Cargando…

Maternal Plasma Fetal DNA Fractions in Pregnancies with Low and High Risks for Fetal Chromosomal Aneuploidies

Recently published international guidelines recommend the clinical use of noninvasive prenatal test (NIPT) for aneuploidy screening only among pregnant women whose fetuses are deemed at high risk. The applicability of NIPT to aneuploidy screening among average risk pregnancies requires additional su...

Descripción completa

Detalles Bibliográficos
Autores principales:	Hudecova, Irena, Sahota, Daljit, Heung, Macy M. S., Jin, Yongjie, Lee, Wing S., Leung, Tak Y., Lo, Yuk Ming Dennis, Chiu, Rossa W.K.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2014
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3938419/ https://www.ncbi.nlm.nih.gov/pubmed/24586333 http://dx.doi.org/10.1371/journal.pone.0088484

Ejemplares similares

FetalQuant(SD): accurate quantification of fetal DNA fraction by shallow-depth sequencing of maternal plasma DNA
por: Jiang, Peiyong, et al.
Publicado: (2016)

Placenta-Derived Fetal Specific mRNA Is More Readily Detectable in Maternal Plasma than in Whole Blood
por: Heung, Macy M. S., et al.
Publicado: (2009)

Enrichment of fetal and maternal long cell‐free DNA fragments from maternal plasma following DNA repair
por: Vong, Joaquim S.L., et al.
Publicado: (2019)

Epigenetic-Genetic Chromosome Dosage Approach for Fetal Trisomy 21 Detection Using an Autosomal Genetic Reference Marker
por: Tong, Yu K., et al.
Publicado: (2010)

Chromosomal phase improves aneuploidy detection in non-invasive prenatal testing at low fetal DNA fractions
por: Genovese, Giulio, et al.
Publicado: (2022)

Noninvasive prenatal screening for fetal common sex chromosome aneuploidies from maternal blood
por: Zhang, Bin, et al.
Publicado: (2017)

A fetal fraction enrichment method reduces false negatives and increases test success rate of fetal chromosome aneuploidy detection in early pregnancy loss
por: Qiao, Longwei, et al.
Publicado: (2022)

Cell-Free Fetal DNA and Cell-Free Total DNA Levels in Spontaneous Abortion with Fetal Chromosomal Aneuploidy
por: Lim, Ji Hyae, et al.
Publicado: (2013)

Cell‐free fetal DNA coming in all sizes and shapes
por: Chiu, Rossa W. K., et al.
Publicado: (2021)

Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies
por: Jiang, Fuman, et al.
Publicado: (2012)

Predictive value of aberrant right subclavian artery for fetal chromosome aneuploidy in women of advanced maternal age
por: Chen, Li-Ping, et al.
Publicado: (2021)

Combining the use of a fetal fraction‐based risk algorithm and probability of an informative redraw in noninvasive prenatal testing for fetal aneuploidy
por: Benn, Peter, et al.
Publicado: (2019)

Noninvasive Prenatal Diagnosis of Fetal Trisomy 21 by Allelic Ratio Analysis Using Targeted Massively Parallel Sequencing of Maternal Plasma DNA
por: Liao, Gary J. W., et al.
Publicado: (2012)

Placental microRNA dataset of monochorionic twin pregnancies with and without selective fetal growth restriction
por: Meng, Meng, et al.
Publicado: (2020)

First trimester diagnosis and screening for fetal aneuploidy
por: Driscoll, Deborah A., et al.
Publicado: (2008)

Screening for fetal aneuploidy and neural tube defects
por: Driscoll, Deborah A., et al.
Publicado: (2009)

Genome-Wide Cell-Free DNA Test for Fetal Chromosomal Abnormalities and Variants: Unrestricted Versus Restricted Reporting
por: Kwan, Angel H. W., et al.
Publicado: (2022)

Not all low fetal fraction cell‐free DNA screening failures are at increased risk for aneuploidy
por: Caldwell, Samantha, et al.
Publicado: (2021)

Screening of Fetal Chromosome Aneuploidies in the First and Second Trimester of 125,170 Iranian Pregnant Women
por: SEYYED KAVOOSI, Elham, et al.
Publicado: (2015)

Non-invasive prenatal testing of fetal chromosomal aneuploidies: validation and clinical performance of the veracity test
por: Kypri, Elena, et al.
Publicado: (2019)

Clinical Practice Guidelines for Prenatal Aneuploidy Screening and Diagnostic Testing from Korean Society of Maternal-Fetal Medicine: (2) Invasive Diagnostic Testing for Fetal Chromosomal Abnormalities
por: Lee, Ji Yeon, et al.
Publicado: (2021)

The correlation between maternal age and fetal sex chromosome aneuploidies: a 8-year single institution experience in China
por: Li, Hongge, et al.
Publicado: (2021)

Prenatal diagnosis of fetal aneuploidies: post-genomic developments
por: Hahn, Sinuhe, et al.
Publicado: (2010)

Prenatal diagnosis of common fetal aneuploidies: Scenario in India
por: Baburao, V., et al.
Publicado: (2013)

Economic evaluation of prenatal screening for fetal aneuploidies in Thailand
por: Wongkrajang, Preechaya, et al.
Publicado: (2023)

Phenotypic findings and pregnancy outcomes of fetal rare autosomal aneuploidies detected using chromosomal microarray analysis
por: Hu, Rong, et al.
Publicado: (2022)

A Method to Quantify Cell-Free Fetal DNA Fraction in Maternal Plasma Using Next Generation Sequencing: Its Application in Non-Invasive Prenatal Chromosomal Aneuploidy Detection
por: Xu, Xu-Ping, et al.
Publicado: (2016)

Fetal mitochondrial DNA in maternal plasma in surrogate pregnancies: Detection and topology
por: Ma, Mary‐Jane L., et al.
Publicado: (2020)

High-Throughput Massively Parallel Sequencing for Fetal Aneuploidy Detection from Maternal Plasma
por: Jensen, Taylor J., et al.
Publicado: (2013)

Maternal antimullerian hormone as a predictor of fetal aneuploidy occurring in an early pregnancy loss
por: Shim, So Hyun, et al.
Publicado: (2015)

An Optimized Method for Accurate Fetal Sex Prediction and Sex Chromosome Aneuploidy Detection in Non-Invasive Prenatal Testing
por: Wang, Ting, et al.
Publicado: (2016)

An adaptive detection method for fetal chromosomal aneuploidy using cell-free DNA from 447 Korean women
por: Kim, Sunshin, et al.
Publicado: (2016)

Targeted cell‐free DNA analysis with microarray quantitation for assessment of fetal sex and sex chromosome aneuploidy risk
por: Jones, K. J., et al.
Publicado: (2018)

The Level of Free Fetal DNA as Precise Noninvasive Marker for Chromosomal Aneuploidies: First Results from BALTIC Region
por: Serapinas, Danielius, et al.
Publicado: (2020)

High Resolution Size Analysis of Fetal DNA in the Urine of Pregnant Women by Paired-End Massively Parallel Sequencing
por: Tsui, Nancy B. Y., et al.
Publicado: (2012)

Motivations for Undertaking DNA Sequencing-Based Non-Invasive Prenatal Testing for Fetal Aneuploidy: A Qualitative Study with Early Adopter Patients in Hong Kong
por: Yi, Huso, et al.
Publicado: (2013)

Performance of Fetal Medicine Foundation algorithm for first trimester preeclampsia screening in an indigenous south Asian population
por: Prasad, Smriti, et al.
Publicado: (2021)

Noninvasive prenatal testing for fetal subchromosomal copy number variations and chromosomal aneuploidy by low‐pass whole‐genome sequencing
por: Yu, Dongyi, et al.
Publicado: (2019)

Performance of Cell-Free DNA Screening for Fetal Common Aneuploidies and Sex Chromosomal Abnormalities: A Prospective Study from a Less Developed Autonomous Region in Mainland China
por: Lai, Yunli, et al.
Publicado: (2021)

Multilevel regression modeling for aneuploidy classification and physical separation of maternal cell contamination facilitates the QF-PCR based analysis of common fetal aneuploidies
por: Noveski, Predrag, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_po7pn57nha43uelrbgbqgp4gqc