Ersan Kalay

CEP152 is a genome maintenance protein disrupted in Seckel syndrome

Ersan Kalay, Gökhan Yigit, Yakup Aslan et al. · Nature Genetics · 2010 · 223 citations · Full text

Genetic Disorder, Genetics, Seckel Syndrome +5

Mutations of ESRRB Encoding Estrogen-Related Receptor Beta Cause Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB35

Rob W.J. Collin, Ersan Kalay, Muhammad Tariq et al. · The American Journal of Human Genetics · 2008 · 128 citations · Full text

Developmental Biology, Genetics, Audiology +7

Mutations in RIPK4 Cause the Autosomal-Recessive Form of Popliteal Pterygium Syndrome

Ersan Kalay, Orhan Sezgın, Vasant Chellappa et al. · The American Journal of Human Genetics · 2011 · 92 citations · Full text

Developmental Biology, Mendelian Disorder, Autosomal-recessive Form +8

Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment

Margit Schraders, Laura Ruiz-Palmero, Ersan Kalay et al. · The American Journal of Human Genetics · 2012 · 91 citations · Full text

Developmental Biology, Genetics, Audiology +10

Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans

Zubair M. Ahmed, Saber Masmoudi, Ersan Kalay et al. · Nature Genetics · 2008 · 84 citations · Full text

Nonsyndromic Deafness, Mendelian Disorder, Genetic Disorder +9