Doç. Dr. SUNA YILMAZ

Yayın Ağı

Makaleler 17

1. The Turkish Short Version of the CSpeech, Spatial, and Qualities of Hearing Scale (SSQ) for Clinical Use: Determining Reliability and Validity for People with and without Hearing Loss on the Basis of SSQ12-A, SSQ12-B, SSQ12-C

ÇILDIR B., KILIÇ S., Ozkisi B., Tokgoz-Yilmaz S.

ENT UPDATES , cilt.11, sa.2, ss.127-133, 2021 (ESCI, TRDizin) Sürdürülebilir Kalkınma

2. Audiological findings in Noonan syndrome

Tokgoz-Yilmaz S., TÜRKYILMAZ M. D., Cengiz F. B., Sjostrand A. P., Kose S. K., Tekin M.

INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY , cilt.89, ss.50-54, 2016 (SCI-Expanded, Scopus)

3. Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss

Bademci G., Cengiz F. B., Foster J., Duman D., Sennaroglu L., Diaz-Horta O., et al.

SCIENTIFIC REPORTS , cilt.6, 2016 (SCI-Expanded, Scopus)

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

Diaz-Horta O., Abad C., SENNAROĞLU L., Foster J., DeSmidt A., Bademci G., et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA , cilt.113, sa.21, ss.5993-5998, 2016 (SCI-Expanded, Scopus)

5. Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort

Bademci G., Foster J., Mahdieh N., Bonyadi M., Duman D., Cengiz F. B., et al.

GENETICS IN MEDICINE , cilt.18, sa.4, ss.364-371, 2016 (SCI-Expanded, Scopus)

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

Diaz-Horta O., Subasioglu-Uzak A., Grati M., DeSmidt A., Foster J., Cao L., et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA , cilt.111, sa.27, ss.9864-9868, 2014 (SCI-Expanded, Scopus)

7. Evidence for genotype-phenotype correlation for OTOF mutations

Yildirim-Baylan M., Bademci G., Duman D., OZTURKMEN-AKAY H., Tokgoz-Yilmaz S., Tekin M.

INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY , cilt.78, sa.6, ss.950-953, 2014 (SCI-Expanded, Scopus)

8. The role of the medial olivocochlear system in the complaints of understanding speech in noisy environments by individuals with normal hearing

Tokgoz-Yilmaz S., Kose S. K., TÜRKYILMAZ M. D., ATAY G.

AURIS NASUS LARYNX , cilt.40, sa.6, ss.521-524, 2013 (SCI-Expanded, Scopus)

9. Evaluation of hearing and speech-language in preschool children: how important, why we should perform?

Tokgoz-Yilmaz S., ÖZCEBE E., TÜRKYILMAZ M. D., Kose A., SENNAROĞLU G., Orhon F., et al.

TURKISH JOURNAL OF PEDIATRICS , cilt.55, sa.6, ss.606-611, 2013 (SCI-Expanded, Scopus)

10. Can Global Field Power be an Objective Tool to Assess Cortical Responses to Acoustic Change? A Study with Cochlear Implant Users

TÜRKYILMAZ M. D., YARALI M., Yagcioglu S., CINAR B. C., Tokgoz-Yilmaz S., ÖZCEBE E., et al.

JOURNAL OF INTERNATIONAL ADVANCED OTOLOGY , cilt.9, sa.3, ss.381-390, 2013 (SCI-Expanded, Scopus)

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

Yariz K. O., Duman D., SECO C. Z., Dallman J., Huang M., PETERS T. A., et al.

AMERICAN JOURNAL OF HUMAN GENETICS , cilt.91, sa.5, ss.872-882, 2012 (SCI-Expanded, Scopus)

12. Recurrent and Private MYO15A Mutations Are Associated with Deafness in the Turkish Population

Cengiz F. B., Duman D., Sirmaci A., Tokgoz-Yilmaz S., Erbek S., OZTUKMEN-AKAY H., et al.

GENETIC TESTING AND MOLECULAR BIOMARKERS , cilt.14, sa.4, ss.543-550, 2010 (SCI-Expanded, Scopus)

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

Sirmaci A., Erbek S., Price J., Huang M., Duman D., Cengiz F. B., et al.

AMERICAN JOURNAL OF HUMAN GENETICS , cilt.86, sa.5, ss.797-804, 2010 (SCI-Expanded, Scopus)

14. Transient evoked otoacoustic emissions and contralateral suppressions in children with auditory listening problems

YALCINKAYA F., Yilmaz S. T., Muluk N. B.

AURIS NASUS LARYNX , cilt.37, sa.1, ss.47-54, 2010 (SCI-Expanded, Scopus)

15. Effect of age on speech recognition in noise and on contralateral transient evoked otoacoustic emission suppression

Tokgoz-Yilmaz S., SENNAROĞLU G., SENNAROĞLU L., Koese S. K.

JOURNAL OF LARYNGOLOGY AND OTOLOGY , cilt.121, sa.11, ss.1029-1034, 2007 (SCI-Expanded, Scopus)

16. Effects of GJB2 genotypes on the audiological phenotype: Variability is present for all genotypes

HISMI B. O., Tokgoz Yilmaz S., INCESULU A., TEKIN M.

INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY , cilt.70, sa.10, ss.1687-1694, 2006 (SCI-Expanded, Scopus)

17. Mitochondrial DNA alterations involving position 961 are not sufficient to explain sensorineural hearing loss

YILMAZ S.

The Mediterranean Journal of Otology , cilt.1, sa.3, ss.110-116, 2005 (Hakemli Dergi)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 3

1. Oto Fasio Servikal OFC Sendromlu İki Vakada Odyolojik ve Oral Motor Bulgular

ALTIN B., UÇAL İ., AKSOY S., YILMAZ S.

8. KOKLEAR İMPLANTASYON OTOLOJİ‐NÖROOTOLOJİ ODYOLOJİ KONGRESİ, Türkiye, 12 - 15 Kasım 2015, (Özet Bildiri)

2. EEG Alpha Power Changes During Sensory Processing in Individuals with Autistic Traits

SİMGE A. Z., GÜRSES E., TUNCALI T., YILMAZ S., HALİSE D. Ö., KALAYCIOĞLU C.

41. ULUSAL FİZYOLOJİ KONGRESİ, 9 - 13 Eylül 2015, (Özet Bildiri)

3. EFFECTS OF CAFFEINE ON SPEECH IN NOISESCORES

ALTIN B., ÇILDIR B., YILMAZ S.

12th Congress of The European Federation of Audiology Societies’ (EFAS), 27 - 30 Mayıs 2015, (Özet Bildiri)

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311

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202

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