Non-invasive Prenatal Testing, What Patients Do Not Learn, May Be Due to Lack of Specialist Genetic Training by Gynecologists and Obstetricians?

Non-invasive prenatal testing for aneuploidy, copy number variants and single gene disorders

(2020) Joe Shaw et al.   REPRODUCTION

Sequencing Shorter cfDNA Fragments Decreases the False Negative Rate of Non-invasive Prenatal Testing

(2020) Ying Xue et al.   Frontiers in Genetics

Rethinking counselling in prenatal screening: An ethical analysis of informed consent in the context of non‐invasive prenatal testing (NIPT)

(2020) Adriana Kater‐Kuipers et al.   BIOETHICS

Non-invasive prenatal testing leading to a maternal diagnosis of Charcot–Marie–Tooth neuropathy

(2020) Camille Kumps et al.   JOURNAL OF HUMAN GENETICS

Screening for Fetal Chromosomal Abnormalities

(2020) et al.   OBSTETRICS AND GYNECOLOGY

Identification of copy number variants by NGS-based NIPT at low sequencing depth

(2020) Xiaoqing Ye et al.   European Journal of Obstetrics & Gynecology and Reproductive Biology

The importance of pre- and post-test counseling for prenatal cell-free DNA screening for common fetal aneuploidies

(2019) Vedran Stefanovic   EXPERT REVIEW OF MOLECULAR DIAGNOSTICS

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

(2019) Olga Žilina et al.   PRENATAL DIAGNOSIS

Result of Prospective Validation of the Trisomy Test® for the Detection of Chromosomal Trisomies

(2019) Sekelska et al.   Diagnostics

More than an information service: are counselling skills needed by genetics professionals in the genomic era?

(2018) Heather Skirton   EUROPEAN JOURNAL OF HUMAN GENETICS

Non-invasive fetal sex diagnosis in plasma of early weeks pregnants using droplet digital PCR

(2018) Elisabetta D’Aversa et al.   MOLECULAR MEDICINE

Discordant non-invasive prenatal testing (NIPT) - a systematic review

(2017) Tanja Schlaikjaer Hartwig et al.   PRENATAL DIAGNOSIS

Using fetal cells for prenatal diagnosis: History and recent progress

(2016) Arthur L. Beaudet   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Validation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations

(2016) Kornelia Neveling et al.   PRENATAL DIAGNOSIS

The implications of non-invasive prenatal testing failures: a review of an under-discussed phenomenon

(2016) Yuval Yaron   PRENATAL DIAGNOSIS

Screening for fetal aneuploidy

(2016) Britton D. Rink et al.   SEMINARS IN PERINATOLOGY

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

(2016) Sian Taylor-Phillips et al.   BMJ Open

Noninvasive Prenatal Testing and Incidental Detection of Occult Maternal Malignancies

(2015) Diana W. Bianchi et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

What Women Want: Lead Considerations for Current and Future Applications of Noninvasive Prenatal Testing in Prenatal Care

(2014) Ruth M. Farrell et al.   BIRTH-ISSUES IN PERINATAL CARE

Maternal Mosaicism Is a Significant Contributor to Discordant Sex Chromosomal Aneuploidies Associated with Noninvasive Prenatal Testing

(2013) Y. Wang et al.   CLINICAL CHEMISTRY

Commercial landscape of noninvasive prenatal testing in the United States

(2013) Ashwin Agarwal et al.   PRENATAL DIAGNOSIS

A method for noninvasive detection of fetal large deletions/duplications by low coverage massively parallel sequencing

(2013) Shengpei Chen et al.   PRENATAL DIAGNOSIS

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

(2013) T. K. Lau et al.   ULTRASOUND IN OBSTETRICS & GYNECOLOGY

Microdeletion and Microduplication Syndromes

(2012) Anja Weise et al.   JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY

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

(2011) Glenn E. Palomaki et al.   GENETICS IN MEDICINE