Academic Journal
Q1Prenatal Diagnosis
About Prenatal Diagnosis
About Prenatal Diagnosis
Prenatal Diagnosis is a peer-reviewed scholarly journal published by John Wiley and Sons Ltd (United Kingdom). It focuses on Q1. Publication coverage spans 1980-2026.
Key indicators: ISSN 1097-0223, 0197-3851; H-index 114.
Understanding This Journal's Metrics
Journal metrics help researchers assess fit, but they must be interpreted in context:
- H-index (114): Exceptionally high — 114 articles have each been cited at least 114 times. This indicates deep, sustained influence in the field.
Publishing in Prenatal Diagnosis
An established venue in its field. The journal welcomes solid, well-executed research. Ensure your manuscript fits the stated scope and follows author guidelines carefully.
- Scope fit: Confirm your research aligns with Q1. Off-scope manuscripts are typically desk-rejected quickly.
- Author guidelines: Follow formatting, reference style, and article-type requirements exactly — non-compliant manuscripts may be returned without review.
- Submission: Submit via the official journal website.
Is This Journal Right for Your Paper?
- Audience match: Will the journal's readers cite and build on your findings?
- Timeline: Higher-tier journals mean longer review and higher rejection risk. Balance prestige against your schedule.
- Indexing: Confirm indexing in Web of Science, Scopus, and PubMed (if biomedical) meets your institutional requirements.
- Open access needs: Check funder mandates and whether the journal offers compliant OA options.
Frequently Asked Questions
What is the ISSN of Prenatal Diagnosis?
1097-0223, 0197-3851.
Who publishes Prenatal Diagnosis?
John Wiley and Sons Ltd.
What are Prenatal Diagnosis's metrics?
H-index 114.
Where do I submit to Prenatal Diagnosis?
Via the official website.
Is Prenatal Diagnosis peer-reviewed?
Yes — it is a peer-reviewed scholarly journal indexed in major academic databases.
Source-backed journal facts
Topics in published research
Prenatal Screening and Diagnostics; Fetal and Pediatric Neurological Disorders; Genomic variations and chromosomal abnormalities; Pregnancy and preeclampsia studies; Congenital Anomalies and Fetal Surgery; Assisted Reproductive Technology and Twin Pregnancy.
OpenAlex classifies topics from published works. These topics are not the publisher’s official aims and scope.
Reported open-access list prices
4,640.00 USD; 3,870.00 EUR; 3,090.00 GBP
APC list prices reported by OpenAlex, which obtains this information from DOAJ. Confirm current charges, taxes, waivers and eligibility with the publisher; this is not a fee quotation.
Source: OpenAlex source record. Retrieved 2026-10-03. Source record updated 2026-10-02. OpenAlex metrics are different from SCImago metrics and the Clarivate Journal Impact Factor.
Journal Metrics
Quartile, SJR and the listed SCImago H-index use the 2025 imported SCImago dataset. A quartile may vary by subject category. Values without a source or reporting year are unverified historical entries. Verify the current Journal Impact Factor with Clarivate or the publisher before using it.
Aims & Scope
The publisher’s official aims and scope have not yet been verified for this profile. Use the journal website to check subject fit and accepted article types before submitting.
Recent Research Articles
Latest publications matched automatically by ISSN.
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Miriam Bertrand, Ute Grasshoff, Cornelia Wiechers, Dennis Witt et al.
2026-10-16 · DOI: 10.1002/pd.70263Standardized Technique for Full Laser Ablation of Feeding Artery in Fetuses With Bronchopulmonary Sequestration and Large Pleural Effusion: Lessons Learned Over 14 Years of Experience
Rogelio Cruz‐Martínez, Miguel Martínez‐Rodríguez, Andrea Peláez‐Jiménez, Abel Guzmán‐Ochoa et al.
2026-10-15 · DOI: 10.1002/pd.70273Microbial Culture Profiles Following Fetal Surgery Versus Spontaneous Preterm Prelabor Rupture of Membranes in Multifetal Gestations
Ohad Houri, Kinneret Tenenbaum Gavish, Bar Narkis, Ofir Sternfeld et al.
2026-10-15 · DOI: 10.1002/pd.70283Transplacental Flecainide and/or Digoxin for Fetal Tachyarrhythmias: Therapeutic Efficacy and Clinical Experience
Mukpradab Darakamas, Sanitra Anuwutnavin, Fuanglada Tongprasert, Wisit Chankhunaphas et al.
2026-10-15 · DOI: 10.1002/pd.70278Genetic Analysis in Monochorionic Diamniotic Twins Discordant for One Fetus With Structural Anomalies
Luyao Cai, Yao Zhang, Yingjun Yang, Gang Zou et al.
2026-10-15 · DOI: 10.1002/pd.70259Non‐Invasive Prenatal Diagnosis of Haemoglobinopathies: From Concept to Clinical Reality
Irene Leonidou, Leila Sallie, Morgan Jean Bell‐Ricketts, Alexandros Abdel Massih et al.
2026-10-15 · DOI: 10.1002/pd.70279First‐Trimester Cell‐Free DNA Screening for Common Trisomies Using Rolling‐Circle Amplification: A Prospective Study
Catalina De Paco Matallana, Javier Sánchez Romero, Miriam Pertegal, Juan Luis Delgado et al.
2026-10-13 · DOI: 10.1002/pd.70260Fetal Ganglionic Eminence Cysts as an Early Neuroimaging Finding for Mitochondrial Dysfunction Caused by a Novel TMEM70 Variant
Sergio Gómez‐Limón, Inés Tamarit, Óscar Toldos, Carmina Bermejo et al.
2026-10-10 · DOI: 10.1002/pd.70270Perinatal Outcomes and Determinants of Elective Embryo Reduction in Trichorionic Triplet Pregnancies
Carlota Rodó, Joaquín Temprado, Silvia Arévalo, Eva Roldán et al.
2026-10-10 · DOI: 10.1002/pd.70277Biological Specificities of Fetal Anemia Induced by Parvovirus B19 Infection
Anaïs Dugas, Paul Maurice, Pierre Olivo‐Marin, Mariam Chelghaf et al.
2026-10-10 · DOI: 10.1002/pd.70266Fetal Postmortem Examination: Confrontation Between the Required, the Needed, and the Accepted
Patricia Ibarra Vilar, Xin Kang, Mieke M. Cannie, Jacques C. Jani et al.
2026-10-10 · DOI: 10.1002/pd.70280Where in the Prenatal Screening Pathway do Ethnic and Socioeconomic Inequalities Occur? A UK Retrospective Cohort Study
Michelle Peter, Dagmar Tapon, Lyn S. Chitty, Melissa Hill et al.
2026-10-09 · DOI: 10.1002/pd.70274Current Practices in Antenatal CMV Testing and Management in Belgium
Elena Costa, Célia Primus‐de Jong, Leen Verleye, Renate Zeevaert et al.
2026-10-08 · DOI: 10.1002/pd.70272From Isolated to Complex: Diagnostic Yield of Chromosomal Microarray and Exome Sequencing in Fetal Growth Restriction
Hadas Miremberg, May Shabat, Maya Stok, Vered Offer Glasner et al.
2026-10-07 · DOI: 10.1002/pd.70258Genetic Investigation of Pregnancies With an Isolated Fetal Pelvic Kidney
Qiu‐Xia Yu, Li Zhen, Qi Tain, Si‐Yun Li et al.
2026-10-07 · DOI: 10.1002/pd.70271Universal Prenatal cfDNA‐Single Gene Disorder Screening for Autosomal Dominant Conditions in a Low‐Risk Cohort: A Cost‐Effectiveness Analysis
Megan E. Bunnell, Claire H. Packer, Sophie Adams, Yael Hoffman Sage et al.
2026-10-05 · DOI: 10.1002/pd.70269Clinical Performance Evaluation of Size‐Selective Placental Cell‐Free DNA Enrichment for Non‐Invasive Prenatal Testing of Fetal Copy Number Variants
Xiaoyi Liu, Xianzhen Cao, Liang Hu, Yanan Liu et al.
2026-10-04 · DOI: 10.1002/pd.70262Prenatal Sonographic Features of Heterozygous DLL1 Single‐Nucleotide Variants and 6q27 Deletions: A Single Referral Center Retrospective Case Series
Xiang‐Yi Jing, Qiu‐Xia Yu, Yong‐Ling Zhang, Jia‐Chun Guo et al.
2026-10-03 · DOI: 10.1002/pd.70265Opportunistic Prenatal Genetic Testing During Fetoscopic Laser Surgery for Twin–Twin Transfusion Syndrome
Jessian L. Munoz, Cara Buskmiller, April D. Adams, Ahmed A. Nassr et al.
2026-10-03 · DOI: 10.1002/pd.70267Reviews
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October 9, 2026 at 9:08 pm
October 2, 2026