Bayram Toraman
Karadeniz Technical University(TR)Adli Tıp Kurumu(TR)
Publications by Year
Research Areas
Microtubule and mitosis dynamics, RNA modifications and cancer, Autism Spectrum Disorder Research, Hearing, Cochlea, Tinnitus, Genetics, Chromosomal and Genetic Variations
Most-Cited Works
- → CEP152 is a genome maintenance protein disrupted in Seckel syndrome(2010)224 cited
- → Mutations in RIPK4 Cause the Autosomal-Recessive Form of Popliteal Pterygium Syndrome(2011)92 cited
- → Involvement ofDFNB59 mutations in autosomal recessive nonsyndromic hearing impairment(2007)68 cited
- → Analysis of centrosome and DNA damage response in PLK4 associated Seckel syndrome(2017)25 cited
- → Novel splice-site and missense mutations in theALDH1A3gene underlying autosomal recessive anophthalmia/microphthalmia(2014)19 cited
- → Investigation of CYP21A2 mutations in Turkish patients with 21-hydroxylase deficiency and a novel founder mutation(2012)13 cited
- → RIPK4 suppresses the TGF‐β1 signaling pathway in HaCaT cells(2019)10 cited
- → Finding underlying genetic mechanisms of two patients with autism spectrum disorder carrying familial apparently balanced chromosomal translocations(2021)7 cited
- → Klinik Enterobacterales İzolatlarında Plazmit Aracılı mcr Kolistin Direnç Geninin Araştırılması(2020)5 cited
- HLA-E*0101/0103X is Associated with Susceptibility to Pemphigus Vulgaris: A Case-control Study.(2017)