Evidence map›Paper›PMID 36980834›Full record

ArticleGenes2023

Prenatal Detection of a

Katarzyna Bzdęga, Anna Kutkowska-Kaźmierczak, Gail H Deutsch, Izabela Plaskota, Marta Smyk, Magdalena Niemiec, Artur Barczyk, Ewa Obersztyn, Jan Modzelewski, Iwona Lipska and 6 more

Open access · goldFull text readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

16 authors at 5 institutions in 2 countries.

Katarzyna BzdęgaChair and Department of Genetics and Pharmaceutical Microbiology, Poznan University of Medical Sciences, 60-806 Poznan, Poland.
Anna Kutkowska-KaźmierczakDepartment of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.ORCID 0000-0001-5295-7363
Gail H DeutschDepartment of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA 98105, USA.
Izabela PlaskotaDepartment of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.
Marta SmykDepartment of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.ORCID 0000-0002-7959-044X
Magdalena NiemiecDepartment of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.ORCID 0000-0002-5485-1607
Artur BarczykDepartment of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.
Ewa ObersztynDepartment of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.
Jan Modzelewski1st Clinic of Obstetrics and Gynecology, Centre of Postgraduate Medical Education, 01-004 Warsaw, Poland.
Iwona LipskaDepartment of Pathomorphology, Wolski Hospital, 01-211 Warsaw, Poland.
Paweł StankiewiczDepartment of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Marzena GajeckaChair and Department of Genetics and Pharmaceutical Microbiology, Poznan University of Medical Sciences, 60-806 Poznan, Poland.ORCID 0000-0001-7468-2604
Małgorzata RydzaniczDepartment of Medical Genetics, Medical University of Warsaw, 02-106 Warsaw, Poland.
Rafał PłoskiDepartment of Medical Genetics, Medical University of Warsaw, 02-106 Warsaw, Poland.
Tomasz SzczapaII Department of Neonatology, Neonatal Biophysical Monitoring and Cardiopulmonary Therapies Research Unit, Poznan University of Medical Science, 60-535 Poznan, Poland.ORCID 0000-0002-5214-2719
Justyna A KarolakChair and Department of Genetics and Pharmaceutical Microbiology, Poznan University of Medical Sciences, 60-806 Poznan, Poland.ORCID 0000-0002-2340-4513
Poznan University of Medical Sciences · PLMedical University of Warsaw · PLBaylor College of Medicine · USPostgraduate School of Molecular Medicine · PLUniversity of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alveolar capillary dysplasia with misalignment of pulmonary veins (ACDMPV) is a lethal lung developmental disorder caused by the arrest of fetal lung formation, resulting in neonatal death due to acute respiratory failure and pulmonary arterial hypertension. Heterozygous single-nucleotide variants or copy-number variant (CNV) deletions involving the

Indexed as

Forkhead Transcription FactorsHydronephrosisPersistent Fetal Circulation SyndromeFetusHumansInfant, NewbornPulmonary AlveoliSequence DeletionForkhead Transcription FactorsFOXF1 protein, human16q24.1alveolar capillary dysplasiagenome sequencinghydronephrosislethal lung developmental disorderprenatal diagnosis

Identifiers

PMID36980834
PMCPMC10048226
OpenAlexW4321787141

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read8
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.