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

Advancements in Prenatal Genetic Screening and Testing: Emerging Technologies and Evolving Applications

13 Oct 2025

Abstract excerpt

Advancements in genomic technologies have transformed prenatal genetic testing, offering more accurate, comprehensive, and noninvasive approaches to reproductive care. This review provides an in-depth overview of current methodologies and emerging innovations, including expanded carrier screening (ECS), cell-free DNA (cfDNA) testing, chromosomal microarray analysis (CMA), and sequencing-based diagnostics. We...

Read the complete abstract on PubMed

Topics

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

Share to Fetal and Pediatric Neurological Disorders
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 41153251
DOI: 10.3390/diagnostics15202579

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 24 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Advancements in Prenatal Genetic Screening and Testing: Emerging Technologies and Evolving ApplicationsPMID 41153251Read ↗

Advancements in Prenatal Genetics: Emerging Technologies and Evolving ApplicationsSemantic proximity Read ↗

Recent advances in prenatal genetic screening and testingSemantic proximity Read ↗

An overview of current prenatal genetic screening and diagnosis guidelinesSemantic proximity Read ↗

Prenatal genetic testing 2: diagnostic testsSemantic proximity Read ↗

Prenatal Whole-Genome Sequencing for Fetal Anomalies: Diagnostic Performance, Challenges, and Clinical Implications.Semantic proximity Read ↗

The evolution of prenatal Whole Exome Sequencing: from cytogenetics to precision medicineSemantic proximity Read ↗

Advances in Prenatal Cell‐Free DNA Screening for Dominant Monogenic Conditions: A Review of Current Progress and Future Directions in Clinical ImplementationSemantic proximity Read ↗

Next-generation sequencing and the impact on prenatal diagnosisSemantic proximity Read ↗

International Society for Prenatal Diagnosis Updated Position Statement on the use of genome‐wide sequencing for prenatal diagnosisSemantic proximity Read ↗

The role of chromosomal microarray and exome sequencing in prenatal diagnosisSemantic proximity Read ↗

The clinical implementation of non‐invasive prenatal diagnosis for single‐gene disorders: challenges and progress madeSemantic proximity Read ↗

Clinical Testing for Genetic Conditions.Semantic proximity Read ↗

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