Academician
IŞIL ÖZER
PROFESÖR
KAFKAS ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Çocuk Metabolizma Hastalıkları (Çocuk Sağlığı ve Hastalıkları)
A quick look at recorded outputs — details below.
- Articles 16
- Projects 0
- Books 0
- Proceedings 0
- Patents 0
- Artistic 0
Scopus (SJR)
Q1
4
Q2
4
Q3
3
Q4
2
WoS (JCR)
Q1
1
Q2
6
Q3
1
Q4
5
TR Index
5
articles
Field+year+type normalized OpenAlex percentiles — not Clarivate ESI / SciVal.
Top 1% articles
0
Top 10% articles
3
Avg percentile
55.3%
Top 1% share
0.0%
Top 10% share
25.0%
Articles
Articles with YÖKSİS and OpenAlex source split; narrow by quartile or TR Index.
Article list
- 2025 Long-Term Outcomes of Chenodeoxycholic Acid Therapy for Cerebrotendinous Xanthomatosis: A Nationwide Study on Prognostic Factors and Treatment Response YÖKSİS SJR Q1 JCR Q2 OpenAlex top 10% OpenAlex 95.8%
- 2024 Clinical, biochemical, and molecular insights into Cerebrotendinous Xanthomatosis: A nationwide study of 100 Turkish individuals YÖKSİS SJR Q2 JCR Q2 OpenAlex top 10% OpenAlex 98.2%
- 2021 Assessing mental health in children and adolescent with MTHFR polymorphisms: psychiatric disorders, executive functioning, and symptom profile in a Turkish clinical sample YÖKSİS SJR Q3 JCR Q4 OpenAlex 1.0%
- 2021 As a Failure to Follow Basic Medical Rules for a Sample, Has a Costly Diagnosis of a Zoonosis. YÖKSİS OpenAlex 49.5%
- 2021 Endoplasmic reticulum stress in leukocytes from phenylketonuric patients YÖKSİS TR Index SJR Q4 JCR Q4 OpenAlex 17.2%
- 2020 Interictal epileptiform discharges on electroencephalography in children with methylenetetrahydrofolate reductase (MTHFR) polymorphisms YÖKSİS SJR Q2 JCR Q2 OpenAlex 70.8%
- 2011 Retrospective approach to methylenetetrahydrofolate reductase mutations in children. YÖKSİS SJR Q2 JCR Q2 OpenAlex 69.9%
- 2011 Molecular genetics and impact of residual in vitro phenylalanine hydroxylase activity on tetrahydrobiopterin responsiveness in Turkish PKU population. YÖKSİS SJR Q1 JCR Q2 OpenAlex top 10% OpenAlex 96.7%
- 2011 Hipofosfatemik raşitizm ile gelen herediter tirozinemili “ onbeş” yaş erkek hasta: Nadir olgu sunumu YÖKSİS TR Index OpenAlex 18.6%
- 2021 Assessing mental health in children and adolescent with MTHFR polymorphisms: psychiatric disorders, executive functioning, and symptom profile in a Turkish clinical sample YÖKSİS SJR Q3 JCR Q4 OpenAlex 1.0%
- 2020 Interictal epileptiform discharges on electroencephalography in children with methylenetetrahydrofolate reductase (MTHFR) polymorphisms YÖKSİS SJR Q2 JCR Q2 OpenAlex 70.8%
- 2013 Obez Çocuklarda Serum B12 Vitamini Seviyelerinin Normal Populasyon İle Karşılaştırılması YÖKSİS TR Index SJR Q4
- 2011 Çocukta İki Traflı Böbrek Taşının Nadir Bir Nedeni: D Vitamini İntoksikasyonu YÖKSİS
- 2011 Hereditary Tyrosinemia Presented by Hypophosphatemic Rickets in Fifteen old Male Patient: A Rare Case Report YÖKSİS TR Index
- 2006 Life threatening hypernatraemic dehydration in breast fed babies YÖKSİS SJR Q1 JCR Q1
- 2006 Risk factors for excess weight loss and hypernatremia in exclusively breast-fed infants YÖKSİS SJR Q1 JCR Q3 OpenAlex 74.5%
- 2005 EXCLUSIVELY BREASTFEEDING AND HYPERNATREMIC DEHYDRATION YÖKSİS SJR Q3 JCR Q4
- 2003 Hafif Zihinsel Geriliği Olan Çocuklarda Genel Sağlık Durumu Değerlendirmesi YÖKSİS TR Index JCR Q4