Akademisyen
AYŞE ESRA MANGUOĞLU
DOÇENT
AKDENİZ ÜNİVERSİTESİ TIP FAKÜLTESİ TEMEL TIP BİLİMLERİ BÖLÜMÜ
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Tıbbi Genetik
Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.
- Makale 35
- Proje 0
- Kitap 0
- Bildiri 77
- Patent 0
- Sanatsal 0
Scopus (SJR)
Q1
7
Q2
6
Q3
2
Q4
6
WoS (JCR)
Q1
3
Q2
3
Q3
7
Q4
12
TR Index
3
makale
Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.
Üst %1 makale
0
Üst %10 makale
0
Ort. yüzdelik
64.3%
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 Evaluation of Expression Levels of Relapse-Associated Survivin, S100A8, GPM6B, NUDT15, AURKA and CASP1 Genes at Time of Diagnosis: A Case-Control Research Study in Childhood Pre-B- Acute Lymphoblastic Leukemia YÖKSİS TR Index SJR Q4 JCR Q4
- 2024 From islet transplantation to beta-cell regeneration: an update on beta-cell-based therapeutic approaches in type 1 diabetes. YÖKSİS SJR Q2 JCR Q3
- 2024 Turkish population-based screening for first identified changes of BRCA1 and BRCA2 genes in breast and/or ovarian cancer patients YÖKSİS SJR Q4 JCR Q4
- 2024 Autophagy dysregulation plays a crucial role in regulatory T-cell loss and neuroinflammation in amyotrophic lateral sclerosis (ALS) YÖKSİS SJR Q1 JCR Q2
- 2019 TCIRG1 and SNX10 gene mutations in the patients with autosomal recessive osteopetrosis YÖKSİS SJR Q1 JCR Q2
- 2019 Enhanced anticancer effect of cetuximab combined with stabilized silver ion solution in EGFR-positive lung cancer cells YÖKSİS SJR Q4 JCR Q4 OpenAlex 61.7%
- 2017 Identification of a constitutional t(119)(q23p13) translocation in an Extranodal Natural Killer T cell Lmyphoma patient YÖKSİS SJR Q2 JCR Q4
- 2016 Pyridoxine Responsive Seizures in Infantile Hypophosphatasia and a Novel Homozygous Mutation in ALPL Gene YÖKSİS TR Index SJR Q2 JCR Q3
- 2016 Evaluation of ETV6 RUNX1 Fusion and Additional Abnormalities Involving ETV6 and or RUNX1 Genes Using FISH Technique in Patients with Childhood Acute Lymphoblastic Leukemia YÖKSİS SJR Q4 JCR Q4 OpenAlex 66.9%
- 2014 PRENATAL DIAGNOSIS OF ISOCHROMOSOME 21p AND ISOCHROMOSOME 21q IN A FETUS WITH DOWN SYNDROME YÖKSİS
- 2013 Absence of the SLC22A12 gene mutation in Turkish population with primary gout disease YÖKSİS SJR Q3 JCR Q3
- 2012 Glikojen depo hastalığı tip III tanılı 10 Türk olgunun mutasyon analizleri dört yeni mutasyonun tanımlanması YÖKSİS TR Index SJR Q4 JCR Q4
- 2012 A patient with Down syndrome with a de novo derivative chromosome 21 YÖKSİS SJR Q1 JCR Q3
- 2012 The value of donor lymphocyte infusions in thalassemia patients at imminent risk of graft rejection following stem cell transplantation YÖKSİS SJR Q1 JCR Q1
- 2011 RLIP76 Gene Variants are not Associated with Drug Response in Turkish Epilepsy Patients YÖKSİS SJR Q4 JCR Q4
- 2011 Genomic Large Rearrangement Screening of BRCA1 and BRCA2 Genes in High Risk Turkish Breast Ovarian Cancer Patients by Using Multiplex Ligation Dependent Probe Amplification Assay YÖKSİS SJR Q1 JCR Q3
- 2010 Germline mutations of BRCA1 and BRCA2 genes in Turkish breast ovarian and prostate cancer patients YÖKSİS SJR Q3 JCR Q3
- 2008 Infantile Spasms Is Associated with Deletion of the MAGI2 Gene on Chromosome 7q11 23 q21 11 YÖKSİS SJR Q1 JCR Q1
- 2007 Combination of Hb Knossos Cod 27 G T and IVSII 745 C G in a Turkish Patient with Beta Thalassemia Major YÖKSİS JCR Q4
- 2007 Short report The AIDIT and IMPACT conference 2006 Outcomes and future directions YÖKSİS