Auditory Processing Differences Correlate With Autistic Traits in Males

ανά Aykan, Simge, Gürses, Emre, Tokgöz-Yılmaz, Suna, Kalaycıoğlu, Canan
Τόπος έκδοσης Front Hum Neurosci (2020)

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

ανά Tokgöz-Yilmaz, Suna, Şahli, Sanem, Fitoz, Suat, Sennaroğlu, Gonca, Tekin, Mustafa
Έκδοση 2011

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

ανά Masterson, John, Yıldırım, Busegül, Gökkaya, Ece, Tokgöz Yılmaz, Suna, Tekin, Mustafa
Τόπος έκδοσης Balkan Med J (2018)

EVIDENCE FOR GENOTYPE-PHENOTYPE CORRELATION FOR OTOFMUTATIONS

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

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

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

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

ανά 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
Τόπος έκδοσης Proc Natl Acad Sci U S A (2019)

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

ανά 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
Έκδοση 2014

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

ανά 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
Τόπος έκδοσης Proc Natl Acad Sci U S A (2016)

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

ανά 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
Έκδοση 2010

SLITRK6 mutations cause myopia and deafness in humans and mice

ανά 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.
Έκδοση 2013

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

ανά 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
Έκδοση 2012

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

ανά 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
Τόπος έκδοσης Genet Med (2015)