(Q28072788)

English

Accuracy of non-invasive prenatal testing using cell-free DNA for detection of Down, Edwards and Patau syndromes: a systematic review and meta-analysis

scientific article

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scholarly article

1 reference

7 references

22 April 2019

25 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

6 July 2020

systematic review

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Accuracy of non-invasive prenatal testing using cell-free DNA for detection of Down, Edwards and Patau syndromes: a systematic review and meta-analysis (English)

1 reference

0 references

chromosomal disease

7 references

22 April 2019

25 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

6 July 2020

7 references

22 April 2019

25 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

6 July 2020

1 reference

2 August 2019

genetic variation

1 reference

14 September 2019

systematic review

1 reference

based on heuristic

inferred from title

Karoline Freeman

object named as

Karoline Freeman

2

0 references

Sian Taylor-Phillips

object named as

Sian Taylor-Phillips

1

0 references

object named as

Jason Madan

6

0 references

object named as

Siobhan Quenby

8

0 references

object named as

Aileen Clarke

9

0 references

Olalekan A. Uthman

object named as

Olalekan A Uthman

5

0 references

author name string

Julia Geppert

3

1 reference

Adeola Agbebiyi

4

1 reference

Angus Clarke

7

1 reference

language of work or name

1 reference

publication date

18 January 2016

8 references

22 April 2019

25 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

6 July 2020

5 references

20 June 2019

30 June 2019

2 August 2019

14 September 2019

6 July 2020

6

1 reference

1

1 reference

e010002

1 reference

copyright license

Creative Commons Attribution

7 references

22 April 2019

25 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

6 July 2020

on focus list of Wikimedia project

0 references

DNA Sequencing versus Standard Prenatal Aneuploidy Screening

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

20 March 2017

Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

20 March 2017

Noninvasive detection of fetal trisomy 21: systematic review and report of quality and outcomes of diagnostic accuracy studies performed between 1997 and 2012

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

20 March 2017

Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

20 March 2017

Diagnostic Accuracy of Noninvasive Detection of Fetal Trisomy 21 in Maternal Blood: A Systematic Review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

20 March 2017

QUADAS-2: a revised tool for the quality assessment of diagnostic accuracy studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

20 March 2017

Noninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

20 March 2017

Bivariate analysis of sensitivity and specificity produces informative summary measures in diagnostic reviews

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

7 April 2017

Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

The feasibility study of non-invasive fetal trisomy 18 and 21 detection with semiconductor sequencing platform

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

Noninvasive prenatal testing: impact on genetic counseling, invasive prenatal diagnosis, and trisomy 21 detection

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

Non-invasive prenatal chromosomal aneuploidy testing--clinical experience: 100,000 clinical samples

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

Initial experience with non-invasive prenatal testing of cell-free DNA for major chromosomal anomalies in a clinical setting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

Single-nucleotide polymorphism-based noninvasive prenatal screening in a high-risk and low-risk cohort

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

Non-invasive prenatal detection of trisomy 13 using a single nucleotide polymorphism- and informatics-based approach.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

Noninvasive prenatal testing goes global

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

A single center's experience with noninvasive prenatal testing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

Validation of targeted sequencing of single-nucleotide polymorphisms for non-invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

Initial clinical laboratory experience in noninvasive prenatal testing for fetal aneuploidy from maternal plasma DNA samples

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

Use of 3x2 tables with an intention to diagnose approach to assess clinical performance of diagnostic tests: meta-analytical evaluation of coronary CT angiography studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

Multivariate meta-analysis: potential and promise

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

Systematic reviews of diagnostic test accuracy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

The diagnostic odds ratio: a single indicator of test performance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

Exploring sources of heterogeneity in systematic reviews of diagnostic tests

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

29 September 2017

Non-invasive prenatal testing for trisomies 21, 18 and 13: clinical experience from 146,958 pregnancies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4735304

2 June 2018

The general public's understanding and perception of direct-to-consumer genetic test results.

1 reference

https://api.crossref.org/works/10.1136%2FBMJOPEN-2015-010002

21 January 2018

Cell-free DNA analysis for noninvasive examination of trisomy

1 reference

https://api.crossref.org/works/10.1136%2FBMJOPEN-2015-010002

21 January 2018

Diagnostic accuracy studies: how to report and analyse inconclusive test results

1 reference

https://api.crossref.org/works/10.1136%2FBMJOPEN-2015-010002

21 January 2018

The performance of tests of publication bias and other sample size effects in systematic reviews of diagnostic test accuracy was assessed.

1 reference

https://api.crossref.org/works/10.1136%2FBMJOPEN-2015-010002

21 January 2018

Clinical application of massively parallel sequencing-based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11,105 pregnancies with mixed risk factors

1 reference

https://api.crossref.org/works/10.1136%2FBMJOPEN-2015-010002

21 January 2018

Cell-free DNA analysis for trisomy risk assessment in first-trimester twin pregnancies.

1 reference

https://api.crossref.org/works/10.1136%2FBMJOPEN-2015-010002

21 January 2018

Noninvasive prenatal diagnosis of common fetal chromosomal aneuploidies by maternal plasma DNA sequencing.

1 reference

https://api.crossref.org/works/10.1136%2FBMJOPEN-2015-010002

21 January 2018

Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing

1 reference

https://api.crossref.org/works/10.1136%2FBMJOPEN-2015-010002

21 January 2018

Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18.

1 reference

https://api.crossref.org/works/10.1136%2FBMJOPEN-2015-010002

21 January 2018

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.

1 reference

https://api.crossref.org/works/10.1136%2FBMJOPEN-2015-010002

21 January 2018

Noninvasive prenatal testing for whole fetal chromosomal aneuploidies: a multicenter prospective cohort trial in Taiwan

1 reference

https://api.crossref.org/works/10.1136%2FBMJOPEN-2015-010002

21 January 2018

Diagnostic accuracy of random massively parallel sequencing for non-invasive prenatal detection of common autosomal aneuploidies: a collaborative study in Europe.

1 reference

https://api.crossref.org/works/10.1136%2FBMJOPEN-2015-010002

21 January 2018

Association of non-invasive prenatal testing and chromosomal microarray analysis for prenatal diagnostics.

1 reference

https://api.crossref.org/works/10.1136%2FBMJOPEN-2015-010002

21 January 2018

Nationwide demonstration project of next-generation sequencing of cell-free DNA in maternal plasma in Japan: 1-year experience

1 reference

https://api.crossref.org/works/10.1136%2FBMJOPEN-2015-010002

21 January 2018

Optimal detection of fetal chromosomal abnormalities by massively parallel DNA sequencing of cell-free fetal DNA from maternal blood

1 reference

https://api.crossref.org/works/10.1136%2FBMJOPEN-2015-010002

21 January 2018

Non-invasive prenatal testing for trisomy 21 based on analysis of cell-free fetal DNA circulating in the maternal plasma.

1 reference

https://api.crossref.org/works/10.1136%2FBMJOPEN-2015-010002

21 January 2018

Meta-analysis of multiple outcomes by regression with random effects.

1 reference

https://api.crossref.org/works/10.1136%2FBMJOPEN-2015-010002

21 January 2018

Clinical application of noninvasive prenatal testing for the detection of trisomies 21, 18, and 13: a hospital experience

1 reference

https://pubmed.ncbi.nlm.nih.gov/26781507

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Non-invasive prenatal testing for fetal aneuploidies in the first trimester of pregnancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/26781507

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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 weeks

1 reference

https://pubmed.ncbi.nlm.nih.gov/26781507

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Performance of screening for aneuploidies by cell-free DNA analysis of maternal blood in twin pregnancies

1 reference

https://pubmed.ncbi.nlm.nih.gov/26781507

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A non-invasive test for prenatal diagnosis based on fetal DNA present in maternal blood: a preliminary study

1 reference

https://pubmed.ncbi.nlm.nih.gov/26781507

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evaluating diagnostic tests: The area under the ROC curve and the balance of errors

1 reference

https://pubmed.ncbi.nlm.nih.gov/26781507

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting

1 reference

https://pubmed.ncbi.nlm.nih.gov/26781507

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome-selective sequencing of maternal plasma cell–free DNA for first-trimester detection of trisomy 21 and trisomy 18

1 reference

https://pubmed.ncbi.nlm.nih.gov/26781507

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Noninvasive prenatal testing of fetal aneuploidies by massively parallel sequencing in a prospective Chinese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/26781507

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Noninvasive prenatal testing of trisomies 21 and 18 by massively parallel sequencing of maternal plasma DNA in twin pregnancies

1 reference

https://pubmed.ncbi.nlm.nih.gov/26781507

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Noninvasive prenatal testing for fetal trisomies in a routinely screened first-trimester population

1 reference

https://pubmed.ncbi.nlm.nih.gov/26781507

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uptake of noninvasive prenatal testing (NIPT) in women following positive aneuploidy screening

1 reference

https://pubmed.ncbi.nlm.nih.gov/26781507

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

European non-invasive trisomy evaluation (EU-NITE) study: a multicenter prospective cohort study for non-invasive fetal trisomy 21 testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/26781507

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/BMJOPEN-2015-010002

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

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