Prenatal Testing
What's New
Last Posted: May 24, 2022
- Systematic evidence-based review: The application of noninvasive prenatal screening using cell-free DNA in general-risk pregnancies
NC Rose et al, Genetics in Medicine, May 23, 2022 - Effectiveness of alternative prenatal genetic counselling methods in a cohort of pregnant women from a low socio-economic population.
Battese Ellis Katie et al. The Australian & New Zealand journal of obstetrics & gynaecology 2022 - Ethically robust reproductive genetic carrier screening needs to measure outcomes that matter to patients
L Dive et al, EJHG, May 18, 2022 - Clinician views and experiences of non-invasive prenatal genetic screening tests in Australia.
McKinn Shannon et al. The Australian & New Zealand journal of obstetrics & gynaecology 2022 - Same performance of exome sequencing before and after fetal autopsy for congenital abnormalities: toward a paradigm shift in prenatal diagnosis?
N Bourgon et al, EJHG, May 16, 2022 - Health economic evaluation of noninvasive prenatal testing and serum screening for down syndrome.
Xiao Gefei et al. PloS one 2022 17(4) e0266718 - Genetic counseling decisions in gestational carrier pregnancies.
Rasouli Melody A et al. Journal of assisted reproduction and genetics 2022 - Noninvasive Prenatal Test Results Indicative of Maternal Malignancies: A Nationwide Genetic and Clinical Follow-Up Study.
Heesterbeek Catharina J et al. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2022 JCO2102260 - Routine noninvasive prenatal screening for fetal Rh D in maternal plasma-A 2-year experience from a single center in Belgium.
Blomme Siska et al. Transfusion 2022 - A study on non-invasive prenatal screening for the detection of aneuploidy.
Chen Yao et al. Ginekologia polska 2022
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About RCH PHGKB
Reproductive and Child Health PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other materials that address the translation of genomic and other precision health discoveries into improved health care and prevention related to reproductive and child Health...more
Content Summary
- NIH Information (4)
- COVID-19 (2)
- Human Genome Epidemiologic Studies (33)
- Human Genomics Translation/Implementation Studies (532)
- Genomic Tests Evidence Synthesis (82)
- Genomic Tests Guidelines (35)
- Tier-Classified Guidelines (9)
- Non-Genomics Precision Health (2)
- State Public Health Genomics Programs (3)
- Reviews/Commentaries (214)
- Tools/Methods (5)
- Ethical/Legal and Social Issues (ELSI) (40)
Common RCH Related Topics
- Attention Deficit/Hyperactivity Disorder
- Autism
- Birth Defects
- Carrier Testing
- Cerebral Palsy
- Congenital heart defects
- Pregnancy loss
- Developmental Disabilities
- Gestational Diabetes
- Hearing loss
- Neural tube defects
- Infant Mortality
- Infertility
- Learning disability
- Newborn Screening
- Preeclampsia
- Prematurity
- Prenatal Testing
- Stillbirth
- Sudden Infant Death Syndrome
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by the CDC Office of Public Health Genomics to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Oct 1, 2021
- Page last updated:May 24, 2022
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