, Jiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Ting HuangDepartment of Medical Genetics, Jiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Qing LuDepartment of Medical Genetics, Jiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Liuyang ZhangDepartment of Medical Genetics, Jiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Yonghua XuDepartment of Medical Genetics, Jiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Yan YangDepartment of Medical Genetics, Jiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Zhen GuoJiangxi Key Laboratory of Birth Defect Prevention and Control, Jiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Huizhen YuanDepartment of Medical Genetics, Jiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Yinqin ShenDepartment of Medical Genetics, Jiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Shuhui HuangDepartment of Medical Genetics, Jiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Bicheng YangDepartment of Medical Genetics, Jiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Yongyi ZouDepartment of Medical Genetics, Jiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Yanqiu LiuDepartment of Medical Genetics, Jiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Jiangxi Maternal and Child Health 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

central China-southern central ChinaHBBhemoglobinopathymutation spectrumprenatal diagnosis

Identifiers

PMID36246595
PMCPMC9554255
OpenAlexW4297540777

What OpenQuestion holds

Textmetadata
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.