Journal Report

Prenatal Diagnosis

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Journal Information
Journal Title
Prenatal Diagnosis
Publisher
John Wiley and Sons Ltd
ISSN
0197-3851
E-ISSN
1097-0223
Database
SCOPUS
Domain
Health Sciences, Life Sciences
Classification History
Year A+ A B C
2026 ✓ ✓
2025 ✓ ✓
2024 ✓ ✓
2023 ✓
2021/2022 ✓ ✓
2020 ✓ ✓
2019 ✓ ✓
2018 ✓
A journal may have more than one classification in the same year. All recorded classifications are displayed.
Recent Articles
Integrated Prenatal Cardiopulmonary Assessment Using Fetal Echocardiography in Isolated Left‐Sided Congenital Diaphragmatic Hernia
Masaya Yamoto, Noboru Inamura, Katsuaki Toyoshima et al.
2026-11-7
DOI: 10.1002/pd.70298
Fetal Cells in Maternal Blood for Noninvasive Prenatal Testing—Is it Still a Distant Star?
Ripudaman Singh, Katarina Ravn, Line Dahl Jeppesen et al.
2026-11-7
DOI: 10.1002/pd.70304
Factors Associated With the Absence of Fetal Autopsy: Perception of Healthcare Professionals From a French Cross‐Sectional Survey
Camille Reyl, Sophie Martin‐Berenguer, Fanny Sauveste et al.
2026-11-4
DOI: 10.1002/pd.70287
Long‐Read Sequencing Resolves a Complex Acrocentric Chromosome Rearrangement and Enables Successful Preimplantation Genetic Testing
Xiao Zhang, Yanhong Lin, Mingyan Huang et al.
2026-11-4
DOI: 10.1002/pd.70299
Long‐Read Sequencing Resolves Phase in Prenatal Congenital Chloride Diarrhea Resulting From Inherited and de novo <i>SLC26A3</i> Variants
Himanshu Goel, Sheridan O'Donnell, Georgina Armstrong et al.
2026-11-3
DOI: 10.1002/pd.70288
Response to Letter to the Editor “Clinical Utility of Nuchal Translucency Measurement in First‐Trimester Ultrasound Screening in a Setting With First‐Tier NIPT for Aneuploidy Screening”
Eline E. R. Lust, Kim Bronsgeest, Monique C. Haak et al.
2026-11-2
DOI: 10.1002/pd.70290
Prenatal Presentation of Muggenthaler‐Chowdhury‐Chioza Syndrome Caused by Compound Heterozygous Variants in <i>HYAL2</i>
Pauline Planté‐Bordeneuve, Anne‐Cécile Leroy‐Tarissi, Marine Tessarech et al.
2026-10-29
DOI: 10.1002/pd.70289
Correction to “Fetal Sylvian Fissure Maturation in Congenital Heart Disease and Its Relation to Expected Brain Arterial Oxygen Saturation: A Longitudinal Study”
2026-10-25
DOI: 10.1002/pd.70261
Extended Non‐Invasive Prenatal Testing for Chromosomal and Monogenic Disorders by Cell‐Free DNA Sequencing: A Blinded Comparison With Amniocentesis
Alvaro Mesoraca, Katia Margiotti, Marco Fabiani et al.
2026-10-20
DOI: 10.1002/pd.70285
Complete Agenesis of the Corpus Callosum and Increased Nuchal Fold in a Fetus With Bainbridge–Ropers Syndrome due to a Likely Pathogenic <i>ASXL3</i> Variant
Shreyasi Sharma, Chanchal Singh, Radhika Aggarwal et al.
2026-10-18
DOI: 10.1002/pd.70284
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Printed: November 9, 2026 06:14