OOIR: Observatory of International Research

Papers

(The TQCC of Journal of Clinical Research in Pediatric Endocrinology is 3. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-05-01 to 2024-05-01.)

Article	Citations
New Features for Child Metrics: Further Growth References and Blood Pressure Calculations	53
Metabolic Bone Disease in Premature Neonates: An Unmet Challenge	37
Traditional and New Methods of Bone Age Assessment-An Overview	28
Triglyceride Glucose Index as a Surrogate Measure of Insulin Sensitivity in a Caucasian Pediatric Population	22
Endocrine Disruptors and Polycystic Ovary Syndrome: Phthalates	21
A New Cause of Obesity Syndrome Associated with a Mutation in the Carboxypeptidase Gene Detected in Three Siblings with Obesity, Intellectual Disability and Hypogonadotropic Hypogonadism	20
Frequency of Celiac Disease and Spontaneous Normalization Rate of Celiac Serology in Children and Adolescent Patients with Type 1 Diabetes	19
Vitamin D Status Across Age Groups in Turkey: Results of 108,742 Samples from a Single Laboratory	18
How Vitamin D Levels of Children Changed During COVID-19 Pandemic: A Comparison of Pre-pandemic and Pandemic Periods	16
A Proposal for the Interpretation of Serum IGF-I Concentration as Part of Laboratory Screening in Children with Growth Failure	15
Has the Frequency of Precocious Puberty and Rapidly Progressive Early Puberty Increased in Girls During the COVID-19 Pandemic?	15
Validity of Six Month L-Thyroxine Dose for Differentiation of Transient or Permanent Congenital Hypothyroidism	13
Detection of <i>SHOX</i> Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature	12
Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: Outcomes of Extended Pilot Study in 241,083 Infants	11
A Novel Missense Mutation in Human Receptor Roundabout-1 <i>(ROBO1)</i> Gene Associated with Pituitary Stalk Interruption Syndrome	11
The Application of Next Generation Sequencing Maturity Onset Diabetes of the Young Gene Panel in Turkish Patients from Trakya Region	10
Association of Exosomal miR-34a with Markers of Dyslipidemia and Endothelial Dysfunction in Children and Adolescents with T1DM	10
A Long-Term Comparison of Presenting Characteristics of Children with Newly Diagnosed Type 1 Diabetes Before and During the COVID-19 Pandemic	10
Association of Total and High Molecular Weight Adiponectin with Components of Metabolic Syndrome in Mexican Children	8
Children with Hashimoto’s Thyroiditis Have Increased Intestinal Permeability: Results of a Pilot Study	8
Nationwide Turkish Cohort Study of Hypophosphatemic Rickets	8
The Clinical Spectrum of Resistance to Thyroid Hormone Alpha in Children and Adults	8
Diagnostic Performance of Neck Circumference and Cut-off Values for Identifying Overweight and Obese Pakistani Children: A Receiver Operating Characteristic Analysis	8
Increased Incidence of Type 1 Diabetes in Children and No Change in the Age of Diagnosis and BMI-SDS at the Onset - is the Accelerator Hypothesis not Working?	8
Urinary NGAL is a Potential Biomarker for Early Renal Injury in Insulin Resistant Obese Non-diabetic Children	7

Current Treatments for Patients with Genetic Obesity	7
Different Potent Glucocorticoids, Different Routes of Exposure but the Same Result: Iatrogenic Cushing’s Syndrome and Adrenal Insufficiency	7
Indonesian National Growth Reference Charts Better Reflect Height and Weight of Children in West Java, Indonesia, than WHO Child Growth Standards	7
Low Complement C1q/TNF-related Protein-13 Levels are Associated with Childhood Obesity But not Binge Eating Disorder	7
Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome	7
A Rare Etiology of 46,XY Disorder of Sex Development and Adrenal Insufficiency: A Case of MIRAGE Syndrome Caused by Mutations in the <i>SAMD9</i> Gene	6
Compound Heterozygous Variants in FAM111A Cause Autosomal Recessive Kenny-Caffey Syndrome Type 2	6
An Evaluation of Glucagon Injection Anxiety and Its Association with the Fear of Hypoglycemia among the Parents of Children with Type 1 Diabetes	6
Very High Incidence of Type 1 Diabetes Among Children Aged Under 15 Years in Tlemcen, Northwest Algeria (2015-2018)	6
Heterozygous Insulin Receptor (INSR) Mutation Associated with Neonatal Hyperinsulinemic Hypoglycaemia and Familial Diabetes Mellitus: Case Series	6
Important Tools for Use by Pediatric Endocrinologists in the Assessment of Short Stature	6
A Case of Familial Male-limited Precocious Puberty with a Novel Mutation	6
Efficacy and Safety of Letrozole in the Management of Constitutional Delay in Growth and Puberty: A Systematic Review and Meta-analysis	6
Long-term Clinical Follow-up of Patients with Familial Hypomagnesemia with Secondary Hypocalcemia	6
Fibroblast Growth Factor 21 Levels and Bone Mineral Density in Metabolically Healthy and Metabolically Unhealthy Obese Children	5
Bisphenol A Exposure in Exclusively Breastfed Infants and Lactating Women: An Observational Cross-sectional Study	5
Cord Blood Levels of Spexin, Leptin, and Visfatin in Term Infants Born Small, Appropriate, and Large for Gestational Age and Their Association with Newborn Anthropometric Measurements	5
Evaluation of Children and Adolescents with Thyroid Nodules: A Single Center Experience	5
Investigating Genetic Mutations in a Large Cohort of Iranian Patients with Congenital Hyperinsulinism	5
Care and Support of Children with Type 1 Diabetes at School: The Turkish Experience	5
Molecular Diagnosis of Monogenic Diabetes and Clinical/Laboratory Features in Turkish Children	5
Treatment Difficulties in Hypomagnesemia Secondary to the Transient Receptor Potential Melastatin 6 Gene: A Case Report with Novel Mutation	5
Are Thyroid Functions Affected in Multisystem Inflammatory Syndrome in Children?	5
Managing Paediatric Growth Disorders: Integrating Technology Into a Personalised Approach	5
TRMT10A Mutation in a Child with Diabetes, Short Stature, Microcephaly and Hypoplastic Kidneys	5
Elevated Pre-injection Basal Luteinizing Hormone Concentrations are Common in Girls Treated for Central Precocious Puberty	5
Diagnostic Value of Bilateral Petrosal Sinus Sampling in Children with Cushing Disease: A Multi-center Study	5
Syndrome of Congenital Insulin Resistance Caused by a Novel INSR Gene Mutation	5
Pediatric Primary Adrenal Insufficiency: A 21-year Single Center Experience	5
Differential Diagnosis of Acromegaly: Pachydermoperiostosis Two New Cases from Turkey	5
Soluble Receptor for Glycation End-products Concentration Increases Following the Treatment of Severe Diabetic Ketoacidosis	5
The Value of Telemedicine for the Follow-up of Patients with New Onset Type 1 Diabetes Mellitus During COVID-19 Pandemic in Turkey: A Report of Eight Cases	5
Clinical and Genetic Characteristics of Patients with Corticosterone Methyloxidase Deficiency Type 2: Novel Mutations in <i>CYP11B2</i>	5
Two Subsequent Metachroneus Solid Tumors: Oncocytic Variant Adrenocortical Carcinoma and Rhabdomyosarcoma of Childhood: Case Report and Literature Review	4
Neonatal Diabetes, Congenital Hypothyroidism, and Congenital Glaucoma Coexistence: A Case of GLIS3 Mutation	4
Factors Affecting Thyroid Elastography in Healthy Children and Patients with Hashimoto’s Thyroiditis	4
Vitamin D Deficiency Prevalence in Late Neonatal Hypocalcemia: A Multicenter Study	4
A Duplication Upstream of SOX9 Associated with <i>SRY</i> Negative 46,XX Ovotesticular Disorder of Sex Development: A Case Report	4
The Effects of Risk Behaviors and Orthorexic Behavior on Glycemic Control in Adolescents with Type 1 Diabetes	4
Precocious Puberty in Boys: A Study Based on Five Years of Data from a Single Center in Northern China	4
The Effectiveness of Sirolimus Treatment in Two Rare Disorders with Nonketotic Hypoinsulinemic Hypoglycemia: The Role of mTOR Pathway	4
The Successful Treatment of Deep Soft-tissue Calcifications with Topical Sodium Thiosulphate and Acetazolamide in a Boy with Hyperphosphatemic Familial Tumoral Calcinosis due to a Novel Mutation in FG	4
Liraglutide Treatment in a Morbidly Obese Adolescent with a MC4R Gene Variant: Side Effects Reduce Success	4
Girls with Premature Thelarche Younger than 3 Years of Age May Have Stimulated Luteinizing Hormone Greater than 10 IU/L	4
Vandetanib in a Child Affected by Neurofibromatosis Type 1 and Medullary Thyroid Carcinoma with Both <i>NF1</i> and Homozygous <i>RET</i> Proto-oncogen Germ-line Mutations	4
IGFA Case Report of Pycnodysostosis Associated with Multiple Pituitary Hormone Deficiencies and Response to Treatment	4
A Rare Cause of Hyperinsulinemic Hypoglycemia: Kabuki Syndrome	4
Specific Functions of Melanocortin 3 Receptor (MC3R)	4
Clinical Management in Systemic Type Pseudohypoaldosteronism Due to <i>SCNN1B</i> Variant and Literature Review	4
Mutations Within the Transcription Factor <i>PROP1</i> in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency	4

Ectopic Posterior Pituitary, Polydactyly, Midfacial Hypoplasia and Multiple Pituitary Hormone Deficiency due to a Novel Heterozygous IVS11-2A>C(c.1957-2A>C) Mutation in the <i>GLI2</i&g	4
Midkine: Utility as a Predictor of Early Diabetic Nephropathy in Children with Type 1 Diabetes Mellitus	4
The Effects of Prehospital Care on Outcome in Pediatric Diabetic Ketoacidosis	4
Epicardial and Perihepatic Fat as Cardiometabolic Risk Predictors in Girls with Turner Syndrome: A Cardiac Magnetic Resonance Study	4
Growth Hormone Treatment and Papilledema: A Prospective Pilot Study	3
A Novel SCNN1A Variation in a Patient with Autosomal-recessive Pseudohypoaldosteronism Type 1	3
Bronchial Carcinoid Tumour as a Rare Cause of Cushing’s Syndrome in Children: A Case Report and Review of Literature	3
Early Onset Diabetes in Two Children due to Progeria, a Monogenic Disease of DNA Repair	3
Expanding the Phenotype of TRMT10A Mutations: Case Report and a Review of the Existing Cases	3
A Novel Mutation in the Thyroglobulin Gene Resulting in Neonatal Goiter and Congenital Hypothyroidism in an Eritrean Infant	3
Hyperinsulinism May Be Underreported in Hypoglycemic Patients with Phosphomannomutase 2 Deficiency	3
Initial Basal and Bolus Rates and Basal Rate Variability During Pump Treatment in Children and Adolescents	3
Mutation Screening and Functional Study of SLC26A4 in Chinese Patients with Congenital Hypothyroidism	3
A Case of Congenital Central Hypothyroidism Caused by a Novel Variant (Gln1255Ter) in <i>IGSF1</i> Gene	3
Evaluation of Thyroid Function Tests in Children with Chronic Liver Diseases	3
Primary Hyperparathyroidism Presenting as Posterior Reversible Encephalopathy Syndrome: A Report of Two Cases	3
46,XY Sex Development Defect due to a Novel Homozygous (Splice Site) c.673_1G>C Variation in the HSD17B3 Gene: Case Report	3
Novel MTTP Gene Mutation in a Case of Abetalipoproteinemia with Central Hypothyroidism	3
Pre-treatment Neutropenia in Children and Adolescents with Autoimmune Hyperthyroidism	3
Evaluation of Glucose Metabolism and Cardiovascular Risk Factors in Prepubertal Girls with Premature Pubarche	3
The Unusual Case of Fibroma of Tendon Sheath in a Young Girl with Turner Syndrome Undergoing Growth Hormone Treatment	3
Left Ventricular Hypertrophy in Patients with X-Linked Hypophosphataemia	3
The IGSF1 Deficiency Syndrome May Present with Normal Free T4 Levels, Severe Obesity, or Premature Testicular Growth	3
Soluble CD40 Ligand Levels in Children with Newly Diagnosed Graves’ Disease	3
Comparison of National Growth Standards for Turkish Infants and Children with World Health Organization Growth Standards	3
Catecholamine-induced Myocarditis in a Child with Pheochromocytoma	3
Transforming Growth Factor-β1 and Receptor for Advanced Glycation End Products Gene Expression and Protein Levels in Adolescents with Type 1 Diabetes Mellitus	3
A Novel Heterozygous ACAN Variant in a Short Patient Born Small for Gestational Age with Recurrent Patellar Dislocation: A Case Report	3
Mild Aromatic L-Amino Acid Decarboxylase Deficiency: As A Reason For Hypoketotic Hypoglycemia In A 4-Year-Old Girl	3
Time to the Peak, Shape of the Curve and Combination of These Glucose Response Characteristics During Oral Glucose Tolerance Test as Indicators of Early Beta-cell Dysfunction in Obese Adolescents	3
Serum Neudesin Levels in Obese Adolescents	3
The Results of 16 Years of Iodization: Assessment of Iodine Deficiency Among School-age Children in Antalya, Turkey	3
Genotype and Phenotype Heterogeneity in Neonatal Diabetes: A Single Centre Experience in Turkey	3