Akademisyen
NÜKET KUTLAY
DOÇENT
ANKARA ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Tıbbi Genetik
Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.
- Makale 32
- Proje 0
- Kitap 0
- Bildiri 52
- Patent 0
- Sanatsal 0
Scopus (SJR)
Q1
4
Q2
9
Q3
9
Q4
4
WoS (JCR)
Q1
0
Q2
3
Q3
5
Q4
17
TR Index
5
makale
Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.
Üst %1 makale
1
Üst %10 makale
3
Ort. yüzdelik
53.9%
Üst %1 payı
4.3%
Üst %10 payı
13.0%
Makaleler
YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.
Makale listesi
- 2021 The association between telomere length and ischemic stroke risk and phenotype YÖKSİS SJR Q1 JCR Q2 OpenAlex 81.7%
- 2021 Molecular testing for thalassemia: discussing the mutations over referral reasons and demographic data YÖKSİS TR Index SJR Q4 JCR Q3 OpenAlex 6.8%
- 2020 New Homozygous Missense MSMO1 Mutation in Two Siblings with SC4MOL Deficiency Presenting with Psoriasiform Dermatitis YÖKSİS SJR Q3 JCR Q4 OpenAlex üst %10 OpenAlex 95.5%
- 2020 Mosaic Small Supernumerary Marker Chromosome Derived From Five Discontinuous Regions of Chromosome 8 in a Patient With Neutropenia and Oral Aphthous Ulcer YÖKSİS SJR Q3 JCR Q4 OpenAlex 1.1%
- 2019 Importance of patient selection criteria in determining diagnostic copy number variations in patients with multiple congenital anomaly/mental retardation YÖKSİS SJR Q2 JCR Q4 OpenAlex 59.6%
- 2018 Use of immunohistochemical versus microsatellite analyses as markers for colorectal cancer YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 19.4%
- 2017 Association Between N363S and BclI Polymorphisms of the Glucocorticoid Receptor Gene (NR3C1) and Glucocorticoid Side Effects During Childhood Acute Lymphoblastic Leukemia Treatment YÖKSİS TR Index SJR Q4 JCR Q4 OpenAlex üst %10 OpenAlex 91.9%
- 2017 Constitutional Trisomy 8 Mosaicism with Persistent Macrocytosis YÖKSİS SJR Q3 JCR Q4 OpenAlex üst %1 OpenAlex 99.3%
- 2017 Akut Miyeloid Lösemide Kromozomal Anomaliler: Tek Merkezden 417 Olgunun Sitogenetik Sonuçları YÖKSİS OpenAlex 54.1%
- 2016 Prognostic impact of RUNX1 and ETV6 gene copy numberon pediatric B cell precursor acute lymphoblastic leukemiawith or without hyperdiploidy YÖKSİS SJR Q2 JCR Q4 OpenAlex 70.3%
- 2016 Unusual Chromosomal RearrangementResulted in Interstitial Monosomy 9p Case Report YÖKSİS SJR Q3 JCR Q4 OpenAlex 81.8%
- 2016 DISTAL TRISOMY 10q DUE TO MATERNAL INSERTIONAL TRANSLOCATION 15 10 A CASE REPORT AND REVIEW OF LITERATURE YÖKSİS SJR Q3 JCR Q4
- 2014 Pure Partial Trisomy 4q Syndrome In A Child With der 9 ins 9 4 q34 3 q26q35 2 mat YÖKSİS SJR Q3 JCR Q4
- 2013 An evaluation of the phenotypic features of fanconi anemia together with DEB/MMC positivity in 199 turkish patients YÖKSİS SJR Q3 JCR Q4
- 2012 Which has greater effects on leukomogenesis in Philadelphia chromosome positive leukemias: fusion or cell type? YÖKSİS SJR Q4 JCR Q4 OpenAlex 16.9%
- 2011 Characteristics and prevalence of non-classical congenital adrenal hyperplasia with a V281l mutation in patients with premature pubarche YÖKSİS SJR Q2 JCR Q4 OpenAlex 51.3%
- 2011 GENETIK ACIDAN TIMOMALAR YÖKSİS OpenAlex 24.2%
- 2010 Bone Fracture Healing with Umbilico-Placental Mononuclear Cells: A Controlled Animal Study YÖKSİS SJR Q2 JCR Q4 OpenAlex 19.5%
- 2010 A Child With Myelodysplastic Syndrome With Hypocellular Fibrosis YÖKSİS SJR Q2 JCR Q3 OpenAlex 53.2%
- 2010 Congenital bilateral parotid gland agenesis in Klinefelter syndrome YÖKSİS SJR Q1 JCR Q2 OpenAlex 78.7%