Evidence map›Paper›PMID 34234805›Full record

ArticleFrontiers in genetics2021

Rapid Trio Exome Sequencing for Autosomal Recessive Renal Tubular Dysgenesis in Recurrent Oligohydramnios.

Shin-Yu Lin, Gwo-Tsann Chuang, Chien-Hui Hung, Wei-Chou Lin, Yung-Ming Jeng, Ting-An Yen, Karine Chang, Yin-Hsiu Chien, Wuh-Liang Hwu, Chien-Nan Lee and 2 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. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

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

12 authors at 1 institution in 1 country.

Shin-Yu LinDepartment of Obstetrics and Gynecology, National Taiwan University Hospital, Taipei, Taiwan.
Gwo-Tsann ChuangDepartment of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.
Chien-Hui HungDepartment of Obstetrics and Gynecology, National Taiwan University Hospital, Taipei, Taiwan.
Wei-Chou LinDepartment of Pathology, National Taiwan University Hospital, Taipei, Taiwan.
Yung-Ming JengDepartment of Pathology, National Taiwan University Hospital, Taipei, Taiwan.
Ting-An YenDepartment of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.
Karine ChangDepartment of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan.
Yin-Hsiu ChienDepartment of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.
Wuh-Liang HwuDepartment of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.
Chien-Nan LeeDepartment of Obstetrics and Gynecology, National Taiwan University Hospital, Taipei, Taiwan.
I-Jung TsaiDepartment of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.
Ni-Chung LeeDepartment of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.
National Taiwan University Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oligohydramnios is not a rare prenatal finding. However, recurrent oligohydramnios is uncommon, and genetic etiology should be taken into consideration. We present two families with recurrent fetal oligohydramnios that did not respond to amnioinfusion. Rapid trio-whole-exome sequencing (WES) revealed mutations in the

Indexed as

AGT geneangiotensinogenautosomal recessive renal tubular dysgenesisoligohydramnioswhole exome sequencing (WES)

Identifiers

PMID34234805
PMCPMC8255961
OpenAlexW3177099697

What OpenQuestion holds

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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.