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Public Health Genomics and Precision Health Knowledge Base (v8.2)
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Last data update: Jan 31, 2023
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all[original query]>>Reproductive Health[Category]
A Bayesian network model for prediction of low or failed fertilization in assisted reproductive technology based on a large clinical real-world data.
Tian Tian et al. Reproductive biology and endocrinology : RB&E 2023 21(1) 8
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Expecting more: the case for incorporating fertility services into comprehensive sickle cell disease care.
Lydia H Pecker et al. The Lancet. Haematology 2023
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Declining Male Sperm Count Is at a Global Crisis Level
Medscape, January 30, 2023
Digital mental health for postpartum women: perils, pitfalls, and promise.
Natalie Feldman et al. NPJ digital medicine 2023 6(1) 11
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How Wearable Sensors Can Support the Research on Foetal and Pregnancy Outcomes: A Scoping Review
A Maugeri et al, JPM, January 2023
Accuracy of Non-Invasive Prenatal Testing for Duchenne Muscular Dystrophy in Families at Risk: A Systematic Review.
Zaninovic Luca et al. Diagnostics (Basel, Switzerland) 2023 13(2)
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Decision-making process about prenatal genetic screening: how deeply do moms-to-be want to know from Non-Invasive Prenatal Testing?
Oliveri Serena et al. BMC pregnancy and childbirth 2023 23(1) 38
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Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death.
Byrne Alicia B et al. Nature medicine 2023
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Informed Consent for Expanded Carrier Screening: Past, Present, and Future.
Rink Britton D et al. Prenatal diagnosis 2023
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Attitudes of professional stakeholders towards implementation of reproductive genetic carrier screening: a systematic review.
Pasquier Laurent et al. European journal of human genetics : EJHG 2023
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Non-invasive prenatal testing for the detection of trisomies 21, 18, and 13 in pregnant women with various clinical indications: A multi-center observational study of 1,854,148 women in China.
Xiang Liangcheng et al. Prenatal diagnosis 2023
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Intergenerational trends in reproduction: Infertility and pregnancy loss.
Woolner Andrea Mf et al. Best practice & research. Clinical obstetrics & gynaecology 2023 102305
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Community Genetics screening in a pandemic: solutions for pre-test education, informed consent, and specimen collection.
Terrill Bronwyn et al. European journal of human genetics : EJHG 2023 1-5
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Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia.
Guzmán-Jiménez Andrea et al. Frontiers in cell and developmental biology 2023 101089782
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Prenatal genetic evaluation of fetuses with structural anomaly: is it time to shift from microarray to exome sequencing as a first-tier test?
Lin X-M et al. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2023 61(1) 119-120
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A Multi-centre Experience of Trans-abdominal Chorionic Villus Sampling in Pakistan.
Baqai Shehla et al. Journal of the College of Physicians and Surgeons--Pakistan : JCPSP 2023 33(1) 37-40
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Experience using singleton exome sequencing of probands as an approach to preconception carrier screening in consanguineous couples.
Abulí Anna et al. Journal of medical genetics 2023
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Bridging the Gap between AZF Microdeletions and Karyotype: Twelve Years' Experience of an Infertility Center.
Kalantari Hamid et al. The world journal of men's health 2023
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Understanding the experiences and perspectives of prenatal screening among a diverse cohort.
Riches Naomi O et al. Prenatal diagnosis 2023
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A systematic review and meta-analysis of cell-free DNA testing for detection of fetal sex chromosome aneuploidy.
Shear Matthew A et al. Prenatal diagnosis 2023
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Maternal Copy Number Imbalances in Non-Invasive Prenatal Testing: Do They Matter?
Hyblova Michaela et al. Diagnostics (Basel, Switzerland) 2022 12(12)
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A decade of non-invasive prenatal screening in Australia: National impact on prenatal screening and diagnostic testing.
Hui Lisa et al. The Australian & New Zealand journal of obstetrics & gynaecology 2022
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The Value of a Comprehensive Genomic Evaluation in Prenatal Diagnosis of Genetic Diseases: A Retrospective Study.
Fu Fang et al. Genes 2022 13(12)
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Development and validation of the prediction models for preeclampsia: a retrospective, single-center, case-control study.
Chen Xuhong et al. Annals of translational medicine 2022 10(22) 1221
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The Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and Implementation.
Archibald Alison D et al. Journal of personalized medicine 2022 12(11)
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Detecting mitochondrial mutations associated with aminoglycoside ototoxicity by noninvasive prenatal testing.
Huang Quanfei et al. Journal of clinical laboratory analysis 2022 e24827
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Real-World Results from Combined Screening for Monogenic Genomic Health Risks and Reproductive Risks in 300 Adults.
Wildin Robert S et al. Journal of personalized medicine 2022 12(12)
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Associated factors with parental pregnancy decision-making and use of consultation after a prenatal congenital heart disease diagnosis.
Chih Wan-Ling et al. Pediatrics and neonatology 2022
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Patients with Recurrent Pregnancy Loss Have Similar Embryonic Preimplantation Genetic Testing Aneuploidy Rates and In Vitro Fertilization Outcomes to Infertility Patients.
Kornfield Molly Siegel et al. F&S reports 2022 3(4) 342-348
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Preimplantation genetic testing for aneuploidies screening is not diagnostic.
Barad David H et al. F&S reports 2022 3(4) 294-295
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Page last reviewed:
Jul 25, 2022
Page last updated:
Jan 31, 2023
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