Ersan Kalay
Karadeniz Technical University(TR)Adli Tıp Kurumu(TR)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Connexins and lens biology, Genetics and Neurodevelopmental Disorders, Chromosomal and Genetic Variations, Microtubule and mitosis dynamics
Most-Cited Works
- → CEP152 is a genome maintenance protein disrupted in Seckel syndrome(2010)224 cited
- → Mutations of ESRRB Encoding Estrogen-Related Receptor Beta Cause Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB35(2008)128 cited
- → Mutations in RIPK4 Cause the Autosomal-Recessive Form of Popliteal Pterygium Syndrome(2011)92 cited
- → Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment(2012)91 cited
- → Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans(2008)86 cited
- → Mutations in thelipoma HMGIC fusion partner-like 5 (LHFPL5)gene cause autosomal recessive nonsyndromic hearing loss(2006)71 cited
- → Involvement ofDFNB59 mutations in autosomal recessive nonsyndromic hearing impairment(2007)68 cited
- → Four novelTMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss(2005)58 cited
- → Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decay(2014)56 cited
- → GJB2 mutations in Turkish patients with ARNSHL: prevalence and two novel mutations(2005)54 cited