Impact Factor
3.47
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
2.69
1,193 total citations
h5-index
35
h5 depth signal
Cited share
69.4%
311 of 448
Total citations
1,193
Citation footprint
Metric signal
2.28
External metric anchor
Self-citation
14.1%
168 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
United States
695
China
313
United Kingdom
239
Netherlands
168
France
164
Citing Fields of Research
Cytogenetics
1,096
Congenital Disorders
1,043
Obstetrics/Gynecology
566
Genetics & Genomics
372
Human Reproduction
255
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
9,493
Articles tracked across the journal lifetime
Indexed publication set
448
311 cited publications
Last 12 months
261
21.8 publications/month
Open access share
46.0%
120 OA publications in the last year
Leading citing country
United States
695 citing publications
Leading citing field
Cytogenetics
1,096 citing publications
Latest tracked publication
20 October 2026
10 recent records available
Coverage & Indexing History
v1n1, 1981-
v1n1, 1981-
Active Coverage
Research Focus & Classification
Indexed Subjects
Congenital Disorders
Cytogenetics
Broad Categories
Obstetrics
Cytogenetics
Congenital Disorders
Cardiology
Obstetrics/Gynecology
Human Reproduction
Abdominal Surgery
MeSH Descriptors
Prenatal Diagnosis
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1002/pd.70285
Open DOI
Extended Non‐Invasive Prenatal Testing for Chromosomal and Monogenic Disorders by Cell‐Free DNA Sequencing: A Blinded Comparison With Amniocentesis
Objective: To determine whether molecular integrated non‐invasive fetal exome sequencing (iNIFS), using clinical exome sequencing of maternal‐plasma cell‐free DNA, concords per pregnancy with paired amniocentesis. Method: Prospective, bl...
02
03
DOI 10.1002/pd.70286
Open DOI
Genome‐Wide NIPT With Fetal‐Fraction Enrichment and BinDel: Clinical Cohort Evaluation of Microdeletion and ‐Duplication Detection
Objective: To evaluate the analytical and clinical performance of fetal fraction (FF) enriched genome‐wide noninvasive prenatal testing (GW‐NIPT) for the detection of clinically relevant copy number variants (CNVs) down to 1 Mb. Methods:...
04
DOI 10.1002/pd.70282
Open DOI
Cost‐Effectiveness of Universal and Contingent NIPT Within a Multi‐Tariff Healthcare System: A Full Incremental Decision‐Analytic Cohort Study
Objective: To compare universal and contingent non‐invasive prenatal testing (NIPT) strategies within a multi‐tariff healthcare system using a full incremental cost‐effectiveness framework and to identify price levels at which universal ...
05
06
DOI 10.1002/pd.70276
Open DOI
Provider Practice and Patient Clinical Follow‐Up Among Patients With Spinal Muscular Atrophy (SMA) Linked‐Variant
Background: The American College of Obstetricians and Gynecologists (ACOG) recommends spinal muscular atrophy (SMA) carrier screening be offered preconception or prenatally. SMA linked‐variant incurs an increased but not absolute risk of...
07
DOI 10.1002/pd.70278
Open DOI
Transplacental Flecainide and/or Digoxin for Fetal Tachyarrhythmias: Therapeutic Efficacy and Clinical Experience
Objective: To assess the efficacy and safety of transplacental flecainide and/or digoxin for fetal tachyarrhythmias when sotalol is unavailable. Method: We evaluated transplacental flecainide, digoxin, or combination therapy in a retrosp...
08
DOI 10.1002/pd.70273
Open DOI
Standardized Technique for Full Laser Ablation of Feeding Artery in Fetuses With Bronchopulmonary Sequestration and Large Pleural Effusion: Lessons Learned Over 14 Years of Experience
Objective: To report on perinatal outcomes and technical aspects of standardized fetal surgery technique with full laser coagulation of the feeding artery in fetuses with bronchopulmonary sequestration and large pleural effusion. Method:...
09
DOI 10.1002/pd.70259
Open DOI
Genetic Analysis in Monochorionic Diamniotic Twins Discordant for One Fetus With Structural Anomalies
Objective: Data concerning the prenatal diagnostic value of exome sequencing (ES) for twins with structural anomalies remain limited. Therefore, this study aimed to investigate the genetic etiology of monochorionic diamniotic (MCDA) twin...
10
DOI 10.1002/pd.70283
Open DOI
Microbial Culture Profiles Following Fetal Surgery Versus Spontaneous Preterm Prelabor Rupture of Membranes in Multifetal Gestations
Objective: To assess microbial culture profiles and antibiotic resistance patterns in pregnancies complicated by preterm prelabor rupture of membranes (PPROM) following fetal surgery compared with spontaneous PPROM without fetal surgery....
Bibliographical & Catalog Notes
Title from cover.
Vol. 10, no. 1 (JAN 1990)19900918 Notice published Printed on acid-free paper