Buchumschlag

Incidental Identification of Potentially Affected Individuals Through Expanded Carrier Screening During Preconception or Early Pregnancy

Fuente: Wiley Open Access

Gespeichert in:

Bibliographische Detailangaben
Hauptverfasser:	Yan Lü, Jiazhen Chang, Yulin Jiang, Xiya Zhou, Na Hao, Yiqing Yu, Mengmeng Li, Kaili Yin, Xueting Yang, Qingwei Qi
Format:	Artículo Open Access
Veröffentlicht:	Wiley 2025
Schlagworte:	Prenatal Diagnosis
Online-Zugang:	Acceder al recurso
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Ähnliche Einträge

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

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)

Fetal Fraction of Cell‐Free DNA and Its Interaction With Maternal Pre‐Pregnancy Body Mass Index on Multiple Adverse Pregnancy Outcomes
von: Xiya Qin, 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)

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

Spinal Muscular Atrophy Carrier Screening: Assessment of Provider Knowledge and Clinical Practice
von: Melissa Riegel, 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)

Screening Positive for Rare Autosomal Aneuploidies Increases Frequency of Adverse Pregnancy Outcomes and Alters Clinical Management
von: Devika Chawla, et al.
Veröffentlicht: (2025)

Diagnostic Yield of Serial PR Interval Screening for Fetal Heart Block in Anti‐SSA/SSB Pregnancies
von: Alyssa Yeung, et al.
Veröffentlicht: (2026)

Free Fetal DNA Testing to Guide Early Intervention in the Management of the Kell Alloimmunized Pregnancy
von: Kenneth J. Moise, et al.
Veröffentlicht: (2026)

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

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

The Potential of Tele‐Ultrasound, Handheld and Self‐Operated Ultrasound in Pregnancy Care: A Systematic Review
von: Shariva S. Kariman, et al.
Veröffentlicht: (2024)

‘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)

Perinatal Outcome of Early‐ and Late‐Onset Selective Fetal Growth Restriction in Monochorionic Diamniotic Twin Pregnancies
von: Li Zhao, et al.
Veröffentlicht: (2026)

Screening and Predictive Biomarkers for Down Syndrome Through Amniotic Fluid Metabolomics
von: Li‐Chao Zhang, et al.
Veröffentlicht: (2024)

Single‐Step Universal First‐Trimester Cytomegalovirus Screening and Valacyclovir Prophylaxis in Pregnancy: A Cost‐Utility Analysis in a High Seroprevalence Setting
von: Zhi Zhen Lim, et al.
Veröffentlicht: (2025)

Combined Cell‐Free DNA Screening for Aneuploidies and Selected Single‐Gene Disorders for Pregnancies With Sonographically Detected Fetal Anomalies: Detection Rate and Residual Risk
von: Thi Lan Anh Luong, et al.
Veröffentlicht: (2024)

Pregnancy Complications in Fetal Congenital Heart Disease: A Result of Common Early Developmental Pathways Rather Than Fetal Hemodynamics
von: Maartje C. Snoep, et al.
Veröffentlicht: (2025)

Cytogenetic and Microarray Analysis Follow‐Up of PGT‐A Mosaic and Sex Discrepant Embryos During Pregnancy: Absence of Confirmation and Follow‐Up Recommendations
von: Laura A. Kline, et al.
Veröffentlicht: (2026)

Confronting the Taboo of Multifetal Pregnancy Reduction: A Qualitative Study of Maternal Decision‐Making in Triplet Pregnancies
von: P. M. van Baar, et al.
Veröffentlicht: (2024)

Prenatal Tympanic Ring Anomaly Without Microtia: A Subtle Clue Toward Severe Early‐Onset Monogenic Disorders
von: Yung Hang Lam, et al.
Veröffentlicht: (2026)

Persistent Uninterpretable or Failed Prenatal Cell‐Free DNA Screening Indicates a High‐Risk Pregnancy and is Associated With Biological Factors Interfering With cfDNA‐Analysis: A Prospective Cohort Study
von: L. Lannoo, et al.
Veröffentlicht: (2025)

Diagnostic Yield of Exome Sequencing for Pregnancies With and Without Fetal Anomalies and for Stillbirth
von: Roni Zemet, et al.
Veröffentlicht: (2025)

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)

Genetic Investigation of Fetal Left‐Right Laterality Defects Identified in the Second Trimester of Pregnancy
von: Qiu‐Xia Yu, et al.
Veröffentlicht: (2026)

Fetal Rapid Eye Movement Sleep Dysfunction as a Potential Early Indicator for NALCN‐Related CLIFAHDD Syndrome: A Case Report
von: Fumiya Fukumori, et al.
Veröffentlicht: (2026)

Maternal Vascular Malperfusion and Anatomic Cord Abnormalities Are Prevalent in Pregnancies With Fetal Congenital Heart Disease
von: Chrystalle Katte Carreon, et al.
Veröffentlicht: (2024)

Sotalol Dose Optimization for Fetal Tachycardia: A Pregnancy Physiologically Based Pharmacokinetic Model Study
von: Hedwig van Hove, et al.
Veröffentlicht: (2026)

Amniocentesis and Risk of Fetal Loss in Dichorionic‐Diamniotic Twin Pregnancy: A Case‐Control Study
von: Sofia Roero, et al.
Veröffentlicht: (2025)

Clinical Utility of Nuchal Translucency Measurement in First‐Trimester Ultrasound Screening in a Setting With First‐Tier NIPT for Aneuploidy Screening
von: Eline E. R. Lust, et al.
Veröffentlicht: (2025)

Incidental Findings Identified by Prenatal Microarray Analysis and Consensus Reporting Criteria of the Catalan Public Health Network XIGENICS
von: Irene Mademont‐Soler, et al.
Veröffentlicht: (2025)

Intrauterine Transfusions in Fetuses Affected by Parvovirus B19: Complications, Challenges and Outcomes
von: Banu Özbakir, et al.
Veröffentlicht: (2026)

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

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)

Heterozygous Beta‐Thalassaemia in Pregnancy: Two Rare Causes of Severe Fetal Anemia Requiring Intrauterine Blood Transfusions
von: Eva van der Meij, et al.
Veröffentlicht: (2024)

The Perspectives and Experiences of Prospective Parents Declining Diagnostic Prenatal Genome Sequencing in Continuing Pregnancies With Fetal Structural Anomalies
von: Lisa S. Weingarten, et al.
Veröffentlicht: (2025)

Assessment of Fetal Cardiac Geometry and Systolic Function in Fetuses With Ventricular Septal Defect During the Second Trimester Using Fetal Heart Quantification Technology
von: Li Hou, et al.
Veröffentlicht: (2025)

CUL3 ‐Related Neurodevelopmental Disorder: Expanding the Prenatal Phenotype
von: Yoel Gofin, et al.
Veröffentlicht: (2026)

Case report of fetus with Lowe syndrome: Expanding the prenatal phenotype
von: Natalie Burrill, et al.
Veröffentlicht: (2024)