Follow
Suna TOKGOZ-YILMAZ, Suna Tokgöz Yılmaz, Tokgoz Yilmaz, S
Suna TOKGOZ-YILMAZ, Suna Tokgöz Yılmaz, Tokgoz Yilmaz, S
Verified email at ankara.edu.tr
Title
Cited by
Cited by
Year
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
1502016
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
1222012
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
762014
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
672010
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
642013
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
592009
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
532010
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
472016
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
442016
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
412010
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
352007
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
312006
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
262019
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
242013
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
232014
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
192019
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
172013
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
112020
Novel variant p.E269K confirms causative role of PLS1 mutations in autosomal dominant hearing loss
O Diaz‐Horta, G Bademci, S Tokgoz‐Yilmaz, S Guo, F Zafeer, CJ Sineni, ...
Clinical genetics 96 (6), 575-578, 2019
112019
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
102012
The system can't perform the operation now. Try again later.
Articles 1–20