Last Posted: Sep 22, 2022
- Multisite assessment of the impact of cell-free DNA-based screening for rare autosomal aneuploidies on pregnancy management and outcomes.
Mossfield Tamara et al. Frontiers in genetics 2022 13975987
- Preimplantation genetic testing for aneuploidy in severe male factor infertility: protocol for a multicenter randomised controlled trial.
Lin Xian-Hua et al. BMJ open 2022 12(7) e063030
- External Validation of a Retinopathy of Prematurity Screening Model Using Artificial Intelligence in 3 Low- and Middle-Income Populations.
Coyner Aaron S et al. JAMA ophthalmology 2022
- The Prediction of Preterm Birth Using Time-Series Technology-Based Machine Learning: Retrospective Cohort Study.
Zhang Yichao et al. JMIR medical informatics 2022 10(6) e33835
- Associations between ambient temperature and risk of preterm birth in Sweden: A comparison of analytical approaches.
de Bont Jeroen et al. Environmental research 2022 113586
- Machine Learning Prediction Models for Neurodevelopmental Outcome After Preterm Birth: A Scoping Review and New Machine Learning Evaluation Framework.
van Boven Menne R et al. Pediatrics 2022
- Prediction of preterm birth using artificial intelligence: a systematic review.
Akazawa Munetoshi et al. Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology 2022 1-7
- The role of the first trimester screen in the face of normal cell free DNA.
Strauss Tirtza Spiegel et al. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2022 1-6
- Inborn Errors of Immunity With Fetal or Perinatal Clinical Manifestations.
Carneiro-Sampaio Magda et al. Frontiers in pediatrics 2022 10891343
- Early Diagnosis and Quantitative Analysis of Stages in Retinopathy of Prematurity Based on Deep Convolutional Neural Networks.
Li Peng et al. Translational vision science & technology 2022 11(5) 17
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
- CDC Information (6)
- NIH Information (2)
- COVID-19 (30)
- CDC Publications (1)
- Human Genome Epidemiologic Studies (342)
- GWAS Studies (6)
- Human Genomics Translation/Implementation Studies (61)
- Genomic Tests Evidence Synthesis (10)
- Genomic Tests Guidelines (3)
- Non-Genomics Precision Health (47)
- Pathogen Advanced Molecular Detection (9)
- State Public Health Genomics Programs (2)
- Reviews/Commentaries (40)
- Tools/Methods (3)
- Ethical/Legal and Social Issues (ELSI) (2)
Common RCH Related Topics
- Attention Deficit/Hyperactivity Disorder
- Birth Defects
- Carrier Testing
- Cerebral Palsy
- Congenital heart defects
- Pregnancy loss
- Developmental Disabilities
- Gestational Diabetes
- Hearing loss
- Neural tube defects
- Infant Mortality
- Learning disability
- Newborn Screening
- Prenatal Testing
- 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.