(Q34496747)

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

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scholarly article

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2 August 2017

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

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2 August 2017

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Jun Wang

34

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author name string

Fuman Jiang

1

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Jinghui Ren

2

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Fang Chen

3

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Yuqiu Zhou

4

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2 August 2017

Jiansheng Xie

5

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2 August 2017

Shan Dan

6

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2 August 2017

Yue Su

7

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2 August 2017

Jianhong Xie

8

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2 August 2017

Baomin Yin

9

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2 August 2017

Wen Su

10

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2 August 2017

Huakun Zhang

11

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2 August 2017

Wei Wang

12

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2 August 2017

Xianghua Chai

13

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2 August 2017

Linhua Lin

14

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2 August 2017

Hui Guo

15

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2 August 2017

Qiyun Li

16

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2 August 2017

Peipei Li

17

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2 August 2017

Yuying Yuan

18

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2 August 2017

Xiaoyu Pan

19

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2 August 2017

Yihan Li

20

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2 August 2017

Lifu Liu

21

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2 August 2017

Huifei Chen

22

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2 August 2017

Zhaoling Xuan

23

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2 August 2017

Shengpei Chen

24

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2 August 2017

Chunlei Zhang

25

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2 August 2017

Hongyun Zhang

26

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2 August 2017

Zhongming Tian

27

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2 August 2017

Zhengyu Zhang

28

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2 August 2017

Hui Jiang

29

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2 August 2017

Lijian Zhao

30

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2 August 2017

Weimou Zheng

31

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2 August 2017

Songgang Li

32

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2 August 2017

Yingrui Li

33

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2 August 2017

Jian Wang

35

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2 August 2017

Xiuqing Zhang

36

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2 August 2017

publication date

1 December 2012

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2 August 2017

BMC Medical Genomics

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2 August 2017

5

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2 August 2017

57

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2 August 2017

Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

Clinical diagnostic testing for the cytogenetic and molecular causes of male infertility: the Mayo Clinic experience

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

Prenatal screening for trisomy 21: recent advances and guidelines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

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=3544640

7 July 2018

Systematic bias in high-throughput sequencing data and its correction by BEADS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

Carrier testing for severe childhood recessive diseases by next-generation sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

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=3544640

7 July 2018

Targeted massively parallel sequencing of maternal plasma DNA permits efficient and unbiased detection of fetal alleles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

Turner's syndrome and pregnancy: has the 45,X/47,XXX mosaicism a different prognosis? Own clinical experience and literature review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

A review of trisomy X (47,XXX)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

Sensitivity of noninvasive prenatal detection of fetal aneuploidy from maternal plasma using shotgun sequencing is limited only by counting statistics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

Clinical practice. Prenatal screening for aneuploidy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

Effects of sex chromosome aneuploidy on male sexual behavior.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

Procedure-related complications of amniocentesis and chorionic villous sampling: a systematic review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

Plasma placental RNA allelic ratio permits noninvasive prenatal chromosomal aneuploidy detection

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

Meiotic segregation of sex chromosomes in mosaic and non-mosaic XYY males: case reports and review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

Cell-free fetal DNA and intact fetal cells in maternal blood circulation: implications for first and second trimester non-invasive prenatal diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

Rapid clearance of fetal DNA from maternal plasma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3544640

7 July 2018

Turner's Syndrome

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-5-57

21 January 2018

Screening for trisomies 21, 18 and 13 by maternal age, fetal nuchal translucency, fetal heart rate, free beta-hCG and pregnancy-associated plasma protein-A.

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-5-57

21 January 2018

Early detection of cell-free fetal DNA in maternal plasma.

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-5-57

21 January 2018

Accurate and robust quantification of circulating fetal and total DNA in maternal plasma from 5 to 41 weeks of gestation.

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-5-57

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-5-57

21 January 2018

Detection and quantification of fetal DNA in maternal plasma by using LightCycler technology

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-5-57

21 January 2018

Presence of fetal DNA in maternal plasma and serum

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-5-57

21 January 2018

Detection of Trisomy 21 by Quantitative Mass Spectrometric Analysis of Single-Nucleotide Polymorphisms

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-5-57

21 January 2018

Noninvasive Prenatal Detection of Fetal Trisomy 18 by Epigenetic Allelic Ratio Analysis in Maternal Plasma: Theoretical and Empirical Considerations

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-5-57

21 January 2018

Choosing the best prenatal screening protocol

1 reference

https://pubmed.ncbi.nlm.nih.gov/23198897

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/23198897

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fetal loss associated with second trimester amniocentesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23198897

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1755-8794-5-57

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

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PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

ResearchGate publication ID

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