Academician
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)
A quick look at recorded outputs — details below.
- Articles 31
- Projects 0
- Books 28
- Proceedings 75
- Patents 0
- Artistic 0
Scopus (SJR)
Q1
7
Q2
7
Q3
7
Q4
1
WoS (JCR)
Q1
4
Q2
7
Q3
6
Q4
8
TR Index
5
articles
Field+year+type normalized OpenAlex percentiles — not Clarivate ESI / SciVal.
Top 1% articles
0
Top 10% articles
1
Avg percentile
44.8%
Top 1% share
0.0%
Top 10% share
3.3%
Articles
Articles with YÖKSİS and OpenAlex source split; narrow by quartile or TR Index.
Article list
- 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 top 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%