Akademisyen
ÖZLEM YALÇIN ÇAPAN
DOKTOR ÖĞRETİM ÜYESİ (Unvan:Doçent)
TEKİRDAĞ NAMIK KEMAL ÜNİVERSİTESİ TIP FAKÜLTESİ TEMEL TIP BİLİMLERİ BÖLÜMÜ
- Ana Dal Fen Bilimleri ve Matematik Temel Alanı
- Yan Dal Moleküler Biyoloji ve Genetik
Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.
- Makale 18
- Proje 0
- Kitap 0
- Bildiri 0
- Patent 0
- Sanatsal 0
Scopus (SJR)
Q1
8
Q2
8
Q3
1
Q4
4
WoS (JCR)
Q1
3
Q2
5
Q3
7
Q4
3
TR Index
5
makale
Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.
Üst %1 makale
0
Üst %10 makale
0
Ort. yüzdelik
56.6%
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
- 2026 FİRİK (FREEKEH) BUĞDAYININ BESİNSEL, ANTİOKSİDAN VE ANTİPROLİFERATİF AKTİVİTESİNİN KARŞILAŞTIRMALI DEĞERLENDİRMESİ YÖKSİS OpenAlex 16.8%
- 2025 Eco-friendly Bacterial Cellulose/Castor Oil Hydrogels: Physicochemical Behavior and Biocompatibility YÖKSİS TR Index SJR Q4 OpenAlex 11.2%
- 2025 Comprehensive in Silico Reclassification of MECP2 Variants of Uncertain Significance in Rett Syndrome: Performance Evaluation and Structural Analysis YÖKSİS SJR Q2 JCR Q3 OpenAlex 21.1%
- 2025 Navigating Uncertainty: Assessing Variants of Uncertain Significance in the CDKL5 Gene for Developmental and Epileptic Encephalopathy Using In Silico Prediction Tools and Computational Analysis YÖKSİS SJR Q2 JCR Q3 OpenAlex 87.5%
- 2024 Exome data of developmental and epileptic encephalopathy patients reveals de novo and inherited pathologic variants in epilepsy-associated genes YÖKSİS SJR Q2 JCR Q2 OpenAlex 85.0%
- 2024 Developmental and epileptic encephalopathy 82 (DEE82) with novel compound heterozygous mutations of GOT2 gene YÖKSİS SJR Q2 JCR Q2 OpenAlex 79.7%
- 2021 HNF1A-MODY Mutations in Nuclear Localization Signal Impair HNF1A-Import Receptor KPNA6 Interactions YÖKSİS SJR Q1 JCR Q3 OpenAlex 46.6%
- 2021 SYNTHESIS, CHARACTERIZATION AND BIOCOMPATIBILITY OF PLANT-OIL BASED HYDROGELS YÖKSİS SJR Q4 OpenAlex 39.0%
- 2021 A Review of Functional Characterization of Single Amino Acid Change Mutations in HNF Transcription Factors in MODY Pathogenesis YÖKSİS SJR Q1 JCR Q3 OpenAlex 88.1%
- 2019 Comparison of Crosslinker Types and Initiation Systems of Thermoresponsive PNIPAM Hydrogels YÖKSİS TR Index OpenAlex 31.2%
- 2017 De novo 8p23.1 deletion in a patient with absence epilepsy YÖKSİS SJR Q2 JCR Q4 OpenAlex 63.5%
- 2016 SCN1A gene sequencing in 46 Turkish epilepsy patients disclosed 12 novel mutations YÖKSİS SJR Q1 JCR Q2 OpenAlex 73.6%
- 2025 Eco-friendly Bacterial Cellulose/Castor Oil Hydrogels: Physicochemical Behavior and Biocompatibility YÖKSİS TR Index SJR Q4 OpenAlex 11.2%
- 2024 Exome data of developmental and epileptic encephalopathy patients reveals de novo and inherited pathologic variants in epilepsy-associated genes YÖKSİS SJR Q2 JCR Q2 OpenAlex 85.0%
- 2021 HNF1A-MODY Mutations in Nuclear Localization Signal Impair HNF1A-Import Receptor KPNA6 Interactions YÖKSİS SJR Q1 JCR Q3 OpenAlex 46.6%
- 2021 Synthesis, Characterization And Biocompatibility Of Plant-Oil Based Hydrogels YÖKSİS TR Index SJR Q4 JCR Q4 OpenAlex 39.0%
- 2020 Whole exome sequencing reveals novel candidate gene variants for MODY YÖKSİS SJR Q2 JCR Q1 OpenAlex 81.1%
- 2016 SCN1A gene sequencing in 46 Turkish epilepsy patients disclosed 12 novel mutations YÖKSİS SJR Q1 JCR Q2 OpenAlex 73.6%
- 2013 A Common VWF Exon 28 Haplotype in the Turkish Population YÖKSİS SJR Q2 JCR Q3 OpenAlex 52.4%
- 2012 Genes and molecular mechanisms involved in the epileptogenesis of idiopathic absence epilepsies YÖKSİS SJR Q1 JCR Q3 OpenAlex 83.5%