Buchumschlag

Disparities in Prenatal Carrier Screening Including Partner Testing by Insurance Status

Fuente: Wiley Open Access

Gespeichert in:

Bibliographische Detailangaben
Hauptverfasser:	Spencer C. Darveau, Isabel Murray, Disha Trivedi, Stephen T. Chasen
Format:	Artículo Open Access
Veröffentlicht:	Wiley 2026
Schlagworte:	Prenatal Diagnosis
Online-Zugang:	Acceder al recurso
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Ähnliche Einträge

Prenatal Diagnosis of Congenital Paraesophageal Hernia With Gastric Volvulus and Postnatal FBN1 Mutation Confirmation
von: Spencer C. Darveau, et al.
Veröffentlicht: (2025)

‘I Could Trust It’: Experiences of Reciprocal Translocation Carriers and Their Partners With Prenatal Cell‐Free DNA Screening for Unbalanced Translocations
von: Marta Cifuentes Ochoa, et al.
Veröffentlicht: (2024)

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

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

Quality of Evidence for Prenatal Down Syndrome Screening: An Umbrella Review
von: Yuehua Zhang, et al.
Veröffentlicht: (2026)

Theoretical Performance of Comprehensive Non‐Invasive Prenatal Screening in Congenital Heart Defects
von: Emily Yang, et al.
Veröffentlicht: (2026)

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

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

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

Blazing the Trail of Non‐Invasive Prenatal Screening Expanded Use: Healthcare Providers' Perspectives
von: Tierry M. Laforce, et al.
Veröffentlicht: (2025)

Prenatal Ultrasound in the Diagnosis of Anorectal Malformations: Correlating Prenatal Signs With Postnatal Outcomes
von: D. Huijgen, et al.
Veröffentlicht: (2024)

Spinal Muscular Atrophy Carrier Screening: Assessment of Provider Knowledge and Clinical Practice
von: Melissa Riegel, et al.
Veröffentlicht: (2025)

Integrating the Continuum of Genetic Testing From Fetus to Neonate: A Review of Prenatal Genetic Testing and the Overlap With Newborn Testing
von: Sarah Harris, et al.
Veröffentlicht: (2025)

Prenatal Screening Via cfDNA – Paired‐End Sequencing Utilizing Fragment Size Information Reduces the Screen Positive Rate for X Chromosome Aneuploidies
von: Susan Hancock, et al.
Veröffentlicht: (2026)

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

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

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

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

Performance of Prenatal Cell‐Free DNA Screening for Foetal Chromosome Aneuploidies and Microdeletion/Microduplication Syndromes: A Retrospective Study of 64,482 Consecutive Cases From a Prenatal Diagnosis Centre in China
von: Feiyan Pan, et al.
Veröffentlicht: (2025)

Artifacts, Not Differences in Sex Development, Are the Predominant Cause of Phenotypic Sex Discordance With Prenatal Cell‐Free DNA Screening: A Review of 33 Cases
von: Qiliang Ding, et al.
Veröffentlicht: (2025)

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

Incidental Identification of Potentially Affected Individuals Through Expanded Carrier Screening During Preconception or Early Pregnancy
von: Yan Lü, et al.
Veröffentlicht: (2025)

Correspondence on “Current Controversy in Prenatal Diagnosis: The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use”
von: Julia Wynn, et al.
Veröffentlicht: (2024)

Evaluation of Maternal Safety Following Prenatal Cell and Gene Therapy for Hemophilia A
von: Quan Minh Pham, et al.
Veröffentlicht: (2026)

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

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

PIGO Gene Variants: New Insights Into Prenatal Diagnosis
von: A. Zambiasi, et al.
Veröffentlicht: (2025)

Analysis of Prenatal Sonographic Features in Rare Fetal Giant Hepatic Hemangioma and Prediction of Prenatal Complications and Prognosis
von: Ling Xu, et al.
Veröffentlicht: (2025)

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

Diagnosis and Management of Prenatal Hereditary Pyropoikilocytosis
von: Connor Hartzell, et al.
Veröffentlicht: (2025)

Improving the Performance of Prenatal Cell‐Free DNA Screening Through Size‐Selective Fetal DNA Enrichment in a Cohort of 71,986 General and High‐Risk Pregnancies
von: Liang Hu, et al.
Veröffentlicht: (2025)

Hemophilia A: An Ideal Disease for Prenatal Therapy
von: Christopher D. Porada, et al.
Veröffentlicht: (2025)

The Arrival of Exome Sequencing in French Prenatal Diagnosis: An Exploratory Qualitative Study Among Professionals in Prenatal Diagnosis Centers: Prenatome‐SHS
von: Charlène Daval, et al.
Veröffentlicht: (2025)

Approaching Universal Prenatal Detection of Significant Cardiovascular Malformations in Nevada
von: William N. Evans, et al.
Veröffentlicht: (2024)

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

Non‐Invasive Prenatal Testing Results, Nuchal Translucency Size, and Second Trimester Resolution Modify First Trimester Cystic Hygroma Outcomes
von: Michelle Joy Wang, et al.
Veröffentlicht: (2025)

Attitudes Toward Prenatal Interventions in the Fanconi Anemia Community
von: Tony Lum, et al.
Veröffentlicht: (2026)

Brain Abnormalities in Prenatally Diagnosed Rubinstein‐Taybi Syndrome
von: Laurence S. Carmant, et al.
Veröffentlicht: (2025)

Prenatal diagnosis of pontocerebellar hypoplasia with postnatal follow‐up
von: Alienor Jaillard, et al.
Veröffentlicht: (2024)

Parental Somatic Mosaicism Detected During Prenatal Diagnosis
von: Natalie J. Chandler, et al.
Veröffentlicht: (2024)