| Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort G Bademci, J Foster, N Mahdieh, M Bonyadi, D Duman, FB Cengiz, ... Genetics in Medicine 18 (4), 364-371, 2016 | 165 | 2016 |
| Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss KO Yariz, D Duman, CZ Seco, J Dallman, M Huang, TA Peters, A Sirmaci, ... The American Journal of Human Genetics 91 (5), 872-882, 2012 | 130 | 2012 |
| FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing O Diaz-Horta, A Subasioglu-Uzak, M Grati, A DeSmidt, J Foster, L Cao, ... Proceedings of the National Academy of Sciences 111 (27), 9864-9868, 2014 | 79 | 2014 |
| A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing loss A Sırmacı, S Erbek, J Price, M Huang, D Duman, FB Cengiz, G Bademci, ... The American Journal of Human Genetics 86 (5), 797-804, 2010 | 72 | 2010 |
| SLITRK6 mutations cause myopia and deafness in humans and mice M Tekin, BA Chioza, Y Matsumoto, O Diaz-Horta, HE Cross, D Duman, ... The Journal of clinical investigation 123 (5), 2094-2102, 2013 | 66 | 2013 |
| Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutations A Sırmacı, D Duman, H Öztürkmen-Akay, S Erbek, A İncesulu, ... International journal of pediatric otorhinolaryngology 73 (5), 699-705, 2009 | 62 | 2009 |
| Recurrent and private MYO15A mutations are associated with deafness in the Turkish population FB Cengiz, D Duman, A Sırmacı, S Tokgöz-Yilmaz, S Erbek, ... Genetic testing and molecular biomarkers 14 (4), 543-550, 2010 | 54 | 2010 |
| ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice O Diaz-Horta, C Abad, L Sennaroglu, J Foster, A DeSmidt, G Bademci, ... Proceedings of the National Academy of Sciences 113 (21), 5993-5998, 2016 | 51 | 2016 |
| Variations in multiple syndromic deafness genes mimic non-syndromic hearing loss G Bademci, FB Cengiz, J Foster Ii, D Duman, L Sennaroglu, O Diaz-Horta, ... Scientific reports 6 (1), 31622, 2016 | 47 | 2016 |
| Transient evoked otoacoustic emissions and contralateral suppressions in children with auditory listening problems F Yalçınkaya, ST Yılmaz, NB Muluk Auris Nasus Larynx 37 (1), 47-54, 2010 | 41 | 2010 |
| Effect of age on speech recognition in noise and on contralateral transient evoked otoacoustic emission suppression ST Yılmaz, G Sennaroğlu, L Sennaroğlu, SK Köse The Journal of Laryngology & Otology 121 (11), 1029-1034, 2007 | 36 | 2007 |
| Effects of GJB2 genotypes on the audiological phenotype: variability is present for all genotypes BÖ Hişmi, ST Yılmaz, A İncesulu, M Tekin International journal of pediatric otorhinolaryngology 70 (10), 1687-1694, 2006 | 34 | 2006 |
| A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss CJ Sineni, M Yildirim-Baylan, S Guo, V Camarena, G Wang, ... Human genetics 138, 1071-1075, 2019 | 29 | 2019 |
| Evidence for genotype–phenotype correlation for OTOF mutations M Yildirim-Baylan, G Bademci, D Duman, H Ozturkmen-Akay, ... International journal of pediatric otorhinolaryngology 78 (6), 950-953, 2014 | 26 | 2014 |
| The role of the medial olivocochlear system in the complaints of understanding speech in noisy environments by individuals with normal hearing S Tokgoz-Yilmaz, SK Kose, MD Turkyilmaz, G Atay Auris Nasus Larynx 40 (6), 521-524, 2013 | 26 | 2013 |
| Dysfunction of GRAP, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss C Li, G Bademci, A Subasioglu, O Diaz-Horta, Y Zhu, J Liu, TG Mitchell, ... Proceedings of the National Academy of Sciences 116 (4), 1347-1352, 2019 | 18 | 2019 |
| Evaluation of hearing and speech-language in preschool children: how important, why we should perform? S Tokgöz-Yılmaz, E Özcebe, MD Türkyılmaz, A Köse, G Sennaroğlu, ... The Turkish Journal of Pediatrics 55 (6), 606-611, 2013 | 18 | 2013 |
| Auditory processing differences correlate with autistic traits in males S Aykan, E Gürses, S Tokgöz-Yılmaz, C Kalaycıoğlu Frontiers in Human Neuroscience 14, 584704, 2020 | 14 | 2020 |
| Children’s auditory performance scale: Turkish validity and reliability M Baydan, F Aslan, S Yılmaz, F Yalçınkaya Hacettepe University Faculty of Health Sciences Journal 7 (1), 32-40, 2020 | 14 | 2020 |
| Computerised Turkish versions of tests for central auditory processing disorder MD Turkyılmaz, S Yılmaz, S Yagcıoglu, M Yaralı, N Celik Journal of Hearing Sciences 2 (1), 30-35, 2012 | 11 | 2012 |