Evidence map›Paper›PMID 31949757›Full record

ArticleInternational journal of clinical and experimental pathology2018

Next-generation sequencing identified genetic variations in families with fetal non-syndromic atrioventricular septal defects.

Jinyu Xu, Qingqing Wu, Li Wang, Jijing Han, Yan Pei, Wenxue Zhi, Yan Liu, Chenghong Yin, Yuxin Jiang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2018. 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
0.2field-weighted citation impact, top 45% 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, 10 citations in OpenAlex.

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

9 authors at 2 institutions in 1 country.

Jinyu XuDepartment of Ultrasound, Beijing Obstetrics and Gynecology Hospital, Capital Medical University Beijing, China.
Qingqing WuDepartment of Ultrasound, Beijing Obstetrics and Gynecology Hospital, Capital Medical University Beijing, China.
Li WangDepartment of Ultrasound, Beijing Obstetrics and Gynecology Hospital, Capital Medical University Beijing, China.
Jijing HanDepartment of Ultrasound, Beijing Obstetrics and Gynecology Hospital, Capital Medical University Beijing, China.
Yan PeiDepartment of Ultrasound, Beijing Obstetrics and Gynecology Hospital, Capital Medical University Beijing, China.
Wenxue ZhiDepartment of Pathology, Beijing Obstetrics and Gynecology Hospital, Capital Medical University Beijing, China.
Yan LiuDepartment of Obstetrics, Beijing Obstetrics and Gynecology Hospital, Capital Medical University Beijing, China.
Chenghong YinDepartment of Internal Medicine, Beijing Obstetrics and Gynecology Hospital, Capital Medical University Beijing, China.
Yuxin JiangDepartment of Ultrasound, Peking Union Medical College Hospital Beijing, China.
Beijing Obstetrics and Gynecology Hospital · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atrioventricular septal defects (AVSDs) account for approximately 5% of all congenital heart disease (CHD). About half of AVSDs are diagnosed in cases with trisomy 21 (Down's syndrome, DS). However, many AVSDs occur sporadically and manifest as non-syndromic. The pathogenesis is complex and has not yet been fully elucidated. In the present study, we applied two advanced applications of next-generation sequencing (NGS) to explore the genetic variations in families with fetal non-syndromic AVSDs. Our study was mainly divided into two steps: (1) low-pass whole-genome sequencing (WGS) was used to detect the genome-wide copy number variations (CNVs) for included subjects; (2) whole-exome sequencing (WES) was used to detect the gene mutations for the subjects without AVSD-associated CNVs. A total of 17 heterozygous de novo CNVs and 19 heterozygous de novo gene mutations were selected, and 15 candidate genes were involved in these variations. Among these heterozygous de novo variations, most have potential pathogenicity for AVSDs, but the others require further investigation to confirm their pathogenicity. Our study not only shows the genetic diversity and the etiological complexity of AVSDs but also shows the rationality and practicability of this sequential genetic detection and analysis strategy.

Indexed as

AVSDcopy number variationgene mutationwhole-exome sequencingwhole-genome sequencing

Identifiers

PMID31949757
PMCPMC6962893
OpenAlexW3013315779

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.