Auditory Processing Differences Correlate With Autistic Traits in Males

gan Aykan, Simge, Gürses, Emre, Tokgöz-Yılmaz, Suna, Kalaycıoğlu, Canan
Cyhoeddwyd yn Front Hum Neurosci (2020)

AUDIOLOGICAL FINDINGS IN OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA (OSMED) ASSOCIATED WITH A NOVEL MUTATION IN COL11A2

gan Tokgöz-Yilmaz, Suna, Şahli, Sanem, Fitoz, Suat, Sennaroğlu, Gonca, Tekin, Mustafa
Cyhoeddwyd 2011

A Novel Variant in SYNE4 Confirms its Causative Role in Sensorineural Hearing Loss

gan Masterson, John, Yıldırım, Busegül, Gökkaya, Ece, Tokgöz Yılmaz, Suna, Tekin, Mustafa
Cyhoeddwyd yn Balkan Med J (2018)

EVIDENCE FOR GENOTYPE-PHENOTYPE CORRELATION FOR OTOFMUTATIONS

gan Yildirim-Baylan, Muzeyyen, Bademci, Guney, Duman, Duygu, Ozturkmen-Akay, Hatice, Tokgoz-Yilmaz, Suna, Tekin, Mustafa
Cyhoeddwyd 2014

A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss

gan Sineni, Claire J., Yildirim-Baylan, Muzeyyen, Guo, Shengru, Camarena, Vladimir, Wang, Gaofeng, Tokgoz-Yilmaz, Suna, Duman, Duygu, Bademci, Guney, Tekin, Mustafa
Cyhoeddwyd yn Hum Genet (2019)

Dysfunction of GRAP, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss

gan Li, Chong, Bademci, Guney, Subasioglu, Asli, Diaz-Horta, Oscar, Zhu, Yi, Liu, Jiaqi, Mitchell, Timothy Gavin, Abad, Clemer, Seyhan, Serhat, Duman, Duygu, Cengiz, Filiz Basak, Tokgoz-Yilmaz, Suna, Blanton, Susan H., Farooq, Amjad, Walz, Katherina, Zhai, R. Grace, Tekin, Mustafa
Cyhoeddwyd yn Proc Natl Acad Sci U S A (2019)

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

gan Diaz-Horta, Oscar, Subasioglu-Uzak, Asli, Grati, M’hamed, DeSmidt, Alexandra, Foster, Joseph, Cao, Lei, Bademci, Guney, Tokgoz-Yilmaz, Suna, Duman, Duygu, Cengiz, F. Basak, Abad, Clemer, Mittal, Rahul, Blanton, Susan, Liu, Xue Z., Farooq, Amjad, Walz, Katherina, Lu, Zhongmin, Tekin, Mustafa
Cyhoeddwyd 2014

ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice

gan Diaz-Horta, Oscar, Abad, Clemer, Sennaroglu, Levent, Foster, Joseph, DeSmidt, Alexandra, Bademci, Guney, Tokgoz-Yilmaz, Suna, Duman, Duygu, Cengiz, F. Basak, Grati, M’hamed, Fitoz, Suat, Liu, Xue Z., Farooq, Amjad, Imtiaz, Faiqa, Currall, Benjamin B., Morton, Cynthia Casson, Nishita, Michiru, Minami, Yasuhiro, Lu, Zhongmin, Walz, Katherina, Tekin, Mustafa
Cyhoeddwyd yn Proc Natl Acad Sci U S A (2016)

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

gan Sırmacı, Aslı, Erbek, Seyra, Price, Justin, Huang, Mingqian, Duman, Duygu, Cengiz, F. Başak, Bademci, Güney, Tokgöz-Yılmaz, Suna, Hişmi, Burcu, Özdağ, Hilal, Öztürk, Banu, Kulaksızoğlu, Sevsen, Yıldırım, Erkan, Kokotas, Haris, Grigoriadou, Maria, Petersen, Michael B., Shahin, Hashem, Kanaan, Moien, King, Mary-Claire, Chen, Zheng-Yi, Blanton, Susan H., Liu, Xue Z., Zuchner, Stephan, Akar, Nejat, Tekin, Mustafa
Cyhoeddwyd 2010

SLITRK6 mutations cause myopia and deafness in humans and mice

gan Tekin, Mustafa, Chioza, Barry A., Matsumoto, Yoshifumi, Diaz-Horta, Oscar, Cross, Harold E., Duman, Duygu, Kokotas, Haris, Moore-Barton, Heather L., Sakoori, Kazuto, Ota, Maya, Odaka, Yuri S., Foster, Joseph, Cengiz, F. Basak, Tokgoz-Yilmaz, Suna, Tekeli, Oya, Grigoriadou, Maria, Petersen, Michael B., Sreekantan-Nair, Ajith, Gurtz, Kay, Xia, Xia-Juan, Pandya, Arti, Patton, Michael A., Young, Juan I., Aruga, Jun, Crosby, Andrew H.
Cyhoeddwyd 2013

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

gan Yariz, Kemal O., Duman, Duygu, Seco, Celia Zazo, Dallman, Julia, Huang, Mingqian, Peters, Theo A., Sirmaci, Asli, Lu, Na, Schraders, Margit, Skromne, Isaac, Oostrik, Jaap, Diaz-Horta, Oscar, Young, Juan I., Tokgoz-Yilmaz, Suna, Konukseven, Ozlem, Shahin, Hashem, Hetterschijt, Lisette, Kanaan, Moien, Oonk, Anne M.M., Edwards, Yvonne J.K., Li, Huawei, Atalay, Semra, Blanton, Susan, DeSmidt, Alexandra A., Liu, Xue-Zhong, Pennings, Ronald J.E., Lu, Zhongmin, Chen, Zheng-Yi, Kremer, Hannie, Tekin, Mustafa
Cyhoeddwyd 2012

Comprehensive Analysis via Exome Sequencing Uncovers Genetic Etiology in Autosomal Recessive Non-Syndromic Deafness in a Large Multiethnic Cohort

gan Bademci, Guney, Foster, Joseph, Mahdieh, Nejat, Bonyadi, Mortaza, Duman, Duygu, Cengiz, F.Basak, Menendez, Ibis, Horta, Oscar Diaz, Shirkavand, Atefeh, Zeinali, Sirous, Subasioglu, Asli, Tokgoz-Yilmaz, Suna, Hernandez, Fabiola Huesca, de la Luz Arenas Sordo, Maria, Dominguez-Aburto, Juan, Hernandez-Zamora, Edgar, Montenegro, Paola, Paredes, Rosario, Moreta, Germania, Vinueza, Rodrigo, Villegas, Franklin, Mendoza Benitez, Santiago, Guo, Shengru, Bozan, Nazim, Tos, Tulay, Incesulu, Armagan, Sennaroglu, Gonca, Blanton, Susan H., Ozturkmen Akay, Hatice, Yildirim-Baylan, Muzeyyen, Tekin, Mustafa
Cyhoeddwyd yn Genet Med (2015)