Cargando…

Validity and Utility of Non-Invasive Prenatal Testing for Copy Number Variations and Microdeletions: A Systematic Review

Valid data on prenatal cell-free DNA-based screening tests for copy number variations and microdeletions are still insufficient. We aimed to compare different methodological approaches concerning the achieved diagnostic accuracy measurements and positive predictive values. For this systematic review...

Descripción completa

Detalles Bibliográficos
Autores principales:	Zaninović, Luca, Bašković, Marko, Ježek, Davor, Katušić Bojanac, Ana
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Systematic Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9224664/ https://www.ncbi.nlm.nih.gov/pubmed/35743413 http://dx.doi.org/10.3390/jcm11123350

Ejemplares similares

Accuracy of Non-Invasive Prenatal Testing for Duchenne Muscular Dystrophy in Families at Risk: A Systematic Review
por: Zaninović, Luca, et al.
Publicado: (2023)

Circulating Cell-Free Tumor Deoxyribonucleic Acid Analysis as a Tool for the Diagnosis and Monitoring of Pediatric Solid Tumors
por: Zaninović, Luca, et al.
Publicado: (2023)

Trends in the treatment of undescended testes: a pediatric tertiary care center experience from Croatia
por: Bašković, Marko, et al.
Publicado: (2022)

The utility of cfDNA in TGCT patient management: a systematic review
por: Krasic, Jure, et al.
Publicado: (2022)

Astaxanthin Relieves Testicular Ischemia-Reperfusion Injury—Immunohistochemical and Biochemical Analyses
por: Bašković, Marko, et al.
Publicado: (2022)

Mast Cells in the Mammalian Testis and Epididymis—Animal Models and Detection Methods
por: Himelreich-Perić, Marta, et al.
Publicado: (2022)

Scrotal cooling as a protective method in tissue preservation after testicular torsion
por: Bašković, Marko, et al.
Publicado: (2021)

Epigenetically inactivated RASSF1A as a tumor biomarker
por: Raos, Dora, et al.
Publicado: (2021)

Non-invasive prenatal testing reveals copy number variations related to pregnancy complications
por: Wu, Guangping, et al.
Publicado: (2019)

Comprehensive Evaluation of Non-invasive Prenatal Screening to Detect Fetal Copy Number Variations
por: Wang, Jing, et al.
Publicado: (2021)

Teratoma Growth Retardation by HDACi Treatment of the Tumor Embryonal Source
por: Krasic, Jure, et al.
Publicado: (2020)

Leydig Cells in Patients with Non-Obstructive Azoospermia: Do They Really Proliferate?
por: Hauptman, Dinko, et al.
Publicado: (2021)

Influence of hyperthermal regimes on experimental teratoma development in vitro
por: Katusic Bojanac, Ana, et al.
Publicado: (2018)

Impact of Preanalytical and Analytical Methods on Cell-Free DNA Diagnostics
por: Krasic, Jure, et al.
Publicado: (2021)

Expanding the application of non-invasive prenatal testing in the detection of foetal chromosomal copy number variations
por: Wang, Chaohong, et al.
Publicado: (2021)

Expanding the Scope of Non-invasive Prenatal Testing to Detect Fetal Chromosomal Copy Number Variations
por: Chen, Songchang, et al.
Publicado: (2021)

Comparison of Bioinformatics Approaches for Fetal Microdeletions and Monogenic Variations Estimation in Non-invasive Prenatal Testing
por: Paul, Lizzy Teleboshe, et al.
Publicado: (2022)

Strategies to minimize false positives and interpret novel microdeletions based on maternal copy-number variants in 87,000 noninvasive prenatal screens
por: Kaseniit, Kristjan Eerik, et al.
Publicado: (2018)

CNV Hotspots in Testicular Seminoma Tissue and Seminal Plasma
por: Raos, Dora, et al.
Publicado: (2021)

Evaluation of the clinical effects of non‐invasive prenatal screening for diseases associated with aneuploidy and copy number variation
por: Zhu, Shaohua, et al.
Publicado: (2023)

Copy number variation and microdeletions of the Y chromosome linked genes and loci across different categories of Indian infertile males
por: Kumari, Anju, et al.
Publicado: (2015)

Evaluation of the clinical utility of extended non-invasive prenatal testing in the detection of chromosomal aneuploidy and microdeletion/microduplication
por: Tian, Weifang, et al.
Publicado: (2023)

Prenatal diagnosis of 913 fetuses samples using copy number variation sequencing
por: Lan, Liubing, et al.
Publicado: (2021)

Investigation on combined copy number variation sequencing and cytogenetic karyotyping for prenatal diagnosis
por: Zhang, Jinman, et al.
Publicado: (2021)

Combined use of karyotyping and copy number variation sequencing technology in prenatal diagnosis
por: Zhang, Suhua, et al.
Publicado: (2022)

Valproate Targets Mammalian Gastrulation Impairing Neural Tissue Differentiation and Development of the Placental Source In Vitro
por: Katušić-Bojanac, Ana, et al.
Publicado: (2022)

Transmembranous and enchondral osteogenesis in transplants of rat limb buds cultivated in serum‐ and protein‐free culture medium
por: Himelreich Perić, Marta, et al.
Publicado: (2022)

High Levels of Sample-to-Sample Variation Confound Data Analysis for Non-Invasive Prenatal Screening of Fetal Microdeletions
por: Chu, Tianjiao, et al.
Publicado: (2016)

Maternal Copy Number Imbalances in Non-Invasive Prenatal Testing: Do They Matter?
por: Hyblova, Michaela, et al.
Publicado: (2022)

In Search of TGCT Biomarkers: A Comprehensive In Silico and Histopathological Analysis
por: Raos, Dora, et al.
Publicado: (2020)

Maternal Xp22.31 copy-number variations detected in non-invasive prenatal screening effectively guide the prenatal diagnosis of X-linked ichthyosis
por: Tang, Xinxin, et al.
Publicado: (2022)

Global DNA methylation and chondrogenesis of rat limb buds in a three-dimensional organ culture system
por: Mužić-Radović, Vedrana, et al.
Publicado: (2022)

Correction: High Levels of Sample-to-Sample Variation Confound Data Analysis for Non-Invasive Prenatal Screening of Fetal Microdeletions
por: Chu, Tianjiao, et al.
Publicado: (2016)

Combining Z-Score and Maternal Copy Number Variation Analysis Increases the Positive Rate and Accuracy in Non-Invasive Prenatal Testing
por: Chen, Liheng, et al.
Publicado: (2022)

A Free Radical Scavenger Ameliorates Teratogenic Activity of a DNA Hypomethylating Hematological Therapeutic
por: Sobočan, Nikola, et al.
Publicado: (2019)

Seminal Plasma Protein N-Glycan Peaks Are Potential Predictors of Semen Pathology and Sperm Chromatin Maturity in Men
por: Maric, Tihana, et al.
Publicado: (2021)

Extended Prophylactic Effect of N-Tert-Butyl-α-Phenylnitron against Oxidative/Nitrosative Damage Caused by the DNA-Hypomethylating Drug 5-Azacytidine in the Rat Placenta
por: Sobočan, Nikola, et al.
Publicado: (2022)

Cell‐based noninvasive prenatal testing (cbNIPT) detects pathogenic copy number variations
por: Hatt, Lotte, et al.
Publicado: (2020)

Analysis of 17 Prenatal Cases with the Chromosomal 1q21.1 Copy Number Variation
por: Wen, Xiaohui, et al.
Publicado: (2022)

Copy number variations and cancer
por: Shlien, Adam, et al.
Publicado: (2009)

Cannot write session to /tmp/vufind_sessions/sess_7mktfpkoqu8ci0n19j3b6kaov0