Impact Factor
2.64
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
1.25
179 total citations
h5-index
17
h5 depth signal
Cited share
57.5%
84 of 146
Total citations
179
Citation footprint
Metric signal
0.96
External metric anchor
Self-citation
2.2%
4 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
United States
519
Canada
111
United Kingdom
41
Spain
35
India
31
Citing Fields of Research
Congenital Disorders
185
Obstetrics/Gynecology
162
Musculoskeletal & Nerve Cancer
139
Oncology
76
Hematology
60
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
2,681
Articles tracked across the journal lifetime
Indexed publication set
146
84 cited publications
Last 12 months
109
9.1 publications/month
Open access share
11.9%
13 OA publications in the last year
Leading citing country
United States
519 citing publications
Leading citing field
Congenital Disorders
185 citing publications
Latest tracked publication
13 October 2026
10 recent records available
Coverage & Indexing History
v1n1, Jan.-Feb. 1998-
v1n1, Jan.-Feb. 1998-
Active Coverage
Research Focus & Classification
Indexed Subjects
Congenital Disorders
Obstetrics/Gynecology
Musculoskeletal & Nerve Cancer
Liver Diseases
Testicular Disorders
Hematology
Issuing & Sponsoring Bodies
Contributor
Society for Pediatric Pathology (U.S.)
Contributor
Paediatric Pathology Society
Contributor
International Paediatric Pathology Association
Contributor
International Association for Pediatric Laboratory Medicine
Broad Categories
Pathology
Pediatrics
Musculoskeletal & Nerve Cancer
Obstetrics/Gynecology
Hematology
Digestive Disorders
Lymphomas
Cytogenetics
MeSH Descriptors
Congenital Abnormalities
Pathology, Clinical
Pediatrics
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1177/10935266261492979
Open DOI
Limb Body Wall Complex: Report of a Discordant Case in a Monozygotic Twin Pregnancy
Limb Body Wall Complex (LBWC) is a rare, severe congenital malformation syndrome characterized by thoracoabdominal wall defects, craniofacial anomalies, and limb and spinal malformations. Its incidence ranges from 0.04 to 3.3 per 10,000 ...
02
DOI 10.1177/10935266261487766
Open DOI
Severe Transient Abnormal Myelopoiesis: A Report of 2 Cases
Transient abnormal myelopoiesis (TAM) occurring in infants with trisomy 21 self-resolves in >90% of cases. In a few infants, there is extensive myeloid proliferation which leads to life threatening symptoms and occasionally fatal outcome...
03
DOI 10.1177/10935266261479810
Open DOI
Fetal Craniopharyngioma: A Rare Prenatal Diagnosis
Adamantinomatous craniopharyngioma (ACP) is a benign epithelial tumor classically diagnosed in childhood and only exceptionally during fetal life. We report a case of prenatally diagnosed ACP at 30 weeks of gestation (WG). Routine third-...
04
DOI 10.1177/10935266261485154
Open DOI
Blastemal-Predominant Primary Extrarenal Nephroblastoma Associated with Lumbosacral Lipomeningocele in an Infant: A Case Report and Focused Review
Primary extrarenal nephroblastoma, or extrarenal Wilms tumor, is an exceptionally rare embryonal tumor outside the kidney. Spinal/lumbosacral involvement is particularly uncommon and may mimic congenital dysraphic lesions. We report a 10...
05
DOI 10.1177/10935266261484295
Open DOI
Omphalocele with Patent Omphalomesenteric Duct and Intestinal Prolapse in a Preterm Neonate: Histopathological Evidence of Incomplete Vitelline Duct Involution
Patent omphalomesenteric duct (OMD) with intestinal prolapse coexisting with omphalocele is an exceptional ventral folding anomaly that may be misdiagnosed as gastroschisis. The vitellointestinal duct normally involutes between the seven...
06
DOI 10.1177/10935266261484282
Open DOI
Pitfalls in Pediatric Supratentorial ZFTA Fusion–Positive Ependymoma: A Clinicopathological Study of 17 Cases
Aims: Supratentorial ependymoma with ZFTA fusion represents a molecularly defined entity with characteristic but heterogeneous histopathological features. In routine diagnostic practice, morphologic diversity and limitations of individua...
07
DOI 10.1177/10935266261478989
Open DOI
Spatial Lineage Divergence at Diagnosis in a Pediatric KMT2A -Rearranged Leukemia Presenting with Concurrent AML and B-LBL
We describe a 1-year-2-month-old boy with KMT2A -rearranged leukemia presenting with concurrent acute myeloid leukemia in bone marrow and B-lymphoblastic leukemia/lymphoma in a right calf mass. Both lesions harbored an identical KMT2A::M...
08
DOI 10.1177/10935266261479959
Open DOI
Prolonged Formalin Fixation Does Not Result in Falsely Elevated Placental Weight
09
DOI 10.1177/10935266261477802
Open DOI
Mixed Vascular Malperfusion: A Hemodynamic Coupling Framework for Placental Vascular Injury
Maternal vascular malperfusion (MVM) and fetal vascular malperfusion (FVM) are traditionally described as individual patterns of placental injury, each pertaining to pathology of either the uteroplacental or fetoplacental circulation. Al...
10
DOI 10.1177/10935266261477804
Open DOI
Fetal Vascular Malperfusion as a Key Association of Dysmorphic Chorionic Villi in the Third Trimester
Objective: Dysmorphic chorionic villi (DCV) are histopathological findings typically associated with chromosomal abnormalities in early pregnancy loss. This study aimed to evaluate the clinical and pathological significance of DCV across...
Bibliographical & Catalog Notes
Title from cover.
Also issued online.
Affiliated with the International Paediatric Pathology Association and the International Association for Pediatric Laboratory Medicine.
Vol. 1, no. 1 (Jan.-Feb 1998)19990106 Notice published Printed on acid-free paper