Suna Tokgöz-Yılmaz

Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort

Güney Bademci, Joseph Foster, Nejat Mahdieh et al. · Genetics in Medicine · 2015 · 158 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +11

Mutations in OTOGL , Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss

Kemal O. Yariz, Duygu Duman, Celia Zazo Seco et al. · The American Journal of Human Genetics · 2012 · 127 citations · Full text

Developmental Biology, Genetics, Audiology +10

FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing

Oscar Diaz‐Horta, Asli Subasioglu-Uzak, M’hamed Grati et al. · Proceedings of the National Academy of Sciences · 2014 · 79 citations · Full text

A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss

Aslı Sırmacı, Seyra Erbek, Justin Price et al. · The American Journal of Human Genetics · 2010 · 72 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +11

SLITRK6 mutations cause myopia and deafness in humans and mice

Mustafa Tekin, Barry A. Chioza, Yoshifumi Matsumoto et al. · Journal of Clinical Investigation · 2013 · 66 citations · Full text

Knockout Mouse, Developmental Biology, Molecular Neuroscience +12