IONA test for first-trimester detection of trisomies 21, 18 and 13.

scientific article published on 21 September 2015

IONA test for first-trimester detection of trisomies 21, 18 and 13. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1002/UOG.15749
P932PMC publication ID5064725
P698PubMed publication ID26387684

P50authorLiona C. PoonQ59160667
P2093author name stringK H Nicolaides
C Francisco
I Fantasia
D Dumidrascu-Diris
P2860cites workDNA Sequencing versus Standard Prenatal Aneuploidy ScreeningQ22250872
Noninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencingQ28742844
DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative studyQ30414408
Non-invasive prenatal detection of trisomy 13 using a single nucleotide polymorphism- and informatics-based approach.Q33578055
Single-nucleotide polymorphism-based noninvasive prenatal screening in a high-risk and low-risk cohortQ34088575
Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencingQ34256640
Validation of targeted sequencing of single-nucleotide polymorphisms for non-invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y.Q34340985
Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidiesQ34496747
Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysisQ35552815
Clinical evaluation of the IONA test: a non-invasive prenatal screening test for trisomies 21, 18 and 13.Q37340255
Screening for fetal aneuploidies at 11 to 13 weeksQ37826399
Initial experience with non-invasive prenatal testing of cell-free DNA for major chromosomal anomalies in a clinical settingQ38419642
Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18.Q40028555
Non-invasive prenatal testing for trisomies 21, 18 and 13: clinical experience from 146,958 pregnancies.Q41566460
Implementation of maternal blood cell-free DNA testing in early screening for aneuploidies.Q43418239
Noninvasive prenatal testing for whole fetal chromosomal aneuploidies: a multicenter prospective cohort trial in TaiwanQ44576378
Optimal detection of fetal chromosomal abnormalities by massively parallel DNA sequencing of cell-free fetal DNA from maternal bloodQ44645735
Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA.Q45026733
First-trimester screening for trisomies 21, 18 and 13 by ultrasound and biochemical testingQ45839764
Cell-free DNA analysis for noninvasive examination of trisomyQ46784231
Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencingQ46816545
Noninvasive prenatal diagnosis of common fetal chromosomal aneuploidies by maternal plasma DNA sequencing.Q46892061
Diagnostic accuracy of random massively parallel sequencing for non-invasive prenatal detection of common autosomal aneuploidies: a collaborative study in Europe.Q51142138
Trisomy 13 detection in the first trimester of pregnancy using a chromosome-selective cell-free DNA analysis method.Q51321305
Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18.Q51349861
A CRITICAL EVALUATION OF SONAR "CROWN-RUMP LENGTH" MEASUREMENTSQ55883094
A robust second-generation genome-wide test for fetal aneuploidy based on shotgun sequencing cell-free DNA in maternal bloodQ56986865
Presence of fetal DNA in maternal plasma and serumQ57075132
Chromosome-selective sequencing of maternal plasma cell–free DNA for first-trimester detection of trisomy 21 and trisomy 18Q61847821
Noninvasive prenatal testing for fetal trisomies in a routinely screened first-trimester populationQ61847837
Screening for trisomies 21, 18 and 13 by cell-free DNA analysis of maternal blood at 10-11 weeks' gestation and the combined test at 11-13 weeksQ85632797
Noninvasive prenatal testing of fetal aneuploidies by massively parallel sequencing in a prospective Chinese populationQ86847268
Non-invasive prenatal testing for fetal aneuploidies in the first trimester of pregnancyQ87418439
P433issue2
P304page(s)184-187
P577publication date2015-12-28
P1433published inUltrasound in Obstetrics and GynecologyQ1817048
P1476titleIONA test for first-trimester detection of trisomies 21, 18 and 13
P478volume47

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cites work (P2860)
Q47618331Genomics-based non-invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women.
Q60046618Improving the calling of non-invasive prenatal testing on 13-/18-/21-trisomy by support vector machine discrimination
Q55438251Noninvasive Prenatal Testing: Comparison of Two Mappers and Influence in the Diagnostic Yield.
Q90259969Prenatal cell-free DNA screening test failures: a systematic review of failure rates, risks of Down syndrome, and impact of repeat testing
Q38973930The IONA® Test: Development of an Automated Cell-Free DNA-Based Screening Test for Fetal Trisomies 13, 18, and 21 That Employs the Ion Proton Semiconductor Sequencing Platform

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