Akademisyen
ELİF ÖZSU
DOÇENT
ANKARA 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 94
- Proje 0
- Kitap 0
- Bildiri 155
- Patent 0
- Sanatsal 0
Scopus (SJR)
Q1
15
Q2
57
Q3
21
Q4
12
WoS (JCR)
Q1
7
Q2
33
Q3
36
Q4
27
TR Index
55
makale
Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.
Üst %1 makale
0
Üst %10 makale
6
Ort. yüzdelik
52.4%
Üst %1 payı
0.0%
Üst %10 payı
6.7%
Makaleler
YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.
Makale listesi
- 2026 SOX17 as a candidate gene for ovarian dysgenesis: functional characterisation of a novel homozygous variant YÖKSİS OpenAlex 39.4%
- 2026 A novel multimorbidity: co-occurrence of neonatal diabetes mellitus and leukocyte adhesion deficiency type 1 in two siblings YÖKSİS SJR Q3 JCR Q3 OpenAlex 33.9%
- 2025 Clinical characteristics, risk stratifications, and long-term follow-up of childhood differentiated thyroid cancer: a single-center experience YÖKSİS SJR Q1 JCR Q2 OpenAlex 9.3%
- 2025 Two Siblings with LRPPRC Mutation: Mitochondrial Complex IV Deficiency: Case Report YÖKSİS SJR Q3 JCR Q4 OpenAlex 15.1%
- 2025 Clinical insights of the TBX19 C.856 C>T variant: acase report and literature review on neonatal isolatedACTH deficiency YÖKSİS SJR Q3 JCR Q3 OpenAlex 14.4%
- 2025 Assessing cortisol levels in non-classical congenitaladrenal hyperplasia: focus on the V281L variant YÖKSİS SJR Q1 JCR Q1 OpenAlex 72.9%
- 2025 Understanding rickets in osteopetrosis via a case:mechanisms and treatment implications YÖKSİS SJR Q3 JCR Q3 OpenAlex 59.2%
- 2025 Adrenal hypoandrogenism in adolescents withpremature ovarian insufficiency YÖKSİS SJR Q3 JCR Q3 OpenAlex 0.2%
- 2025 Wolcott–Rallison syndrome: late-onset diabetes, multiple epiphyseal dysplasia, and acute liver failure – a case report YÖKSİS SJR Q3 JCR Q3 OpenAlex 74.7%
- 2025 Close relationship, similar phenotype of GATA4 and NR5A1 mutations: gonadal dysgenesis and puberty development YÖKSİS SJR Q2 JCR Q2 OpenAlex 78.3%
- 2025 Molecular Characterization and Phenotype-Genotype Correlation of Childhood Thyroid Nodules and Cancers: A Study of 62 Patients YÖKSİS SJR Q1 JCR Q1 OpenAlex 34.1%
- 2025 Monogenic diabetes: the role of mitochondrial dysfunction and endoplasmic reticulum stress YÖKSİS SJR Q2 JCR Q2 OpenAlex 19.3%
- 2025 The Impact of an Adolescent-Friendly Approach on Metabolic Control in Adolescents with Type 1 Diabetes in Türkiye YÖKSİS SJR Q2 JCR Q1 OpenAlex 31.1%
- 2025 Long-Term Follow-up of a Case with TBX19 Mutation, a Rare Cause of Isolated ACTH Deficiency and Literature Review YÖKSİS TR Index SJR Q2 JCR Q2 OpenAlex 10.6%
- 2025 Insights Into Pediatric Non-congenital Adrenal Hyperplasia: A Review Based on 5 Different Rare Cases with Primary Adrenal Insufficiency YÖKSİS TR Index SJR Q2 JCR Q2 OpenAlex 5.1%
- 2025 Pubertal characteristics, final height, and associated factors in patients with nonclassical congenital adrenal hyperplasia: a single center experience YÖKSİS SJR Q3 JCR Q3 OpenAlex 19.0%
- 2024 Comprehensive Insights into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes with a Multicenter Approach YÖKSİS TR Index SJR Q2 JCR Q3 OpenAlex 83.8%
- 2024 Mitotically Active Follicular Nodule in Early Childhood: A Case Report with A Novel Mutation in the Thyroglobulin Gene YÖKSİS TR Index SJR Q2 JCR Q3 OpenAlex 21.0%
- 2024 Exploring Multiple Endocrinological Issues and Dysautonomia in a Rare Case: Hypoparathyroidism in MIRAGE Syndrome YÖKSİS TR Index SJR Q2 JCR Q3 OpenAlex 70.4%
- 2024 Assessment of the Admission and Follow-up Characteristics of Children Diagnosed with Secondary Osteoporosis YÖKSİS TR Index SJR Q2 JCR Q3 OpenAlex 65.1%