Evidence map›Paper›PMID 35186825›Full record

ReviewFrontiers in pediatrics2021

Unraveling the Genetics of Congenital Diaphragmatic Hernia: An Ongoing Challenge.

Erwin Brosens, Nina C J Peters, Kim S van Weelden, Charlotte Bendixen, Rutger W W Brouwer, Frank Sleutels, Hennie T Bruggenwirth, Wilfred F J van Ijcken, Danielle C M Veenma, Suzan C M Cochius-Den Otter and 8 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in pediatrics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 19 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

18 authors at 2 institutions in 2 countries.

Erwin BrosensDepartment of Clinical Genetics, Erasmus MC Sophia Children's Hospital, Rotterdam, Netherlands.
Nina C J PetersDivision of Obstetrics and Fetal Medicine, Department of Obstetrics and Gynecology, Erasmus MC Sophia Children's Hospital, Rotterdam, Netherlands.
Kim S van WeeldenDepartment of Clinical Genetics, Erasmus MC Sophia Children's Hospital, Rotterdam, Netherlands.
Charlotte BendixenUnit of Pediatric Surgery, Department of General, Visceral, Vascular and Thoracic Surgery, University Hospital Bonn, Bonn, Germany.
Rutger W W BrouwerCenter for Biomics, Erasmus MC Sophia Children's Hospital, Rotterdam, Netherlands.
Frank SleutelsDepartment of Clinical Genetics, Erasmus MC Sophia Children's Hospital, Rotterdam, Netherlands.
Hennie T BruggenwirthDepartment of Clinical Genetics, Erasmus MC Sophia Children's Hospital, Rotterdam, Netherlands.
Wilfred F J van IjckenCenter for Biomics, Erasmus MC Sophia Children's Hospital, Rotterdam, Netherlands.
Danielle C M VeenmaDepartment of Clinical Genetics, Erasmus MC Sophia Children's Hospital, Rotterdam, Netherlands.
Suzan C M Cochius-Den OtterDepartment of Pediatric Surgery and Intensive Care, Erasmus MC Sophia Children's Hospital, Rotterdam, Netherlands.
Rene M H WijnenDepartment of Pediatric Surgery and Intensive Care, Erasmus MC Sophia Children's Hospital, Rotterdam, Netherlands.
Alex J EgginkDivision of Obstetrics and Fetal Medicine, Department of Obstetrics and Gynecology, Erasmus MC Sophia Children's Hospital, Rotterdam, Netherlands.
Marieke F van DoorenDepartment of Clinical Genetics, Erasmus MC Sophia Children's Hospital, Rotterdam, Netherlands.
Heiko Martin ReutterInstitute of Human Genetics, University Hospital of Bonn, Bonn, Germany.
Robbert J RottierDepartment of Pediatric Surgery and Intensive Care, Erasmus MC Sophia Children's Hospital, Rotterdam, Netherlands.
J Marco SchnaterDepartment of Pediatric Surgery and Intensive Care, Erasmus MC Sophia Children's Hospital, Rotterdam, Netherlands.
Dick TibboelDepartment of Pediatric Surgery and Intensive Care, Erasmus MC Sophia Children's Hospital, Rotterdam, Netherlands.
Annelies de KleinDepartment of Clinical Genetics, Erasmus MC Sophia Children's Hospital, Rotterdam, Netherlands.
Erasmus MC - Sophia Children’s Hospital · NLUniversity Hospital Bonn · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital diaphragmatic hernia (CDH) is a congenital structural anomaly in which the diaphragm has not developed properly. It may occur either as an isolated anomaly or with additional anomalies. It is thought to be a multifactorial disease in which genetic factors could either substantially contribute to or directly result in the developmental defect. Patients with aneuploidies, pathogenic variants or

Indexed as

congenitalcounselingdevelopmentdiaphragmdiscordant monozygotic twinforegutgeneticshernia

Identifiers

PMID35186825
PMCPMC8852845
OpenAlexW4213289290

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.