JCRPE Journal of Clinical Research in Pediatric Endocrinology
JCRPE Journal of Clinical Research in Pediatric Endocrinology is a journal indexed in SJR in Endocrinology and Endocrinology, Diabetes and Metabolism with an H index of 50. It is an CC BY-NC-ND Journal with a Single blind Peer Review review system, and It has a price of 90 €. The scope of the journal is focused on pediatrics, endocrinology, metabolism, clinical research. It has an SJR impact factor of 0,607 and it has a best quartile of Q2. It is published in English. It has an SJR impact factor of 0,607.
Metrics
Scimago and CountryOfPapers database fields
SJR Impact
0,607
H-index
50
Docs (year)
71
Docs 3y
194
Total refs
2035
Cites 3y
318
Citable 3y
184
Cites/Doc 2y
1.5
Ref/Doc
28.66
Immediate OA
90 €
Embargoed OA
NPD
Non OA / Submission
- €
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Researcher reviews
Best articles by citations
An Unusual Presentation of Carney Complex
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View moreCirculating Insulin-like Growth Factor Binding Protein-4
View moreCeliac Disease and Autoimmune Thyroid Disease in Children with Type 1 Diabetes Mellitus: Clinical and HLA-Genotyping Results-Original Article
View moreCan Nesfatin-1 Predict Hypertension in Obese Children?
View moreAtypical Presentation of Hashimoto's Disease in an Adolescent: Thyroid-Associated Ophthalmopathy
View moreAtherogenic Lipid Profile and Systolic Blood Pressure are Associated with Carotid Artery Intima-media Thickness in Children with Turner Syndrome
View moreAssociations of Prenatal and Perinatal Factors with Cortisol Diurnal Pattern and Reactivity to Stress at Preschool Age Among Children Living in Poverty
View moreAssociation Between the Corrected QT Interval and Carotid Artery Intima-Media Thickness in Obese Children
View moreAssessment of Bisphenol A Levels in Preschool Children: Results of a Human Biomonitoring Study in Ankara, Turkey
View moreAromatase Inhibitors to Augment Height: Continued Caution and Study Required
View moreAromatase Deficiency in Two Siblings with 46,XX Karyotype Raised as Different Genders: A Novel Mutation (p.R115X) in the CYP19A1 Gene
View moreAn Unusual Presentation of Parathyroid Adenoma in an Adolescent: Calcific Achilles Tendinitis
View moreA Case of Central Precocious Puberty Due to Concomitant Hypothalamic Hamartoma and Juvenile Pilocytic Astrocytoma
View moreAn Unusual Presentation of 46,XY Pure Gonadal Dysgenesis: Spontaneous Breast Development and Menstruation
View moreAn Unusual Combination of Klinefelter Syndrome and Growth Hormone Deficiency in a Prepubertal Child
View moreAn Iranian Patient with Maroteaux Type Acromesomelic Dysplasia, Showing no Involvement of Distal Lower Limbs
View moreAl-Awadi/Raas-Rothschild Syndrome in a Newborn with Additional Anomalies
View moreAcceleration of Puberty During Growth Hormone Therapy in a Child with Septo-Optic Dysplasia
View moreA Rare Cause of Precocious Puberty: Hepatoblastoma
View moreA Novel Mutation in the Arginine Vasopressin Receptor 2 Gene Causing Congenital Nephrogenic Diabetes Insipidus
View moreA novel missense mutation in human Receptor Roundabout-1 (ROBO1) gene associated with pituitary stalk interruption syndrome
View moreA Neurofibromatosis Noonan Syndrome Patient Presenting with Abnormal External Genitalia
View moreA Deep Intronic HADH Splicing Mutation (c.636+471G>T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course
View more