Literature DB >> 27732785

Noninvasive Prenatal DNA Testing: The Vanguard of Genomic Medicine.

Lisa Hui1,2,3, Diana W Bianchi4,5,6.   

Abstract

Noninvasive prenatal DNA testing is the vanguard of genomic medicine. In only four years, this screening test has revolutionized prenatal care globally and opened up new prospects for personalized medicine for the fetus. There are widespread implications for increasing the scope of human genetic variation that can be detected before birth, and for discovering more about maternofetal and placental biology. These include an urgent need to develop pretest education for all pregnant women and consistent post-test management recommendations for those with discordant test results. The reduction in invasive testing has had downstream effects on specialist training and caused many countries to re-examine their national approaches to prenatal screening. Finally, the accumulating datasets of genomic information on pregnant women and their fetuses raise ethical issues regarding consent for future data mining and intellectual property.

Entities:  

Keywords:  cell-free DNA analysis; copy-number variants (CNVs); noninvasive prenatal screening; pregnancy; sex chromosome aneuploidy

Mesh:

Substances:

Year:  2016        PMID: 27732785     DOI: 10.1146/annurev-med-072115-033220

Source DB:  PubMed          Journal:  Annu Rev Med        ISSN: 0066-4219            Impact factor:   13.739


  12 in total

Review 1.  Liquid Biopsy Applications in the Clinic.

Authors:  Dake Chen; Tao Xu; Shubin Wang; Howard Chang; Tao Yu; Yu Zhu; Jian Chen
Journal:  Mol Diagn Ther       Date:  2020-04       Impact factor: 4.074

2.  [France and Great-Britain at the age of genomic medicine: new ethical challenges in reproductive medicine].

Authors:  Ruth Horn
Journal:  Med Sci (Paris)       Date:  2019-02-18       Impact factor: 0.818

3.  A Capabilities Approach to Prenatal Screening for Fetal Abnormalities.

Authors:  Greg Stapleton; Wybo Dondorp; Peter Schröder-Bäck; Guido de Wert
Journal:  Health Care Anal       Date:  2019-12

Review 4.  Personalized Medicine and the Power of Electronic Health Records.

Authors:  Noura S Abul-Husn; Eimear E Kenny
Journal:  Cell       Date:  2019-03-21       Impact factor: 41.582

Review 5.  Feto-Maternal Microchimerism: The Pre-eclampsia Conundrum.

Authors:  Sinuhe Hahn; Paul Hasler; Lenka Vokalova; Shane Vontelin van Breda; Nandor Gabor Than; Irene Mathilde Hoesli; Olav Lapaire; Simona W Rossi
Journal:  Front Immunol       Date:  2019-03-29       Impact factor: 7.561

6.  Just choice: a Danielsian analysis of the aims and scope of prenatal screening for fetal abnormalities.

Authors:  Greg Stapleton; Wybo Dondorp; Peter Schröder-Bäck; Guido de Wert
Journal:  Med Health Care Philos       Date:  2019-12

7.  Noninvasive prenatal diagnosis of β-thalassemia by relative haplotype dosage without analyzing proband.

Authors:  Haoxian Li; Bole Du; Fuman Jiang; Yulai Guo; Yang Wang; Chunsheng Zhang; Xiaojing Zeng; Yuhuan Xie; Shuming Ouyang; Yexing Xian; Min Chen; Weiqiang Liu; Xiaofang Sun
Journal:  Mol Genet Genomic Med       Date:  2019-09-30       Impact factor: 2.183

8.  Termination of pregnancy for fetal anomalies: Parents' preferences for psychosocial care.

Authors:  Frederike H W Dekkers; Attie T J I Go; Luuk Stapersma; Alex J Eggink; Elisabeth M W J Utens
Journal:  Prenat Diagn       Date:  2019-05-21       Impact factor: 3.050

9.  'Small cost to pay for peace of mind': Women's experiences with non-invasive prenatal testing.

Authors:  Hilary Bowman-Smart; Julian Savulescu; Cara Mand; Christopher Gyngell; Mark D Pertile; Sharon Lewis; Martin B Delatycki
Journal:  Aust N Z J Obstet Gynaecol       Date:  2019-02-06       Impact factor: 2.100

10.  Population-based impact of noninvasive prenatal screening on screening and diagnostic testing for fetal aneuploidy.

Authors:  Lisa Hui; Briohny Hutchinson; Alice Poulton; Jane Halliday
Journal:  Genet Med       Date:  2017-05-18       Impact factor: 8.822

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