Evidence map›Paper›PMID 35846127›Full record

ArticleFrontiers in genetics2022

Non-Invasive Prenatal Diagnosis of Monogenic Disorders Through Bayesian- and Haplotype-Based Prediction of Fetal Genotype.

Jia Li, Jiaqi Lu, Fengxia Su, Jiexia Yang, Jia Ju, Yu Lin, Jinjin Xu, Yiming Qi, Yaping Hou, Jing Wu and 19 more

Abstract 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
–field-weighted citation impact
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.

  1. Article
  2. Review
  3. Article
  4. 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

29 authors.

Jia LiBGI Genomics, BGI-Shenzhen, Shenzhen, China.
Jiaqi LuMedical Genetics Centre, Guangdong Women and Children's Hospital, Guangzhou Medical University, Guangzhou, China.
Fengxia SuBGI-Shenzhen, Shenzhen, China.
Jiexia YangPrenatal Diagnosis Centre, Guangdong Women and Children's Hospital, Guangzhou, China.
Jia JuBGI-Shenzhen, Shenzhen, China.
Yu LinBGI-Shenzhen, Shenzhen, China.
Jinjin XuBGI-Shenzhen, Shenzhen, China.
Yiming QiPrenatal Diagnosis Centre, Guangdong Women and Children's Hospital, Guangzhou, China.
Yaping HouPrenatal Diagnosis Centre, Guangdong Women and Children's Hospital, Guangzhou, China.
Jing WuPrenatal Diagnosis Centre, Guangdong Women and Children's Hospital, Guangzhou, China.
Wei HePrenatal Diagnosis Centre, Guangdong Women and Children's Hospital, Guangzhou, China.
Zhengtao YangBGI-Shenzhen, Shenzhen, China.
Yujing WuBGI-Shenzhen, Shenzhen, China.
Zhuangyuan TangBGI-Shenzhen, Shenzhen, China.
Yingping HuangBGI-Shenzhen, Shenzhen, China.
Guohong ZhangBGI-Shenzhen, Shenzhen, China.
Ying YangBGI-Shenzhen, Shenzhen, China.
Zhou LongBGI-Shenzhen, Shenzhen, China.
Xiaofang ChengBGI-Shenzhen, Shenzhen, China.
Ping LiuBGI-Shenzhen, Shenzhen, China.
Jun XiaBGI-Shenzhen, Shenzhen, China.
Yanyan ZhangBGI-Shenzhen, Shenzhen, China.
Yicong WangBGI-Shenzhen, Shenzhen, China.
Fang ChenBGI-Shenzhen, Shenzhen, China.
Jianguo ZhangBGI Genomics, BGI-Shenzhen, Shenzhen, China.
Lijian ZhaoBGI Genomics, BGI-Shenzhen, Shenzhen, China.
Xin JinBGI-Shenzhen, Shenzhen, China.
Ya GaoBGI-Shenzhen, Shenzhen, China.
Aihua YinPrenatal Diagnosis Centre, Guangdong Women and Children's Hospital, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

fetal genomemassively parallel sequencingmonogenic diseasenon-invasive prenatal diagnosissingle nucleotide variations

Identifiers

PMID35846127
PMCPMC9283829

What OpenQuestion holds

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Registered trials

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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.