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Akademisyen

GÜLAY KARAGÜZEL

PROFESÖR

KARADENİZ TEKNİK ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ

  • Ana Dal Sağlık Bilimleri Temel Alanı
  • Yan Dal Çocuk Endokrinolojisi (Çocuk Sağlığı ve Hastalıkları)

Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.

  • Makale 115
  • Proje 0
  • Kitap 20
  • Bildiri 77
  • Patent 0
  • Sanatsal 0
Scopus (SJR) Q1 26 Q2 36 Q3 15 Q4 4
WoS (JCR) Q1 14 Q2 17 Q3 31 Q4 19
TR Index 23 makale

Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.

Üst %1 makale 0
Üst %10 makale 9
Ort. yüzdelik 61.7%
Üst %1 payı 0.0%
Üst %10 payı 10.6%

Makaleler

YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.

Dizin filtreleri

Toplam 115 yayın

Scopus (SJR)
Q1 26 Q2 36 Q3 15 Q4 4
WoS (JCR)
Q1 14 Q2 17 Q3 31 Q4 19
TR Index
23 makale

Makale listesi

  1. 2026 The role of sclerostin and osteoprotegerin in bone metabolism in children with congenital adrenal hyperplasia European Journal of Pediatrics DOI 10.1007/s00431-026-07245-2 YÖKSİS SJR Q1 JCR Q1 OpenAlex 70.2%
  2. 2025 Central precocious puberty in boys; diagnosis, treatment and follow-up: a nation-wide study Endocrine DOI 10.1007/s12020-025-04382-w YÖKSİS SJR Q2 JCR Q3 OpenAlex 84.7%
  3. 2025 A synonymous single nucleotide variant on the FAM20C gene causes non-lethal Raine syndrome HUMAN MOLECULAR GENETICS DOI 10.1093/hmg/ddaf129 YÖKSİS SJR Q1 JCR Q2 OpenAlex 74.6%
  4. 2025 Pubertal stage significantly and independently impacts C-peptide levels at type 1 diabetes diagnosis along with body mass index and age EUROPEAN JOURNAL OF PEDIATRICS DOI 10.1007/s00431-025-06046-3 YÖKSİS SJR Q1 JCR Q1 OpenAlex 88.5%
  5. 2025 Genetic heterogeneity in pediatric short stature: insights from whole exome sequencing and snp- array analyses in a Turkish cohort European Journal of Pediatrics DOI 10.1007/s00431-025-06529-3 YÖKSİS SJR Q1 JCR Q1 OpenAlex 73.8%
  6. 2025 Two New Families With TAF13 Variant Presenting With Syndromic 46,XY Disorder of Sex Development: Expanding the Clinical Phenotype American Journal of Medical Genetics Part A DOI 10.1002/ajmg.a.64183 YÖKSİS SJR Q2 JCR Q4 OpenAlex 14.8%
  7. 2024 Clinical and genetic characteristics of patients with monocarboxylate transporter-8 deficiency: a multicentre retrospective study European Journal of Pediatrics DOI 10.1007/s00431-024-05931-7 YÖKSİS SJR Q1 JCR Q1 OpenAlex 70.3%
  8. 2024 Natural history of ENPP1 deficiency: Nationwide Turkish Cohort Study of autosomal‐recessive hypophosphataemic rickets type 2 Clinical Endocrinology DOI 10.1111/cen.15028 YÖKSİS SJR Q2 JCR Q3 OpenAlex 77.4%
  9. 2024 A triple molecular diagnosis in a Turkish individual with hypotrichosis, deafness, and diabetes Clinical Dysmorphology DOI 10.1097/MCD.0000000000000499 YÖKSİS SJR Q3 JCR Q4 OpenAlex 4.8%
  10. 2024 Role of ERα and Aromatase in Juvenile Gigantomastia The Journal of Clinical Endocrinology & Metabolism DOI 10.1210/clinem/dgae019 YÖKSİS SJR Q1 JCR Q1 OpenAlex 87.9%
  11. 2023 Rare Causes of Recurrent Acute Liver Failure In Children: Infantile Liver Failure Syndromes Georg Thieme Verlag KG DOI 10.1055/a-1937-9397 YÖKSİS SJR Q3 JCR Q3 OpenAlex 2.4%
  12. 2023 Risk Factors and Clinical Characteristics of Metabolic Bone Disease of Prematurity AMERICAN JOURNAL OF PERINATOLOGY DOI doi: 10.1055/s-0041-1729559 YÖKSİS SJR Q2 JCR Q2 OpenAlex 74.7%
  13. 2023 De novo Pure Partial Trisomy 6p Associated with Facial Dysmorphism, Developmental Delay, Brain Anomalies, and Primary Congenital Hypothyroidism S. Karger AG DOI 10.1159/000525393 YÖKSİS SJR Q4 JCR Q4 OpenAlex 64.3%
  14. 2022 Increased severe cases and new-onset type 1 diabetes among children presenting with diabetic ketoacidosis during first year of COVID-19 pandemic in Turkey Frontiers in Pediatrics DOI 10.3389/fped.2002.926013 YÖKSİS SJR Q1 JCR Q2 OpenAlex 19.3%
  15. 2022 Increased Severe Cases and New-Onset Type 1 Diabetes Among Children Presenting With Diabetic Ketoacidosis During First Year of COVID-19 Pandemic in Turkey FRONTIERS IN PEDIATRICS DOI 10.3389/fped.2022.926013 YÖKSİS SJR Q1 JCR Q2 OpenAlex 86.1%
  16. 2022 Successful therapeutic plasma exchange in a case with extremely severe hypertriglyceridemia secondary to diabetic ketoacidosis concomitant with type IX glycogen storage disease. Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis DOI 10.1016/j.transci.2021.103289 YÖKSİS SJR Q3 JCR Q4 OpenAlex 12.2%
  17. 2022 A long-term comparison of presenting characteristics of children with newly diagnosed type 1 diabetes before and during the COVID-19 pandemic Journal of Clinical Research in Pediatric Endocrinology DOI 10.4274/jcrpe.galenos.2022.2021-10-2 YÖKSİS TR Index SJR Q2 JCR Q3 OpenAlex üst %10 OpenAlex 91.6%
  18. 2022 Preservation of c-peptide levels in children with new-onset type 1 diabetes: a comparison based on body mass index Yeni tanı tip 1 diyabetli çocuklarda korunmuş c-peptid düzeyleri: vücut kütle indeksine dayalı bir karşılaştırma Turkish Journal of Diabetes and Obesity Türkiye Diyabet ve Obezite Dergisi DOI 10.25048/tudod.1059061 YÖKSİS TR Index OpenAlex 63.0%
  19. 2022 The relationship between long-term glycemic control and partial remission in type 1 diabetes: a retrospective study Tip 1 diyabette uzun dönem glisemik kontrol ile remisyon dönemi arasındaki ilişki: retrospektif bir çalışma Turkish Journal of Diabetes and Obesity Türkiye Diyabet ve Obezite Dergisi DOI 10.25048/tudod.1170939 YÖKSİS TR Index OpenAlex 22.9%
  20. 2022 Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked Syndrome in Two Siblings: Same Mutation But Different Clinical Manifestations at Onset J Clin Res Pediatr Endocrinol DOI 10.4274/jcrpe.galenos.2021.2021.0005 YÖKSİS TR Index SJR Q2 JCR Q3 OpenAlex 70.9%

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