Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

PIEZO1 is the most common monogenic etiology of non‐immune hydrops fetalis detected by prenatal exome sequencing

30 Oct 2023

Abstract excerpt

OBJECTIVE: To clarify the relevance of PIEZO1 variants detected by prenatal exome in the context of non-immune hydrops fetalis (NIHF). METHODS: A systematic review of prenatal exome studies from 1/1/2000-8/1/2022 was performed. Thirty-six studies met the inclusion criteria. PIEZO1 variants were categorized by disease mode (dominant (AD) versus recessive (AR)) and classified by the American College of Medical...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Blood properties and coagulation
Share to Erythrocyte Function and Pathophysiology
Share to Parvovirus B19 Infection Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 37902181
DOI: 10.1002/pd.6451

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

PIEZO1 is the most common monogenic etiology of non‐immune hydrops fetalis detected by prenatal exome sequencingPMID 37902181Read ↗

Value of Exome Sequencing in Diagnosis and Management of Recurrent Non-immune Hydrops Fetalis: A Retrospective AnalysisSemantic proximity Read ↗

Non-immune hydrops fetalis caused by PIEZO1 compound heterozygous deletions detected only by exome sequencing.Semantic proximity Read ↗

Perinatal presentations of nonimmune hydrops fetalis due to biallelic pathogenic variants in PIEZO1: underdiagnosed?Semantic proximity Read ↗

The many etiologies of nonimmune hydrops fetalis diagnosed by exome sequencingSemantic proximity Read ↗

Utility of fetal whole exome sequencing in the etiological evaluation and outcome of nonimmune hydrops fetalisSemantic proximity Read ↗

Identification of novel PIEZO1 variants using prenatal exome sequencing and correlation to ultrasound and autopsy findings of recurrent hydrops fetalisSemantic proximity Read ↗

RASopathies are the most common set of monogenic syndromes identified by exome sequencing for nonimmune hydrops fetalis: A systematic review and meta-analysis.Semantic proximity Read ↗

Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis.Semantic proximity Read ↗

Nonimmune hydrops fetalis: Genetic analysis and clinical outcomeSemantic proximity Read ↗

Fetal hydrops and the Incremental yield of Next‐generation sequencing over standard prenatal Diagnostic testing ( FIND ) study: prospective cohort study and meta‐analysisSemantic proximity Read ↗

Diagnostic yield using whole‐genome sequencing and in‐silico panel of 281 genes associated with non‐immune hydrops fetalis in clinical settingSemantic proximity Read ↗

High diagnosis rate for nonimmune hydrops fetalis with prenatal clinical exome from the Hydrops-Yielding Diagnostic Results of Prenatal Sequencing (HYDROPS) StudySemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.