Creating basis for introducing non‐invasive prenatal testing in the Estonian public health setting-Reference-Cited by-同舟云学术

Creating basis for introducing non‐invasive prenatal testing in the Estonian public health setting

Published:2019-11-06 Issue:13 Volume:39 Page:1262-1268
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:de
Short-container-title:Prenatal Diagnosis

Author:

Žilina Olga¹,Rekker Kadri²³,Kaplinski Lauris¹,Sauk Martin¹,Paluoja Priit²,Teder Hindrek²⁴,Ustav Eva‐Liina³⁵,Tõnisson Neeme⁶⁷,Reimand Tiia⁴⁷,Ridnõi Konstantin⁸⁹,Palta Priit⁶¹⁰,Vermeesch Joris Robert¹¹,Krjutškov Kaarel²¹²¹³,Kurg Ants¹,Salumets Andres²³⁴¹⁴^ORCID

Affiliation:

1. Institute of Molecular and Cell BiologyUniversity of Tartu Tartu Estonia

2. Competence Centre on Health Technologies Tartu Estonia

3. Department of Obstetrics and Gynaecology, Institute of Clinical MedicineUniversity of Tartu Tartu Estonia

4. Institute of Bio‐ and Translational MedicineUniversity of Tartu Tartu Estonia

5. Women's ClinicTartu University Hospital Tartu Estonia

6. Institute of GenomicsUniversity of Tartu Tartu Estonia

7. Department of Clinical GeneticsTartu University Hospital Tartu Estonia

8. Center for Perinatal Care, Women's Clinic, East‐Tallinn Central Hospital Tallinn Estonia

9. Department of Clinical Genetics, Institute of Clinical MedicineUniversity of Tartu Tartu Estonia

10. Institute for Molecular Medicine Finland (FIMM)University of Helsinki Helsinki Finland

11. Centre for Human GeneticsUniversity Hospital Leuven Department of Human Genetics, KU Leuven Leuven Belgium

12. Department of Biosciences and Nutrition, Karolinska Institutet Huddinge Sweden

13. Molecular Neurology Research ProgramUniversity of Helsinki and Folkhälsan Institute of Genetics Helsinki Finland

14. Department of Obstetrics and GynecologyUniversity of Helsinki and Helsinki University Hospital Helsinki Finland

Funder

Ettevõtluse Arendamise Sihtasutus

Eesti Teadusagentuur

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.5578

Reference25 articles.

1. Noninvasive prenatal testing: the future is now;Norwitz ER;Reviews in Obstetrics and Gynecology,2013

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

4. Analysis of cell-free fetal DNA in maternal blood for detection of trisomy 21, 18 and 13 in a general pregnant population and in a high risk population - a systematic review and meta-analysis

5. DNA sequencing of maternal plasma to detect Down syndrome: An international clinical validation study

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Association between low fetal fraction in cell‐free DNA screening and fetal chromosomal aberrations: A systematic review and meta‐analysis;Prenatal Diagnosis;2023-05-17

2. BinDel: software tool for detecting clinically significant microdeletions in low-coverage WGS-based NIPT samples;2022-09-23

3. Prenatal diagnosis of a 46,XY karyotype female fetus with an SRY-associated gonadal dysgenesis, conceived through an intracytoplasmic sperm injection: a case report;BMC Pregnancy and Childbirth;2022-02-05

4. Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples;PLOS Computational Biology;2021-12-20

5. From late fatherhood to prenatal screening of monogenic disorders: evidence and ethical concerns;Human Reproduction Update;2021-07-30