Putative origins of cell-free DNA in humans: a review of active and passive nucleic acid release mechanisms
S Grabuschnig, AJ Bronkhorst, S Holdenrieder… - International journal of …, 2020 - mdpi.com
Through various pathways of cell death, degradation, and regulated extrusion, partial or
complete genomes of various origins (eg, host cells, fetal cells, and infiltrating viruses and …
complete genomes of various origins (eg, host cells, fetal cells, and infiltrating viruses and …
Diagnosis and treatment of fetal cardiac disease: a scientific statement from the American Heart Association
MT Donofrio, AJ Moon-Grady, LK Hornberger… - Circulation, 2014 - Am Heart Assoc
Background—The goal of this statement is to review available literature and to put forth a
scientific statement on the current practice of fetal cardiac medicine, including the diagnosis …
scientific statement on the current practice of fetal cardiac medicine, including the diagnosis …
Analysis of cell‐free DNA in maternal blood in screening for fetal aneuploidies: updated meta‐analysis
MM Gil, MS Quezada, R Revello… - … in obstetrics & …, 2015 - Wiley Online Library
Objective To review clinical validation or implementation studies of maternal blood cell‐free
(cf) DNA analysis and define the performance of screening for fetal trisomies 21, 18 and 13 …
(cf) DNA analysis and define the performance of screening for fetal trisomies 21, 18 and 13 …
Accuracy of non-invasive prenatal testing using cell-free DNA for detection of Down, Edwards and Patau syndromes: a systematic review and meta-analysis
S Taylor-Phillips, K Freeman, J Geppert, A Agbebiyi… - BMJ open, 2016 - bmjopen.bmj.com
Objective To measure test accuracy of non-invasive prenatal testing (NIPT) for Down,
Edwards and Patau syndromes using cell-free fetal DNA and identify factors affecting …
Edwards and Patau syndromes using cell-free fetal DNA and identify factors affecting …
[HTML][HTML] DNA sequencing versus standard prenatal aneuploidy screening
DW Bianchi, RL Parker, J Wentworth… - New England journal …, 2014 - Mass Medical Soc
Background In high-risk pregnant women, noninvasive prenatal testing with the use of
massively parallel sequencing of maternal plasma cell-free DNA (cfDNA testing) accurately …
massively parallel sequencing of maternal plasma cell-free DNA (cfDNA testing) accurately …
Non-invasive prenatal testing: a review of international implementation and challenges
M Allyse, MA Minear, E Berson, S Sridhar… - … journal of women's …, 2015 - Taylor & Francis
Noninvasive prenatal genetic testing (NIPT) is an advance in the detection of fetal
chromosomal aneuploidies that analyzes cell-free fetal DNA in the blood of a pregnant …
chromosomal aneuploidies that analyzes cell-free fetal DNA in the blood of a pregnant …
Non‐invasive prenatal testing for trisomies 21, 18 and 13: clinical experience from 146 958 pregnancies
H Zhang, Y Gao, F Jiang, M Fu, Y Yuan… - … in Obstetrics & …, 2015 - Wiley Online Library
Objectives To report the clinical performance of massively parallel sequencing‐based non‐
invasive prenatal testing (NIPT) in detecting trisomies 21, 18 and 13 in over 140 000 clinical …
invasive prenatal testing (NIPT) in detecting trisomies 21, 18 and 13 in over 140 000 clinical …
Transcriptome analysis using next-generation sequencing
KO Mutz, A Heilkenbrinker, M Lönne, JG Walter… - Current opinion in …, 2013 - Elsevier
Up to date research in biology, biotechnology, and medicine requires fast genome and
transcriptome analysis technologies for the investigation of cellular state, physiology, and …
transcriptome analysis technologies for the investigation of cellular state, physiology, and …
Fetal fraction in maternal plasma cell‐free DNA at 11–13 weeks' gestation: relation to maternal and fetal characteristics
G Ashoor, A Syngelaki, LCY Poon… - … in Obstetrics & …, 2013 - Wiley Online Library
Objective To examine the possible effects of maternal and fetal characteristics on the fetal
fraction in maternal plasma cell‐free (cf) DNA at 11–13 weeks' gestation and estimate the …
fraction in maternal plasma cell‐free (cf) DNA at 11–13 weeks' gestation and estimate the …
Single-nucleotide polymorphism–based noninvasive prenatal screening in a high-risk and low-risk cohort
E Pergament, H Cuckle, B Zimmermann… - Obstetrics & …, 2014 - journals.lww.com
OBJECTIVE: To estimate performance of a single-nucleotide polymorphism–based
noninvasive prenatal screen for fetal aneuploidy in high-risk and low-risk populations on …
noninvasive prenatal screen for fetal aneuploidy in high-risk and low-risk populations on …