In case you missed it: The Prenatal Diagnosis editors bring you the most significant advances of 2019-Reference-Cited by-同舟云学术

In case you missed it: The Prenatal Diagnosis editors bring you the most significant advances of 2019

Published:2020-01-29 Issue:3 Volume:40 Page:287-293
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenatal Diagnosis

Author:

Chitty LS¹^ORCID,Hui L²,Ghidini A³^ORCID,Levy B⁴,Deprest J⁵,Van Mieghem T⁶,Bianchi DW⁷

Affiliation:

1. London North Genomic Laboratory, Great Ormond Street NHS Foundation Trust, and Genetics and Genomic MedicineUCL Great Ormond Street Institute of Child Health London UK

2. Department of Obstetrics and GynaecologyUniversity of Melbourne Melbourne Victoria Australia

3. Antenatal Testing CentreInova Alexandria Hospital Alexandria VA

4. Departments of Pathology and Cell BiologyColumbia University New York NY

5. Departments of Obstetrics and GynaecologyUniversity Hospitals Leuven Leuven Belgium

6. Department of Obstetrics and GynaecologyMount Sinai Hospital and University of Toronto Toronto Ontario Canada

7. Eunice Kennedy Shriver National Institute of Child Health and Human DevelopmentNational Institutes of Health Bethesda MD

Funder

NIHR Biomedical Research Centre, Royal Marsden NHS Foundation Trust/Institute of Cancer Research

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.5632

Reference62 articles.

1. Free fetal DNA in maternal plasma in anembryonic pregnancies: confirmation that the origin is the trophoblast

2. Predominant Hematopoietic Origin of Cell-free DNA in Plasma and Serum after Sex-mismatched Bone Marrow Transplantation

3. The impact of maternal plasma DNA fetal fraction on next generation sequencing tests for common fetal aneuploidies

4. HuiL BianchiDW. Fetal fraction and noninvasive prenatal testing: what clinicians need to know. Prenat Diagn2019; dos:https://doi.org/10.1002/pd.5620

5. Comparing methods for fetal fraction determination and quality control of NIPT samples

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1. Counseling in a Changing World of Genetics;Prenatal Diagnostic Testing for Genetic Disorders;2023

2. Detection of 46, XY Disorder of Sex Development (DSD) Based on Plasma Cell-Free DNA and Targeted Next-Generation Sequencing;Genes;2021-11-25

3. The fetus in the age of the genome;Human Genetics;2021-08-23

4. Comprehensive non-invasive prenatal screening for pregnancies with elevated risks of genetic disorders: protocol for a prospective, multicentre study;BMJ Open;2021-08

5. Prediction of preterm birth in nulliparous women using logistic regression and machine learning;PLOS ONE;2021-06-30