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

What does next-generation sequencing mean for prenatal diagnosis?

Biomarkers in medicine - 1 Jan 2014

Manegold-Brauer Gwendolin, Hahn Sinuhe, Lapaire Olav

Abstract excerpt

The ability to gain genetic information from the fetus in the mother's blood during pregnancy has been a long desired goal of research in prenatal medicine. The detection of fetal DNA in maternal blood, coupled with the development of the powerful techniques of next-generation sequencing finally transferred this analysis into clinical practice. Following the commercial introduction of noninvasive prenatal testing...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Aberrations
Share to High-Throughput Nucleotide Sequencing
Share to Polymorphism, Single Nucleotide

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pregnancy

Share to Prenatal Care

Share to Prenatal Diagnosis

Share to Sequence Analysis, DNA

Source

Identifiers

PMID: 24796613
DOI: 10.2217/bmm.14.18

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

What does next-generation sequencing mean for prenatal diagnosis?PMID 24796613Read ↗

Clinical Perspective of Cell-Free DNA Testing for Fetal AneuploidiesSemantic proximity Read ↗

[Cell-free nucleic acid-based non-invasive prenatal diagnosis of fetal aneuploidies].Semantic proximity Read ↗

Non-Invasive Prenatal Testing: Current Perspectives and Future ChallengesSemantic proximity Read ↗

Cell-Free Fetal DNA and Non-Invasive Prenatal Diagnosis of Chromosomopathies and Pediatric Monogenic Diseases: A Critical Appraisal and Medicolegal RemarksSemantic proximity Read ↗

Amplification-free sequencing of cell-free DNA for prenatal non-invasive diagnosis of chromosomal aberrationsSemantic proximity Read ↗

PREIMPLANTATION GENETIC TESTING: Non-invasive prenatal testing for aneuploidy, copy-number variants and single-gene disordersSemantic proximity Read ↗

Cell-Free DNA Testing for Fetal Chromosomal Anomalies in clinical practice: Austrian-German-Swiss Recommendations for non-invasive prenatal tests (NIPT)Semantic proximity Read ↗

Non invasive prenatal diagnosis of fetal aneuploidy using cell free fetal DNASemantic proximity Read ↗

Noninvasive Prenatal Genetic Screening Using Cell-free DNASemantic proximity Read ↗

Non-invasive prenatal diagnosis: progress and potentialSemantic 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 ↗

Non-invasive prenatal diagnosis of aneuploidies: new technologies and clinical applicationsSemantic proximity Read ↗

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