Akademisyen
ERGÜL BERBER
PROFESÖR
İSTANBUL AREL ÜNİVERSİTESİ FEN-EDEBİYAT FAKÜLTESİ MOLEKÜLER BİYOLOJİ VE GENETİK BÖLÜMÜ
- Ana Dal Fen Bilimleri ve Matematik Temel Alanı
- Yan Dal Biyoloji
Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.
- Makale 25
- Proje 0
- Kitap 0
- Bildiri 1
- Patent 0
- Sanatsal 0
Scopus (SJR)
Q1
3
Q2
8
Q3
2
Q4
1
WoS (JCR)
Q1
1
Q2
6
Q3
2
Q4
5
TR Index
3
makale
Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.
Üst %1 makale
0
Üst %10 makale
0
Ort. yüzdelik
61.5%
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
- 2022 Gene therapy in haemophilia: literature review and regional perspectives for Turkey YÖKSİS SJR Q2 JCR Q2 OpenAlex 84.8%
- 2018 Exploring the role of miRNAs in the diagnosis of MODY3 YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 55.6%
- 2017 Functional characterisation of the type 1 von Willebrand disease candidate VWF gene variants: p. M771I, p. L881R and p. P1413L YÖKSİS SJR Q2 JCR Q3 OpenAlex 59.7%
- 2014 Spontaneous thrombosis in a patient with factor XI deficiency homozygous for the p Cys398Tyr mutation YÖKSİS OpenAlex 1.2%
- 2012 The Molecular Genetics of von Willebrand Disease YÖKSİS TR Index SJR Q4 JCR Q4 OpenAlex 58.2%
- 2012 Higher Expression of the Novel Gene Upregulated Gene 4 in Two Acute Lymphoblastic Leukemia Patients with Poor Prednisolone Response YÖKSİS SJR Q2 JCR Q4 OpenAlex 67.2%
- 2009 Characterization of the genetic basis of FXI deficiency in two Turkish patients YÖKSİS SJR Q1 JCR Q2 OpenAlex 52.0%
- 2006 Sequencing of the factor 8 F8 coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations and one rediagnosis of von Willebrand s disease type 2N YÖKSİS SJR Q1 JCR Q2 OpenAlex 73.0%
- 2022 Gene therapy in haemophilia: literature review and regional perspectives for Turkey YÖKSİS SJR Q2 JCR Q2 OpenAlex 84.8%
- 2020 Whole exome sequencing reveals novel candidate gene variants for MODY YÖKSİS SJR Q2 JCR Q1
- 2018 Molecular genetic analysis of FXI gene in 14 Turkish FXI deficiency patients: identification of novel and recurrent mutations and inheritance of the mutations within the family YÖKSİS SJR Q2 JCR Q2
- 2018 Exploring the role of miRNAs in the diagnosis of MODY3. YÖKSİS TR Index SJR Q3 JCR Q4
- 2017 Functional Characterization of the Type 1 VWD candidate VWF gene variants: p.M771I, p.L881R and p.P1413L YÖKSİS SJR Q2 JCR Q3
- 2015 Identification of novel vwf gene mutations in the Turkish type 2 VWD patient population YÖKSİS
- 2014 An assessment of the pathogenic significance of the R924Q von Willebrand factor substitution YÖKSİS
- 2014 Molecular Characterization of FXI Deficiency YÖKSİS
- 2014 Founder von Willebrand factor haplotype associated with type 1 von Willebrand disease YÖKSİS
- 2014 DNA microarray analysis for the detection of mutations in hemophilia A YÖKSİS
- 2014 Organisational design of non governmental organisations related to hemophilia An example from Turkey YÖKSİS
- 2014 Spontaneous thrombosis in a patient with factor XI deficiency homozygous for the p Cys398Tyr mutation YÖKSİS