Impact Factor
3.48
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
3.19
681 total citations
h5-index
31
h5 depth signal
Cited share
67.4%
151 of 224
Total citations
681
Citation footprint
Metric signal
3.80
External metric anchor
Self-citation
3.1%
21 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
United States
226
United Kingdom
95
Germany
89
Italy
77
Netherlands
65
Citing Fields of Research
Endocrinology & Metabolism
673
Diabetes
212
Adrenal Dysfunction
171
Cytogenetics
139
Congenital Disorders
95
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
4,497
Articles tracked across the journal lifetime
Indexed publication set
224
151 cited publications
Last 12 months
158
13.2 publications/month
Open access share
42.4%
67 OA publications in the last year
Leading citing country
United States
226 citing publications
Leading citing field
Endocrinology & Metabolism
673 citing publications
Latest tracked publication
16 October 2026
10 recent records available
Coverage & Indexing History
v73n1, 2010-
v73n1, 2010-
Research Focus & Classification
Indexed Subjects
Endocrinology & Metabolism
Diabetes
Adrenal Dysfunction
Issuing & Sponsoring Bodies
Contributor
European Society for Paediatric Endocrinology
Contributor
Sociedade Latino-Americana de Endocrinologîa Pediátrica
Broad Categories
Endocrinology
Pediatrics
Endocrinology & Metabolism
Diabetes
Adrenal Dysfunction
Cytogenetics
MeSH Descriptors
Adolescent
Child
Endocrine System Diseases
Infant
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1159/hrp/adaag044
Open DOI
Reconsidering the Interpretation of Thyroid Cancer Risk in Pediatric Hashimoto Thyroiditis
02
DOI 10.1159/hrp/adaag030
Open DOI
Clinical and genetic heterogeneity of Triple A syndrome: a multicenter study
Triple A syndrome (AAAS) is a rare autosomal recessive neuroendocrine disorder caused by pathogenic variants in the AAAS gene and characterized by marked clinical heterogeneity. In this multicenter retrospective study, we analyzed 23 pat...
03
DOI 10.1159/hrp/adaag039
Open DOI
Calcium Overload in Trisomy 21: An Underrecognized Cause of Persistent Hypercalcaemia - A Case Report
Introduction: Calcium overload in trisomy 21 is a rare and underrecognized cause of persistent parathyroid hormone (PTH)-independent hypercalcaemia in infants and young children with Down syndrome. Characteristic features include hyperca...
04
DOI 10.1159/hrp/adaag040
Open DOI
Weight Maintenance Following Discontinuation of Semaglutide in an Adolescent with Antipsychotic-Associated Weight Gain: A Case Report
Introduction: Antipsychotic-induced weight gain (AIWG) presents a significant clinical challenge in pediatric psychiatry, often leading to Class II or III obesity and metabolic comorbidities. While treatment with metformin is the current...
05
DOI 10.1159/hrp/adaag041
Open DOI
Thyroid Abnormalities in a Prospective Longitudinal Cohort of Pediatric Patients following SARS-CoV-2 infection
Introduction Thyroid dysfunction has been reported in adults and children following COVID-19. We evaluated thyroid function in children following SARS-CoV-2 infection compared to uninfected controls over at least one year of follow up. M...
06
07
DOI 10.1159/hrp/adaag021
Open DOI
Long-Acting PEG-rhGH in Short Children Born SGA in China: 4-Year Results from a Randomized Phase 2 Study
Introduction Children born small for gestational age (SGA) who failed to achieve catch-up growth are at risk of persistent short stature and associated metabolic complications. Daily recombinant human growth hormone (rhGH) therapy improv...
08
DOI 10.1159/hrp/adaag036
Open DOI
Expert Recommendations on Insulin Injection Technique and Education for the Pediatric and Young Adult Population with Diabetes: FITTER Forward Youth
Rates of type 1 diabetes (T1D) and type 2 diabetes (T2D) in the pediatric population have risen over the past two decades. Insulin therapy remains critical for diabetes management, and proper injection technique has been shown to improve...
09
DOI 10.1159/hrp/adaag038
Open DOI
Sustained Glycemic Outcomes in Children: A Three-Year Real-World Follow-Up of the MiniMed™ 780G System
Introduction Automated insulin delivery systems have shown promise in bridging the gap between achieving international glycemic targets and the burden associated with achieving such outcomes. This is especially important in children and ...
10
DOI 10.1159/hrp/adaag033
Open DOI
Clinical Features and Short-Term Growth Hormone Outcomes in Maternal UPD of Chromosome 20: Five Chinese Patients and a Literature Review
Background: Maternally derived uniparental disomy of chromosome 20 [UPD(20)mat], also known as Mulchandani–Bhoj–Conlin syndrome (MBCS), is a rare imprinting disorder with fewer than 30 cases documented to date. It is characterized by pre...
Bibliographical & Catalog Notes
Description based on v. 73, no. 1, 2010; title from cover.
Latest issue consulted: v. 73, no. 1, 2010.
Also issued online.