Ahmet Karagüzel

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 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

The frequency of chromosomal abnormalities in patients with reproductive failure

Figen Celep, Ahmet Karagüzel, Mehmet Özeren et al. · European Journal of Obstetrics & Gynecology and Reproductive Biology · 2006 · 74 citations

Infertility, Andrology, Fertility +9

Mutations in the<i>lipoma HMGIC fusion partner-like 5 (LHFPL5)</i>gene cause autosomal recessive nonsyndromic hearing loss

Ersan Kalay, Yun Li, Abdullah Üzümcü et al. · Human Mutation · 2006 · 71 citations

Mendelian Disorder, Genetic Disorder, Genetics +13