Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents
Yan, Denise, Tekin, Demet, Bademci, Guney, Foster, Joseph, Cengiz, F. Basak, Kannan-Sundhari, Abhiraami, Guo, Shengru, Mittal, Rahul, Zou, Bing, Grati, Mhamed, Kabahuma, Rosemary I., Kameswaran, Mohan, Lasisi, Taye J., Adedeji, Waheed A., Lasisi, Akeem O., Menendez, Ibis, Herrera, Marianna, Carranza, Claudia, Maroofian, Reza, Crosby, Andrew H., Bensaid, Mariem, Masmoudi, Saber, Behnam, Mahdiyeh, Mojarrad, Majid, Feng, Yong, Duman, Duygu, Mawla, Alex M., Nord, Alex S., Blanton, Susan H., Liu, Xue Z., Tekin, Mustafa
Published in Human genetics (01.08.2016)
Published in Human genetics (01.08.2016)
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Journal Article
FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing
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
Published in Proceedings of the National Academy of Sciences - PNAS (08.07.2014)
Published in Proceedings of the National Academy of Sciences - PNAS (08.07.2014)
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Journal Article
ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice
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
Published in Proceedings of the National Academy of Sciences - PNAS (24.05.2016)
Published in Proceedings of the National Academy of Sciences - PNAS (24.05.2016)
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Journal Article
SLITRK6 mutations cause myopia and deafness in humans and mice
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, 2nd, 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
Published in The Journal of clinical investigation (01.05.2013)
Published in The Journal of clinical investigation (01.05.2013)
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Journal Article
Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort
Bademci, Guney, Foster, Joseph, Mahdieh, Nejat, Bonyadi, Mortaza, Duman, Duygu, Cengiz, F.Basak, Menendez, Ibis, Diaz-Horta, Oscar, Shirkavand, Atefeh, Zeinali, Sirous, Subasioglu, Asli, Tokgoz-Yilmaz, Suna, Huesca-Hernandez, Fabiola, 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
Published in Genetics in medicine (01.04.2016)
Published in Genetics in medicine (01.04.2016)
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Journal Article
Analysis of NPHS2 mutations in Turkish steroid-resistant nephrotic syndrome patients
Ozçakar, Z Birsin, Cengiz, F Başak, Cakar, Nilgün, Uncu, Nermin, Kara, Nazli, Acar, Banu, Yüksel, Selçuk, Ekim, Mesiha, Tekin, Mustafa, Yalçinkaya, Fatoş
Published in Pediatric nephrology (Berlin, West) (01.08.2006)
Published in Pediatric nephrology (Berlin, West) (01.08.2006)
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Journal Article
A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss
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
Published in American journal of human genetics (14.05.2010)
Published in American journal of human genetics (14.05.2010)
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Journal Article
Targeted Resequencing of Deafness Genes Reveals a Founder MYO15A Variant in Northeastern Brazil
Manzoli, Gabrielle N., Bademci, Guney, Acosta, Angelina X., Félix, Têmis M., Cengiz, F.Basak, Foster, Joseph, Da Silva, Danniel S. Dias, Menendez, Ibis, Sanchez‐Pena, Isalis, Tekin, Demet, Blanton, Susan H., Abe‐Sandes, Kiyoko, Liu, Xue Zhong, Tekin, Mustafa
Published in Annals of human genetics (01.11.2016)
Published in Annals of human genetics (01.11.2016)
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Journal Article
Recurrent and private MYO15A mutations are associated with deafness in the Turkish population
Cengiz, F Basak, Duman, Duygu, Sirmaci, Asli, Tokgöz-Yilmaz, Suna, Erbek, Seyra, Oztürkmen-Akay, Hatice, Incesulu, Armagan, Edwards, Yvonne J K, Ozdag, Hilal, Liu, Xue Z, Tekin, Mustafa
Published in Genetic testing and molecular biomarkers (01.08.2010)
Published in Genetic testing and molecular biomarkers (01.08.2010)
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Journal Article
GJB2 Mutations in Mongolia: Complex Alleles, Low Frequency, and Reduced Fitness of the Deaf
Tekin, Mustafa, Xia, Xia‐Juan, Erdenetungalag, Radnaabazar, Cengiz, Filiz Basak, White, Thomas W., Radnaabazar, Janchiv, Dangaasuren, Begzsuren, Tastan, Hakki, Nance, Walter E., Pandya, Arti
Published in Annals of human genetics (01.03.2010)
Published in Annals of human genetics (01.03.2010)
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Journal Article
Spectrum of DNA variants for nonsyndromic deafness in a large cohort from multiple continents
Yan, Denise, Tekin, Demet, Bademci, Guney, Foster, Joseph, Cengiz, F. Basak, Kannan-Sundhari, Abhiraami, Guo, Shengru, Mittal, Rahul, Zou, Bing, Grati, Mhamed, Kabahuma, Rosemary I., Kameswaran, Mohan, Lasisi, Taye J, Adedeji, Waheed A, Lasisi, Akeem O., Menendez, Ibis, Herrera, Marianna, Carranza, Claudia, Maroofian, Reza, Crosby, Andrew H., Bensaid, Mariem, Masmoudi, Saber, Behnam, Mahdiyeh, Mojarrad, Majid, Feng, Yong, Duman, Duygu, Mawla, Alex M., Nord, Alex S., Blanton, Susan H., Liu, Xuezhong, Tekin, Mustafa
Published in Human genetics (25.06.2016)
Published in Human genetics (25.06.2016)
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