Akademisyen
ROJAN İPEK
DOÇENT
DİCLE ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Çocuk Nörolojisi (Çocuk Sağlığı ve Hastalıkları)
Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.
- Makale 34
- Proje 0
- Kitap 28
- Bildiri 75
- Patent 0
- Sanatsal 0
Scopus (SJR)
Q1
7
Q2
7
Q3
7
Q4
1
WoS (JCR)
Q1
4
Q2
7
Q3
6
Q4
8
TR Index
5
makale
Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.
Üst %1 makale
0
Üst %10 makale
1
Ort. yüzdelik
44.8%
Üst %1 payı
0.0%
Üst %10 payı
3.3%
Makaleler
YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.
Makale listesi
- 2026 Effects of newborn screening and nusinersen on survival and functional outcomes in spinal muscular atrophy with two SMN2 copies: A nationwide multicentre real-world study from Turkey YÖKSİS SJR Q1 JCR Q1 OpenAlex 78.1%
- 2025 Genotypic and Phenotypic Characterization of Axonal Charcot–Marie–Tooth Disease in Childhood: Identification of One Novel and Four Known Mutations YÖKSİS SJR Q2 JCR Q2 OpenAlex 60.3%
- 2025 A Case Report of a New Variant Associated with Vici Syndrome in a Turkish Infant; EPG5 Frameshift Variant YÖKSİS OpenAlex 69.9%
- 2025 The fourth family in the world with a novel variant in the ATP5MK gene: four siblings with complex V (ATP synthase) deficiency YÖKSİS SJR Q3 JCR Q4 OpenAlex 65.7%
- 2025 Evaluation of posterior ocular structures in pediatric migraine patients with and without aura YÖKSİS SJR Q3 JCR Q3 OpenAlex 14.9%
- 2025 Can Headache Be a Symptom of Celiac Disease?: A University Hospital Experience YÖKSİS TR Index OpenAlex 65.4%
- 2024 Çocuk Acil Polikliniğine Kanama Şikayeti ile Başvuran Hastaların Değerlendirilmesi: Tek Merkez Deneyimi YÖKSİS OpenAlex 5.6%
- 2024 Biallelic NAA60 variants with impaired N-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 98.4%
- 2024 COL12A1 Gene Variant and a Review of the Literature: A Case Report of Ullrich Congenital Muscular Dystrophy YÖKSİS SJR Q3 JCR Q4 OpenAlex 58.7%
- 2024 A Multicenter Study of Self-Limited Epilepsy With Centrotemporal Spikes: Effectiveness of Antiseizure Medication With Respect to Spike-Wave Index YÖKSİS SJR Q1 JCR Q2 OpenAlex 69.4%
- 2024 Could headache in children be a biomarker for dyslipidemia? YÖKSİS SJR Q2 JCR Q3 OpenAlex 11.3%
- 2024 Two Sibling Cases of Spastic Paraplegia-45 with a Novel Pathogenic Variant in NT5C2 Gene: Concomitant RYR1 Gene in One Sibling YÖKSİS SJR Q3 JCR Q4 OpenAlex 1.7%
- 2024 Evaluation of Etiological Causes and Demographic Characteristics of Neonatal Seizure in Adiyaman University Training And Research Hospital, Türkiye: A Retrospective Study YÖKSİS OpenAlex 22.8%
- 2024 Çocuklarda D vitamini ile migren arasındaki ilişkinin değerlendirilmesi YÖKSİS TR Index OpenAlex 20.6%
- 2024 Alterations in the tear film and ocular surface in pediatric migraine patients YÖKSİS SJR Q2 JCR Q2 OpenAlex 9.4%
- 2023 A Rare Case of Rotavirus-related Acute Benign Myositis YÖKSİS SJR Q1 JCR Q1 OpenAlex 46.6%
- 2023 Case Report of Two Siblings Diagnosed with Osteogenesis Imperfecta Type XV with a New Mutation in the WNT1 Gene and Review of the Literature YÖKSİS SJR Q4 JCR Q4 OpenAlex 58.9%
- 2023 Vitamin D Levels in Children Presenting with Breath-Holding Spells: An Example of A University Hospital YÖKSİS TR Index OpenAlex 16.0%
- 2023 The relationship between febrile seizure and hematological parameters in children YÖKSİS TR Index OpenAlex 23.1%
- 2022 Pyridoxine-dependent Epilepsy caused by a Novel homozygous mutation in PLPBP Gene YÖKSİS SJR Q2 JCR Q2 OpenAlex 58.1%