Scientific work
Prof. Dr. Gönül Çatlı
217 publications. The source of the information is stated next to each publication.
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Long-term clinical outcomes of primary adrenal insufficiency caused by homozygous CYP11A1 p.R451W variant
European Journal of Endocrinology, 2026
DOI 10.1093/ejendo/lvag110 PMID 42340003 Open-access full textSource: OpenAlex
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Genotype-Phenotype Correlation Analysis and Identification of a Novel Variant in Children with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
The Journal of Pediatric Research, 2026
DOI 10.4274/jpr.galenos.2026.07448 Source: OpenAlex
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Is oxytocin related to psychiatric symptoms in adolescents with obesity?
Journal of Pediatric Endocrinology and Metabolism, 2025
DOI 10.1515/jpem-2024-0583 PMID 39953894 Open-access full textSource: OpenAlex
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SUN-202 Nerve Conduction Studies May Predict the Natural Course of Mild Subclinical Hypothyroidism in Children
Journal of the Endocrine Society, 2025
DOI 10.1210/jendso/bvaf149.1828 Source: OpenAlex
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Could the Use of Pacifiers in Infancy Be Associated with Binge Eating Disorder and Obesity in Adolescents?
Journal of College of Physicians And Surgeons Pakistan, 2025
DOI 10.29271/jcpsp.2025.12.1574 PMID 41351092 Open-access full textSource: OpenAlex
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Evaluation of Family Functioning and Eating Attitudes in Adolescents Diagnosed with Obesity with and without Binge Eating Disorder and Their Comparison with Healthy Adolescents
Çocuk ve Gençlik Ruh Sağlığı Dergisi / Turkish Journal of Child and Adolescent Mental Health, 2024
DOI 10.4274/tjcamh.galenos.2024.72687 1 citation (OpenAlex) Open-access full textSource: OpenAlex
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Genetic Findings in Short Turkish Children Born to Consanguineous Parents
Hormone Research in Paediatrics, 2024
DOI 10.1159/000539696 PMID 38838658 3 citations (Europe PMC) Open-access full textSource: OpenAlex
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Androgen receptor CAG repeat polymorphism might be a possible cause of familial constitutional delay of growth and puberty
Journal of Endocrinological Investigation, 2024
DOI 10.1007/s40618-024-02502-3 PMID 39570490 1 citation (Europe PMC) Source: OpenAlex
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6687 New indication for monogenic diabetes genetic testing in children – implication for routine clinical practice
British Society for Paediatric Endocrinology and Diabetes Meeting (BSPED), 2024
DOI 10.1136/archdischild-2024-rcpch.361 Source: OpenAlex
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Does Voiding Cystouretrography Cause Thyroid Dysfunction in Pediatric Patients with Chronic Kidney Disease?
Research Square, 2024
DOI 10.21203/rs.3.rs-5296155/v1 Open-access full textSource: OpenAlex
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Clinical features, diagnosis and treatment outcomes of Cushing's disease in children: A multicenter study
Clinical Endocrinology, 2023
DOI 10.1111/cen.14980 PMID 37814958 4 citations (Europe PMC) Source: OpenAlex
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POU6F2 mutation in humans with pubertal failure alters GnRH transcript expression
Frontiers in Endocrinology, 2023
DOI 10.3389/fendo.2023.1203542 PMID 37600690 12 citations (Europe PMC) Open-access full textSource: OpenAlex
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Resting Electroencephalography Differences Between Eyes-Closed and Eyes-Open Conditions in Children with Subclinical Hypothyroidism
Turkish Archives of Pediatrics, 2023
DOI 10.5152/turkarchpediatr.2022.22144 PMID 36598209 1 citation (Europe PMC) Open-access full textSource: OpenAlex
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Evaluation of the effects of insulin resistance on ECG parameters in obese children.
PubMed, 2023
DOI 10.26355/eurrev_202309_33797 PMID 37782187 2 citations (Europe PMC) Source: OpenAlex
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Sensory and Sensorimotor Gating in Children with Subclinical Hypothyroidism
The Anatolian Journal of General Medical Research, 2023
DOI 10.4274/terh.galenos.2021.68815 1 citation (OpenAlex) Open-access full textSource: OpenAlex
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Clinical Characteristics of Children with Combined Pituitary Hormone Deficiency and the Effects of Growth Hormone Treatment
Klinische Pädiatrie, 2023
DOI 10.1055/a-2186-9304 PMID 38049102 Source: OpenAlex
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Are serum MOTS-c levels and MOTS-c m.1382A>C polymorphism related to polycystic ovary syndrome?
Archives of Endocrinology and Metabolism, 2023
DOI 10.20945/2359-4292-2026-0031 PMID 41945630 Open-access full textSource: OpenAlex
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Genotype of congenital adrenal hyperplasia patients with testicular adrenal rest tumor
European Journal of Medical Genetics, 2022
DOI 10.1016/j.ejmg.2022.104654 PMID 36343887 6 citations (Europe PMC) Open-access full textSource: OpenAlex
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Atypical STAT5B deficiency, severe short stature and mild immunodeficiency associated with a novel homozygous STAT5B Variant
Molecular and Cellular Endocrinology, 2022
DOI 10.1016/j.mce.2022.111799 PMID 36265659 8 citations (Europe PMC) Open-access full textSource: OpenAlex
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Are Thyroid Functions Affected in Multisystem Inflammatory Syndrome in Children?
Journal of Clinical Research in Pediatric Endocrinology, 2022
DOI 10.4274/jcrpe.galenos.2022.2022-4-7 PMID 35770945 6 citations (Europe PMC) Open-access full textSource: OpenAlex
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The effect of breast milk nesfatin-1 and ghrelin levels on growth in infants with SGA
The Turkish Journal of Pediatrics, 2022
DOI 10.24953/turkjped.2021.1075 PMID 35611412 2 citations (Europe PMC) Source: OpenAlex
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Asfotase Alfa Treatment in a 2-year-old Girl with Childhood Hypophosphatasia
The Journal of Pediatric Research, 2022
DOI 10.4274/jpr.galenos.2021.51333 Source: OpenAlex
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Elevated neurotensin levels among obese adolescents may be related to emotion dysregulation and impulsivity: a cross-sectional, case-control study
The Turkish Journal of Pediatrics, 2022
DOI 10.24953/turkjped.2021.1437 PMID 35611414 2 citations (Europe PMC) Open-access full textSource: OpenAlex
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Leptin and leptin receptor gene polymorphisms in obese and healthy children
Çukurova medical journal (Online)/Çukurova medical journal, 2022
DOI 10.17826/cumj.977534 Source: OpenAlex
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A rare endocrinological complication of chronic kidney disease
The Turkish Journal of Pediatrics, 2022
DOI 10.24953/turkjped.2020.3601 PMID 35611427 Source: OpenAlex
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Evaluation of Thyroid Function Tests in Children With Covid-19
Research Square, 2022
DOI 10.21203/rs.3.rs-1433666/v1 Open-access full textSource: OpenAlex
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MKRN3 Gene Mutation in a Case of Familial Central Precocious Puberty
Güncel Pediatri, 2022
DOI 10.4274/jcp.2022.02439 Open-access full textSource: OpenAlex
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Virilizing Adrenocortical Carcinoma Oncocytic Variant in a Child with Heterosexual Precocious Puberty and a Literature Review
The Journal of Pediatric Research, 2022
DOI 10.4274/jpr.galenos.2022.05579 Source: OpenAlex
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A childhood primary hyperparathyroidism due to parathyroid adenoma: Atypical presenting with leg pain and normocalcemia
Pediatric Academic Case Reports, 2022
DOI 10.61107/pacr.2022.001 Source: OpenAlex
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Clinical and Hormonal Profiles Correlate With Molecular Characteristics in Patients With 11β-Hydroxylase Deficiency
The Journal of Clinical Endocrinology & Metabolism, 2021
DOI 10.1210/clinem/dgab225 PMID 33830237 28 citations (Europe PMC) Open-access full textSource: OpenAlex
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Oxytocin receptor gene polymorphism and low serum oxytocin level are associated with hyperphagia and obesity in adolescents
International Journal of Obesity, 2021
DOI 10.1038/s41366-021-00876-5 PMID 34091593 13 citations (Europe PMC) Source: OpenAlex
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Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinics
Diabetologia, 2021
DOI 10.1007/s00125-021-05597-y PMID 34686905 20 citations (Europe PMC) Open-access full textSource: OpenAlex
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Diagnostic Value of Bilateral Petrosal Sinus Sampling in Children with Cushing Disease: A Multi-center Study
Journal of Clinical Research in Pediatric Endocrinology, 2021
DOI 10.4274/jcrpe.galenos.2021.2021.0152 PMID 34538049 9 citations (Europe PMC) Open-access full textSource: OpenAlex
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Early and late diagnoses of 17β‐Hydroxysteroid dehydrogenase type‐3 deficiency in two unrelated patients
Andrologia, 2021
DOI 10.1111/and.14017 PMID 33586216 4 citations (Europe PMC) Open-access full textSource: OpenAlex
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The relationship of carotid intima-media thickness with anthropometric and metabolic parameters in patients with classic congenital adrenal hyperplasia
TURKISH JOURNAL OF MEDICAL SCIENCES, 2021
DOI 10.3906/sag-2001-57 PMID 33486914 2 citations (Europe PMC) Open-access full textSource: OpenAlex
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Childhood-onset mild diabetes caused by a homozygous novel variant in the glucokinase gene
HORMONES, 2021
DOI 10.1007/s42000-021-00330-1 PMID 34697762 3 citations (Europe PMC) Source: OpenAlex
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High serum neurotensin level in obese adolescents is not associated with metabolic parameters, hyperphagia or food preference
Journal of Pediatric Endocrinology and Metabolism, 2021
DOI 10.1515/jpem-2021-0031 PMID 34147046 1 citation (Europe PMC) Source: OpenAlex
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Monogenik Obezite Ön Tanısı ile İncelenen Hastaların Klinik, Laboratuvar ve Genetik Sonuçlarının Değerlendirilmesi
Güncel Pediatri, 2021
DOI 10.4274/jcp.2021.0008 Open-access full textSource: OpenAlex
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Gecikmiş Puberte: Kızlarda Gecikmiş Puberte, Tanı ve Tedavisi
2021
Source: OpenAlex
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Revisiting Classical 3β-hydroxysteroid Dehydrogenase 2 Deficiency: Lessons from 31 Pediatric Cases
The Journal of Clinical Endocrinology & Metabolism, 2020
DOI 10.1210/clinem/dgaa022 PMID 31950145 20 citations (Europe PMC) Open-access full textSource: OpenAlex
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The Spectrum From Classic to Non-Classic 11β-Hydroxylase Deficiency
SSRN Electronic Journal, 2020
DOI 10.2139/ssrn.3712924 Open-access full textSource: OpenAlex
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Can ocular changes be detected early in children and adolescents with type 1 diabetes mellitus without retinopathy by using optical biometry and optical coherence tomography?
International Ophthalmology, 2020
DOI 10.1007/s10792-020-01430-4 PMID 32488589 6 citations (Europe PMC) Source: OpenAlex
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Can we use copeptin as a biomarker for masked hypertension or metabolic syndrome in obese children and adolescents?
Journal of Pediatric Endocrinology and Metabolism, 2020
DOI 10.1515/jpem-2020-0240 PMID 33581704 7 citations (Europe PMC) Source: OpenAlex
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Comparison of the effectiveness of simple carbohydrates on hypoglycemic episodes in children and adolescents with type 1 diabetes mellitus: A randomized study in a diabetes camp
Pediatric Diabetes, 2020
DOI 10.1111/pedi.13077 PMID 32662200 4 citations (Europe PMC) Open-access full textSource: OpenAlex
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Does fludrocortisone treatment cause hypomagnesemia in children with primary adrenal insufficiency?
TURKISH JOURNAL OF MEDICAL SCIENCES, 2020
DOI 10.3906/sag-2008-167 PMID 33155789 Open-access full textSource: OpenAlex
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Konjenital Hiperinsülinemik Hipoglisemi Tanılı Hastalarda Klinik ve Genetik Özellikler ile Tedavi Sonuçları: Tek Merkez Deneyimi
Bursa Uludag University - AVESIS, 2020
DOI 10.32941/pediatri.841408 Source: OpenAlex
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Clinical, Genetic Features and Treatment Results in Patients with Congenital Hyperinsulinemic Hypoglycemia: A Single Center Experience
Güncel Pediatri, 2020
DOI 10.4274/jcp.2020.0029 Source: OpenAlex
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Nationwide Turkish Cohort Study of Hypophosphatemic Rickets
Journal of Clinical Research in Pediatric Endocrinology, 2019
DOI 10.4274/jcrpe.galenos.2019.2019.0098 PMID 31514490 11 citations (Europe PMC) Open-access full textSource: OpenAlex
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Evaluation of Molecular Characteristics and Steroid Metabolomics in a Large Cohort of Children with 3β-Hydroxysteroid Dehydrogenase 2 Deficiency
58th Annual ESPE Meeting (ESPE 2019), 2019
Source: OpenAlex
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Ambulatory blood pressure monitoring parameters in obese children and adolescents with masked hypertension
Blood Pressure Monitoring, 2019
DOI 10.1097/mbp.0000000000000402 PMID 31567187 12 citations (Europe PMC) Source: OpenAlex