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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Public Health Genomics Branch
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Precision Health Database
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Apr 23, 2024
. (Total: 63653 Documents since 2012)
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all[original query]>>Reproductive Health[Category]
Expanding Access to Noninvasive Prenatal Diagnosis for Monogenic Conditions to Consanguineous Families.
Britt Hanson et al. Clin Chem 2024
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Prenatal screening after preimplantation genetic testing for aneuploidy: time to evaluate old strategies.
María Gabriela Palacios-Verdú et al. Reprod Biomed Online 2024 48(6) 103761
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Accepting or declining preconception expanded carrier screening: An exploratory study with 407 couples.
Ariane J A G Van Tongerloo et al. J Genet Couns 2024
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Parental questions about sex chromosome aneuploidies regarding sex, gender, and sexual orientation as reported by genetic counselors in a prenatal setting.
Sarah Burzynski et al. J Genet Couns 2024
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Toward clinical exomes in diagnostics and management of male infertility
C Lillepea et al, AJHG, April 15, 2024
Clinical application value of pre-pregnancy carrier screening in Chinese Han childbearing population.
Li Tan et al. Mol Genet Genomic Med 2024 12(4) e2425
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Non-invasive prenatal test identifies circulating cell-free DNA chromosomal abnormalities derived from clonal hematopoiesis in aggressive hematological malignancies.
Valentina Giudice et al. Clin Exp Med 2024 24(1) 69
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Ultrasonographic Fetal Nuchal Translucency Measurements and Cytogenetic Outcomes.
Kara Bellai-Dussault et al. JAMA Netw Open 2024 7(3) e243689
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A rapid PCR-free next-generation sequencing method for comprehensive diagnosis of chromosome disease syndromes in prenatal samples.
Hong Su et al. Medicine (Baltimore) 2024 103(13) e37610
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Preparing for the bedside-optimizing a postpartum depression risk prediction model for clinical implementation in a health system.
Yifan Liu et al. J Am Med Inform Assoc 2024
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Predictive value of ultrasonic artificial intelligence in placental characteristics of early pregnancy for gestational diabetes mellitus.
Huien Zhou et al. Front Endocrinol (Lausanne) 2024 151344666
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Equitable Artificial Intelligence in Obstetrics, Maternal-Fetal Medicine, and Neonatology.
Ryan M McAdams et al. Obstet Gynecol 2024
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Parsimonious Waveform-derived Features consisting of Pulse Arrival Time and Heart Rate Variability Predicts the Onset of Septic Shock.
Moamen M Soliman et al. Biomed Signal Process Control 2024 92
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Prevalence of common autosomal recessive mutation carriers in women in the Southern Vietnam following the application of expanded carrier screening.
Xuan-Hong To-Mai et al. Sci Rep 2024 14(1) 7461
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Ready for polygenic risk scores? An analysis of regulation of preimplantation genetic testing in European countries.
M Siermann et al. Hum Reprod 2024
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Machine learning-enabled maternal risk assessment for women with pre-eclampsia (the PIERS-ML model): a modelling study.
Tünde Montgomery-Csobán et al. Lancet Digit Health 2024 6(4) e238-e250
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Pregnancy advances your 'biological' age - but giving birth turns it back.
Saima Sidik et al. Nature 2024
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Artificial intelligence in imaging in the first trimester of pregnancy: a systematic review.
Emma Umans et al. Fetal Diagn Ther 2024
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Predicting risk of preterm birth in singleton pregnancies using machine learning algorithms.
Qiu-Yan Yu et al. Front Big Data 2024 71291196
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Clinical experience of next generation sequencing based expanded carrier screening in high-risk couples from a tertiary healthcare center in Pakistan.
Fizza Akbar et al. Prenat Diagn 2024
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Researchers one step closer to preventing preeclampsia
Medical XPress, APA, March 14, 2024
Prenatal Genome-Wide Sequencing analysis (Exome or Genome) in detecting pathogenic Single Nucleotide Variants in fetal Central Nervous System Anomalies: systematic review and meta-analysis.
Enrica Marchionni et al. Eur J Hum Genet 2024
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Evaluation of Nanopore Sequencing on Polar Bodies for Routine Pre-Implantation Genetic Testing for Aneuploidy.
Anna Oberle et al. Clin Chem 2024
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Clinical value of screening prenatal ultrasound combined with chromosomal microarrays in prenatal diagnosis of chromosomal abnormalities.
Hongru Jiang et al. J Matern Fetal Neonatal Med 2024 37(1) 2324348
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'Something that helped the whole picture': Experiences of parents offered rapid prenatal exome sequencing in routine clinical care in the English National Health Service.
Hannah McInnes-Dean et al. Prenat Diagn 2024
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Performance of cell-free DNA testing for common fetal trisomies in triplet pregnancies.
Hoda Zakaria et al. Prenat Diagn 2024
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Enhancing gestational diabetes mellitus risk assessment and treatment through GDMPredictor: a machine learning approach.
J Xing et al. J Endocrinol Invest 2024
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What importance do donors and recipients attribute to the nuclear DNA-related genetic heritage of oocyte donation?
A Mayeur et al. Hum Reprod 2024
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Clinical utility of polygenic risk scores for embryo selection: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG).
Theresa A Grebe et al. Genet Med 2024 101052
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Prediction of pregnancy-related complications in women undergoing assisted reproduction, using machine learning methods.
Chen Wang et al. Fertil Steril 2024
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 23, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
,
National Center on Birth Defects and Developmental Disabilities
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