Academician
BAYRAM TORAMAN
DOKTOR ÖĞRETİM ÜYESİ
KARADENİZ TEKNİK ÜNİVERSİTESİ TIP FAKÜLTESİ TEMEL TIP BİLİMLERİ BÖLÜMÜ
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Tıbbi Biyoloji
A quick look at recorded outputs — details below.
- Articles 28
- Projects 0
- Books 0
- Proceedings 17
- Patents 0
- Artistic 0
Scopus (SJR)
Q1
16
Q2
6
Q3
2
Q4
2
WoS (JCR)
Q1
10
Q2
6
Q3
6
Q4
4
TR Index
12
articles
Field+year+type normalized OpenAlex percentiles — not Clarivate ESI / SciVal.
Top 1% articles
1
Top 10% articles
2
Avg percentile
51.2%
Top 1% share
3.7%
Top 10% share
7.4%
Articles
Articles with YÖKSİS and OpenAlex source split; narrow by quartile or TR Index.
Article list
- 2026 Molecular modeling and clinical characterization of a CYP17A1 variant (p. Asp298Asn) causing 17α-hydroxylase/17, 20-lyase deficiency in two siblings YÖKSİS SJR Q3 JCR Q4 OpenAlex 38.1%
- 2025 LZTR1 interacts with AIFM3 protein and negatively regulates Ras signaling by downregulating SHOC2 and phosphorylated p90RSK protein levels in apoptosis YÖKSİS TR Index OpenAlex 13.7%
- 2025 AIFM3 Has Pro-apoptotic, Whereas LZTR1 Has Bilateral Functions In The Intrinsic Apoptosis Pathway YÖKSİS TR Index OpenAlex 18.2%
- 2025 A synonymous single nucleotide variant on the FAM20C gene causes non-lethal Raine syndrome YÖKSİS SJR Q1 JCR Q2 OpenAlex 74.6%
- 2024 Genetically determined plasma trefoil factor-3 levels are causally associated with the risk of ulcerative colitis: a Mendelian randomization study YÖKSİS TR Index OpenAlex 21.7%
- 2022 Is the MTHFR C677T variant a genetic risk factor in the etiology of autism spectrum disorder? Is it alone or by combined with rare variants of the PHGDH gene? Running Title: Is the MTHFR C677T a genetic risk factor for autism? YÖKSİS TR Index OpenAlex 7.0%
- 2022 Two male patients from an extended seven generation Turkish family diagnosed with Renpenning syndrome: identifying the causative mutation and review of the literature YÖKSİS TR Index OpenAlex 4.0%
- 2021 A novel homozygous RIPK4 variant in a family with severe Bartsocas-Papas syndrome YÖKSİS SJR Q2 JCR Q3 OpenAlex 48.0%
- 2021 Finding underlying genetic mechanisms of two patients with autism spectrum disorder carrying familial apparently balanced chromosomal translocations YÖKSİS SJR Q2 JCR Q2 OpenAlex 80.0%
- 2020 Klinik Enterobacterales İzolatlarında Plazmit Aracılı mcr Kolistin Direnç Geninin Araştırılması YÖKSİS TR Index SJR Q4 JCR Q4 OpenAlex 26.9%
- 2020 RIPK4 suppresses the TGF-Beta1 signaling pathway in HaCaT cells YÖKSİS SJR Q2 JCR Q3 OpenAlex 64.4%
- 2017 Analysis of centrosome and DNA damage response in PLK4 associated Seckel syndrome YÖKSİS SJR Q1 JCR Q2 OpenAlex 86.2%
- 2014 Novel splice site and missense mutations in the ALDH1A3 gene underlying autosomal recessive anophthalmia microphthalmia YÖKSİS SJR Q1 JCR Q1 OpenAlex 83.4%
- 2013 Investigation of CYP21A2 mutations in Turkish patients with 21 hydroxylase deficiency and a novel founder mutation YÖKSİS SJR Q1 JCR Q3 OpenAlex 47.3%
- 2012 Mutations in RIPK4 Cause the Autosomal Recessive Form of Popliteal Pterygium Syndrome YÖKSİS SJR Q1 JCR Q1 OpenAlex 89.4%
- 2010 CEP152 is a genome maintenance protein disrupted in Seckel syndrome YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.1%
- 2007 Involvement ofDFNB59 mutations in autosomal recessive nonsyndromic hearing impairment YÖKSİS SJR Q1 JCR Q1 OpenAlex 70.3%
- 2026 Could vector-derived cadherin mimicry contribute to pemphigus vulgaris? An immunogenetic and in silico study involving HLA-DRB104:02 and 14:01 YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 92.6%
- 2026 LZTR1 Loss Reduces Vimentin Expression and Motility in Hep3B Hepatocellular Carcinoma Cells YÖKSİS SJR Q1 JCR Q1 OpenAlex 87.0%
- 2025 A synonymous single nucleotide variant on the FAM20C gene causes non-lethal Raine syndrome YÖKSİS SJR Q1 JCR Q2 OpenAlex 74.5%