Copertina

Integrating the Continuum of Genetic Testing From Fetus to Neonate: A Review of Prenatal Genetic Testing and the Overlap With Newborn Testing

Fuente: Wiley Open Access

Salvato in:

Dettagli Bibliografici
Autori principali:	Sarah Harris, Neeta L. Vora
Natura:	Artículo Open Access
Pubblicazione:	Wiley 2025
Soggetti:	Prenatal Diagnosis
Accesso online:	Acceder al recurso
Tags:	Aggiungi Tag Nessun Tag, puoi essere il primo ad aggiungerne!!

Documenti analoghi

Cranial, Renal, and Skeletal Anomalies in a Fetus With a Pathogenic Variant in the TAFAZZIN Gene
di: Cordelia R. Muir, et al.
Pubblicazione: (2025)

Prenatal Detection of TGFBR1 Variant Associated With Severe Ventriculomegaly and Loeys–Dietz Syndrome
di: Mia B. Hodges, et al.
Pubblicazione: (2025)

Can Prenatal Ultrasound and Genetic Testing Reliably Exclude Non‐Isolated Clubfoot?
di: Jana M. de Vries, et al.
Pubblicazione: (2025)

The Ultrasound and Genetic Characteristics of Fetuses With Laterality Defects—A Prenatal Cohort in Asian Population
di: Wu Yi, et al.
Pubblicazione: (2025)

Application of Genetic Origin Analysis of Copy Number Variations in Non‐Invasive Prenatal Testing
di: Jing Wang, et al.
Pubblicazione: (2024)

Novel Missense Variant in the FGFR1 Gene Associated With Prenatal Diagnosis of Hartsfield Syndrome
di: Mia B. Hodges, et al.
Pubblicazione: (2025)

Prenatal Diagnosis of Arthrogryposis Multiplex Congenita (AMC): Ultrasound and Genetic Findings in 69 Fetuses From 67 Unrelated Families
di: Tingting Yao, et al.
Pubblicazione: (2026)

Novel Missense Variant in the SMARCD1 Gene as the Cause of Coffin–Siris Syndrome 11 in a Fetus With Ambiguous Genitalia and Multiple Dysmorphic Features
di: Rachel A. Veazey, et al.
Pubblicazione: (2024)

Comparing the Introduction and Implementation of Noninvasive Prenatal Testing (NIPT) in Japan, the Netherlands, and the United States: An Integrative Review
di: Chloe Connor, et al.
Pubblicazione: (2025)

Potential of Nanopore Long Read Sequencing for Determining CTG Repeat Lengths in the DMPK1 Gene During Prenatal or Preimplantation Genetic Testing
di: Yui Shichiri, et al.
Pubblicazione: (2025)

Reproductive Decision‐Making Among BRCA1/2 Pathogenic Variants Carriers and Physicians: Attitudes Toward Preimplantation and Prenatal Genetic Testing
di: Marta D'Alonzo, et al.
Pubblicazione: (2026)

Prenatal Diagnostic Testing for Adult‐Onset Neurodegenerative Disease
di: Maya Rawal, et al.
Pubblicazione: (2025)

Clinically Significant Genetic Results in Fetuses With Isolated Horseshoe Kidney
di: Qiu‐Xia Yu, et al.
Pubblicazione: (2026)

Genetic Diagnosis and Clinical Features of Fetuses With Congenital Diaphragmatic Hernia
di: Yan Lü, et al.
Pubblicazione: (2024)

Risk of Genetic Abnormality in Fetuses With Unilateral Versus Bilateral Pleural Effusions
di: Brian Burnett, et al.
Pubblicazione: (2024)

A Decade of Prenatal Genetic Diagnostics: Insights From 1949 Cases at a Medical Genetics Facility in South India
di: Roopadarshini Balasubramanian, et al.
Pubblicazione: (2025)

Severe Early‐Onset Fetal Growth Restriction: The Yield of Antenatal and Postnatal Genetic Testing
di: Matthew H. Mossayebi, et al.
Pubblicazione: (2026)

Optical Genome Mapping for Prenatal Diagnosis in Fetuses With Structural Anomalies
di: Yiyun Xu, et al.
Pubblicazione: (2025)

Disparities in Prenatal Carrier Screening Including Partner Testing by Insurance Status
di: Spencer C. Darveau, et al.
Pubblicazione: (2026)

Placental and Fetal Brain Volumes in Congenital Heart Disease Are Smallest Among Fetuses With Genetic Abnormalities
di: Sonali Ajwani, et al.
Pubblicazione: (2025)

High Risk for Rare Autosomal Trisomies Detected by Non‐Invasive Prenatal Testing: Prenatal Diagnosis and Pregnancy Outcomes
di: Zihan Jiang, et al.
Pubblicazione: (2026)

Diagnosed After Birth—But Detectable Before? A Cohort Study of Prenatal Testing Potential
di: Allison Schartman, et al.
Pubblicazione: (2026)

Sex Ratios at Birth Following Non‐Invasive Prenatal Testing in Victoria, Australia
di: Hilary Bowman‐Smart, et al.
Pubblicazione: (2026)

Exome Sequencing of Fetuses With Intracranial Hemorrhage Unravels Novel Causative Genes and an Extreme Genetic Heterogeneity
di: Thibault Coste, et al.
Pubblicazione: (2025)

Fetal Pancreas in Growth Restriction: A Prenatal Window Into Metabolic and Genetic Risk
di: Hadas Miremberg, et al.
Pubblicazione: (2025)

Prenatal Diagnosed Agenesis of the Corpus Callosum: Identifying the Underlying Genetic Etiologies
di: Xing Wei, et al.
Pubblicazione: (2024)

The Intersection Between Genetic Reproductive Carrier Screening and Genomic Newborn Screening: Implications for Clinical Practice
di: Lilian Downie, et al.
Pubblicazione: (2025)

Clinical and Molecular Features of Ciliopathies Diagnosed by Prenatal Exome Sequencing in Fetuses With Ultrasound Abnormalities
di: Xiaofan Zhu, et al.
Pubblicazione: (2025)

Monocentric Study on the Performance of Noninvasive Prenatal Testing on Cell‐Free DNA for the Detection of Monosomy X
di: Kelly Steinfort, et al.
Pubblicazione: (2024)

Genetic Investigation of Fetuses With Isolated Unilateral Renal Agenesis Identified on Second Trimester Ultrasound: A Single Referral Center Experience
di: Yong‐Ling Zhang, et al.
Pubblicazione: (2025)

Prenatal Screening for Fetal X‐Linked Ichthyosis: A Large Cohort Study Combining Non‐Invasive Prenatal Testing and Maternal Serum Unconjugated Estriol Analysis
di: Miao Han, et al.
Pubblicazione: (2026)

Differences in Prenatal and Postnatal Phenotypic Evaluations in Patients With Congenital Anomalies and Known Genetic Diagnoses
di: Nicole Horton, et al.
Pubblicazione: (2025)

Prenatal and Perinatal Outcomes in Fetuses With Macrocystic Congenital Pulmonary Airway Malformations: Thoracoamniotic Shunting Versus Expectant Management
di: Laurence Sophie Carmant, et al.
Pubblicazione: (2026)

Prenatal Exome Sequencing Analysis in Fetuses With Structural Anomalies: A Multicenter Prospective Cohort Study With Practical Implications
di: Yulin Jiang, et al.
Pubblicazione: (2025)

The Clinical Utility of Sequence‐Based Genetic Testing for Fetal Edema Following Non‐Diagnostic Microarray Results: A Population‐Based Cohort Study
di: Victoria M. Allen, et al.
Pubblicazione: (2026)

Confined Placental Mosaicism Detected With Non‐Invasive Prenatal Testing: Is There an Association Between Mosaic Ratio and Pregnancy Outcome?
di: Geerke M. Eggenhuizen, et al.
Pubblicazione: (2024)

Use of Prenatal Exome Sequencing: Opinion Statement of the French Federation of Human Genetics Working Group
di: Guillaume Cogan, et al.
Pubblicazione: (2024)

Clinical Implications of Noninvasive Prenatal Testing Failures Due to Low Fetal Fraction: Associations With Adverse Maternal and Fetal Outcomes
di: Yuan Ren, et al.
Pubblicazione: (2025)

Hereditary Spherocytosis: A Case Series Spanning Prenatal Detection to Neonatal Care
di: Carly M. Smith, et al.
Pubblicazione: (2026)

Prenatal Diagnosis of a KIDINS220 De Novo Heterozygous Variant in a Fetus With a Complex CNS Anomaly
di: Hadas Miremberg, et al.
Pubblicazione: (2024)