R01DC009645/DC/NIDCD NIH HHS/United States[Grant Number] - Search Results

Year	Number of Results
2010	1
2011	3
2012	8
2013	4
2014	6
2015	6
2016	3
2019	2
2020	1
2024	0

1

Autosomal recessive nonsyndromic deafness genes: a review.

Duman D, Tekin M. Duman D, et al. Front Biosci (Landmark Ed). 2012 Jun 1;17(6):2213-36. doi: 10.2741/4046. Front Biosci (Landmark Ed). 2012. PMID: 22652773 Free PMC article. Review.

2

Whole-exome sequencing and its impact in hereditary hearing loss.

Atik T, Bademci G, Diaz-Horta O, Blanton SH, Tekin M. Atik T, et al. Genet Res (Camb). 2015 Mar 31;97:e4. doi: 10.1017/S001667231500004X. Genet Res (Camb). 2015. PMID: 25825321 Free PMC article. Review.

3

Next-generation sequencing in genetic hearing loss.

Yan D, Tekin M, Blanton SH, Liu XZ. Yan D, et al. Genet Test Mol Biomarkers. 2013 Aug;17(8):581-7. doi: 10.1089/gtmb.2012.0464. Epub 2013 Jun 5. Genet Test Mol Biomarkers. 2013. PMID: 23738631 Free PMC article. Review.

4

GPSM2 mutations in Chudley-McCullough syndrome.

Diaz-Horta O, Sirmaci A, Doherty D, Nance W, Arnos K, Pandya A, Tekin M. Diaz-Horta O, et al. Am J Med Genet A. 2012 Nov;158A(11):2972-3. doi: 10.1002/ajmg.a.35636. Epub 2012 Sep 14. Am J Med Genet A. 2012. PMID: 22987632 Free PMC article. No abstract available.

5

The Generation of Zebrafish Mariner Model Using the CRISPR/Cas9 System.

Zou B, Desmidt AA, Mittal R, Yan D, Richmond M, Tekin M, Liu XZ, Lu Z. Zou B, et al. Anat Rec (Hoboken). 2020 Mar;303(3):556-562. doi: 10.1002/ar.24221. Epub 2019 Jul 18. Anat Rec (Hoboken). 2020. PMID: 31260171 Free article.

6

Evidence for genotype-phenotype correlation for OTOF mutations.

Yildirim-Baylan M, Bademci G, Duman D, Ozturkmen-Akay H, Tokgoz-Yilmaz S, Tekin M. Yildirim-Baylan M, et al. Int J Pediatr Otorhinolaryngol. 2014 Jun;78(6):950-3. doi: 10.1016/j.ijporl.2014.03.022. Epub 2014 Mar 28. Int J Pediatr Otorhinolaryngol. 2014. PMID: 24746455 Free PMC article.

7

Unique spectrum of GJB2 mutations in Mexico.

de la Luz Arenas-Sordo M, Menendez I, Hernández-Zamora E, Sirmaci A, Gutiérrez-Tinajero D, McGetrick M, Murphy-Ruiz P, Leyva-Juárez X, Huesca-Hernández F, Dominguez-Aburto J, Tekin M. de la Luz Arenas-Sordo M, et al. Int J Pediatr Otorhinolaryngol. 2012 Nov;76(11):1678-80. doi: 10.1016/j.ijporl.2012.08.005. Epub 2012 Aug 24. Int J Pediatr Otorhinolaryngol. 2012. PMID: 22925408

8

Hearing Assessment in Zebrafish During the First Week Postfertilization.

Yao Q, DeSmidt AA, Tekin M, Liu X, Lu Z. Yao Q, et al. Zebrafish. 2016 Apr;13(2):79-86. doi: 10.1089/zeb.2015.1166. Epub 2016 Jan 26. Zebrafish. 2016. PMID: 26982161 Free PMC article.

9

Comprehensive genetic testing can save lives in hereditary hearing loss.

Tekin D, Tutar E, Ozturkmen Akay H, Blanton S, Foster J 2nd, Tekin M. Tekin D, et al. Clin Genet. 2015 Feb;87(2):190-1. doi: 10.1111/cge.12376. Epub 2014 Apr 2. Clin Genet. 2015. PMID: 24689698 Free PMC article. No abstract available.

10

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

Sineni CJ, Yildirim-Baylan M, Guo S, Camarena V, Wang G, Tokgoz-Yilmaz S, Duman D, Bademci G, Tekin M. Sineni CJ, et al. Hum Genet. 2019 Oct;138(10):1071-1075. doi: 10.1007/s00439-019-02037-1. Epub 2019 Jun 7. Hum Genet. 2019. PMID: 31175426 Free PMC article.

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