Akademisyen
SELAHADDİN TEKEŞ
PROFESÖR
DİCLE ÜNİVERSİTESİ TIP FAKÜLTESİ TEMEL TIP BİLİMLERİ BÖLÜMÜ
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Tıbbi Biyoloji
Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.
- Makale 86
- Proje 0
- Kitap 1
- Bildiri 86
- Patent 0
- Sanatsal 0
Scopus (SJR)
Q1
7
Q2
8
Q3
9
Q4
5
WoS (JCR)
Q1
3
Q2
5
Q3
8
Q4
14
TR Index
5
makale
Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.
Üst %1 makale
0
Üst %10 makale
0
Ort. yüzdelik
43.4%
Üst %1 payı
0.0%
Üst %10 payı
0.0%
Makaleler
YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.
Makale listesi
- 2025 Association of CD40 gene polymorphisms rs1883832 and rs4810485 with familial mediterranean fever in pediatric patients YÖKSİS SJR Q4 JCR Q4 OpenAlex 11.1%
- 2025 Phenotypic and Fertility Variability in Klinefelter Syndrome: Evidence of Natural Fatherhood in Non- Mosaic 47,XXY Men and Rare 48,XXYY Cases YÖKSİS
- 2025 A Comprehensive Perspective on Febrile Seizures in Children: A Prospective Cohort Study with Evaluation of Clinical, Laboratory, and Genetic Features YÖKSİS SJR Q2 JCR Q1 OpenAlex 84.7%
- 2025 Pediatrik Diyabetik Hastalarda Paraoksonaz Gen Polimorfizm Analizi YÖKSİS OpenAlex 22.5%
- 2025 Association of CD40 gene polymorphisms rs1883832 and rs4810485 with familial mediterranean fever in pediatric patients YÖKSİS JCR Q4 OpenAlex 6.0%
- 2025 Differentiating between oligospermic men and fertile men using aniline blue staining, a marker for sperm chromatin defects YÖKSİS OpenAlex 7.4%
- 2024 The relationship between primary ovarian insufficiency and gene variations: a prospective case-control study YÖKSİS SJR Q2 JCR Q2 OpenAlex 61.1%
- 2024 The clinical and demographic characteristics of patients with late-diagnosed cerebrotendinous xanthomatosis in a Turkish population YÖKSİS SJR Q1 JCR Q1 OpenAlex 23.7%
- 2024 Prevalence of HLA B27 in Patients Diagnosed with Ankylosing Spondylitis (AS) in Diyarbakır, Southeastern Region of Turkey YÖKSİS SJR Q3 JCR Q3 OpenAlex 65.7%
- 2024 A Newborn With Restrictive Dermatopathy: A Case Report YÖKSİS OpenAlex 14.3%
- 2024 Clinical Application of Whole-exome Sequencing Analysis in Childhood Epilepsy YÖKSİS SJR Q3 JCR Q3 OpenAlex 80.8%
- 2022 Analysis of beta globin gene mutations in Diyarbakir YÖKSİS SJR Q4 JCR Q4 OpenAlex 48.5%
- 2022 Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium YÖKSİS SJR Q2 JCR Q3 OpenAlex 75.1%
- 2022 Çocuk Ailesel Akdeniz Ateşi Hastalarında MEFV Mutasyonlarının Dağılımı: Türkiye\u2019nin Güneydoğusunda Tek Merkezli Çalışma YÖKSİS OpenAlex 42.5%
- 2022 Hematolojik Kanser Tanılı Hastaların Kemik İliği Örneklerindeki Kromozomal Anomaliler: Tek Merkezden 109 Olgunun FISH Sonuçları YÖKSİS OpenAlex 56.8%
- 2021 Crystalline gene mutations in Turkish children with congenital cataracts YÖKSİS SJR Q2 JCR Q3 OpenAlex 44.0%
- 2021 Assessment of second-trimester amniocentesis cases: 10-year experience of a tertiary center YÖKSİS TR Index OpenAlex 3.5%
- 2020 Glycogen Storage Disease Type IIIa Presenting with Hyperglycemia: A Novel Mutation YÖKSİS TR Index OpenAlex 16.3%
- 2014 The Tumor Necrosis Factor A TNF A Gene 308 G A Polymorphism and the Tumor Necrosis Factor Related Apoptosis Inducing Ligand Trail Gene Polymorphisms in Behcet S Disease YÖKSİS SJR Q4 JCR Q4 OpenAlex 67.6%
- 2014 Seroprevalence of serum HBsAg positivity and hepatitis delta virus infection among blood donors in Southeastern Turkey YÖKSİS OpenAlex 79.9%