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Precision Health Database


Genomics & Health Impact Scan Database|Search|PHGKB

Last data update: Jan 31, 2023. (Total: 52373 Documents since 2012)
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Query Trace: 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
Expecting more: the case for incorporating fertility services into comprehensive sickle cell disease care.
Lydia H Pecker et al. The Lancet. Haematology 2023
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
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)
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
Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death.
Byrne Alicia B et al. Nature medicine 2023
Informed Consent for Expanded Carrier Screening: Past, Present, and Future.
Rink Britton D et al. Prenatal diagnosis 2023
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
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
Intergenerational trends in reproduction: Infertility and pregnancy loss.
Woolner Andrea Mf et al. Best practice & research. Clinical obstetrics & gynaecology 2023 102305
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
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
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
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
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
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
Understanding the experiences and perspectives of prenatal screening among a diverse cohort.
Riches Naomi O et al. Prenatal diagnosis 2023
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
Maternal Copy Number Imbalances in Non-Invasive Prenatal Testing: Do They Matter?
Hyblova Michaela et al. Diagnostics (Basel, Switzerland) 2022 12(12)
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
The Value of a Comprehensive Genomic Evaluation in Prenatal Diagnosis of Genetic Diseases: A Retrospective Study.
Fu Fang et al. Genes 2022 13(12)
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
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)
Detecting mitochondrial mutations associated with aminoglycoside ototoxicity by noninvasive prenatal testing.
Huang Quanfei et al. Journal of clinical laboratory analysis 2022 e24827
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)
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
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
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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